Khunamornpong Surapan, Siriaunkgul Sumalee, Suprasert Prapaporn, Chitapanarux Imjai
Department of Pathology, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Gynecol Oncol. 2005 Apr;97(1):238-42. doi: 10.1016/j.ygyno.2004.12.054.
Yolk sac tumor (YST) of the vulva is extremely rare. Seven cases of vulvar YST have been reported to the literature. Due to the rarity of tumors, the appropriate choice of treatment may remain unclear.
A 30-year-old woman presented with a 3.5-cm right labial mass. Excisional biopsy showed YST with predominant solid pattern. Three weeks after excision, right inguinal lymph node biopsy revealed metastatic tumor. The serum alpha-fetoprotein (AFP) was not elevated. Cisplatin-based chemotherapy was administered, followed by pelvic and groin irradiation. The patient was free of disease 90 months after the diagnosis.
Local excision of tumor with adjuvant cisplatin-based chemotherapy can be justified for vulvar YST. Inguinal lymphadenectomy is recommended because metastasis may occur early. Adjuvant radiation therapy may help to control the disease. Tumor size of 5 cm or less may be a favorable prognostic factor. Serum AFP level may not be a sensitive marker for follow-up of vulvar YST.
外阴卵黄囊瘤(YST)极为罕见。文献报道了7例外阴YST。由于肿瘤罕见,合适的治疗选择可能仍不明确。
一名30岁女性出现一个3.5厘米的右侧阴唇肿物。切除活检显示为以实性为主型的YST。切除术后三周,右侧腹股沟淋巴结活检显示有转移性肿瘤。血清甲胎蛋白(AFP)未升高。给予了以顺铂为基础的化疗,随后进行盆腔和腹股沟放疗。诊断后90个月患者无疾病。
对于外阴YST,肿瘤局部切除并辅以顺铂为基础的化疗是合理的。建议行腹股沟淋巴结切除术,因为可能早期就发生转移。辅助放疗可能有助于控制疾病。肿瘤大小5厘米或更小可能是一个有利的预后因素。血清AFP水平可能不是外阴YST随访的敏感标志物。