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隐源性纤维性肺泡炎的预后

The prognosis of cryptogenic fibrosing alveolitis.

作者信息

Stack B H, Choo-Kang Y F, Heard B E

出版信息

Thorax. 1972 Sep;27(5):535-42. doi: 10.1136/thx.27.5.535.

Abstract

The course of cryptogenic fibrosing alveolitis (CFA) in 96 patients is described. The mean survival from the onset of the first symptom until death was 47·4 months in all the 59 fatal cases, 49·6 months in those dying from CFA only, and 48·4 months in those dying from CFA in whom the course of the illness was not influenced by corticosteroids. There was a wide variation in the natural course of the disorder, varying from death within a year of the onset of symptoms in five patients to prolonged survival with slow or arrested progress in four patients not treated with corticosteroids. Most patients died from CFA but five developed bronchial carcinoma and two died after lung biopsy. The main factor influencing the prognosis was the effectiveness of corticosteroid drugs. Only 16% of the treated patients had a worthwhile (grade 2) response to these drugs and the five-year survival of this group was 67%. In those patients in whom the course of the illness was uninfluenced by corticosteroids the five-year survival rate was only 20%. The histological appearances on lung biopsy gave a rough guide to the likely effect of corticosteroid therapy. Other factors influencing the prognosis were the degree of dyspnoea on presentation, the vital capacity, and the presence of arterial hypoxaemia. Patients who had had symptoms for more than four years before the first hospital attendance had a relatively good prognosis. By contrast, neither the extent of radiographic abnormality nor the presence of circulating rheumatoid and antinuclear factors influenced subsequent survival.

摘要

本文描述了96例隐源性纤维性肺泡炎(CFA)患者的病程。在59例死亡病例中,从首次出现症状到死亡的平均生存期为47.4个月,仅死于CFA的患者为49.6个月,疾病进程未受皮质类固醇影响、死于CFA的患者为48.4个月。该疾病的自然病程差异很大,5例患者在症状出现后1年内死亡,4例未接受皮质类固醇治疗的患者生存期延长,病情进展缓慢或停滞。大多数患者死于CFA,但5例发生支气管癌,2例在肺活检后死亡。影响预后的主要因素是皮质类固醇药物的疗效。仅16%的接受治疗的患者对这些药物有显著(2级)反应,该组患者的五年生存率为67%。在疾病进程未受皮质类固醇影响的患者中,五年生存率仅为20%。肺活检的组织学表现可为皮质类固醇治疗的可能效果提供大致指导。其他影响预后的因素包括就诊时的呼吸困难程度、肺活量和动脉血氧不足的存在。首次就诊前有症状超过4年的患者预后相对较好。相比之下,影像学异常的程度以及循环中类风湿因子和抗核因子的存在均不影响后续生存。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf32/470541/e96d24456ffc/thorax00125-0027-a.jpg

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