Encyclopaedia of tumour-associated familial disorders. Part I: from AIMAH to CHIME syndrome

Cancer is associated with a wide range of hereditary disorders. Recognizing these disorders in cancer patients may be of great importance for the medical management of both patients and their relatives. Conversely, recognizing the fact that cancer may develop as a complication of a particular hereditary disorder which has already been diagnosed may be important for the same reason. The Familial Cancer Database (FaCD) is a web-based application which has been developed at our department with the intention to assist clinicians and genetic counsellors in making a genetic differential diagnosis in cancer patients, as well as in becoming aware of the tumour spectrum associated with hereditary disorders that have already been diagnosed in their patients. This encyclopaedia is published in parts and discusses the disorders included in the FaCD database in alphabetical order. It lists names, synonyms, OMIM number, mode of inheritance, associated genes, phenotype, clinical discussion and references. The purpose of presenting this encyclopaedia in paper format is simply that we hope that you as clinicians and researchers find it helpful to browse through it and familiarize yourself even better with the scope of genetic disorders that have been associated with increased tumour risk.


A Ab bs st tr ra ac ct t
Cancer is associated with a wide range of hereditary disorders. Recognizing these disorders in cancer patients may be of great importance for the medical management of both patients and their relatives. Conversely, recognizing the fact that cancer may develop as a complication of a particular hereditary disorder which has already been diagnosed may be important for the same reason. The Familial Cancer Database (FaCD) is a web-based application (www.facd.info) which has been developed at our department with the intention to assist clinicians and genetic counsellors in making a genetic differential diagnosis in cancer patients, as well as in becoming aware of the tumour spectrum associated with hereditary disorders that have already been diagnosed in their patients. This encyclopaedia is published in parts and discusses the disorders included in the FaCD database in alphabetical order. It lists names, synonyms, OMIM number, mode of inheritance, associated genes, phenotype, clinical discussion and references. The purpose of presenting this encyclopaedia in paper format is simply that we hope that you as clinicians and researchers find it helpful to browse through it and familiarize yourself even better with the scope of genetic disorders that have been associated with increased tumour risk.

I In nt tr ro od du uc ct ti io on n
Cancer is associated with a wide range of hereditary disorders. Recognizing these disorders in cancer patients may be of great importance for the medical management of both patients and their relatives. Conversely, recognizing the fact that cancer may develop as a complication of a particular hereditary disorder which has already been diagnosed may be important for the same reason. The Familial Cancer Database (FaCD) is a web-based application (www.facd.info) which has been developed at the Department of Genetics of the University Medical Center Groningen, The Netherlands, with the intention to assist clinicians and genetic counsellors in making a genetic differential diagnosis in cancer patients, as well as in becoming aware of the tumour spectrum associated with hereditary disorders that have already been diagnosed in their patients. This encyclopaedia is published in parts and discusses the disorders included in the FaCD database in alphabetical order. It lists names, synonyms, genes involved, phenotype, brief clinical discussion and references. The following classes of disorders have been included in this paper: hereditary disorders certainly or Encyclopaedia of tumour-associated familial disorders. Part I: from AIMAH to CHIME syndrome possibly associated with increased cancer risk (e.g. Lynch syndrome) and familial clustering of particular types of cancer e.c.i. (for example familial occurrence of salivary gland tumours). If some fields are not listed for a particular disorder, for example 'Non-tumour features', then those fields are empty for that disorder. Especially in rare syndromes it can be difficult to decide whether or not a particular tumour type truly belongs to the phenotype of that disorder. Those tumours have been classified below as 'Tumour features (possible)' in the descriptions of the phenotypes. The purpose of presenting this encyclopaedia in paper format is that we hope that you as clinicians and researchers find it helpful to browse through it and familiarize yourself even better with the scope of genetic disorders that have been associated with increased tumour risk.
A Ab bb br re ev vi ia at ti io on ns s u us se ed d: : AD -autosomal dominant AR -autosomal recessive CGD -contiguous gene deletion CI -confidence interval de novo -de novo mutation Impr -subject to genomic imprinting Multifact -multifactorial inheritance OMIM number -the number of the disorder in Online Mendelian Inheritance in Men Pat -paternal RR -relative risc SIR -standarized incidence ratio Upd -uniparental disomy XLR or XLD -X-linked recessive or dominant, respectively ? -reflects uncertainty with respect to mode of inheritance A AC CT TH H--i in nd de ep pe en nd de en nt t m ma ac cr ro on no od du ul la ar r a ad dr re en na al l h hy yp pe er rp pl la as si ia a S Sy yn no on ny ym m: : AIMAH, Cushing's disease, adrenal, familial M Mo od de e o of f i in nh he er ri it ta an nc ce e: : spor/AD O OM MI IM M n nu um mb be er r: : 219080 G Ge en ne es s: : GNAS1, mapped to 20q13.2 T Tu um mo ou ur r f fe ea at tu ur re es s: : macronodular adrenal hyperplasia N No on n--t tu um mo ou ur r f fe ea at tu ur re es s: : adrenal dysplasia adrenal hyperplasia C Co om mm me en nt t AIMAH cases are usually sporadic, causing Cushing's disease generally in the 5 th or 6 th decade.

C Co om mm me en nt t
Familial clustering of ALL has been observed [1][2][3]. Becker et al. [4] reported a 4-generation Irish family with childhood onset acute T-cell leukaemia/ lymphoblastic T-cell lymphoma in 9 relatives, which to the authors suggested autosomal dominant inheritance with reduced penetrance.
Dearden et al. [5] studied HLA-DQB1 alleles in children with ALL because of the suggestion that ALL may be caused by HLA-regulated susceptibility to an unidentified neonatal infection. They observed a significant excess of the DQB1*05 allele (RR 2.5) and in particular of certain amino acid motifs (not restricted to that allele). Polymorphisms in the GSTM1 and CYP1A1 genes, encoding xenobiotic-metabolizing enzymes, have been found to be associated with an Rolf H. Sijmons increased relative risk of childhood ALL [6]. A germline heterozygous truncating mutation in the gene for Fanconi anaemia type C has been detected in 2 sibs with T-ALL; 1 of the sibs subsequently developed AML [7]. In general, there appears to be no increase in ALL risk to siblings of patients. Risk may even be decreased and it has been speculated that immunization of mothers to leukaemia-specific antigens may occur which can enhance elimination of pre-leukaemic cells in utero [8].
A Ac cu ut te e m my ye el lo oc cy yt ti ic c l le eu uk ka ae em mi ia a w wi it th h p po ol ly yp po os si is s c co ol li i a an nd d c co ol lo on n c ca an nc ce er r M Mo od de e o of f i in nh he er ri it ta an nc ce e: : AR? O OM MI IM M n nu um mb be er r: : 246470 T Tu um mo ou ur r f fe ea at tu ur re es s: : bladder polyps colorectal cancer leukaemia, acute myeloblastic (AML, M2) C Co om mm me en nt t Two brothers with consanguineous parents were reported by Greenberg et al. [1] to have developed multiple colorectal adenomatous polyps, early-onset colorectal cancer, acute myeloblastic leukaemia, and (in one of the brothers) papillary bladder tumours. This could have been a case of bi-allelic MMR gene mutations. ADA, mapped to 20q13.11 T Tu um mo ou ur r f fe ea at tu ur re es s: : Burkitt's lymphoma Hodgkin's disease leukaemia, acute non-Hodgkin's lymphoma N No on n--t tu um mo ou ur r f fe ea at tu ur re es s: : adenosine deaminase deficiency agammaglobulinaemia immunodeficiency skeletal dysplasia C Co om mm me en nt t A substantial percentage of (apparently) autosomal recessive severe combined immunodeficiency is caused by deficiency of adenosine deaminase. Dysplastic skeletal changes (typically of costochondral junctions) occur frequently in patients with ADA deficiency. Most cases are diagnosed in the first year [1]. As in other types of severe combined immune deficiency, there is an increased risk of developing malignancies of the haemato-lymphoproliferative type [2][3][4][5]. There appears to be no increased cancer risk for heterozygotes of the mutant gene [6].
