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伪装成原发性骨肿瘤的双相性恶性胸膜间皮瘤

Biphasic Malignant Pleural Mesothelioma Masquerading as a Primary Skeletal Tumor.

作者信息

Gleason James Benjamin, Tashtoush Basheer, Diacovo Maria Julia

机构信息

Department of Pulmonary and Critical Care Medicine, Cleveland Clinic Florida, 2950 Cleveland Clinic Boulevard, Weston, FL 33331, USA.

Department of Pathology and Laboratory Medicine, Cleveland Clinic Florida, 2950 Cleveland Clinic Boulevard, Weston, FL 33331, USA.

出版信息

Case Rep Pulmonol. 2016;2016:7560929. doi: 10.1155/2016/7560929. Epub 2016 Aug 31.

Abstract

Biphasic malignant pleural mesothelioma is a rare malignant tumor, usually presenting as a pleural-based mass in a patient with history of chronic asbestos exposure. We herein report a case of a 41-year-old man who presented with chest pain and had a chest computed tomography (CT) scan suggestive of a primary skeletal tumor originating from the ribs (chondrosarcoma or osteosarcoma), with no history of asbestos exposure. CT-guided core needle biopsies were diagnosed as malignant sarcomatoid mesothelioma. Surgical resection and chest wall reconstruction were performed, confirming the diagnosis and revealing a secondary histologic component (epithelioid), supporting the diagnosis of biphasic malignant mesothelioma.

摘要

双相性恶性胸膜间皮瘤是一种罕见的恶性肿瘤,通常表现为有慢性石棉接触史患者的胸膜肿块。我们在此报告一例41岁男性,他因胸痛就诊,胸部计算机断层扫描(CT)显示提示为起源于肋骨的原发性骨肿瘤(软骨肉瘤或骨肉瘤),无石棉接触史。CT引导下的粗针活检诊断为恶性肉瘤样间皮瘤。进行了手术切除和胸壁重建,进一步证实了诊断,并发现了次要组织学成分(上皮样),支持双相性恶性胸膜间皮瘤的诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0851/5021854/5743304c7461/CRIPU2016-7560929.001.jpg

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