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Reed's Syndrome
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Autores
Orientador(es)
Resumo(s)
Multiple cutaneous and uterine leiomyomatosis (MCUL), also known as Reed's syndrome, is a rare genodermatosis, with an autosomal dominant pattern of inheritance. It results from a germline heterozygous mutation of fumarate hydratase gene, that is classified as a tumor suppressor gene. Hereditary leiomyomatosis and renal cell cancer is characterized by the association of MCUL with renal cell carcinoma. We report a case of a 57-year-old woman, with multiple cutaneous leiomyomas as the presenting sign of Reed's syndrome.
Descrição
Palavras-chave
Leiomiomatose Síndromes Neoplásicas Hereditárias Neoplasias da Pele Neoplasias Uterinas
Contexto Educativo
Citação
Indian J Dermatol. 2018 May-Jun;63(3):261-263.