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缬沙坦诱发血管性水肿1例罕见病例。

A Rare Case of Valsartan-Induced Angioedema.

作者信息

Abadir Sandra, Ipalawatte Harendra, Takher Jasprit

机构信息

Internal Medicine, Los Robles Regional Medical Center, Thousand Oaks, USA.

出版信息

Cureus. 2025 Jun 9;17(6):e85623. doi: 10.7759/cureus.85623. eCollection 2025 Jun.

DOI:10.7759/cureus.85623
PMID:40636633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12240215/
Abstract

Angioedema of the face and neck is a rare but potentially life-threatening condition induced by angiotensin-converting enzyme (ACE) inhibitors. While ACE inhibitors are commonly implicated, recent reports suggest angiotensin II receptor blockers (ARBs) may also trigger angioedema. This case report highlights the development of angioedema in a patient on valsartan, an ARB, emphasizing the importance of recognizing ARBs as a potential cause of this condition, even in patients with no prior history of swelling. A 77-year-old male with coronary artery disease, hypertension, and type 2 diabetes presented to the emergency department with sudden-onset tongue swelling and difficulty breathing. The patient had been on valsartan for several years without any prior episodes of swelling. Upon examination, he had significant tongue swelling, and multiple hemorrhagic blisters were observed. Laboratory results indicated mild inflammation and C1 esterase inhibitor levels were normal, supporting a diagnosis of non-hereditary angioedema. Treatment included steroids, epinephrine, and diphenhydramine. Valsartan was discontinued and replaced with nifedipine. The patient improved, and the swelling resolved without airway obstruction. This case underscores the need for heightened awareness of angioedema induced by ARBs like valsartan. Early recognition and discontinuation of the offending medication are key to successful management. In drug-induced angioedema without airway compromise, supportive care is typically sufficient, and the condition is self-limiting. Proper identification of the cause and timely intervention are crucial to avoid life-threatening complications.

摘要

面部和颈部血管性水肿是一种由血管紧张素转换酶(ACE)抑制剂引起的罕见但可能危及生命的疾病。虽然ACE抑制剂通常是引发因素,但最近的报告表明血管紧张素II受体阻滞剂(ARB)也可能引发血管性水肿。本病例报告强调了一名服用ARB缬沙坦的患者发生血管性水肿的情况,强调了即使在没有既往肿胀病史的患者中,认识到ARB是这种疾病的潜在病因的重要性。一名77岁男性,患有冠状动脉疾病、高血压和2型糖尿病,因突发舌肿胀和呼吸困难就诊于急诊科。该患者服用缬沙坦数年,之前没有任何肿胀发作史。检查时,他的舌头明显肿胀,观察到多个出血性水疱。实验室结果显示有轻度炎症,C1酯酶抑制剂水平正常,支持非遗传性血管性水肿的诊断。治疗包括使用类固醇、肾上腺素和苯海拉明。停用缬沙坦,换用硝苯地平。患者病情好转,肿胀消退,未出现气道梗阻。本病例强调了提高对缬沙坦等ARB引起的血管性水肿认识的必要性。早期识别并停用致病药物是成功治疗的关键。在无气道受累的药物性血管性水肿中,支持性治疗通常就足够了,这种情况是自限性的。正确识别病因并及时干预对于避免危及生命的并发症至关重要。

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