手淫诱发的预震:IgG4相关疾病中的一例无痛性主动脉夹层

IF 1.9 Q2 EMERGENCY MEDICINE Clinical and Experimental Emergency Medicine Pub Date : 2024-03-15 DOI:10.15441/ceem.23.182
Charles Sanky, Nidhish Sasi
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引用次数: 0

摘要

本病例涉及一名 59 岁男性,既往有高血压、慢性肾功能不全和继发于 IgG4 相关疾病的自身免疫性胰腺炎病史,长期服用类固醇。患者在手淫时突然感到头晕、双手刺痛和下颌发紧。他被发现患有 A 型主动脉夹层。这是首例记录 IgG4 相关疾病患者非典型、无痛性主动脉夹层表现的病例。这篇文章探讨了 IgG4 相关疾病的纤维炎症后遗症如何会导致主动脉表现,并讨论了在遇到出现不典型症状的患者时考虑包括主动脉综合征在内的更广泛鉴别的重要性。
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Masturbation-Induced Presyncope: A Case of Painless Aortic Dissection in IgG4-Related Disease.

This case concerns a 59-year-old male with a past medical history of hypertension, chronic renal insufficiency, and autoimmune pancreatitis secondary to IgG4-related disease, on chronic steroids. The patient experienced acute onset of lightheadedness, a tingling sensation to both hands, and jaw tightness while masturbating. He was found to have a Type A aortic dissection. This is the first case of its kind to document an atypical, painless aortic dissection presentation in a patient with IgG4-related disease. This piece explores how fibroinflammatory sequelae of IgG4-related disease can result in aortic manifestations and discusses the importance of considering a broader differential including aortic syndrome when encountering patients presenting with atypical symptoms.

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来源期刊
CiteScore
2.80
自引率
10.50%
发文量
59
期刊最新文献
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