R Re ef fe er re en nc ce es s This infantile immunodeficiency in males is characterized by an isolated B-cell defect and these cells are absent in the vast majority of patients. Lymphoid tissue (adenoid, tonsils) is either absent or hypoplastic. There is approximately an incidence of 1.5-6% of malignancies in this disorder, mainly involving the haematopoietic-lymphoid system [1][2][3][4][5][6][7][8][9]. Patients also have an increased risk of developing colorectal cancer [10,11]. Lung cancer was diagnosed in a 32-year-old non-smoking male with the disorder [12]. Gastric cancer associated with chronic atrophic gastritis [13,14].
A Ai ic ca ar rd di i s sy yn nd dr ro om me e M Mo od de e o of f i in nh he er ri it ta an nc ce e: : XLD O OM MI IM M n nu um mb be er r: : 304050 G Ge en ne es s: : AIC, mapped to Xp22 T Tu um mo ou ur r f fe ea at tu ur re es s ( (p po os ss si ib bl le e) ): : angiosarcoma choroid plexus papilloma colorectal polyps gastric polyps hepatoblastoma lipoma medulloblastoma palate, benign teratoma of parapharyngeal embryonal cell cancer A Al la ag gi il ll le e s sy yn nd dr ro om me e S Sy yn no on ny ym m: : ALGS1, ALGS2, Alagille-Watson syndrome M Mo od de e o of f i in nh he er ri it ta an nc ce e: : AD/AR? O OM MI IM M n nu um mb be er r: : 118450 G Ge en ne es s: : JAG1, mapped to 20p12 NOTCH2, mapped to 1p13-p11 T Tu um mo ou ur r f fe ea at tu ur re es s: : hepatocellular cancer T Tu um mo ou ur r f fe ea at tu ur re es s ( (p po os ss si ib bl le e) ): : thyroid cancer, papillary Wilms' tumour (nephroblastoma) N No on n--t tu um mo ou ur r f fe ea at tu ur re es s: : bile ducts, paucity of intrahepatic chin, triangular embryotoxon posterior eyes, deeply set frontal bossing/prominent forehead hypertelorism midface, flat/hypoplastic nose, long straight philtrum, short pulmonary artery stenosis vertebral anomalies C Co om mm me en nt t Hallmarks of this disorder are: paucity of intrahepatic bile ducts leading to cholestasis, peripheral pulmonary artery stenosis, vertebral arch defects, poor linear growth, a characteristic facies and embryotoxon posterior in the eye [1]. Hepatocellular cancer has been reported in a number of cases [2][3][4][5], and papillary thyroid cancer [6] and Wilms' tumour in one case [7]. 6 A Al lp ph ha a--1 1--a an nt ti it tr ry yp ps si in n d de ef fi ic ci ie en nc cy y M Mo od de e o of f i in nh he er ri it ta an nc ce e: : AD O OM MI IM M n nu um mb be er r: : 107400 G Ge en ne es s: : PI, mapped to 14q32.1 T Tu um mo ou ur r f fe ea at tu ur re es s: : hepatocellular cancer T Tu um mo ou ur r f fe ea at tu ur re es s ( (p po os ss si ib bl le e) ): : colorectal cancer lung/bronchial cancer N No on n--t tu um mo ou ur r f fe ea at tu ur re es s: : liver cirrhosis lung emphysema C Co om mm me en nt t This disorder is caused by deficiency of alpha-1antitrypsin (= protease inhibitor = anti-elastase) and is characterized by emphysema and juvenile or adult liver cirrhosis. The severity of the disease depends on the specific combination of alleles and very likely also on the influence of exogenous factors such as smoking. The homozygous null allele combination causes the most severe disease, followed by the ZZ combination. Risk of hepatocellular cancer is increased, possibly only in males [1,2] and depending on allele type [3]. It has been reported in children [4]. Alpha-1-antitrypsin deficiency/haplosufficiency may also act as a co-risk factor for lung cancer [5]. Yang et al. [6] estimated a 20-fold increase in risk of developing colorectal cancer (with microsatellite instability, MSI-H) among smokers who carry alpha-1-antitrypsin deficiency alleles.
R Re ef fe er re en nc ce es s  This disorder is characterized by the persistence of high AFP, due to a mutation in the AFP gene [1,2]. Staples et al. [3] reported high serum AFP in a 23-yearold man with a testicular seminoma as well as in his 3 sisters, mother and maternal aunt. He also had hereditary spherocytosis. Hart et al. [4] and Cochran et al. [5] reported a yolk sac tumour in a 20-year-old male and a 20-month-old male with HPAFP, respectively. Although the association is probably purely coincidental, it is important to stress that HPAFP may confuse management in patients with testicular or liver tumours, or other conditions where AFP levels are of diagnostic or screening importance. If HPAFP is not recognized in these conditions, then this may lead to inappropriate medical decisions. Testing parental levels of AFP has been advised for cases where persistent (mild) elevation of AFP following resection of localized germ cell tumours has been observed, before deciding on chemotherapy [5].
R Re ef fe er re en nc ce es s C Co om mm me en nt t Alport syndrome is characterized by haematuric nephropathy, in most cases leading to renal failure (usually progressive), sensorineural deafness and ocular anomalies (maculopathy and anterior lenticonus). Some patients with Alport syndrome develop diffuse leiomyomatosis (especially of the oesophagus and less often the vulva and other anatomical sites). These patients also frequently have severe cataracts. The oesophageal leiomyomas appear to develop earlier among boys (average age 6 years compared to 14 years in girls) [1][2][3][4].
Alport syndrome is genetically heterogeneous. The specific subset of patients/families with Alport syndrome and leiomyomatosis is associated with deletions extending from within the COL4A5 gene to the neighbouring COL4A6 gene [5,6]. Multiple giant gastro-oesophageal leiomas have been reported in the absence of such a detectable deletion [7]. R Re ef fe er re en nc ce es s A Am me en no or rr rh ho oe ea a--g ga al la ac ct to or rr rh ho oe ea a s sy yn nd dr ro om me e T Tu um mo ou ur r f fe ea at tu ur re es s: : non-seminoma seminoma testicular gonadoblastoma testicular Sertoli-Leydig cell tumour N No on n--t tu um mo ou ur r f fe ea at tu ur re es s: : male (46,XY) pseudohermaphroditism C Co om mm me en nt t Mutations in the androgen receptor coding gene on the X chromosome cause pseudo-hermaphroditism in the XY individual through androgen insensitivity. External genitals are female. The gonads are undescended testes and may be intra-abdominal, inguinal, or labial. Mullerian structures (including uterus) are absent, because of AMH production by the testicles [1].
