Development of Dermatomyositis after Pfizer BioNTeh COVID-19 Vaccine: A Case Report.

IF 1.1 Q4 PHARMACOLOGY & PHARMACY Current drug safety Pub Date : 2024-01-01 DOI:10.2174/1574886318666230614164607
Imen Aouintia, Wiem Daly, Ghozlane Lakhoua, Widd Kaabi, Ons Charfi, Sana Debbeche, Sarrah Kastalli, Ahmed Zaiem, Sihem El Aidli
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Abstract

Introduction: The Coronavirus Disease 2019 (COVID-19) pandemic led to the fast development of vaccines, which is considered a medical advance in healthcare. With the extensive vaccination campaign performed worldwide, many adverse events following immunization (AEFI) were reported. Most of them were flu-like symptoms, mild and self-limiting. However, serious adverse events, such as dermatomyositis (DM), an idiopathic autoimmune connective tissue disease, have also been reported.

Case presentation: In this report, we describe a case of skin erythema, edema, and diffuse myalgia attributed at first to Pfizer BioNTeh, COVID-19 vaccination, given the temporal relationship and the absence of significant medical history. The causality assessment score was I1B2. However, after completing the etiological assessment, an invasive breast carcinoma was identified, and we retained the diagnosis of paraneoplastic DM.

Conclusion: This study underlines the importance of completing the etiological assessment before attributing any adverse reaction to vaccination to maintain optimal patient care.

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辉瑞 BioNTeh COVID-19 疫苗引发皮肌炎:病例报告。
导言:2019 年冠状病毒病(COVID-19)大流行促使疫苗迅速发展,这被认为是医疗保健领域的一大进步。随着全球范围内广泛开展疫苗接种活动,许多免疫接种后不良事件(AEFI)被报道出来。其中大多数是类似流感的症状,症状轻微且有自限性。但也有严重不良事件的报道,如皮肌炎(DM),这是一种特发性自身免疫性结缔组织疾病:在本报告中,我们描述了一例皮肤红斑、水肿和弥漫性肌痛病例,考虑到时间关系和无重要病史,起初将其归因于辉瑞 BioNTeh COVID-19 疫苗接种。因果关系评估得分为 I1B2。然而,在完成病因评估后,发现了浸润性乳腺癌,我们保留了副肿瘤性 DM 的诊断:本研究强调了在将任何不良反应归因于疫苗接种之前完成病因学评估的重要性,以保持对患者的最佳护理。
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来源期刊
Current drug safety
Current drug safety PHARMACOLOGY & PHARMACY-
CiteScore
2.10
自引率
0.00%
发文量
112
期刊介绍: Current Drug Safety publishes frontier articles on all the latest advances on drug safety. The journal aims to publish the highest quality research articles, reviews and case reports in the field. Topics covered include: adverse effects of individual drugs and drug classes, management of adverse effects, pharmacovigilance and pharmacoepidemiology of new and existing drugs, post-marketing surveillance. The journal is essential reading for all researchers and clinicians involved in drug safety.
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