Hereditary Cancer in Clinical Practice

, 10:15

Diagnostic and pathogenetic role of café-au-lait macules in nevoid basal cell carcinoma syndrome

  • Giovanni Ponti
  • Aldo Tomasi
  • Lorenza Pastorino
  • Cristel Ruini
  • Carmelo Guarneri
  • Victor Desmond Mandel
  • Stefania Seidenari
  • Giovanni Pellacani
Open AccessCase report

DOI: 10.1186/1897-4287-10-15

Cite this article as:
Ponti, G., Tomasi, A., Pastorino, L. et al. Hered Cancer Clin Pract (2012) 10: 15. doi:10.1186/1897-4287-10-15

Abstract

Café au lait spots (CALS) are common dermatologic findings that can at the same time arise in a variety of pathologic conditions such as Neurofibromatosis type 1 (NF1), together with numerous hereditary syndromes for which they represent either diagnostic criteria or associated elements (McCune Albright, Silver-Russell, LEOPARD, Ataxia-Telangiectasia). A review of the literature also revealed two cases of association with NBCCS. We report here the case of a female proband with CALS associated to Nevoid Basal Cell Carcinoma Syndrome (NBCCS) with known PTCH1 germline mutation (C.1348-2A>G) who had been misdiagnosed with NF1 in her childhood because of 5 CALS and cutaneous nodules. The patient presented a giant cell tumor of the skin, palmar and calcaneal epidermoidal cystic nodules, odontogenic keratocystic tumors and deformity of the jaw profile. Her family history brought both her brother and father to our attention because of the presence of KCOTs diagnosed at early age: after genetic testing, the same PTCH1 germline mutation was identified in the three family members. Clinical criteria are used for discerning NF1 diagnosis (size, number and onset age), while there are no definite guidelines concerning CALS except for their presence. In our experience, we have noted an association of CALS with NBCCS; this seems interesting because we already know clinical criteria are a dynamic entity and can be modified by epidemiologic evidences.

Keywords

Café au lait spotsNevoid basal cell carcinoma syndromePTCH1 mutationNeurofibromatosis type 1GenodermatosesHereditary cancer syndrome

Abbreviations

BCC

Basal cell carcinoma

CALS

Café-au-lait spots

KCOT

Keratocystic odontogenic tumor

NBCCS

Nevoid basal cell carcinoma syndrome

NF1

Neurofibromatosis type 1.

Background

Café au lait spots (CALS) are cutaneous hyper pigmented flat macules or patches (>1 cm) that usually appear in childhood and tend to increase in number and size until puberty[1]. They’re colored in various shades of brown and located anywhere on the body, independent from sun exposure, especially on face, scalp, palms, soles and external genitalia. Although a single CALS is a common finding in Caucasian children (10-20%)[2], an increasing number is much less frequent: 6 CALS represent a threshold for the diagnosis of Neurofibromatosis type 1[3, 4]. NF1 isn’t the only disease associated to CALS, that appear in multiple pathologic conditions for which they represent either diagnostic criteria or just associated signs: McCune-Albright syndrome, LEOPARD syndrome, Ataxia telangiectasia syndrome and many more (see Table1)[5]. They’re a common finding of metabolic disease such as Gaucher syndrome and they were also reported in patients in two cases of Nevoid Basal Cell Carcinoma Syndrome (NBCCS).
Table 1

Syndromes associated with café-au-lait macules

Syndrome

Gene or Locus

Cutaneous Clinical Features

Systemic Clinical Features

NF1

NF1

Multiple café-au-lait (>6), skin-fold freckling, cutaneous and plexiform neurofbromas

Macrocephaly, optic pathway glioma, skeletal dysplasia

NF2

NF2

Café-au-lait macules seen but not a criterion for diagnosis, neurofibromas

Acoustic neuromas, schwannomas, meningiomas, juvenile posterior subcapsular lenticular opacity

Multiple familial Café-au-lait

Unknown

Multiple café-au-lait

Without other stigmata of NF1

Legius (NF-1 like) syndrome

SPREAD1

Multiple café-au-lait, skin-fold freckling

Without other stigmata of NF1

McCune Albright syndrome

GNAS1

Segmental café-au-lait

Precocious puberty, other endocrinopathies, polyostotic fibrous dysplasia

Constitutional MMR deficiency syndrome

MLH1, MSH2, MSH6, PMS2

Multiple café-au-lait

Adenomatous colonic polyps, multiple malignancies (medulloblastoma, lymphoma, glioblastoma)

Ring chromosome syndrome

Choromosomes 7,11,12,15,17

Multiple café-au-lait

Microcephaly, mental retardation, short stature

Leopard/multiple lentigenes syndrome

PTPN11

Café-au-lait, café-noir, lentigines

Cardiac conduction defects, ocular hypertelorism, pulmonary stenosis, growth retardation, hearing loss

