Internal Medicine
Online ISSN : 1349-7235
Print ISSN : 0918-2918
ISSN-L : 0918-2918
CASE REPORTS
Pulmonary Alveolar Proteinosis with Ulcerative Colitis
Noriho SakamotoShota NakashimaHiroshi IshimotoTomoyuki KakugawaAtsuko HaraHirokazu YuraTakuto MiyamuraSeiko NakamichiYasushi ObaseYuji IshimatsuHiroshi Mukae
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JOURNAL OPEN ACCESS

2018 Volume 57 Issue 18 Pages 2705-2708

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Abstract

A 65-year-old Japanese man was referred to our hospital for the further assessment of cough and dyspnea. He had a history of ulcerative colitis for which he was receiving treatment. Chest computed tomography showed a crazy-paving pattern. His bronchoalveolar lavage fluid had a milky appearance, and a transbronchial lung biopsy specimen revealed acellular periodic acid-Schiff stain-positive bodies. The serum anti-granulocyte macrophage-colony stimulating factor (GM-CSF) antibody titer was elevated. The diagnosis was autoimmune pulmonary alveolar proteinosis (PAP). There are few reports of autoimmune PAP in patients with ulcerative colitis. Some reports suggest that PAP and inflammatory bowel disease might have a common pathogenesis involving the anti-GM-CSF antibody.

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© 2018 by The Japanese Society of Internal Medicine
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