Sex cord hamartomas and Sertoli cell adenomas are common findings in AIS, with a prevalence of 63 and 23%, respectively, observed in one series of 43 patients [2]. Patients with AIS show an increased frequency of testicular malignancies with risks estimated between 2 and 33%; 2-10% might be the most realistic estimate. Seminoma [3][4][5][6][7][8] and sex-cord stromal tumours (particularly Sertoli-cell tumours) [9][10][11][12][13][14] are the most common tumour types observed. Gonadoblastoma [15] and non-seminomas (yolk sac tumour [16], embryonal carcinoma [17]) have been reported as well. Familial clustering of multiple (non-infiltrating) angiolipomas has been reported a few times, the most extensive family being that published by Kumar et al. [1]. In that family the angiolipomas were well encapsulated and located on the upper part of the body. Hapnes et al. [2] reported on a case with angiolipomas located close to joints and extending deep between muscle, tendons and joint capsules. Abbasi et al. reported an 80-year-old man with a 50-year history of asymptomatic, subcutaneous masses on the arms, trunk, and legs. His father and maternal grandmother had a history of similar lesions [3]. The distinction from familial multiple lipomatosis is not completely certain. Familial angiolipomatosis may sometimes be clinically confused with neurofibromatosis type 1 (NF1). Interestingly, Cina et al. [4] reported the occurrence of Lisch nodules (a typical feature of NF1) in familial angiolipomatosis.
A Ar rr rh he en no ob bl la as st to om ma a a an nd d t th hy yr ro oi id d a ad de en no om ma a, , f fa am mi il li ia al l S Sy yn no on ny ym m: : including arrhenoblastoma, familial clustering M Mo od de e o of f i in nh he er ri it ta an nc ce e: : AD O OM MI IM M n nu um mb be er r: : 107950 T Tu um mo ou ur r f fe ea at tu ur re es s: : ovarian Sertoli-Leydig cell tumour thyroid adenoma T Tu um mo ou ur r f fe ea at tu ur re es s ( (p po os ss si ib bl le e) ): : hamartomatous polyps in small intestine ovarian mucinous cystadenoma Wilm's tumour N No on n--t tu um mo ou ur r f fe ea at tu ur re es s: : thyroid hyperplasia/goitre C Co om mm me en nt t A number of families with multiple cases of ovarian Sertoli-Leydig cell tumours (arrhenoblastomas) have been reported. In some of these families (multiple) thyroid adenomas were also present in some of the relatives with ovarian tumours as well as in relatives without these tumours [1,2]. A mucinous cystadenoma was reported twice in these families and one case of Wilms' tumour was reported [1]. In the proband published by O'Brien et al. [2], a hamartous polyp was removed from the small intestine at the age of 3 months. Could this disorder be a variant of Cowden syndrome or Peutz-Jeghers syndrome? R Re ef fe er re en nc ce es s A At ta ax xi ia a t te el la an ng gi ie ec ct ta as si ia a S Sy yn no on ny ym m: : AT, Louis-Bar syndrome M Mo od de e o of f i in nh he er ri it ta an nc ce e: : AR O OM MI IM M n nu um mb be er r: : 208900 G Ge en ne es s: : ATM, mapped to 11q22.3 T Tu um mo ou ur r f fe ea at tu ur re es s: : astrocytoma breast cancer colon cancer gastric cancer glioma of the brain hepatocellular cancer histiocytosis (reticuloendotheliosis), malignant Hodgkin's disease laryngeal cancer leukaemia, acute lymphoblastic (ALL) leukaemia, chronic lymphocytic (CLL) non-Hodgkin's lymphoma ovarian cancer (i.e. epithelial origin) parotid gland cancer skin cancer, basal cell skin cancer, squamous cell thyroid cancer T Tu um mo ou ur r f fe ea at tu ur re es s ( (p po os ss si ib bl le e) ): : leiomyosarcoma of the uterus ovarian dysgerminoma ovarian fibroma ovarian gonadoblastoma seminoma uterine leiomyoma N No on n--t tu um mo ou ur r f fe ea at tu ur re es s: : café-au-lait spots cerebellar ataxia growth deficiency hypogonadism immunodeficiency increased chromosomal breakage increased/persistent serum AFP ionizing radiation sensitivity, increased mutagen sensitivity, increased oculocutaneous telangiectasia strabismus thymus hypoplasia/aplasia C Co om mm me en nt t Progressive ataxia usually develops during infancy. Telangiectasia occurs usually first in the bulbar conjunctivae and later over the bridge of the nose, auricles and other areas. Growth deficiency commonly presents during late infancy/childhood. Mental deficiency is a feature in about half of cases [1]. Neoplasms develop in approximately 10 percent of patients, especially lymphoid tumours. Many patients do not survive to adulthood, lung infections and neurological complications being the main cause of death. Non-Hodgkin's lymphoma (mostly of the histological subtype associated with 14q translocations), acute lymphoblastic leukaemia and Hodgkin's disease (mostly of lymphocytic depletion type) are the most frequent neoplasms in AT patients [2]. Myeloid tumours are absent [3]. The increase in lymphoid malignancy is caused by both B-and T-cell tumours [3,4]. T-cell tumours may develop at any age and may be T-ALL, T-cell lymphoma or T-cell prolymphocytic leukaemia [3]. The recognition of lymphomas may be delayed due to confusion with known infectious complications in AT [5]. A wide range of other neoplasms have been reported, including gastric cancer, colon cancer, chronic lymphoblastic leukaemia, brain tumours, craniopharyngioma, liver cancer, laryngeal cancer, leiomyoma and leiomyosarcoma of the uterus, dysgerminoma, fibroadenoma and gonadoblastoma of the ovaries, testicular seminoma and basal cell and squamous cell skin cancer [5][6][7][8][9][10][11][12][13].
Inheriting one mutated copy of the AT gene (ATM) increases breast cancer risk in females, and may turn out to contribute significantly to the total breast cancer burden. However, data are inconclusive as to the magnitude of this contribution and strength of this risk factor [14][15][16][17][18][19][20][21][22][23][24][25]. Broeks et al. [26] found the relatively high percentage of 8.5% ATM mutation carriers in a group of 82 breast cancer patients selected for early onset (<45 years), long-term survival and bilaterality. Baynes et al. showed that it is unlikely that common ATM variants increase breast cancer risk [27]. Johnson et al. confirmed this and argued that it is rather a combination of variants in different genes (ATM, BRCA1, BRCA2) that confers an increased breast cancer risk [28]. However, single rare ATM alleles may still confer a substantially increased breast cancer risk [29]. Balleine et al. reported that breast cancer occurring in carriers of ATM variants is not associated with distinctive histopathological features [30].
Fibroblast cultures of AT heterozygotes show increased radiosensitivity and given the fact that breast cancer is a complication well known to occur in longterm survivors of Hodgkin's disease who received mantle-field irradiation, it has been questioned whether germline mutations in ATM contributed to this increase of breast cancer risk. Studies by Broeks et al. [31] and Nichols et al. [32] did not support a major contribution of germline ATM mutations to the breast cancer risk in these types of patients. The same was true for contralateral breast cancer risk after radiation therapy for the first breast tumour, as reported by Shafman et al. [33].
