水痘带状疱疹病毒引发成人过敏性紫癜1例报告

IF 1.1 Q4 INFECTIOUS DISEASES
IDCases Pub Date : 2025-01-01 DOI:10.1016/j.idcr.2025.e02174
Kevin Chung , Natasha Priya Dyal , Sandhya Nagarakanti
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引用次数: 0

摘要

本病例报告强调了一名37岁的女性,她在出现癫痫发作、精神状态改变和弥漫性点疹以及腹股沟附近的水疱性病变后被转移到亚利桑那州的梅奥诊所接受治疗。她接受了广谱抗菌药物治疗。脑脊液检测显示淋巴细胞增多和蛋白水平升高,PCR检测证实水痘带状疱疹病毒(VZV)感染。脑部MRI显示慢性微出血,表明播散性VZV继发血管炎。皮肤科会诊和随后的皮肤病变活检显示白细胞分裂性血管炎伴IgA沉积,与过敏性紫癜(HSP)一致。从皮疹中提取的vzv阳性PCR进一步证实了诊断。该病例是首次报道的VZV诱导成人热休克病例。虽然该患者没有HSP并发症,但在某些情况下,早期识别和有针对性的治疗是必要的,以防止病情恶化。这个病例强调了维持广泛的鉴别诊断的重要性,以及活检病变对迅速识别高危患者不常见情况的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Varicella zoster virus triggering Henoch–Schonlein Purpura in an adult: A case report
This case reports highlights a 37-year-old woman who was transferred to Mayo Clinic Arizona for care after development of seizures, altered mental status, and a diffuse petechial rash, along with vesicular lesions near the groin. She received broad-spectrum antimicrobial therapy. CSF testing showed lymphocytic pleocytosis and elevated protein levels, and PCR testing confirmed varicella zoster virus (VZV) infection. MRI of the brain demonstrated chronic microhemorrhages, indicative of vasculitis secondary to disseminated VZV. Dermatology consultation and subsequent biopsy of the skin lesions revealed leukocytoclastic vasculitis with IgA deposition, consistent with Henoch-Schonlein Purpura (HSP). A VZV-positive PCR from the rash further corroborated the diagnosis. This case highlights the first reported instance of VZV induced HSP in an adult. Although this patient had no complications from HSP, early recognition and targeted treatment are necessary in some cases to prevent severe conditions. This case underscores the importance of maintaining a broad differential diagnosis and the importance of biopsy lesions for prompt recognition of uncommon conditions in high-risk patients.
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来源期刊
IDCases
IDCases INFECTIOUS DISEASES-
CiteScore
2.60
自引率
6.70%
发文量
300
审稿时长
10 weeks
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