A Case of Bronchiolitis Interstitial Pneumonitis. |
Su Young Chi, Kyoung Ho Ryu, Dae Hun Lim, Hong Joon Shin, Hee Jung Ban, In Jae Oh, Yong Soo Kwon, Kyu Sik Kim, Sung Chul Lim, Young Chul Kim, Yoo Duk Choi, Sang Yun Song, Hyun Ju Seon |
1Department of Internal Medicine, Chonnam National University Medical School, Gwangju, Korea. yskwon@chonnam.ac.kr 2Department of Pathology, Chonnam National University Medical School, Gwangju, Korea. 3Department of Thoracic and Cardiovascular Surgery, Chonnam National University Medical School, Gwangju, Korea. 4Department of Radiology, Chonnam National University Medical School, Gwangju, Korea. |
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Abstract |
Bronchiolitis interstitial pneumonitis (BIP), an unclassified and newly described interstitial pneumonia, has a combined feature of prominent bronchiolitis, interstitial inflammation, and fibrosis. It is distinct from bronchiolitis obliterans or bronchiolitis obliterans organizing pneumonia (BOOP). BIP has a better prognosis than common cases of interstitial pneumonia. However, BIP has a poorer prognosis than BOOP. BIP's response to corticosteroids is not as successful as BOOP's response to this treatment. We encountered the case of a 31-year-old woman with BIP with an initial presentation of dyspnea and a cough that had lasted for 3 months. The patient's chest CT scan demonstrated patchy ground glass opacities and multiple ill-defined centrilobular nodules in both lungs, suggesting military tuberculosis or nontuberculous mycobacterial infection. A video-assisted thoracoscopic lung biopsy resulted in the diagnosis of BIP. Clinical symptoms, pulmonary lesions, and pulmonary function tests were improved after oral glucocorticoid therapy. |
Key Words:
Interstitial lung diseases, Bronchiolitis, Bronchiolitis obliterans |
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