A Au ut to oi im mm mu un ne e l ly ym mp ph ho op pr ro ol li if fe er ra at ti iv ve e s sy yn nd dr ro om me e, , t ty yp pe e I I S Sy yn no on ny ym m: : Canale-Smith syndrome, ALPS type I (including: ALPS1A, ALPS1B), including autoimmune lymphoproliferative disease (ALD) M Mo od de e o of f i in nh he er ri it ta an nc ce e: : AD O OM MI IM M n nu um mb be er r: : 601859, 134637 G Ge en ne es s: : APT1/FAS, mapped to 10q24.1 T Tu um mo ou ur r f fe ea at tu ur re es s: : Burkitt lymphoma Hodgkin's disease non-Hodgkin's lymphoma T Tu um mo ou ur r f fe ea at tu ur re es s ( (p po os ss si ib bl le e) ): : hepatocellular cancer N No on n--t tu um mo ou ur r f fe ea at tu ur re es s: : autoimmune disease C Co om mm me en nt t This disorder develops in early childhood because of a defective lymphocyte apoptosis. It is characterized by non-malignant lymphadenopathy, splenomegaly and autoimmune disease [1]. In the majority of patients a heterozygous mutation in APT1 has been detected. APT1 encodes the Fas protein, which is a mediator of lymphocyte apoptosis. Of 46 ALPS1 patients with APT1 mutations studied at the NIH, 6 (13%) developed a lymphoma: Hodgkin's, Burkitt's, follicular lymphoma or non-Hodgkin's lymphoma [2,3]. A case of hepatocellular carcinoma has also been reported. In general, risk for non-Hodgkin's lymphoma and Hodgkin's disease is increased.
Ramenghi et al. [4] reported an ALPS-like disorder, which they referred to as autoimmune lymphoproliferative disease (ALD), associated with decreased Fas function in the absence of detectable Fas mutations. Hodgkin's disease was reported by them to have occurred in one of these ALD families and the frequency of cancer in general was increased in the families' maternal lines.
R Re ef fe er re en nc ce es s  T Tu um mo ou ur r f fe ea at tu ur re es s ( (p po os ss si ib bl le e) ): : breast cancer meningioma thyroid adenoma thyroid cancer N No on n--t tu um mo ou ur r f fe ea at tu ur re es s: : cornea, prominent nerves deafness gross motor delay high birth weight hypotonia joint laxity lipid storage myopathy of proximal muscles macrocephaly mental deficiency pectus excavatum pigmented macules on glans and shaft of penis scoliosis seizures vulvar lentigines C Co om mm me en nt t Lipid storage myopathy, pigmented macules on glans and shaft of penis and vulva, intestinal hamartous (juvenile type) polyps and neurodevelopmental delay are the typical features [1][2][3][4][5][6][7][8][9]. A clinical overlap with Cowden disease has been noted and indeed germline mutations in the PTEN gene, involved in Cowden disease, have been detected in this disorder. It should therefore be considered as a variant of Cowden syndrome [10][11][12][13][14][15]. DiLiberti [10] has recently proposed the nomenclature PTEN-MATCHS (macrocephaly, autosomal dominant, thyroid disease, cancer, hamartomata, skin abnormalities) to cover the clinical spectrum associated with germline PTEN mutations. BBS1, mapped to 11q13 BBS10, mapped to 12q BBS11, mapped to 9q33.1 BBS12, mapped to 4q27 BBS2, mapped to 16q21 BBS3, mapped to 3p12-q13 BBS4, mapped to 15q22.3 BBS5, mapped to 2q31 BBS6/MKKS, mapped to 20p12 BBS7, mapped to 4q27 BBS8, mapped to 14q32.11 BBS9, mapped to 7p14 T Tu um mo ou ur r f fe ea at tu ur re es s ( (p po os ss si ib bl le e) ): : renal cell cancer, clear-cell N No on n--t tu um mo ou ur r f fe ea at tu ur re es s: : brachydactyly, of feet brachydactyly, of hands deafness, conductive dental abnormalities hypogonadism mental deficiency obesity polydactyly, postaxial renal anomalies renal dysplasia rod-cone dystrophy C Co om mm me en nt t Barrett's oesophagus and oesophageal adenocarcinoma are complications of gastroesophageal reflux [1], which may show familial clustering, as has been demonstrated by Romero et al. [2]. These authors reported that reflux symptoms were significantly more prevalent among parents and siblings of patients with oesophageal adenocarcinoma and/or Barrett's oesophagus than among controls. Other authors have reported familial cases as well. Hampel et al. [3] reported on 3 families and suggested that Barrett's oesophagus families possibly are at an increased risk of developing extra-oesophageal cancer (notably of the digestive tract) as well. More recently more familial clusters have been reported [4][5][6][7][8] and family history is an acknowledged risk factor. Chak et al. showed that a family history of Barrett's oesophagus can be confirmed in 7.3% of persons presenting with Barrett's oesophagus, adenocarcinoma of the oesophagus, or adenocarcinoma of the gastroesophageal junction [5]. Linkage analyses are underway [9].  In this disorder, multiple nevoid basal cell cancers (NBCC) typically start to appear at the age of puberty, although they have been reported to occur as early as 3 years of age. The NBCCs may manifest anywhere on the skin, but mainly on the face, neck and upper trunk. A typical facies is often present (70%), featuring frontoparietal bossing, broad nasal bridge and prognathism. Skeletal anomalies are often detected (e.g. 80% of patients are diagnosed with keratocysts of the jaw before the age of 30), as well as palmoplantar skin pits (87% of patients [1]). Mental deficiency occurs in a few cases [1][2][3][4].
Patients with the syndrome have an increased risk of developing secondary tumours in the field of radiation treatment. A conservative estimate of the new mutation rate in basal cell nevus syndrome is 14% [4]. Fukushima et al. [23] reported the occurrence of a meningioma after radiation treatment for a medulloblastoma.
The gene for basal cell nevus syndrome has been identified as the human homologue of the Drosophila patched gene [24,25]. Diagnostic criteria: two major criteria or one major + two minor criteria should be present.  The influence of a family history of skin cancer on basal cell skin cancer (BCC) risk is controversial. Two studies could not demonstrate a familial risk factor [1,2]. However, Wallberg et al. [3] found a family history of skin cancer (not further specified) among siblings and/or parents to be the strongest risk factor (RR 10.9) of 12 factors tested. The authors could not explain this risk by correcting for hereditary pigmentary characteristics, such as skin type, eye and hair colour, which are known to be associated with melanoma as well as non-melanoma skin cancer risk [4]. Hogan et al. [5] also found that a family history of skin cancer was associated with an increased risk of developing BCC (RR 1.22). In their series of 538 BCC patients and matched controls, they also observed a significantly lower age at diagnosis in those BCC patients with a family history of skin cancer compared with those who did not. In a case-control study of similar size, Naldi et al. [6] confirmed the significant association of BCC and a family history of skin cancer (odds ratio 6.7). In a population-based cohort study of twins, the co-twin of a twin affected with BCC cancer was shown to have an increased BCC risk (RR 7-8); however, zygosity did not influence this risk [7,8]. In general, BCC in children in the absence of known genetic conditions is rare, but has been diagnosed at the age of 4 years and older [9].
Polymorphisms of members of the glutathione-Stransferase and cytochrome P450 enzyme families have been associated with an increased risk of developing (multiple) BCC [10][11][12].
For squamous cell skin cancer (SCC), a positive family history of skin cancer in general also increases SCC risk, as has been calculated by Hogan et al. [13], Gamble et al. [14] and Hemminki and Dong [15]. The latter study from the Swedish Family-Cancer Database reported SIRs of 2.4 for invasive SCC and 2.8 for invasive SCC in the offspring of parents with SCC. SIR for SCC in offspring of parents with multiple SCC was 70% higher than in offspring of parents with single SCC. The authors also reported a familial association between SCC and skin and ocular melanoma.

C Co om mm me en nt t
This syndrome is characterized by multiple basal cell cancers developing mainly on the face, from the second decade. The skin shows follicular atrophoderma (resembling ice pick marks), especially on the face, hands, elbows and feet. Sweating is decreased and hypotrichosis is another characteristic. The term follicular atrophoderma appears inappropriate because the skin histology does not show atrophy [1][2][3][4][5][6][7]. The disorder has been mapped to Xq [8].
