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阴蒂上皮样血管内皮瘤:一例伴有免疫组化和超微结构结果的病例报告

Epithelioid hemangioendothelioma of the clitoris: a case report with immunohistochemical and ultrastructural findings.

作者信息

Strayer S A, Yum M N, Sutton G P

机构信息

Department of Pathology, Indiana University School of Medicine, Indianapolis 46202-5280.

出版信息

Int J Gynecol Pathol. 1992 Jul;11(3):234-9. doi: 10.1097/00004347-199207000-00011.

DOI:10.1097/00004347-199207000-00011
PMID:1399230
Abstract

A 30-year-old woman was referred for evaluation of a small nodule of the clitoris. This was subsequently diagnosed as epithelioid hemangioendothelioma. This rare vascular tumor of intermediate malignancy has not been previously described in the vulva. The patient underwent a modified radical vulvectomy and bilateral inguinal lymph node dissection, and subsequently received photon therapy. She is alive with no evidence of disease 27 months after diagnosis.

摘要

一名30岁女性因阴蒂小结节前来接受评估。该结节随后被诊断为上皮样血管内皮瘤。这种罕见的中间恶性度血管肿瘤此前尚未在外阴有过描述。患者接受了改良根治性外阴切除术及双侧腹股沟淋巴结清扫术,随后接受了光子治疗。诊断后27个月,她仍存活且无疾病证据。

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Epithelioid hemangioendothelioma of the clitoris: a case report with immunohistochemical and ultrastructural findings.阴蒂上皮样血管内皮瘤:一例伴有免疫组化和超微结构结果的病例报告
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Spindle and histiocytoid (epithelioid) hemangioendothelioma. Primary in lymph node.梭形细胞和组织细胞样(上皮样)血管内皮瘤。原发于淋巴结。
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引用本文的文献

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Rare Malignant Tumors of Clitoris-a Case Report.阴蒂罕见恶性肿瘤——病例报告
Indian J Surg. 2014 Jun;76(3):230-3. doi: 10.1007/s12262-013-0950-0. Epub 2013 Jul 30.