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一名特发性腹膜后纤维化患者的纵隔纤维化

Mediastinal fibrosis in a patient with idiopathic retroperitoneal fibrosis.

作者信息

Bahler Clinton, Hammoud Zane, Sundaram Chandru

机构信息

Department of Urology, Indiana University School of Medicine, Indianapolis, Indiana, USA.

出版信息

Interact Cardiovasc Thorac Surg. 2008 Apr;7(2):336-8. doi: 10.1510/icvts.2007.166033. Epub 2008 Jan 24.

Abstract

Combined idiopathic retroperitoneal-mediastinal fibrosis is rare. We report a case of mediastinal fibrosis that followed the onset of retroperitoneal fibrosis by six years. A 61-year-old asymptomatic woman was diagnosed with idiopathic mediastinal fibrosis in December of 2006 after discovering a 1.4 cm thick prevascular mass encasing the aortic arch. In August of 2001 the patient had been diagnosed with retroperitoneal fibrosis, which was successfully treated surgically. An axillary thoracotomy found dense adhesions that fixed the arch of the aorta to the adjacent lung. Mediastinal biopsies were consistent with idiopathic fibrosis. We describe the imaging of this case and briefly review the literature.

摘要

特发性腹膜后-纵隔联合纤维化较为罕见。我们报告一例纵隔纤维化病例,该病例在腹膜后纤维化发病六年之后出现。一名61岁无症状女性于2006年12月被诊断为特发性纵隔纤维化,此前发现一个1.4厘米厚的血管前肿块包绕主动脉弓。该患者曾于2001年8月被诊断为腹膜后纤维化,已通过手术成功治疗。腋下开胸手术发现致密粘连,将主动脉弓固定于相邻肺组织。纵隔活检结果符合特发性纤维化。我们描述了该病例的影像学表现并简要回顾了相关文献。

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