医学
结节性多动脉炎
网状利维多
坏死性血管炎
病理
血管炎
支气管肺泡灌洗
肺
肺活检
系统性血管炎
活检
内科学
疾病
作者
Hiroshi Ishii,Yoshinori Kawabata,Hiroaki Oka,Kosaku Komiya,Atsuko Iwata,Jun‐ichi Kadota
出处
期刊:The journal of the Japanese Respiratory Society
日期:2011-04-01
卷期号:49 (4): 298-303
摘要
Abstract A 71-year-old man was admitted due to persistent pyrexia of over 2 weeks duration, dry cough, and chest computed tomographic (CT) findings of interstitial pneumonia. On admission, his body temperature was 38.0 degrees C, and there was mild livedo reticularis observed on the trunk and skin of the extremities. Fine crackles were detected in the lower lung fields. Laboratory examinations showed high levels of an inflammatory reaction and a positive rheumatoid factor, but the findings were negative for any other autoantibodies, including the antineutrophil cytoplasmic antibody. His bronchoalveolar lavage fluid revealed an increase in CD4+ lymphocytes. A biopsy specimen of the abdominal skin showed necrotizing vasculitis of the muscular arteries. Lung biopsy specimens showed necrotizing and granulomatous vasculitis of the pulmonary arteries in the usual interstitial pneumonia pattern, with numerous lymphoid follicles. Therefore, a diagnosis of polyarteritis nodosa was clinically and pathologically established. This case of interstitial pneumonia associated with polyarteritis nodosa was difficult to discriminate from microscopic polyarteritis.
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