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一名携带因子V莱顿杂合突变的女孩患爱泼斯坦-巴尔病毒相关皮肤坏死性血管炎

Epstein-Barr virus-related cutaneous necrotizing vasculitis in a girl heterozygous for factor V Leiden.

作者信息

Guerriero Cristina, Moretta Gaia, Bersani Giulia, Valentini Piero, Gatto Antonio, Rigante Donato

机构信息

Institute of Dermatology, Catholic University of Sacred Heart, Rome, Italy.

Institute of Pediatrics, Catholic University of Sacred Heart, Rome, Italy.

出版信息

J Dermatol Case Rep. 2017 Dec 1;11(2):25-28. doi: 10.3315/jdcr.2017.1245.

Abstract

BACKGROUND

Necrotizing vasculitides are basically characterized by vessel wall neutrophil infiltration and necrosis and they can occur as a primary process or secondary to an underlying disease. Although Henoch-Schönlein purpura (HSp) is the more frequent primary vasculitis in childhood, sometimes it has to be distinguished from other secondary vasculitides induced by infections, drugs, vaccines, or immune-mediated disorders.

MAIN OBSERVATIONS

We report a case of a 14-year-old girl with cutaneous necrotizing vasculitis, appearing in the course of acute Epstein-Barr virus infection. Physical examination revealed highly aching erythematous-purple lesions with reticular edges localized on the back of feet. Pain was non-responsive to ibuprofen and required administration of tapentadol and pregabalin. The patient was also heterozygous for factor V Leiden that might have contributed to the development of cutaneous painful lesions.

CONCLUSIONS

To our knowledge this is the first documented pediatric case of necrotizing vasculitis associated with acute EBV infection in a girl heterozygous for factor V Leiden. In this patient the severity of skin manifestations might have been influenced by the concomitant factor V Leiden, which gave rise to hypercoagulability and occlusive vasculopathy with markedly severe pain, a symptom rather infrequent in other childhood vasculitides.

摘要

背景

坏死性血管炎的基本特征是血管壁中性粒细胞浸润和坏死,可作为原发性疾病出现,也可继发于潜在疾病。虽然过敏性紫癜(HSp)是儿童期较常见的原发性血管炎,但有时必须将其与由感染、药物、疫苗或免疫介导性疾病引起的其他继发性血管炎相鉴别。

主要观察结果

我们报告一例14岁女孩,在急性EB病毒感染过程中出现皮肤坏死性血管炎。体格检查发现足部背部有边界呈网状的高度疼痛的红斑紫色病变。布洛芬对疼痛无效,需要使用曲马多和普瑞巴林。该患者还存在因子V莱顿突变杂合子,这可能促使了皮肤疼痛性病变的发生。

结论

据我们所知,这是首例记录在案的与急性EB病毒感染相关的坏死性血管炎儿科病例,该女孩为因子V莱顿突变杂合子。在该患者中,皮肤表现的严重程度可能受到同时存在的因子V莱顿突变的影响,这导致了高凝状态和闭塞性血管病,并伴有明显严重的疼痛,这是其他儿童血管炎中较少见的症状。

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