A case of pediatric serum sickness like reaction (SSLR) after a 2-month re-exposure to amoxicillin.

IF 2.6 4区 医学 Q2 ALLERGY
Devyani Bakshi, Xinxin Tang, Susan Waserman
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引用次数: 0

Abstract

Background: Serum-sickness like reactions (SSLRs) to amoxicillin have been documented in the medical literature. Beta-lactams are important and commonly used medications especially in the pediatric population. Often, SSLRs present within days of and during first exposure/ingestion to the offending agent. We described a unique case of a 4-year-old boy who presented with symptoms of amoxicillin SSLR following his second course of amoxicillin with only 2 months and 10 days between his second and first course.

Case presentation: A 4-year-old boy presented to hospital with a pruritic rash on day 7 of a 10-day course of amoxicillin for otitis media accompanied by fever (38.7 degrees Celsius). On day 7 of his second course of amoxicillin, which was separated from his first course by only 2 months and 10 days, his mother noticed erythematous, raised, pruritic lesions with central clearing on his sternum. He presented to the ED with emesis, progression of the rash to his torso, back, legs, and face, hypotension, angioedema, and joint pain. His bloodwork demonstrated a leukocytosis of 18.6 × 109 g/L with neutrophilic predominance and thrombocytosis with a platelet count of 653 × 109 g/L. He was treated with 5 mg oral cetirizine daily and 1 mg/kg oral prednisone which improved his rash and angioedema. He was managed with up to 4 times the usual dose of cetirizine. He was assessed in our outpatient clinic as an outpatient and penicillin skin testing was unremarkable. A diagnosis of a probable SSLR to amoxicillin was made.

Conclusion: We report an unusual presentation of SSLR following re-exposure to amoxicillin. Our case highlights that patients with previous asymptomatic exposure to amoxicillin can develop SSLR with repeat exposure. Although it is not uncommon for children to develop amoxicillin SSLRs after previous exposure to the drug, this case is unique because of its short time course of 2 months and 10 days months between drug courses. Penicillins are commonly used in the pediatric population. Therefore, it is important to correctly characterize adverse drug reactions to broaden our understanding of SSLRs, prevent unnecessary avoidance of the triggering agent, and improve patient management.

一例再次接触阿莫西林两个月后出现的小儿血清病样反应(SSLR)。
背景:阿莫西林引起的类似血清病反应(SSLR)在医学文献中已有记载。β-内酰胺类药物是重要的常用药物,尤其是在儿童群体中。通常情况下,SSLR 会在首次接触/摄入违禁药物的几天内出现。我们描述了一例独特的病例,一名 4 岁男孩在服用阿莫西林第二个疗程后出现阿莫西林 SSLR 症状,而第二个疗程与第一个疗程之间仅相隔 2 个月零 10 天:一名 4 岁男孩在服用阿莫西林治疗中耳炎 10 天疗程后的第 7 天出现瘙痒性皮疹,并伴有发烧(38.7 摄氏度)。他的第二个阿莫西林疗程与第一个疗程相隔仅 2 个月零 10 天,在第二个疗程的第 7 天,他的母亲发现他的胸骨上出现了红斑、隆起、瘙痒性皮损,中央清亮。他因呕吐、皮疹扩展到躯干、背部、腿部和脸部、低血压、血管性水肿和关节疼痛而来到急诊室。他的血常规显示白细胞增多为 18.6 × 109 g/L,其中中性粒细胞占多数,血小板增多,血小板计数为 653 × 109 g/L。他每天口服 5 毫克西替利嗪和 1 毫克/千克口服泼尼松,皮疹和血管性水肿症状有所改善。他服用的西替利嗪剂量是平时的 4 倍。我们在门诊对他进行了评估,青霉素皮试结果无异常。诊断结果为阿莫西林可能引起的 SSLR:结论:我们报告了一起再次接触阿莫西林后出现 SSLR 的不寻常病例。我们的病例突出表明,以前无症状接触过阿莫西林的患者在再次接触后可能会出现 SSLR。虽然以前接触过阿莫西林的儿童发生阿莫西林 SSLR 的情况并不少见,但本病例的独特之处在于其病程短,仅为 2 个月,且两个疗程之间相隔 10 天。青霉素类是儿科常用药物。因此,正确描述药物不良反应的特征对于拓宽我们对 SSLR 的认识、防止不必要地避免使用诱发药物以及改善患者管理非常重要。
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来源期刊
CiteScore
4.30
自引率
3.70%
发文量
96
审稿时长
12 weeks
期刊介绍: Allergy, Asthma & Clinical Immunology (AACI), the official journal of the Canadian Society of Allergy and Clinical Immunology (CSACI), is an open access journal that encompasses all aspects of diagnosis, epidemiology, prevention and treatment of allergic and immunologic disease. By offering a high-visibility forum for new insights and discussions, AACI provides a platform for the dissemination of allergy and clinical immunology research and reviews amongst allergists, pulmonologists, immunologists and other physicians, healthcare workers, medical students and the public worldwide. AACI reports on basic research and clinically applied studies in the following areas and other related topics: asthma and occupational lung disease, rhinoconjunctivitis and rhinosinusitis, drug hypersensitivity, allergic skin diseases, urticaria and angioedema, venom hypersensitivity, anaphylaxis and food allergy, immunotherapy, immune modulators and biologics, immune deficiency and autoimmunity, T cell and B cell functions, regulatory T cells, natural killer cells, mast cell and eosinophil functions, complement abnormalities.
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