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腹膜后肉瘤:两例罕见的肠穿孔病因

Retroperitoneal sarcoma: a rare cause of intestinal perforation in two cases.

作者信息

Kopplin Lj, Kim Ja

机构信息

Department of Genetics, Case Western Reserve University, Cleveland, OH.

Division of Surgical Oncology, Department of Surgery, University Hospitals Case Medical Center, Cleveland, OH.

出版信息

J Surg Case Rep. 2011 May 1;2011(5):3. doi: 10.1093/jscr/2011.5.3.

Abstract

Retroperitoneal sarcoma is a rare malignancy often insidious in onset. At initial presentation, abdominal mass, pain or obstructive symptoms are the most common complaints. Here we present two patients who presented with abdominal discomfort and were discovered to have retroperitoneal sarcomas with secondary intestinal perforation. Perforation is a rare complication of retroperitoneal sarcoma, but one with the potential to significantly affect patient outcomes. Both patients underwent surgical resection and pathological characterization of their malignancies. The discovery of intestinal perforation during workup necessitates initiation of empirical antibiotic coverage and prompt surgical intervention.

摘要

腹膜后肉瘤是一种罕见的恶性肿瘤,起病往往隐匿。初次就诊时,腹部肿块、疼痛或梗阻症状是最常见的主诉。在此,我们报告两名患者,他们均因腹部不适就诊,经检查发现患有腹膜后肉瘤并伴有继发性肠穿孔。穿孔是腹膜后肉瘤的一种罕见并发症,但有可能显著影响患者的预后。两名患者均接受了手术切除及恶性肿瘤的病理特征分析。在检查过程中发现肠穿孔需要开始经验性抗生素覆盖并及时进行手术干预。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab19/3649246/ab1176400142/jscr-2011-5-3fig1.jpg

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