Dermal Hyperneury and Multiple Sclerotic Fibromas in Multiple Endocrine Neoplasia Type 2A Syndrome

• Published in: JAMA dermatology (Chicago, Ill.) Vol. 153; no. 12; p. 1298
• Main Authors: Alegría-Landa, Victoria, Jo-Velasco, Margarita, Robledo, Mercedes, Requena, Luis
• Format: Journal Article
• Language: English
• Published: United States 01-12-2017
• Subjects: Adult; Carcinoma, Medullary - congenital; Carcinoma, Medullary - genetics; Carcinoma, Medullary - pathology; Female; Fibroma - genetics; Fibroma - pathology; Genetic Testing; Germ-Line Mutation; Humans; Middle Aged; Multiple Endocrine Neoplasia Type 2a - complications; Multiple Endocrine Neoplasia Type 2a - genetics; Multiple Endocrine Neoplasia Type 2a - pathology; Phenotype; Proto-Oncogene Proteins c-ret - genetics; Skin Diseases - genetics; Skin Diseases - pathology; Skin Neoplasms - genetics; Skin Neoplasms - pathology; Thyroid Neoplasms - genetics; Thyroid Neoplasms - pathology
• ISSN: 2168-6084
• DOI: 10.1001/jamadermatol.2017.3959

Multiple endocrine neoplasia type 2 (MEN 2) syndrome is an autosomal dominant, hereditary cancer disorder caused by germline mutations in the RET (formerly MEN2A, MEN2B) proto-oncogene located on chromosomal band 10q11.21. Two distinct clinical forms have been described as the following phenotypes: multiple endocrine neoplasia type 2A (MEN 2A) and multiple endocrine neoplasia type 2B (MEN 2B) syndromes. The common and necessary nexus that defines these 2 phenotypes is the presence of medullary thyroid carcinoma (MTC). The familial MTC type of MEN 2 syndrome was included within the spectrum of MEN 2A syndrome. Cutaneous manifestations of MEN 2A syndrome include macular amyloidosis, whereas MEN 2B syndrome is traditionally linked to multiple mucosal neuromas.
To describe a family with cutaneous manifestations not previously described in patients with MEN 2A syndrome and to discuss the association of this disorder with Cowden syndrome.
Clinicopathologic correlation of cutaneous lesions and genetic studies in 11 members of a family with familial MTC.
Cutaneous lesions were histopathologically and immunohistochemically studied. Genetic screening for a germline mutation at the RET gene was performed in 11 family members.
Identification of cutaneous lesions not previously described in patients with MEN 2A syndrome.
This family of 11 individuals with familial MTC type of MEN 2A syndrome demonstrated the moderate risk RET p.Val804Met (protein valine at residue 804 replaced by methionine) genetic mutation, with 2 of the relatives presenting with dermal hyperneury, cutaneous lesions classically described in MEN 2B syndrome, and 1 relative also showing multiple sclerotic fibromas, a cutaneous manifestation of PTEN (phosphatase and tensin homologue) hamartoma-tumor syndrome.
Dermal hyperneury and multiple sclerotic fibromas should be added to the list of cutaneous manifestations of patients with the familial MTC type of MEN 2A syndrome.