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对类固醇或细胞毒性疗法无反应的脱屑性纤维性肺泡炎。

Desquamative fibrosing alveolitis unresponsive to steroid or cytotoxic therapy.

作者信息

Barnes S E, Godfrey S, Millward-Sadler G H, Roberton N R

出版信息

Arch Dis Child. 1975 Apr;50(4):324-7. doi: 10.1136/adc.50.4.324.

Abstract

A case of desquamative fibrosing alveolitis beginning in early infancy is described. The disease was characterized by tachypnoea, hypoxia relieved by O2, absence of signs in the chest or clubbing, and radiological and physiological evidence of hyperinflation. The diagnosis was made by needle biopsy of the lung. Treatment with steroids and immunosuppression was without effect and the infant died at 9 months. The disease has a high mortality in infancy, only 2 out of 9 reported cases having survived. The difference from the usual course in adults and older children is noted.

摘要

本文描述了一例始于婴儿早期的脱屑性纤维性肺泡炎病例。该疾病的特征为呼吸急促、吸氧可缓解的低氧血症、胸部无体征或杵状指,以及影像学和生理学上的肺过度充气证据。通过肺穿刺活检做出诊断。使用类固醇和免疫抑制治疗无效,患儿于9个月时死亡。该疾病在婴儿期死亡率很高,9例报告病例中仅有2例存活。文中指出了其与成人及大龄儿童常见病程的差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/852b/1544432/96e1f27c615e/archdisch00842-0083-a.jpg

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