Almeida, FTSantos, R PCarvalho, SDBrito, C2018-07-062018-07-062018Indian J Dermatol. 2018 May-Jun;63(3):261-263.http://hdl.handle.net/10400.23/1265Multiple 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.engLeiomiomatoseSíndromes Neoplásicas HereditáriasNeoplasias da PeleNeoplasias Uterinasjournal article10.4103/ijd.IJD_69_18