Cowden syndrome

PTEN

Café-au-lait spots, Facial trichilemmomas, soft tissue tumors (lipomas, neuromas)

Cobblestoning of the oral mucosa, gastrointestinal polyps, breast carcinoma, thyroid adenoma and cancer

Banayan-Riley- Ruvalcaba syndrome

PTEN

Pigmented genital macules, Facial trichilemmomas

Oral papillomas, gastrointestinal polyps, Macrocephaly, vascular anomalies

WEAK ASSOCIATION

   

NAME (naevi, atrial mixoma, ephelides) syndrome

Unknown

Naevi, ephelides

Atrial mixoma

Ataxia teleangectasia

ATM

Cutaneous and ocular teleangectasias

Cerebellar ataxia, immunodeficiency, hypogonadism, lymphoreticular malignancy

Epidermal Nevus syndrome

Unknown

Linear epidermal nevus

Mental retardation, seizures, movement disorders

Turner Syndrome

X-chromosomal anomalies (XO karyotupe or Xp deletion)

Cutaneous lymphatic malformations

Short stature, broad chest, low hairline, low-set ears and webbed necks, swelling, gonadal dysfunction, congenital heart disease, hypothyroidism.

Silver-Russel Syndrome

Unknown

Multiple café au lait macules

Short stature, craniofacial and body asymmetry, microcephaly, congenital cardiac defects

Fanconi Anemia

FANCA, FANCB/C/D locus on chromosome 3, FANCE/F/G/H

Hyper- and hypopigmentation of the skin, mucocutaneous squamous cell carcinomas

Bone marrow failure, multiple congenital anomalies, mental retatrdation, microcephaly

Westerhof Syndrome

unknown

Hypopigmented and hyperpigmented macules

Retarded growth and mental deficiency

MEN1/Men2B

RET

Multiple malignancies

 

Bloom syndrome

RECQL3

Hypo- and hyper-pigmented spots; telangiectasias

Mental retardation, short stature

Gaucher Disease

Chromosome 1

Yellowish-brown skin pigmentation

Astenia, diarrhoea, ataxia, splenomegalia, hemorrhagies, muscolar atrophia,

Hunter Disease

X-linked

Skin eruptions

Macrocephaly, mental retardation, valvular dysfunction

Watson Syndrome

NF1

Axillary/inguinal freckling

Mental retardation, short stature, pulmonary valvular stenosis, Lisch nodules

Case presentation

We present here an association between NBCCS and café-au-lait spots, the case of a 23 year old female patient born in 1989, originally examined in the Department of Pediatrics at the age of 10. General and skin examination revealed 4 café-au-lait spots, palmar and calcaneal cystic nodules and deformity of the jaw profile (see Figure1). One of the nodules was excised and histopathological examination set the diagnosis of giant cell tumor. Neurofibromatosis type 1 was the first diagnosis although the patient didn’t completely fulfill the criteria. Later, the patient presented jaw keratocystic odontogenic tumors (KCOTs) that were surgically removed and histologically evaluated. Her family history brought both her brother and father to our attention because of the presence of KCOTs in all of them; they were tested for PTCH1 gene mutation under suspicion of Gorlin syndrome: diagnosis was made after the discovery of the same PTCH1 gene germline mutation (C.1348-2A>G). The brother presented KCOTs diagnosed at the age of 15, while the father presented KCOTs diagnosed at the age of 16, so that we hypothesized the presence of a “Gorlin syndrome with KCOTs only”, while a BCC was discovered on the father’s arm was after the dermatologic follow-up to determine whether this was just a sporadic skin tumor or the sign of a full phenotype.
https://static-content.springer.com/image/art%3A10.1186%2F1897-4287-10-15/MediaObjects/13053_2012_Article_405_Fig1_HTML.jpg
Figure 1

Clinical features and genealogic tree of NBCCS’ probands.

Conclusion

Nevoid basal cell carcinoma syndrome (NBCC; also known as Gorlin syndrome; OMIM #109400), inherited in an autosomal dominant pattern, is characterized by a very wide spectrum of peculiar clinical manifestations. The most common features include multiple basal cell carcinomas, KCOTs, palmar and/or plantar pits and skeletal abnormalities (i.e. fused, bifid or splayed ribs). According to Kimonis et al., two major or one major and two minor criteria should contemporary exist in order to confirm the diagnosis of NBCCS[6]. Most individuals present developmental defects, such as intracranial calcification, calcifications of the falx cerebri, and a variety of other benign or malignant tumors, including ovarian fibroma, medulloblastoma, rhabdomyosarcomas and cardiac fibromas[7]. The major criteria included multiple BCCs or one BCC before 30 years, keratocysts of the jaw, palmar/plantar pits and lamellar calcification of the falx cerebri on skull radiograph. Minor criteria included spina bifida occulta or other vertebral anomalies, brachymetacarpaly in at least one limb, hypertelorism or telecanthus, frontal bossing, rib anomalies (bifid, synostosed, hypoplastic), ovarian fibroma, medulloblastoma, flame shaped lucencies in the phalanges, and brachymetacarpaly in the 4 limbs. One diagnosis was also established by the presence of a first degree relative with NBCC and one major or two minor criteria.[7].

