以气道为中心的间质纤维化:一种不寻常的表现。

The Indian journal of chest diseases & allied sciences Pub Date : 2022-11-17 DOI:10.5005/ijcdas-58-2-139

Prajay Lunia, V. Karkhanis, G. Amonkar, J. Joshi

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摘要

以气道为中心的间质性纤维化(ACIF)是一种组织学类型罕见的间质性肺疾病(ILDs)。其特点是主要气道受累，伴有小叶中心纤维化、细支气管周围皮化生和细支气管中心炎性改变。我们报告一例女性患者，其表现为气胸和中枢性尿囊症，经肺活检诊断为ACIF。

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Airway-centered Interstitial Fibrosis: An Unusual Presentation.

Airway-centered interstitial fibrosis (ACIF) is described as one of the interstitial lung diseases (ILDs) with rare histologic patterns. It is characterised by predominant airway involvement with centrilobular fibrosis, peribronchiolar metaplasia and bronchiolocentric inflammatory changes. We report the case of a female who presented with pneumothorax and central diabetes insipidus, diagnosed as ACIF on lung biopsy.

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The Indian journal of chest diseases & allied sciences

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