Please use this identifier to cite or link to this item:
|Type:||Artigo de periódico|
|Title:||Congenital perineal lipoma presenting as ambiguous genitalia|
|Abstract:||Background: Congenital perineal lipoma is extremely rare and may lead to a misdiagnosis of ambiguous genitalia. Case Reports: We report on two girls referred to our service for ambiguous genitalia. Patient 1 (17 clays old) and patient 2 (2 months old) had Unremarkable gestational and perinatal histories. Both had normal female external genitalia and a 46,XX karyotype. Patient 1 had a polypoid, protruding 3.0 x 2.0 x 1.5-cm phallic-like mass arising at the inferior border of the left labium majora, and patient 2 had a similar mass of 1.5 x 1.5 x 1.0 cm at the same site and an imperforate anus. In both cases the mass was removed and found to be a lipoma. Discussion: To our knowledge, perineal lipoma has been reported only in eleven girls, nine of them with associated anorectal malformation. Migration and fusion of the labioscrotal folds and formation of the urorectal septum are sirnultaneous developmental events occurring in the same region, which may explain the association of perineal lipoma and anorectal malformations.|
|Editor:||Georg Thieme Verlag Kg|
|Citation:||European Journal Of Pediatric Surgery. Georg Thieme Verlag Kg, v. 18, n. 4, n. 269, n. 271, 2008.|
|Appears in Collections:||Unicamp - Artigos e Outros Documentos|
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.