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Triple Calamity in a Smoker: Idiopathic Pulmonary Fibrosis, Chronic Pulmonary Aspergillosis, and Lung Adenocarcinoma.

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Cureus 2026 Vol.18(1) p. e102539
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출처

PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
환자: IPF presenting with new cavitary or progressive lesions
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
He was managed with antifungal, antifibrotic, and systemic chemotherapy following a multidisciplinary discussion. This rare coexistence highlights the complex diagnostic and therapeutic challenges in patients with IPF presenting with new cavitary or progressive lesions.

Sahoo S, Patro M, Mohapatra PR, Sable M, Hallur VK, Panigrahi MK

📝 환자 설명용 한 줄

We report, to the best of our knowledge, the first case of idiopathic pulmonary fibrosis (IPF) with concomitant chronic pulmonary aspergillosis (CPA) and lung adenocarcinoma in a 62-year-old male smok

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BibTeX ↓ RIS ↓
APA Sahoo S, Patro M, et al. (2026). Triple Calamity in a Smoker: Idiopathic Pulmonary Fibrosis, Chronic Pulmonary Aspergillosis, and Lung Adenocarcinoma.. Cureus, 18(1), e102539. https://doi.org/10.7759/cureus.102539
MLA Sahoo S, et al.. "Triple Calamity in a Smoker: Idiopathic Pulmonary Fibrosis, Chronic Pulmonary Aspergillosis, and Lung Adenocarcinoma.." Cureus, vol. 18, no. 1, 2026, pp. e102539.
PMID 41769627

Abstract

We report, to the best of our knowledge, the first case of idiopathic pulmonary fibrosis (IPF) with concomitant chronic pulmonary aspergillosis (CPA) and lung adenocarcinoma in a 62-year-old male smoker. The patient presented with a dry cough for three years and intermittent hemoptysis for the last year. The radiological evaluation suggested IPF and bilateral lung masses with an air-crescent sign, which progressively increased in size. Subsequent investigations, including bronchoscopy and transthoracic biopsy, confirmed the presence of the triple calamity of IPF, CPA, and lung cancer. He was managed with antifungal, antifibrotic, and systemic chemotherapy following a multidisciplinary discussion. This rare coexistence highlights the complex diagnostic and therapeutic challenges in patients with IPF presenting with new cavitary or progressive lesions.

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