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小儿阴道卵黄囊瘤1例罕见病例

A Rare Case of Pediatric Vaginal Yolk Sac Tumor.

作者信息

Lightfoot Michelle A, Bilgutay Aylin N, Kirsch Andrew J

机构信息

Department of Pediatric Urology, Children's Healthcare of Atlanta and Emory University School of Medicine, Atlanta, GA.

Department of Pediatric Urology, Children's Healthcare of Atlanta and Emory University School of Medicine, Atlanta, GA.

出版信息

Urology. 2018 Sep;119:137-139. doi: 10.1016/j.urology.2018.01.007. Epub 2018 Mar 13.

Abstract

A 14-month-old girl was evaluated for intermittent vaginal bleeding. Vaginoscopy revealed a friable tumor, and biopsy results confirmed a yolk sac tumor. Alpha-fetoprotein was elevated (1386 ng/mL) at diagnosis but quickly normalized with chemotherapy. The patient remained tumor-free 12 months after diagnosis without the need for radical surgery. Although rare, malignant tumors of the vagina must be included in the differential diagnosis of prepubertal girls who present with vaginal bleeding. Primary yolk sac tumor of the vagina is seen in girls less than 3 years of age and is treated with chemotherapy with or without surgical excision. Prognosis is good with appropriate treatment.

摘要

一名14个月大的女童因间歇性阴道出血接受评估。阴道镜检查发现一个易碎的肿瘤,活检结果证实为卵黄囊瘤。诊断时甲胎蛋白升高(1386 ng/mL),但化疗后迅速恢复正常。诊断后12个月,患者无肿瘤,无需进行根治性手术。尽管罕见,但对于出现阴道出血的青春期前女孩,阴道恶性肿瘤必须列入鉴别诊断。阴道原发性卵黄囊瘤见于3岁以下女童,治疗采用化疗,可联合或不联合手术切除。适当治疗后预后良好。

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A Rare Case of Pediatric Vaginal Yolk Sac Tumor.小儿阴道卵黄囊瘤1例罕见病例
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