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巨大孤立性纤维瘤源于大网膜。

Giant solitary fibrous tumor arising from greater omentum.

机构信息

Liang Zong, Ping Chen, Guang-Yao Wang, Qun-Shan Zhu, Department of Gastrointestinal Surgery, Subei People's Hospital, Yangzhou University, Yangzhou 225001, Jiangsu Province, China.

出版信息

World J Gastroenterol. 2012 Nov 28;18(44):6515-20. doi: 10.3748/wjg.v18.i44.6515.

Abstract

Extrathoracic solitary fibrous tumors (SFTs) have been described at almost every anatomic location of human body, but reports of SFT in the abdominal cavity are rare. We herein present a rare case of SFT originating from greater omentum. Computed tomography revealed a 15.8 cm × 21.0 cm solid mass located at superior aspect of stomach. Open laparotomy confirmed its mesenchymal origin. Microscopically, its tissue was composed of non-organized and spindle-shaped cells exhibiting atypical nuclei, which were divided up by branching vessel and collagen bundles. Immunohistochemical staining showed that this tumor was negative for CD117, CD99, CD68, cytokeratin, calretinin, desmin, epithelial membrane antigen, F8 and S-100, but positive for CD34, bcl-2, α-smooth muscle actin and vimentin. The patient presented no evidence of recurrence during follow-up. SFT arising from abdominal cavity can be diagnosed by histological findings and immunohistochemical markers, especially for CD34 and bcl-2 positive cases.

摘要

胸腔外孤立性纤维瘤(SFT)几乎可发生于人体的任何解剖部位,但发生于腹腔的 SFT 较为罕见。本文报道了 1 例源自大网膜的 SFT。计算机断层扫描显示胃上方有一 15.8cm×21.0cm 的实性肿块。剖腹探查证实其为间叶来源。显微镜下,肿瘤组织由非组织化的梭形细胞构成,细胞核异型性明显,被分支状血管和胶原束分隔。免疫组化染色显示该肿瘤 CD117、CD99、CD68、细胞角蛋白、钙视网膜蛋白、结蛋白、上皮膜抗原、F8 和 S-100 均阴性,而 CD34、bcl-2、α-平滑肌肌动蛋白和波形蛋白阳性。随访期间患者无复发证据。通过组织学发现和免疫组化标志物,尤其是 CD34 和 bcl-2 阳性病例,可诊断发生于腹腔的 SFT。

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