The genetics of BWS are relatively complex. Cooper et al. analysed genotype-cancer phenotype associations and concluded that the risk of neoplasia was significantly higher in UPD and IC1 defect cases than in IC2 defect and CDKN1C mutation cases. Cancer risk for all patients was estimated at 9% at age 5 years, and 24% in the UPD subgroup. UPD including WT1 was associated with renal neoplasia. In contrast, Wilms' tumour risk in the IC2 defect subgroup appears to be small [20]. Rump et al. concluded that increased tumour risk in BWS is typically associated with loss of imprinting of H19 [21].
R Re ef fe er re en nc ce es s B Bi ia al ll le el li ic c m mi is sm ma at tc ch h r re ep pa ai ir r g ge en ne e m mu ut ta at ti io on ns s a as ss so oc ci ia at te ed d e ea ar rl ly y o on ns se et t c ca an nc ce er r S Sy yn no on ny ym m: : childhood cancer syndrome M Mo od de e o of f i in nh he er ri it ta an nc ce e: : AR G Ge en ne es s: : MLH1, mapped to 3p21.3 MSH2, mapped to 2p21-p22 MSH6, mapped to 2p16 PMS2, mapped to 7p22 T Tu um mo ou ur r f fe ea at tu ur re es s: : astrocytoma colorectal cancer endometrial cancer glioblastoma (multiforme) leukaemia, acute leukaemia, acute lymphoblastic (ALL) leukaemia, acute myeloid (AML, including ANLL) leukaemia, chronic myeloid (CML) medulloblastoma non-Hodgkin's lymphoma oligodendroglioma T Tu um mo ou ur r f fe ea at tu ur re es s ( (p po os ss si ib bl le e) ): : ovarian sarcoma (including pPNET of ovary) Wilms' tumour (nephroblastoma) N No on n--t tu um mo ou ur r f fe ea at tu ur re es s: : axillary freckling café-au-lait spots N No on n--t tu um mo ou ur r f fe ea at tu ur re es s ( (p po os ss si ib bl le e) ): : immunodeficiency C Co om mm me en nt t Multiple café-au-lait spots, axillary freckling and early onset colorectal cancer, oligopolyposis, leukaemia (ALL, AML, AL-not specifed, CML), non-Hodgkin's lymphoma, brain tumours (glioblastoma, astrocytoma, oligodendroglioma medulloblastoma), Wilms' tumour, ovarian neuroectodermal tumour, endometrial cancer and sometimes IgA-deficiency have been observed in patients with biallelic mutations of the mismatch repair (MMR) genes MLH1, MSH2, MSH6 and PMS2 [1][2][3][4][5][6][7][8][9][10][11].
There is overlap with HNPCC (associated with single inherited MMR mutations) and Turcot syndrome (brain tumours and colorectal polyps).

C Co om mm me en nt t
This condition is characterized by the presence of 3 types of benign skin tumours: fibrofolliculomas, trichodiscomas and acrochordons [1][2][3][4], although its has been questioned whether acrochordons truly belong to this hereditary disorder [5]. Spontaneous pneumothorax and cystic lung disease is another feature of BHD [6].
In one large family with this disorder, medullary thyroid cancer was diagnosed in several relatives, 2 of them also presenting with skin tumours. It may have been a coincidental co-segregation of familial medullary thyroid cancer (see that entry) and Birt-Hogg-Dubé syndrome. Benign and malignant adenomatous colon polyps have been reported in patients with this disorder and with what some consider to be a variant of Birt-Hogg-Dubé syndrome: Hornstein-Knickenberg syndrome, which is characterized by multiple perifollicular fibromas [7][8][9][10]. Renal tumours (single or multiple, unilateral or bilateral) of various histology have been observed in Birt-Hogg-Dubé syndrome: oncocytoma, chromophobe carcinoma and clear cell as well papillary renal cell carcinomas [11][12][13].
B Bl la ad dd de er r, , u ur re et te er r, , r re en na al l p py ye el lu um m c ca an nc ce er r, , f fa am mi il li ia al l c cl lu us st te er ri in ng g o of f M Mo od de e o of f i in nh he er ri it ta an nc ce e: : multifact? G Ge en ne es s: : many low penetrant gene mutations have been reported, we do not list them separately here T Tu um mo ou ur r f fe ea at tu ur re es s: : renal pyelum cancer ureter cancer urinary bladder cancer N No on n--t tu um mo ou ur r f fe ea at tu ur re es s ( (p po os ss si ib bl le e) ): : t(5;20)(p15;q11) (constitutional) C Co om mm me en nt t Familial clustering of bladder cancer has been reported [1][2][3][4][5] and may occur in approximately 4% of cases [6]. Kantor et al. [6] demonstrated that having an affected first-degree relative increases the risk of bladder cancer. These authors reported relative risks of 2.7, 1.7 and 1.3 depending on the age at diagnosis of the tumour: below age 45, ages 45-64 and 65 and older, respectively. Cigarette smoking in the setting of a family history of bladder cancer was shown to strongly increase the risk of developing this tumour. Relative risks of up to 28.1 in heavy smokers (60 + cigarettes/day) were calculated as compared to a RR of 2.1 in heavy smokers with a negative family history. Non-smokers with a positive family history still had a RR of 1.5 and this observation of a familial component independent of smoking was supported by the findings of Kramer et al. [7], who reported a RR of 1.8 for a similar group. Piper et al. [8] found bladder or renal cancer in first-degree relatives not to be a risk factor for bladder cancer in young women (<50 years). A family history of cancer in general has been reported to be a risk factor in the development of bladder cancer [2].
Having blood type A or HLA types Cw4 and B5 increases the risk of developing this tumour [9]. Inherited variation in the metabolism of (pro)carcinogens, related to smoking and other environmental exposures, also influences the risk of bladder cancer, e.g. activities of glutathione-S-transferase, N-acetyltransferase and those of the cytochrome P450 group [10][11][12][13]. Also, certain alleles of the Hras1 minisatellite locus are associated with an increased tumour risk at this anatomical site [14]. More mutations have been reported, not listed in this brief overview. A small number of published families suggest the existence of a rare autosomal dominant predisposition to urinary tract cancer [3,5,15]. Familial clustering of transitional cell carcinomas (TCC) at different sites of the urinary tract has been observed [5,16,17], including familial cancer of the ureter [18]. A germline translocation (5;20)(p15;q11) has been observed in a 29-year-old man with TCC bladder cancer. His mother had been diagnosed with a similar tumour (she was not karyotyped) [19]. T Tu um mo ou ur r f fe ea at tu ur re es s: : breast cancer cervical cancer colon cancer gastric cancer hepatocellular cancer laryngeal cancer leukaemia, acute lymphoblastic (ALL) leukaemia, acute myeloid (AML, including ANLL) lymphoma, malignant (non-Hodgkin's and/or Hodgkin's) oral cancer skin cancer, basal cell Wilms' tumour (nephroblastoma) T Tu um mo ou ur r f fe ea at tu ur re es s ( (p po os ss si ib bl le e) ): : colorectal adenomatous polyps external auditory canal cancer medulloblastoma myelodysplastic syndrome (MDS) osteosarcoma skin cancer, squamous cell vaginal cancer N No on n--t tu um mo ou ur r f fe ea at tu ur re es s: : clinodactyly growth deficiency hyperpigmentation of the skin hypopigmentation of the skin immunodeficiency increased chromosomal breakage increased sister chromatid exchange long small facies mutagen sensitivity, increased UV hypersensitivity UV radiation sensitivity, increased N No on n--t tu um mo ou ur r f fe ea at tu ur re es s ( (p po os ss si ib bl le e) ): : bone marrow monosomy 7 karyotype C Co om mm me en nt t Clinical features of this disorder are [1][2][3][4]: short stature, dolichocephaly, excessive number of neoplasms (see below), characteristic facies (malar hypoplasia, prominent nose, small mandible, protuberant prominent ears), UV hypersensitivity of the skin (lesions appear mainly in the face and back of hand/forearms), patchy hyperpigmentation (café-au-lait spots) and areas of hypopigmentation of the skin (predominantly on the trunk), variable degree of vomiting and diarrhoea during infancy, diabetes mellitus, azoospermia and early menopause, immunodeficiency, average to low-average intelligence, sometimes mental retardation. Cytogenetic studies show increased sister-chromatid exchange and excessive number of chromatid gaps and breaks. Neoplasms reported in Bloom syndrome (in decreasing frequency): non-Hodgkin's lymphoma, skin cancer (predominantly basal cell type), acute lymphocytic and acute myelocytic leukaemia, breast cancer, colon (diagnosed as early as age 16 [5]) and rectal cancer, oesophageal cancer, tongue cancer, laryngeal cancer, cervical cancer and endometrial cancer, tongue cancer, external auditory canal cancer, Wilms' tumour, osteogenic sarcoma, medulloblastoma and meningioma, tonsillar cancer, retinoblastoma and myelodysplastic syndrome (associated with monosomy 7 [6]). Wang et al. [7] reported a 37-year-old man with ulcerative colitis complicated by colon cancer. Lowy et al. observed colonic polyposis in a Bloom syndrome patient [8]. More recently hepatocellular cancer and vaginal cancer were reported [9,10].
