A Case of Tegafur-Uracil-Induced Interstitial Lung Disease Presenting as Hypersensitivity Pneumonitis

This report describes the case of a 77-year-old man undergoing chemotherapy for synchronous lung cancer and rectal cancer. After receiving tegafur-uracil (UFT) plus leucovorin in combination with bevacizumab for rectal cancer, he developed exertional dyspnea. Chest computed tomography revealed diffuse bilateral centrilobular nodules and ground-glass opacities, suggesting a hypersensitivity pneumonia (HP) pattern of drug-induced interstitial lung disease (DI-ILD), and he was therefore admitted for further evaluation and treatment. Bronchoalveolar lavage demonstrated an increased lymphocyte fraction with a decreased CD4/CD8 ratio, and a drug-induced lymphocyte stimulation test was positive only for UFT. Based on the clinical course and these findings, the patient was diagnosed with UFT-induced interstitial lung disease. His respiratory condition improved rapidly following corticosteroid therapy. DI-ILD associated with UFT is rare, and to the best of our knowledge, no previous reports have described an HP pattern on imaging. We therefore report this case with a review of the relevant literature.

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Publication Details

Journal
Cureus
Published
2026-02-16
DOI
https://doi.org/10.7759/cureus.103741
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
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article

A Case of Tegafur-Uracil-Induced Interstitial Lung Disease Presenting as Hypersensitivity Pneumonitis

Takumi Kiwamoto, Manato Taguchi, Kai Kawashima, Nobuyuki Hizawa et al.
Cureus
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
article

A Case of Tegafur-Uracil-Induced Interstitial Lung Disease Presenting as Hypersensitivity Pneumonitis

Takumi Kiwamoto, Manato Taguchi, Kai Kawashima, Nobuyuki Hizawa, Kazuhumi Yoshida
article en

Abstract

This report describes the case of a 77-year-old man undergoing chemotherapy for synchronous lung cancer and rectal cancer. After receiving tegafur-uracil (UFT) plus leucovorin in combination with bevacizumab for rectal cancer, he developed exertional dyspnea. Chest computed tomography revealed diffuse bilateral centrilobular nodules and ground-glass opacities, suggesting a hypersensitivity pneumonia (HP) pattern of drug-induced interstitial lung disease (DI-ILD), and he was therefore admitted for further evaluation and treatment. Bronchoalveolar lavage demonstrated an increased lymphocyte fraction with a decreased CD4/CD8 ratio, and a drug-induced lymphocyte stimulation test was positive only for UFT. Based on the clinical course and these findings, the patient was diagnosed with UFT-induced interstitial lung disease. His respiratory condition improved rapidly following corticosteroid therapy. DI-ILD associated with UFT is rare, and to the best of our knowledge, no previous reports have described an HP pattern on imaging. We therefore report this case with a review of the relevant literature.

CureusVol. 18(2)
University of Tsukuba (JP)
Good health and well-being
Openalex Percentile: Top 54%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
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