[Diffuse interstitial lung disease and connective tissue diseases: study of seven cases in Dakar].

Dakar medical Pub Date : 2008-01-01
S Diallo, D Dia, S Fall, Ad Kâne, M Sané, M Thiam, A Pouye, P S Mbaye, M M Kâ, T Moréira-Diop
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引用次数: 0

Abstract

Introduction: The diagnosis of diffuse interstitial lung disease non specific in connective tissue disease is difficult because of many differential diagnoses. Lung involvement can affect functional or vital prognosis. We report 7 cases.

Cases: We collected data from 60 years old mean patients. Pulmonary localisation was diagnosed after 19 years of evolution of the auto-immune disease. Discovering circumstances were dyspnea and chronic cough. The radiographic and scannographic signs were diffuse because of long diagnosis delay. The underlying auto immune disease was scleroderma, rheumatoid arthritis, Sjögren's syndrome, ankylosing spondylitis, Sharp's syndrome, and multiple autoimmune syndrome. The main treatment was corticosteroids and respiratory physiotherapy.

Conclusion: Throughout these 7 cases we discuss clinical, radiological and evolutive aspects and we focus on the need of early diagnosis for a better prognosis.

[弥漫间质性肺病和结缔组织病:达喀尔7例研究]。
弥漫性间质性肺疾病非特异性结缔组织病的诊断困难,因为许多鉴别诊断。肺部受累可影响功能或生命预后。我们报告了7例。病例:我们收集了60岁平均患者的数据。经过19年自身免疫性疾病的发展,肺部定位被诊断出来。发现情况为呼吸困难和慢性咳嗽。由于诊断延误时间长,影像学和扫描征象呈弥漫性。潜在的自身免疫性疾病是硬皮病、类风湿性关节炎、Sjögren综合征、强直性脊柱炎、夏普综合征和多发性自身免疫性综合征。主要治疗方法为皮质类固醇和呼吸物理治疗。结论:在这7例病例中,我们讨论了临床、放射学和进化方面的问题,并强调早期诊断的必要性,以获得更好的预后。
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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