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[外阴侵袭性血管黏液瘤。病例报告及文献复习]

[Aggressive angiomyxoma of the vulva. Case report and literature review].

作者信息

Nava Flores Elda Lizeth, Alvarez Blanco Mario A, Figueroa Vadillo Jazmín, Cruz Ortiz Humberto

机构信息

División de Medicina, Hospital General de México, OD.

出版信息

Ginecol Obstet Mex. 2009 Oct;77(10):487-90.

Abstract

Aggressive angiomyxoma is a rare vulvovaginal, perineal or pelvic mesenchymal neoplasm with a marked tendency to local recurrence but does not metastasize. A case of an aggressive angiomyxoma of vulva in a 39-years-old women with an illness of one year prior to examination, with a slow and progressive growth of the left vulvar region, without other symptoms. During physical examination, a piriform tumor of 15x10 cm was found, located on the left labia majora, soft tissue dependent. Wide resection of the tumor were performed. Hystopathology reported an aggressive angiomyxoma of the vulva, with tumor in resection margins. The patient was treated with a 65Gy postsurgical radiotherapy and gosereline 3.6 mg monthly, during 6 cycles. Aggressive angiomyxoma is a rare neoplasm 150 cases has been reported. The treatment is surgical resection. Radiotherapy and hormonal adyuvant is not fully stablished.

摘要

侵袭性血管黏液瘤是一种罕见的发生于外阴阴道、会阴或盆腔的间叶性肿瘤,具有明显的局部复发倾向,但不发生转移。一名39岁女性,在检查前患病1年,左侧外阴区域缓慢进行性生长,无其他症状,诊断为外阴侵袭性血管黏液瘤。体格检查发现一个15×10 cm的梨形肿瘤,位于左侧大阴唇,与软组织相连。对肿瘤进行了广泛切除。组织病理学报告为外阴侵袭性血管黏液瘤,切除边缘有肿瘤。患者接受了65Gy的术后放疗,并每月注射戈舍瑞林3.6 mg,共6个周期。侵袭性血管黏液瘤是一种罕见肿瘤,已报道150例。治疗方法为手术切除。放疗和激素辅助治疗尚未完全确立。

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