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巨大会阴孤立性纤维瘤:一例罕见病例报告

Giant Perineal Solitary Fibrous Tumor: A Rare Case Report.

作者信息

Melo Petronio Augusto de Souza, Yoshino Bonifaci Ana Maria, Crochik Fabio da Silva, Murta Claudio Bovolenta, Claro Joaquim Francisco de Almeida, Manzano Joao Padua

机构信息

Division of Urology, Men's Health Centre, Hospital Brigadeiro, Sao Paulo, SP, Brazil.

Division of Pathology, Men's Health Centre, Hospital Brigadeiro, Sao Paulo, SP, Brazil.

出版信息

Case Rep Urol. 2017;2017:4876494. doi: 10.1155/2017/4876494. Epub 2017 Mar 2.

Abstract

. Solitary fibrous tumor (SFT) is a fibroblastic mesenchymal tumor that was initially described from the pleura but currently arises at almost every anatomic site. It is usually benign, and surgical resection is curative. SFT involving the perineum is extremely rare. This is the third case report of a perineal SFT in the literature. . We reported an uncommon case of a 64-year-old man presenting with a huge perineal mass that started growing 3 years before his arrival in our service. He was asymptomatic. A contrast-enhanced CT scan revealed a heterogeneous well-circumscribed perineal mass with soft-tissue density. Invasion of the surrounding organs, distal metastasis, and lymph node swelling were absent. The complete resection of mass was done successfully. The specimen was a 23.0 × 14.0 × 8.0 cm encapsulated tumor. Mass weight was 1,170 g. After pathological analysis, we confirmed that the mass was a solitary fibrous tumor. The diagnosis was based on clinical findings and histological morphology and immunohistochemistry study. . SFTs are usually indolent tumors with a favorable prognosis. The perineal location is extremely rare. Complete resection of the mass is the treatment of choice.

摘要

孤立性纤维瘤(SFT)是一种成纤维细胞性间叶组织肿瘤,最初是从胸膜描述而来,但目前几乎在每个解剖部位都有发生。它通常是良性的,手术切除可治愈。累及会阴的SFT极为罕见。这是文献中第三例会阴SFT的病例报告。我们报告了一例罕见病例,一名64岁男性,出现巨大会阴肿物,该肿物在他前来我院就诊前3年开始生长。他没有症状。增强CT扫描显示一个边界清晰的异质性会阴肿物,呈软组织密度。未见周围器官侵犯、远处转移及淋巴结肿大。成功地完整切除了肿物。标本是一个23.0×14.0×8.0厘米的包膜肿瘤。肿物重量为1170克。经过病理分析,我们确认该肿物为孤立性纤维瘤。诊断基于临床表现、组织形态学及免疫组化研究。SFT通常是惰性肿瘤,预后良好。会阴部位极为罕见。肿物完整切除是首选治疗方法。

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