Khalid Nauman, Chhabra Lovely, Ahmad Sarah Aftab, Umer Affan, Spodick David H
Saint Louis University, Saint Louis, Missouri.
University of Connecticut School of Medicine, Hartford, Connecticut.
Methodist Debakey Cardiovasc J. 2015 Oct-Dec;11(4):250-252. doi: 10.14797/mdcj-11-4-250.
We describe herein a 48-year-old Caucasian woman with a history of autoimmune polyglandular syndrome type 2 who presented with pericarditis, pericardial effusion, and pericardial tamponade preceded by acute adrenal crisis in the setting of normal thyroid function. The case highlights the importance of a rare yet important complication of autoimmune polyglandular syndrome type 2 that mandates early recognition and intervention.
我们在此描述一名48岁的白种女性,她有2型自身免疫性多腺体综合征病史,在甲状腺功能正常的情况下,先出现急性肾上腺危象,随后出现心包炎、心包积液和心包填塞。该病例突出了2型自身免疫性多腺体综合征一种罕见但重要的并发症的重要性,这种并发症需要早期识别和干预。