Our proband meets the diagnostic criteria for Gorlin syndrome since she presents two major criteria: multiple histologically proven odontogenic keratocysts occurred before the age of 20 and family history of NBCCS (father and brother). Moreover, molecular characterization reported the same germline PTCH1 mutation, C.1348-2A>G[8, 9]; we had hypothesized this mutation was related to a NBCCS subset with keratocysts only, until we discovered the presence of one basal cell carcinoma in the proband’s father. The entire family, which has been identified by a clinical approach starting from the KCOTs (8), is still under strict dermatologic follow-up.

We present here the case of an association between NBCCS and café au lait spots; the family history was peculiarly interesting since the proband was initially misdiagnosed with NF1 due the presence of 5 café-au-lait spots, which represent a common dermatologic finding either sporadic or associated to genodermatoses and other hereditary syndromes such as NF1, McCune-Albright syndrome and LEOPARD syndrome.

CALS vary from innocent findings to stigmata that connect different hereditary and sporadic syndromes. Histopathologically, they are nests of pigmented melanocytes, cells of neuroectodermal origin that migrate during the embryonic development: for this reason they sometimes have a somatotopic distribution, sometimes they follow dermatomes[10]. They might for this reason relate to different neoplasms of common embryonic origin, not only in genodermatoses as NF1 but also in many other syndromes. We do not know how frequent is the presence of café-au-lait spots in Gorlin syndrome, but it might be interesting to further analyze this skin feature that might be useful in the detection of NBCCS. The literature review reported the case of a 10 year-old child diagnosed with NBCCS presenting CALS and neck pits[11], and a family composed by women and her two sons with NBCCS and CALS[12]. In general, CALS range from the spectrum of innocent finding to that of an alarm bell for suspecting a hereditary syndrome; the threshold between the two is a clinical criteria, comprehending their number, their size and their onset age, at least in NF1, since in the majority of other syndromes there are no specific guidelines concerning CALS except for their presence. In our experience, we have noted an association of CALS with NBCCS; this seems interesting because we already know clinical criteria are a dynamic entity and can be modified by epidemiologic evidences, as it’s now happening to ameloblastoma in NBCCS diagnosis[13]. Further clinical study will be necessary for the complete characterization of the clinical association between CALS and NBCCS.

Consent

Peripheral blood samples were collected from the proband and her first-degree relatives. Molecular analysis of PTCH1 was performed as previously described[14].Written informed consent, agreeing to peripheral blood sampling and genetic analysis, was obtained from each patient. Molecular analysis of PTCH1 was performed. The PTCH1 cDNA sequence from GenBank (Accession number U59464.1) was used as a reference sequence, where the A of the ATG translation initiation start site represents nucleotide +1. An Institutional Review Board (IRB) approval was obtained and the study in which the patients were enrolled was conducted according to the Declaration of Helsinki Principles. All patients provided their written informed consent for the management of personal data and for publication of their photographs before participating into the study. A copy of the written consent is available for review on request.

Acknowledgments

The authors thank all colleagues who provided assistance: Luca Fabbiani, Silvana Ciardo and Sandro Radighieri.

Supplementary material

13053_2012_405_MOESM1_ESM.pdf (610 kb)
Authors’ original file for figure 1

Copyright information

© Ponti et al.; licensee BioMed Central Ltd. 2012

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Authors and Affiliations

  • Giovanni Ponti
    • 1
  • Aldo Tomasi
    • 1
  • Lorenza Pastorino
    • 2
  • Cristel Ruini
    • 3
  • Carmelo Guarneri
    • 3
  • Victor Desmond Mandel
    • 3
  • Stefania Seidenari
    • 3
  • Giovanni Pellacani
    • 3
  1. 1.Department of Clinical and Diagnostic Medicine and Public Health, University Hospital of Modena and Reggio EmiliaUniversity of Modena and Reggio EmiliaModenaItaly
  2. 2.Department of Internal Medicine and Medical Specialties (DiMI)University of GenoaGenoaItaly
  3. 3.Department of Surgical, Medical, Odontoiatric and Morphological Sciences, with Transplantation, Oncological and Regenerative Medicine interests, Division of Dermatology, University Hospital of Modena and Reggio EmiliaUniversity of Modena and Reggio EmiliaModenaItaly