[Diagnostic and therapeutic difficulties in mediastinal fibromatosis. Case report].

Małgorzata Edyta Wojtyś, Jacek Alchimowicz, Piiotr Waloszczyk, Norbert Wójcik, Tomasz Grodzki
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引用次数: 0

Abstract

Mediastinal fibromatosis is a very rare mesenchymal tumor originated from fibrous tissue. A case of 26-year old men with mediastinal tumor causes respiratory insufficiency and dysphagia is described. This sympthoms occured due to esophageal impression and infiltration with occlusion of main left bronchus by mediastinal tumor. Ethiology of the tumor was established based on histopathology assesment of the tissue samples taken during explorative thoracotomy after 3 years and many other diagnostic procedures undertaken. The authors describe difficulties in diagnosis of mediastinal tumors, especially those rare observed.

纵隔纤维瘤病的诊断和治疗难点。病例报告)。
摘要纵隔纤维瘤病是一种罕见的起源于纤维组织的间质肿瘤。本文报告一例26岁男性纵隔肿瘤导致呼吸功能不全及吞咽困难。这种症状是由于纵隔肿瘤阻塞左主支气管的食道压迫和浸润所致。肿瘤的病理学是基于3年后探查性开胸术中组织样本的组织病理学评估和许多其他诊断程序而建立的。作者描述了诊断纵隔肿瘤的困难,特别是那些罕见的观察。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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