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Indian J Cancer ; 2007 Apr-Jun; 44(2): 87-9
Artigo em Inglês | IMSEAR | ID: sea-50337

RESUMO

Aggressive angiomyxoma is a rare, locally invasive mesenchymal tumor, occurring predominantly in the pelvic-perineal region of adults and carries a high risk for local relapse and hence the need to differentiate it from the other mesenchymal tumors occurring in this region. Presentation as a pedunculated polyp, like in our case, is unusual for this rare tumor. Except for positive surgical margins, there are no clinical or histological means for predicting the tumor recurrence. A diligent long-term follow-up is mandatory. Though rare, this tumor needs to be considered in the differential diagnosis of vulval polyps.


Assuntos
Adulto , Diagnóstico Diferencial , Feminino , Humanos , Imuno-Histoquímica , Leiomioma/patologia , Mixoma/diagnóstico , Pólipos/diagnóstico , Receptores de Progesterona/metabolismo , Neoplasias Vulvares/diagnóstico
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