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家族性地中海热并发大量心包填塞

Familial Mediterranean Fever Complicated By Massive Cardiac Tamponade.

作者信息

Melo Lara, Patail Haris, Gautam Garima, Braish Julie, Ozimek David

机构信息

Internal Medicine, University of Connecticut Health, Farmington, USA.

Leukemia, MD Anderson Cancer Center, Houston, USA.

出版信息

Cureus. 2023 Dec 7;15(12):e50137. doi: 10.7759/cureus.50137. eCollection 2023 Dec.

Abstract

Familial Mediterranean fever (FMF) is a hereditary, autosomal recessive auto-inflammatory disorder characterized by recurrent attacks of fever and serositis. While arthritis, pleuritis, peritonitis, and pericarditis are common in FMF, large pericardial effusions with cardiac tamponade as a sequelae of FMF are considered rare.  We report a case of an 83-year-old female with a history of FMF who presented with chest pain. She was found to have acute pericarditis complicated by hemodynamically significant pericardial tamponade that was subsequently treated with an urgent pericardiocentesis followed by colchicine.

摘要

家族性地中海热(FMF)是一种遗传性常染色体隐性自身炎症性疾病,其特征为反复发热和浆膜炎发作。虽然关节炎、胸膜炎、腹膜炎和心包炎在FMF中很常见,但作为FMF后遗症的伴有心脏压塞的大量心包积液被认为很罕见。我们报告一例83岁有FMF病史的女性,她因胸痛就诊。发现她患有急性心包炎并伴有血流动力学显著的心包压塞,随后接受了紧急心包穿刺术并服用秋水仙碱进行治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/517a/10771347/dbb033f3bdf0/cureus-0015-00000050137-i01.jpg

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