B Bl lu ue e r ru ub bb be er r b bl le eb b n ne ev vu us s s sy yn nd dr ro om me e S Sy yn no on ny ym m: : Bean syndrome M Mo od de e o of f i in nh he er ri it ta an nc ce e: : AD/spor O OM MI IM M n nu um mb be er r: : 112200 T Tu um mo ou ur r f fe ea at tu ur re es s: : gastrointestinal polypoid haemangioma hepatic haemangioma joint capsules, haemangioma in lung haemangioma splenic haemangioma subcutaneous haemangioma T Tu um mo ou ur r f fe ea at tu ur re es s ( (p po os ss si ib bl le e) ): : leukaemia, chronic lymphocytic (CLL) medulloblastoma renal cell cancer N No on n--t tu um mo ou ur r f fe ea at tu ur re es s: : cutaneous nevi, haemangiomatous (blue rubber blebs) C Co om mm me en nt t The hallmarks of this disease are the presence of multiple bladder-like haemangiomas (blue rubber blebs) on the skin, especially on the trunk and arms. The intestinal polypous haemangiomas may cause bleeding. Haemangiomas may be found in a wide range of tissues (spleen, lungs, joint capsules etc.) [1][2][3]. Chronic lymphocytic leukaemia (at age 66) and renal cell cancer (at age 57) were reported in a male with this disorder [4]. Medulloblastoma was reported in a 21-year old affected woman [5]. This condition may be identical to familial venous malformation syndrome. The neoplasms were originally classified as fibrosarcomas, but later reclassified as malignant fibrous histiocytomas. Approximately 35% of gene carriers develop these malignant tumours. Earlyonset cataract was documented in some of the patients and mental retardation was seen in a minority of cases [1,2]. This syndrome maps to 9p21-22 [3,4]. T Tu um mo ou ur r f fe ea at tu ur re es s ( (p po os ss si ib bl le e) ): : breast cancer colon cancer gastric cancer Hodgkin's disease leukaemia malignant melanoma, cutaneous C Co om mm me en nt t Familial occurrence of brain tumours has predominantly been reported in sibs, but in some cases the tumours have been found in successive generations [1][2][3][4][5]. The most frequent tumours in these clusters are astrocytoma, medulloblastoma [6,7] and glioblastoma [8]. Less frequently, choroid plexus papillomas [9], ependymomas [10] and sarcomas [11] have been reported. Figures on the percentage of brain tumours that are familial are rare. Estimates for astrocytomas range from less than 1 to 14% [12]. In the Swedish Family-Cancer Database, which included 2060 childhood brain tumours, 1.3% of brain tumour patients had a parent with nervous system cancer. Some studies conclude that a family history of brain tumours or cancer in general does not significantly contribute to glioma risk in adults and brain tumour risk in children [13][14][15][16][17]. Others found that the occurrence of childhood brain tumour is associated with an increased risk of developing central nervous system tumours, leukaemia and childhood tumours in relatives [18][19][20]. One study found a particularly strong association between parental meningioma and brain astrocytoma in the offspring [20]. Malmer et al. [26] studied cancer risk in the first-degree relatives of Swedish astrocytoma patients and found an increased risk for astrocytomas (relative risk 2.1) but not for other primary brain tumours in these relatives.
Hill et al. reported that in individuals with a family history of a brain cancer or a brain tumour, risk of glioma was 1.6 and 3.0, respectively, in comparison with those without such family histories. Increased risks were also reported for a family history of stomach (RR 2.2), colon (RR 1.4), or prostate cancer (RR 2.1) or Hodgkin's disease (RR 2.4) [21]. In another paper they reported that risk of meningioma was increased among those with a family history of a benign brain tumour (RR 4.5) or melanoma (RR 4.2). A family history of breast cancer was associated with an elevated meningioma risk among participants aged 18 to 49 years (RR 3.9) but a reduced risk among older individuals [22].
In general, the familial clustering of gliomas may be associated with a range of congenital malformations and is a genetically heterogeneous group [2]. Relatives of patients with Ewing sarcoma or prostate cancer are at increased risk of developing brain tumours [23,24]. Significantly more colon cancer was observed in firstdegree relatives of children with brain tumours, although absolute numbers were small [25]. Interestingly, another study reported a significant decrease in colon (and breast) cancer risk for firstdegree relatives of astrocytoma patients [26]. Certain variants of enzymes involved in (pro)carcinogen metabolism have been found to be associated with an increased risk of astrocytomas and meningiomas, e.g. GSTT1, GSTM1 and CYP2D6 [27]. A small fraction of familial clustering of gliomas may be attributed to germline TP53 mutations [28][29][30][31]. colorectal cancer endometrial cancer ovarian cancer (i.e. epithelial origin) prostate cancer N No on n--t tu um mo ou ur r f fe ea at tu ur re es s: : breast, proliferative disease mutagen sensitivity, increased C Co om mm me en nt t Given the high risk of breast cancer in women [1], familial occurrence of breast cancer is not rare. A family history of breast cancer has been reported in 14 to 30% of female breast cancer patients [2,3]. Familial male breast cancer is rare [4][5][6]. Having a relative with breast cancer is one of the strongest risk factors for this tumour [7][8][9][10]. A RR of 34.7 of developing breast cancer has been reported in monozygotic twins of women in whom breast cancer had occurred before age 35 [11]. In general, the risk of breast cancer in relatives does not appear to depend heavily on the gender of their affected family member [12][13][14][15]. Compared with the general population, breast cancer is also found more frequently in women with family history of ovarian, endometrial, colorectal and/or prostate cancer and vice versa [16][17][18][19][20][21][22][23][24]. One study reported a RR of 5.6 for parotid cancer in firstdegree relatives of breast cancer patients [25].
