Aspergilloma Coexisting With Idiopathic Pulmonary Fibrosis: A Rare Clinical Entity

被引:0
作者
Athish, K. K. [1 ]
Guruprasad, T. J. [2 ]
Padmanabha, Spurthy [3 ]
Harshitha, K. R. [3 ]
机构
[1] Sri Devaraj Urs Acad Higher Educ & Res, Internal Med, Kolar, India
[2] Sri Devaraj Urs Acad Higher Educ & Res, Resp Med, Kolar, India
[3] Sri Devaraj Urs Acad Higher Educ & Res, Pulmonol, Kolar, India
关键词
interstitial lung disease; usual interstitial pneumonia (uip); traction bronchiectasis; cystic bronchiectasis; idiopathic pulmonary fibrosis; pulmonary aspergilloma;
D O I
10.7759/cureus.59323
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aspergilloma also known as fungal ball or mycetoma, is a saprophytic mycotic infection caused by Aspergillus species which usually colonizes pre-existing cavitary or cystic lesions in the lung. Here, we have a rare case of idiopathic pulmonary fibrosis (IPF) with bilateral bronchiectasis complicated by aspergilloma. Although the existence of aspergilloma is common in pre-existing lung cavities, its coexistence in patients with IPF is a rarity, and the incidence of such cases in the literature remains sparse. Here is an interesting case report of aspergilloma co -existing with IPF. This article comprehensively analyzes the existing literature depicting similar associations and the possible etiology for the development of aspergilloma in patients with IPF.
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