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复发性多软骨炎伴严重主动脉瓣关闭不全。

Relapsing polychondritis with severe aortic insufficiency.

作者信息

Manna R, Annese V, Ghirlanda G, Pennestri F, Greco A V, Pala M A, Bochicchio G B, Magaro M

出版信息

Clin Rheumatol. 1985 Dec;4(4):474-80. doi: 10.1007/BF02031904.

Abstract

Relapsing polychondritis (RP) is a rare disease characterized by auricular, nasal and respiratory tract chondritis, ocular inflammation, inflammatory polyarthritis and cardiovascular abnormalities. Here we describe a patient with a five-year history of mild nasal and auricular chondritis, which suddenly developed into a severe aortic insufficiency with rest dyspnea. The pathogenesis and the management of this rare connective tissue disease are discussed.

摘要

复发性多软骨炎(RP)是一种罕见疾病,其特征为耳廓、鼻和呼吸道软骨炎、眼部炎症、炎性多关节炎以及心血管异常。在此,我们描述一名有五年轻度鼻和耳廓软骨炎病史的患者,其突然发展为伴有静息呼吸困难的严重主动脉瓣关闭不全。本文讨论了这种罕见结缔组织病的发病机制及治疗。

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