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表现为胸内肿瘤的腹外硬纤维瘤:病例报告及文献综述

Extra-abdominal desmoid tumor presenting as an intrathoracic tumor: case report and literature review.

作者信息

Takeshima Y, Nakayori F, Nakano T, Shimizu K, Yamashita Y, Toge T, Inai K

机构信息

Second Department of Pathology, Hiroshima University School of Medicine, Japan.

出版信息

Pathol Int. 2001 Oct;51(10):824-8. doi: 10.1046/j.1440-1827.2001.01262.x.

Abstract

A case of an extra-abdominal desmoid tumor presenting as an intrathoracic tumor (intrathoracic desmoid tumor) in a 46-year-old woman is reported. The tumor originated in the left chest wall and protruded into the left pleural cavity. Simple resection was carried out. The tumor, measuring 13 x 9 x 7 cm, was solid, gray-tan in color, and covered with parietal pleura. Histologically, the tumor was composed of a hypocellular arrangement of spindle-shaped cells with a fibromyxoid background. In some areas, keloid-like hyalinized collagen fibers proliferated, and a perivascular hypercellular area was seen. Immunohistochemical analysis showed that the cytoplasms of the tumor cells were strongly positive for vimentin, and some tumor cells were positive for alpha-smooth muscle actin, but all tumor cells were negative for CD34. These findings were consistent with the characteristics of an intrathoracic desmoid tumor. The differential diagnoses, in particular solitary fibrous tumor and tumors with a myofibroblastic nature, are discussed.

摘要

报告了一例46岁女性患者,其腹外硬纤维瘤表现为胸腔内肿瘤(胸腔内硬纤维瘤)。肿瘤起源于左胸壁并突入左胸腔。进行了单纯切除术。肿瘤大小为13×9×7cm,质地坚实,呈灰棕色,表面覆盖有脏层胸膜。组织学上,肿瘤由梭形细胞的低细胞排列构成,背景为纤维黏液样。在一些区域,瘢痕疙瘩样玻璃样变性的胶原纤维增生,可见血管周围细胞增多区域。免疫组织化学分析显示,肿瘤细胞的细胞质波形蛋白呈强阳性,一些肿瘤细胞α平滑肌肌动蛋白呈阳性,但所有肿瘤细胞CD34均为阴性。这些发现与胸腔内硬纤维瘤的特征相符。讨论了鉴别诊断,特别是孤立性纤维瘤和具有肌成纤维细胞性质的肿瘤。

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