尼日利亚一例继发于特发性肺纤维化的肺源性心脏病罕见病例。
A rare case of cor pulmonale secondary to idiopathic pulmonary fibrosis in Nigeria.
作者信息
Anakwue Raphael Chinedu, Chijioke Chioli Paschal, Iloanusi Nneka Ifeyinwa
机构信息
Department of Medicine, University of Nigeria Teaching Hospital, Enugu, Nigeria.
出版信息
BMJ Case Rep. 2011 Jun 29;2011:bcr0420114061. doi: 10.1136/bcr.04.2011.4061.
Abstract
Idiopathic pulmonary fibrosis (IPF) is a rarely reported disease in Nigeria. Cor pulmonale, one of the complications of this type of diffuse parenchymal lung disease is even rarer. The authors present a Nigerian patient with IPF with a classical high-resolution CT features, managed in our centre together with associated problems.
摘要
特发性肺纤维化（IPF）在尼日利亚是一种鲜有报道的疾病。肺心病作为这类弥漫性实质性肺病的并发症之一，更为罕见。本文作者介绍了一名具有典型高分辨率CT特征的尼日利亚IPF患者，该患者在我们中心接受治疗，同时伴有相关问题。
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