| Literature DB >> 14736600 |
C Poncelet1, J Boccara, F Walker-Combrouze, O Féraud, P Madelenat.
Abstract
Liposarcoma of the vulva is a rare entity. This unusual localization with atypical clinical and histological appearance may induce diagnostic and treatment delay. We report the 13th case shown in the literature in a 31-year-old woman initially treated for a vulvar lipoma. Arguments based on clinical short term recurrence, histological infiltrating adipocytes, and cytogenentical findings evoked well-differentiated liposarcoma. Even though cytogenetic abnormalities, involving MDM2 and CDK4 genes, have been found, a certainty in malignity diagnosis could be difficult. In these cases, treatment decision may be uneasy. This case report recalls difficulties encountered in uterine hypercellular leiomyomas.Entities:
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Year: 2004 PMID: 14736600 DOI: 10.1016/j.gyobfe.2003.11.003
Source DB: PubMed Journal: Gynecol Obstet Fertil ISSN: 1297-9589