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原发性胸膜上皮样血管内皮瘤压迫心肌。

Primary pleural epithelioid hemangioendothelioma compressing the myocardium.

作者信息

Yu Lei, Gu Tianxiang, Xiu Zongyi, Shi Enyi, Zhao Xiaoqi

机构信息

Department of Cardiac Surgery, The First Affiliated Hospital of China Medical University, Shenyang, P.R. China.

出版信息

J Card Surg. 2013 May;28(3):266-8. doi: 10.1111/jocs.12094. Epub 2013 Apr 1.

Abstract

Epithelioid haemangioendothelioma (EH) is a rare malignant tumor of vascular origin that usually arises in bone, liver, soft tissue, or lung. EH originating in the pleura has been less frequently described. We describe an uncommon case of pleural EH compressing the myocardium in a 39-year-old woman. The patient was diagnosed with pleural EH confirmed by surgery and immunohistochemistry. She sustained stable disease 14 months after the diagnosis and her symptoms improved after systemic chemotherapy with carboplatine and etoposide. Complete surgical excision of pleural EH followed chemotherapy may prolong survival.

摘要

上皮样血管内皮瘤(EH)是一种罕见的血管源性恶性肿瘤,通常发生于骨骼、肝脏、软组织或肺部。起源于胸膜的EH较少见。我们描述了一例39岁女性胸膜EH压迫心肌的罕见病例。该患者经手术及免疫组化确诊为胸膜EH。诊断后14个月病情稳定,经卡铂和依托泊苷全身化疗后症状改善。化疗后完整切除胸膜EH可能延长生存期。

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