Basgul A, Gokaslan H, Kavak Z N, Eren F T, Bozkurt N
Department of Obstetrics and Gynecology, Marmara University School of Medicine, Istanbul, Turkey.
Eur J Gynaecol Oncol. 2006;27(4):395-8.
Endodermal sinus tumor (EST) or primary yolk sac tumor (YST) of the vulva is extremely rare and a highly malignant germ cell tumor. Only nine cases of vulvar YST have been reported to the world literature to date. We present the tenth case of endodermal sinus tumor of the vulva.
A 32-year-old white virgin presented with a 3.5 cm right labial mass without any other signs or symptoms. Excisional biopsy showed YST with a predominantly solid pattern. Unilateral hemivulvectomy with bilateral inguinal lymphadenectomy was performed. Six months after surgery there was a recurrence. She was treated with three courses of the BEP regimen (bleomycin, etoposide, cisplatin). The patient refused to take any further treatment including radiotherapy. The serum alpha-fetoprotein (AFP) was not elevated at the initial diagnosis however it was elevated during recurrence. The patient is alive with the disease 42 months after the first appearance of the vulvar mass.
外阴内胚窦瘤(EST)或原发性卵黄囊瘤(YST)极为罕见,是一种高度恶性的生殖细胞肿瘤。迄今为止,世界文献中仅报道了9例外阴YST病例。我们报告第10例外阴内胚窦瘤病例。
一名32岁的白人处女,右侧阴唇有一个3.5厘米的肿块,无任何其他体征或症状。切除活检显示为主要呈实性模式的YST。行单侧半外阴切除术及双侧腹股沟淋巴结清扫术。术后6个月复发。她接受了三个疗程的BEP方案(博来霉素、依托泊苷、顺铂)治疗。患者拒绝接受包括放疗在内的任何进一步治疗。初始诊断时血清甲胎蛋白(AFP)未升高,但复发时升高。自外阴肿块首次出现42个月后,该患者带瘤生存。