Publication: Aspergilloma and Idiopathic Pulmonary Fibrosis: A Rare Coexistence.
Program
Authors
Authors
Bircan, Hacı Ahmet
Akcan, Ahmet
Advisor
Language
Type
Publisher
Journal Title
Journal ISSN
Volume Title
Abstract
Pulmonary aspergilloma (mycetoma) usually is a saprophytic fungal infection due to aspergillus species which is colonized and grows into pre-existing cystic/ cavitary lesions resulting from pulmonary tuberculosis or fibrotic sarcoidosis, or other fibro-cavitary diseases including interstitial lung diseases. Idiopathic pulmonary fibrosis (IPF) is a rare, chronic, progressive fibrotic lung disease, characterized by the histological pattern of usual interstitial pneumonia. Heavy smoker, diabetic, a 69-year-old male patient was admitted to our clinic with complaints of dry cough, fever, dyspnea on exertion and weight loss. The diagnosis was made as coexisting of pulmonary aspergilloma and IPF according to findings on HRCT. Hereby, we wanted to present this rare case regarding of coexisting of the development of Aspergillus infection and idiopathic pulmonary fibrosis in the light of the literature.
Description
Source:
Keywords:
Keywords
Citation
Bircan H. A. , Akcan A., -Aspergilloma and Idiopathic Pulmonary Fibrosis: A Rare Coexistence.-, Süleyman Demirel Üniversitesi Tıp Fakültesi Dergisi, cilt.28, sa.2, ss.351-354, 2021