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1例与使用氨氯地平相关的特发性血管性水肿罕见病例。

A Rare Case of Idiopathic Angioedema Associated With Amlodipine Use.

作者信息

Kent Nicole, Allikesam Kishan K, Ly Austin, Veerasammy Melanie, Avula Sai K

机构信息

Medicine, Alabama College of Osteopathic Medicine, Dothan, USA.

Internal Medicine, Sri Venkateswara Medical College, Tirupati, IND.

出版信息

Cureus. 2025 Jul 10;17(7):e87661. doi: 10.7759/cureus.87661. eCollection 2025 Jul.

Abstract

Angioedema is a self-limited, non-pitting edema of subcutaneous or submucosal tissues often affecting the face, lips, oral cavity, and airway. It may be histamine or bradykinin-mediated and is most commonly triggered by allergic reactions, medications, or systemic conditions. Drug-induced angioedema is frequently associated with angiotensin-converting enzyme (ACE) inhibitors, whereas calcium channel blockers (CCBs) like amlodipine are rarely implicated. This case report describes a rare case of recurrent angioedema in a hypertensive patient, ultimately attributed to amlodipine, and underscores the importance of a thorough evaluation and medication review in persistent idiopathic angioedema. A 63-year-old male patient with a history of hypertension, hyperlipidemia, and obstructive sleep apnea presented with recurrent episodes of tongue swelling and dyspnea beginning one week after the initiation of ramipril and amlodipine. Ramipril was initially suspected and discontinued, yet symptoms persisted despite multiple antihypertensive regimen changes and negative evaluations for hereditary angioedema and carcinoid syndrome. Allergy testing indicated idiopathic histaminergic angioedema, and a variety of symptomatic treatments provided limited relief. Ultimately, discontinuation of amlodipine in November 2024 resulted in the complete resolution of angioedema, with no recurrence noted over the next few months of subsequent follow-up. The Naranjo Algorithm is a structured, 10-question tool used to determine the likelihood that an adverse drug reaction (ADR) is actually caused by a specific medication. It assesses factors such as the timing of the reaction, alternative causes, drug levels, and response to dechallenge or rechallenge, which determines if an ADR is definite, probable, possible, or doubtful. Retrospective assessment using this algorithm yielded a score of 7, indicating a probable ADR. This case highlights amlodipine as a rare but important cause of drug-induced angioedema. It emphasizes the need for careful medication review in patients with unexplained, recurrent angioedema and the benefit of considering less common etiologies when standard evaluations are inconclusive. Prompt recognition and discontinuation of the offending agent can result in full resolution and prevent unnecessary morbidity.

摘要

血管性水肿是一种自限性的皮下或黏膜下组织非凹陷性水肿,常累及面部、嘴唇、口腔和气道。它可能由组胺或缓激肽介导,最常见的触发因素是过敏反应、药物或全身性疾病。药物性血管性水肿常与血管紧张素转换酶(ACE)抑制剂有关,而像氨氯地平这样的钙通道阻滞剂(CCB)很少涉及。本病例报告描述了一名高血压患者罕见的复发性血管性水肿病例,最终归因于氨氯地平,并强调了在持续性特发性血管性水肿中进行全面评估和药物审查的重要性。一名63岁男性患者,有高血压、高脂血症和阻塞性睡眠呼吸暂停病史,在开始使用雷米普利和氨氯地平一周后出现反复发作的舌肿胀和呼吸困难。最初怀疑是雷米普利并停用,但尽管多次改变抗高血压治疗方案且遗传性血管性水肿和类癌综合征的评估结果为阴性,症状仍持续存在。过敏测试显示为特发性组胺能性血管性水肿,多种对症治疗仅提供了有限的缓解。最终,2024年11月停用氨氯地平后,血管性水肿完全消退,在随后几个月的随访中未再复发。Naranjo算法是一种结构化的10个问题工具,用于确定药物不良反应(ADR)实际上是否由特定药物引起。它评估反应时间、替代原因、药物水平以及撤药或再激发反应等因素,以确定ADR是肯定、很可能、可能还是可疑。使用该算法进行回顾性评估得分为7分,表明很可能是药物不良反应。本病例突出了氨氯地平作为药物性血管性水肿罕见但重要的原因。它强调了对不明原因复发性血管性水肿患者进行仔细药物审查的必要性,以及在标准评估无定论时考虑不太常见病因的益处。及时识别并停用致病药物可实现完全缓解并预防不必要的发病。

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