Epstein-Barr病毒与皮肤多发性肌炎相关1例报告

A. C. Fernandes, Francisco Brilhante Neto, Laura Aragão, Cítara Queiroz, M. Vieira, A. Moura
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摘要

Epstein-Barr病毒(EBV)是一种疱疹病毒科的DNA病毒,在世界95%的人口中以潜伏形式存在。这种病毒感染B淋巴细胞,从而促进周期性再激活的持续性感染。EBV可能是自身免疫性疾病病因学中的一个强大的环境因素,一旦其病毒蛋白参与改变宿主的免疫系统,导致自身耐受性丧失和肿瘤的发展。目的:报告一例EBV患者与皮肤多发性肌炎的发展相关。病例报告:女孩,5岁,表现为上肢和下肢延伸区红斑鳞状病变。在随访期间,患者的母亲返回,涉及儿童恶化,主诉周期性发烧,上呼吸道感染,在过去三周内,与行走困难和坐下困难相关的病变恶化。体格检查显示咽扁桃体炎、宫颈、腋窝及腹股沟腺肿大及肝肿大。四肢皮肤及掌指关节、指间关节呈鳞状、瘙痒性红斑,骨盆肌无力,膝、踝关节痛。在接受肌肉活检后,它呈现出皮肤多发性肌炎的模式,并开始使用甲氨蝶呤进行免疫抑制。因此,患者在临床和实验室方面对单核细胞增多症和皮肤多发性肌炎的症状有所改善。患者继续接受专科治疗和运动物理治疗。结论:在自身免疫性疾病易感人群中,应重视病毒成分(如爱泼斯坦-巴尔病毒)对皮肤多发性肌炎发病机制的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epstein-Barr virus associated with dermatopolymyositis: a case report
INTRODUCTION: The Epstein-Barr virus (EBV) is a DNA virus of the Herpesviridae family, which exists in the latent form in 95% of the world population. This virus infects the B lymphocytes, which promotes a persistent infection with periodic reactivations. EBV is probably a strong environmental factor in etiology of autoimmune diseases, once its viral proteins are involved in altering the host’s immune system, causing loss of self-tolerance and development of neoplasms. OBJECTIVE: To report a case of a patient with EBV associated with the development of dermatopolymyositis. CASE REPORT: Girl, 5 years, presenting erythematous-scaly lesions in extending region in upper and lower limbs. During follow-up, the patient’s mother returns referring worsening of the child, complaining of periodic fever, infection of upper airways and worsening of the lesions associated with difficulty of ambulation as well as difficulty of sitting in the past three weeks. Physical examination showed pharyngotonsillitis, cervical, axillary and inguinal adenomegalies and hepatomegaly. The limbs skin presented scaly and pruritic erythematous macules as well as on the metacarpophalangeal and interphalangeal joints, weakness of the pelvic muscles and arthralgia in the knees and ankles. After undergoing muscle biopsy, it presented a pattern for dermatopolymyositis, and imunosupression was initiated with methotrexate. Therefore, the patient improved clinically and laboratory regarding mononucleosis and the symptoms of dermatopolymyositis. The patient continues in specialized treatment and motor physiotherapy. CONCLUSION: Attention should be payed to the influence of viral component, such as the Epstein-Barr virus, on the pathogenesis of dermatopolymyositis in individuals genetically predisposed to autoimmune diseases.
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