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Interface in English. Medical references retain their original language; bilingual names and selected translations are provided.

中英关联术语

特发性肺纤维化

Idiopathic Pulmonary Fibrosis

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A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change.

中文名称索引;定义为 MeSH 英文原文,尚未逐条译审。MESH:D054990 · MeSH 2026。

Courtesy of the U.S. National Library of Medicine. Annual snapshot; later updates may not be reflected. NLM does not endorse this service.

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