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表现为阴蒂肿瘤的原发性外阴淋巴瘤。

Primary vulvar lymphoma presenting as a clitoral tumor.

作者信息

Ferrando-Marco J, Martorell M A, Carrato A, Navarro J T

机构信息

Department of Pathology, Valencia University and General Hospital, Spain.

出版信息

Acta Obstet Gynecol Scand. 1992 Oct;71(7):543-6. doi: 10.3109/00016349209041448.

DOI:10.3109/00016349209041448
PMID:1332376
Abstract

We report a case of malignant large cleaved cell vulvar lymphoma predominantly affecting the clitoris, in a 60 year-old woman. In a review of the literature, female genital tract lymphomas of vulvar location are exceptional. Histologically, these tumors must be differentiated from pseudolymphomatous lesions. In the present case (Stage IE), response to chemotherapy was good and the patient remains asymptomatic after three years of follow-up.

摘要

我们报告一例主要累及阴蒂的恶性大裂细胞外阴淋巴瘤病例，患者为一名60岁女性。在文献回顾中，外阴部位的女性生殖道淋巴瘤较为罕见。从组织学上看，这些肿瘤必须与假性淋巴瘤性病变相鉴别。在本病例（IE期）中，化疗反应良好，患者在随访三年后仍无症状。

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