Abstract
Vulvar tümörler nadir görülür, vulvar sarkomlar ise tüm vulvar
tümörlerin %1-2’sini oluflturur. Biz klini¤imizde palyatif radyoterapi
alan ve agresif seyreden bir vulvar alveoler tip rabdomyosarkom vakas›n›
sunmay› amaçlad›k. Yirmi yafl›nda hasta genital bölgede flifllik
flikayetiyle baflvurmufltu. Radikal hemivulvektomi ve sa¤ inguinal
lenfadenoktomi yap›lan hastan›n postoperatif patoloji raporu alveoler
rabdomyosarkom olarak raporlanm›flt›. Postoperatif kemoterapi ve
radyoterapi alan hastan›n tedavinin tamamlanmas›ndan bir ay sonra
exitus oldu. Nadir görülen ve agresif seyreden vulvar alveoler rabdomyosarkom
vakas› sunulmufl ve literatür bilgileri eflli¤inde tedavisi
ve prognozu tart›fl›lm›flt›r.
Abstract
Vulvar tumors are uncommon, among them vulvar sarcomas represent
only 1-2% of all vulvar malignancies. We aimed to present an
agressive vulvar alveolar type rhabdomyosarcoma that was treated
with palliative radiotherapy at our clinic. A 20-years-old patient presented
with a mass on genitalia. Radical hemivulvectomy and inguinal
lymphadenectomy was performed and postoperative histopathology
was reported as alveolar rhabdomyosarcoma. Postoperative chemotherapy
and radiotherapy was administered, one month after
completion of treatment she died. A case of vulvar alveolar rhabdomyosarcoma
which is uncommon and agressive is presented and the
treatment and prognosis is discussed with the literature review.
Details
| Other ID | JA98JE94PN |
|---|---|
| Journal Section | Case Report |
| Authors | |
| Publication Date | January 1, 2009 |
| Submission Date | January 1, 2009 |
| Published in Issue | Year 2009 Volume: 12 Issue: 1 |