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以肠套叠形式表现的小肠原发性恶性纤维组织细胞瘤:病例报告

Primary malignant fibrous histiocytoma of the small intestine presenting as an intussusception: report of a case.

作者信息

Kotan Cetin, Kosem Mustafa, Alici Süleyman, Ilhan Mahmut, Tuncer Ilyas, Harman Mustafa

机构信息

Department of Surgery, Yüzüncü Yil University School of Medicine, YYU Tip Fakültesi, Genel Cerrahi AD, 65200 Van, Turkey.

出版信息

Surg Today. 2002;32(12):1091-5. doi: 10.1007/s005950200221.

Abstract

Malignant fibrous histiocytoma occurs most commonly in the extremities and trunk, but rarely in the visceral organs. Malignant fibrous histiocytoma of the small intestine is an extremely rare condition. To our knowledge, only ten cases of primary tumors involving the small intestine have been described up to now. Among them only one case has been reported to lead to intussusception. This case report documents the appearance of a storiform-pleomorphic type primary malignant fibrous histiocytoma of the ileum, which led to intussusception, in a 58-year-old man with a 3-month history of dyspepsia, weight loss, general fatigue, and nonspecific abdominal pain. The patient was well with no sign of disease at 8 months after surgery. The clinical and pathologic characteristics of malignant fibrous histiocytoma of the small intestine as found in the literature are also reviewed.

摘要

恶性纤维组织细胞瘤最常发生于四肢和躯干,但很少发生在内脏器官。小肠恶性纤维组织细胞瘤是一种极其罕见的病症。据我们所知,截至目前仅有十例累及小肠的原发性肿瘤的报道。其中仅有一例被报道导致肠套叠。本病例报告记录了一名58岁男性患者,患有消化不良、体重减轻、全身乏力和非特异性腹痛3个月,其回肠出现 storiform-pleomorphic 型原发性恶性纤维组织细胞瘤并导致肠套叠。患者术后8个月情况良好,无疾病迹象。文中还回顾了文献中发现的小肠恶性纤维组织细胞瘤的临床和病理特征。

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