医学
毛细支气管炎
闭塞性细支气管炎
心脏病学
内科学
肺
呼吸系统
肺移植
出处
期刊:Chest
[Elsevier]
日期:2022-07-01
卷期号:162 (1): 179-183
标识
DOI:10.1016/j.chest.2022.02.045
摘要
Paraneoplastic autoimmune multiorgan syndrome (PAMS), also known as “paraneoplastic pemphigus,” is a rare life-threatening autoimmune disease triggered by an underlying neoplasm. It is characterized by painful erosive stomatitis and a polymorphous mucocutaneous eruption.1 A subset of patients with PAMS manifest pulmonary involvement characterized by progressive airflow obstruction related to constrictive (obliterative) bronchiolitis (also known as bronchiolitis obliterans).2
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