Depending on the number of affected relatives, the degree of kinship and the age at onset of the tumours, the empirical risk of developing breast cancer in a female relative may be close to 50% (even higher if she already has children with breast cancer). Several models have been developed to estimate breast cancer risk in a specific family situation. Those by Gail et al. [26][27][28][29][30], focussing on white females who are being examined annually, and by Claus et al. [21,31,32] are the ones most widely used in clinical practice. Users should be aware of the specific limitations of these models [33]. For example, the risk tables may need to be adapted for use in different countries and or ethnic groups to account for differences in genetic background and exogenous risk factors [34]. The Claus model includes first-and second-degree relatives, as opposed to the Gail model, which looks at first-degree relatives only. However, the latter method also takes into account the risk factors of age at menarche, age at first live birth and number of previous biopsies.
Given a positive or negative family history of breast cancer, other known risk factors may differ in their contribution to overall risk. Colditz et al. [35] reported on an adverse effect of first pregnancy among women with a family history of breast cancer that was approximately 50% greater in magnitude than among women without a family history. Past use of oral contraceptives and use of postmenopausal hormones and history of benign breast disease showed similar relative risks between the two groups. Sellers et al. concluded the same with regard to hormone replacement therapy in women with a family history of breast cancer [36]. However, with respect to benign breast disease, Dupont et al. [37] found that fibroadenomas have an increased effect on breast cancer risk in patients with a family history of breast cancer compared to patients without a family history of breast cancer. In addition, Skolnick et al. [38] analyzed families with a clustering of breast cancer and suggested that genetic susceptibility may cause both proliferative benign breast disease and breast cancer in those kindreds. Among women aged 30-49 years, a family history of breast cancer was associated with an increased risk of ductal carcinoma-in-situ (DCIS), and among those aged 50 and older it was associated with an increased risk of both DCIS and invasive breast cancer [39]. Egan et al. [40] demonstrated a stronger inverse association of high parity with breast cancer risk in women who reported first-degree relatives with breast cancer compared with women who did not have affected first-degree relatives. In a study by Schouten et al. [41], family history of breast cancer was not correlated with survival.
Chromosomes of breast cancer patients (and some of their unaffected relatives) with a family history of breast cancer are more sensitive to the action of the mutagen bleomycin compared with sporadic breast cancer patients [42], hinting at the involvement of genes responsible for DNA repair. Anderson reported a father and daughter both diagnosed with carcinoid of the appendix (at age 42 and 15 years, respectively) [1]. Moertel and Dockerty [2] reported on a 2-generation family with (multiple) intestinal carcinoids. One of the affected women developed breast cancer at age 53 while her mother had done so at age 47. Other tumours in that family included nasopharyngeal fibrosarcoma (age 5) and lung cancer (age 42), possibly suggesting Li-Fraumeni-like syndrome (see that entry). Additional cases of familial intestinal carcinoids have been published [3][4][5][6][7][8] . An unknown proportion of these and other cases of familial carcinoid might very well be caused by germline mutations in MEN1, the gene associated with multiple endocrine neoplasia type 1. Perkins et al. [9] studied the family history of patients with carcinoid tumours of the lung and demonstrated that the proportion of distant metastasis in these patients was significantly higher among those with a positive family history of cancer (in general). Babovic-Vuksanovic et al. [10] studied the occurrence of cancer in first-degree relatives of 245 gastrointestinal carcinoid patients. For first-degree relatives, only the risk for carcinoid was increased (p<0.0001, life-time risk 1.5%).
Oliveira et al. reported pulmonary carcinoid in two affected sibs and in a mother and daughter. No other signs of MEN1 were present in these two families [11].

C Co om mm me en nt t
Hallmarks of CFC are a typical facies, congenital heart defects (predominantly pulmonary stenosis and ASD), growth failure and ectodermal anomalies. There is clinical and molecular overlap with Noonan syndrome and Costello syndrome. These disorders share disruption of the RAS/MAPK signalling pathway [1][2][3].
Van den Berg and Hennekam [4] reported a 5-yearold girl with CFC who was diagnosed with ALL and Makita reported another case [5]. Bisogno et al. [6] described a 20-month-old boy with CFC and an (embryonal) rhabdomyosarcoma. A hepatoblastoma was reported by Al-Rahawan [7].
C Ca ar rn ne ey y c co om mp pl le ex x S Sy yn no on ny ym m: : Carney syndrome, NAME syndrome, LAMB syndrome, familial myxoma syndrome M Mo od de e o of f i in nh he er ri it ta an nc ce e: : AD O OM MI IM M n nu um mb be er r: : 160980 G Ge en ne es s: : CNC2, mapped to 2p15-p16 PRKAR1A, mapped to 17q22-q24 T Tu um mo ou ur r f fe ea at tu ur re es s: : adrenocortical disease, primary pigmented nodular (PPNAD) breast myxoma cardiac myxoma ductal adenoma of the breast ear canal myxoma gastrointestinal schwannoma pituitary gland tumour schwannoma (neurilemmoma), peripheral nerve schwannoma of the bone schwannoma, psammomatous melanotic schwannomas of the (posterior) spinal nerve roots skin myxoma testicular Sertoli-Leydig cell tumour thyroid cancer, follicular uterine leiomyoma T Tu um mo ou ur r f fe ea at tu ur re es s ( (p po os ss si ib bl le e) ): : cervical mesenchymal tumour, atypical colorectal adenomas peripheral nerve tumour pheochromocytoma teratoma, benign cystic (dermoid cyst) of the ovary vestibular schwannoma N No on n--t tu um mo ou ur r f fe ea at tu ur re es s: : blue nevi, café-au-lait spots lentiginosis (spotty pigmentation) lips, pigmentation of oral mucosa, pigmentation of N No on n--t tu um mo ou ur r f fe ea at tu ur re es s ( (p po os ss si ib bl le e) ): : oesophagus, Barrett's C Co om mm me en nt t More than 200 patients have been reported, half of them familial cases. Patients present with spotty multiple small brown to black macules (lentiginosis) on the skin and mucosae (67% of patients). Other pigmented lesions are cafe-au-lait spots, (epithelioid) blue nevi (19% of patients) and less frequently psammomatous melanotic schwannoma (neurilemmoma) [1]. Primary pigmented nodular adrenocortical disease (PPNAD) leading to Cushing's disease is also typical for the syndrome (found in 33% of patients).
A range of tumours can be found in Carney complex, including myxomas of the heart (in 30-61% of patients), breasts (20%), skin (37%) (of the eyelids in 25%) and external ear canal, testicular tumours (30%): testicular large cell calcifying Sertoli tumours (LCCST) and (less frequently) Leydig cell tumours, growth hormone producing pituitary adenomas (11%) and schwannomas of the upper GI tract, bone, Rolf H. Sijmons sympatic chain and the skin (as mentioned above) (total % schwannomas found in Carney complex: 11). Thyroid gland involvement is common (11%), ranging from follicular hyperplasia to cancer [2][3][4]. Nwokoro et al. [5] reported an affected 34-year-old woman from a Carney complex family, who in addition to features typical for this disorder also developed an atypical mesenchymal tumour of the cervix, neoplastic colonic polyps and Barrett's oesophagus.
There is evidence for genetic heterogeneity in Carney complex [4,[6][7][8]. In some families, linkage analysis may help in identifying affected relatives [9]. Germline mutations in the PRKAR1A gene have been detected in approximately 45% of Carney complex cases and can also be found in isolated familial myxoma and familial or isolated cases of PPNAD [10][11][12].
