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Title: Type 2 segmental manifestation of congenital multiple glomangiomas. Author: Allombert-Blaise CJ, Batard ML, Ségard M, Martin de Lassalle E, Brevière GM, Piette F. Journal: Dermatology; 2003; 206(4):321-5. PubMed ID: 12771473. Abstract: Congenital multiple glomus tumors are extremely rare, and less than 20 cases have been well documented. We report an uncommon case of congenital multiple glomangiomas with a segmental manifestation in a 9-year-old girl. Since birth, the child had presented asymptomatic angiomatous macules arranged in a segmental pattern on the neck and trunk. During a follow-up period of 9 years, disseminated smaller papulonodular lesions developed on both arms and the left leg with a segmental distribution. Histopathology of congenital and acquired lesions confirmed the diagnosis of glomangiomas. The family history was negative for glomus tumors. This type of presentation supports the recently described type 2 segmental manifestation of multiple glomus tumors, with a segmental involvement of congenital early developing lesions.[Abstract] [Full Text] [Related] [New Search]