Criteria [4,5,13] -2 of the following should be present: a) heart myxoma, b) breast myxoma (myxoid mammary fibroadenoma), c) skin myxoma, d) primary pigmented nodular adrenocortical disease, e) GH-secreting pituitary tumour, f) psammomatous melanotic schwannoma (PMS), g) ductal adenoma of the breast, h) large-cell calcifying Sertoli cell tumour of the testes (LCCST), i) spotty pigmentation if it is: multiple, present in a characteristic distribution (vermilion border of the lips, conjunctivae, external genitalia), not dependent on exposure to sunlight, and has histology consistent with lentigo rather than ephelide (freckle). The presence of adrenocortical rest tumours is regarded as corroboratory evidence for the diagnosis [12].
Unfortunately, the name Carney syndrome is used by some to refer to the Carney complex, whereas others use it to refer to Carney triad, which is a completely different disorder.
C Ca ar rn ne ey y t tr ri ia ad d S Sy yn no on ny ym m: : Carney syndrome M Mo od de e o of f i in nh he er ri it ta an nc ce e: : spor/multifact? O OM MI IM M n nu um mb be er r: : 604287 T Tu um mo ou ur r f fe ea at tu ur re es s: : adrenal adenoma oesophageal leiomyoma oesophageal stromal tumour gastric leiomyosarcoma gastric stromal sarcoma paraganglioma, chromaffin (extra-adrenal pheochromocytoma) pulmonary chondroma small intestine, stromal tumour of T Tu um mo ou ur r f fe ea at tu ur re es s ( (p po os ss si ib bl le e) ): : exostoses leiomyosarcoma of the uterus parathyroid adenoma renal angiomyolipomas C Co om mm me en nt t The combination of gastric stromal sarcoma, extraadrenal paraganglioma and pulmonary chondroma is referred to as the Carney triad. Carney reviewed the 79 reported cases [1]. Approximately 85% of Carney triad patients are female. Age of onset ranged from 7 to 48 years (82% diagnosed before age 30); 78% of the reported cases do not present with the complete triad but show only 2 of the 3 features, the paragangliomas being the least frequent component. Although most cases are sporadic, 2 patients have been reported each with a sibling who had one of the tumours of the triad [1]. Gastric stromal sarcomas are usually the presenting tumour. The name (epithelioid) leiomyosarcoma was used in the past to refer to these tumours, but smooth muscle markers have not been identified in all cases; hence the change to 'stromal sarcomas'. The chondromas (diagnosed between 12 and 49 years) are multiple unilateral in 24% and bilateral in 13% of cases and may be recognized more than 15 years earlier and more than 20 years later than the leiomyosarcomas. After surgery for the chondromas, one or more new tumours developed in 56% of patients. The paragangliomas (diagnosed between age 12 to 48 years) are generally catecholamine secreting; they are present in multiple sites in 22% and may undergo malignant change. Silent adrenocortical adenomas were present in 13% of the patients and are considered part of the disorder. Other tumours observed were: oesophageal leiomyoma and stromal tumour, duodenal (multiple) stromal tumours, uterine leiomyosarcoma, bony exostosis, renal angiomyolipoma, parathyroid adenomas, gluteal myoma [1][2][3][4][5][6][7].
Unfortunately, the name Carney syndrome is used by some to refer to the Carney triad, whereas others use it to refer to Carney complex (or LAMB or NAME syndrome), which is a completely different disorder.

Rolf H. Sijmons
C Ce er re eb br ra al l s sa ar rc co om ma a, , f fa am mi il li ia al l c cl lu us st te er ri in ng g o of f M Mo od de e o of f i in nh he er ri it ta an nc ce e: : multifact?/AR?/AD? O OM MI IM M n nu um mb be er r: : 117600 T Tu um mo ou ur r f fe ea at tu ur re es s: : brain, sarcoma of the C Co om mm me en nt t Gainer et al. [1] reported four cases of cerebral fibrosarcomas occurring in two families: an affected father (age at diagnosis 73 years) and daughter (at 59 years); and a family with two affected sisters (diagnosed at age 64 and 69 years).
R Re ef fe er re en nc ce es s C Ce er rv vi ic ca al l c ca an nc ce er r, , f fa am mi il li ia al l c cl lu us st te er ri in ng g o of f M Mo od de e o of f i in nh he er ri it ta an nc ce e: : multifact? G Ge en ne es s: : various low penetrant gene mutations have been reported, we do not list them separately here T Tu um mo ou ur r f fe ea at tu ur re es s: : cervical cancer ovarian cancer (i.e. epithelial origin) T Tu um mo ou ur r f fe ea at tu ur re es s ( (p po os ss si ib bl le e) ): : anal cancer hepatocellular cancer lung/bronchial cancer lymphoma, malignant (non-Hodgkin's and/or Hodgkin's) oral cancer rectal cancer skin cancer urinary bladder cancer C Co om mm me en nt t Familial clustering of cervical cancer has been reported [1][2][3][4]. An estimated 15% of patients with this tumour have at least one affected first-degree relative [1]. It has been calculated that having a first-degree relative with cervical cancer is associated with a RR of 3 of developing squamous cell cancer of the cervix, a RR of 10 of developing adenosquamous cancer at this site and no increased risk of developing cervical adenocarcinoma [1]. No other studies have confirmed these detailed findings so far. Data from the Swedish Family-Cancer Database showed a cervical cancer RR of 2.0 for daughters of affected mothers [5]. In a more recent and more detailed analysis the following figures were reported [6]: daughters of mothers with in situ cancer had a RR of 1.7 of developing in situ and RR of again 1.7 of invasive cancer. Daughters of mothers with invasive cervical cancer had a RR of 1.6 of developing in situ cancer and a RR of 2.0 of developing invasive cancer. The following other cancer types in mothers increased the risk for in situ and/or invasive cervical cancer in their daughters: lung, liver, urinary bladder and oral cancer. The following cancer types in daughters increased the risk for in situ and/or invasive cervical cancer in their mothers: lymphoma, ovarian, oral, skin and anorectal cancer.
An analysis of large Mormon families did not show increased risks of cervical cancer in women with an affected sister [7]. However, an excess of cervical cancer was observed in first-degree relatives of patients with early-onset bladder cancer (RR 2.32). A family history of cancer in general was no risk factor for cervical cancer in a Yugoslavian and a Japanese cohort [8,9]. A study of Finnish patients with borderline ovarian tumours and their relatives demonstrated a RR of 7.8 for cervical cancer in the mothers of index cases [10]. In a Swedish twin study, the increase in risk of cervical cancer tended to be greater if monozygotic rather than dizygotic twins were affected [11].
inclusions in all white blood cells and of giant melanosomes in melanocytes. The majority of patients develop a lymphoproliferative disorder during the accelerated phase of the disease, which was demonstrated by Argyle et al. [1] to be a NHL T-cell lymphoma. The patients generally die in early childhood due to recurrent infections, although a lateonset type has been reported. An ovarian sclerosing stormal tumour has been detected in a girl with CHS [2]. The CHS gene has been identified [3]. lower face swelling rib cysts associated with multinucleated giant cells C Co om mm me en nt t This benign self-limiting disorder is characterized by swelling of the lower face, associated with multiple cystic changes in the jaw and anterior end of ribs. Biopsies of these skeletal lesions show multinucleated giant cells. Onset is around the 3 rd -4 th year of life and it progresses until the late teens [1][2][3]. Some cases may behave very aggressively [4][5][6]. Mangion et al. reported the occurrence of an osteosarcoma in the irradiated jaw of one of their patients [7].