Serum Sickness-Like Reaction Associated with Epstein – Barr Virus: Clinical Case

V. V. Ivanchikov, N. Murashkin, E. T. Ambarchian, A. Kuzminova
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Abstract

Background. Annular dermatoses are a group of diseases with major clinical manifestation of rashes of relevant form. This manifestation pattern causes difficulties in diagnosis. The case of rarely diagnosed annular dermatosis is presented: serum siknesslike reaction (SSLR) triggered by the Epstein – Barr virus (EBV). Clinical case description. Patient D., 8 years old girl, noted abdominal pain 3 weeks before hospitalization, and later numerous polymorphic rashes (erythematous macules, urticarial elements), swelling and pain in joints. Self-treatment with non-steroidal anti-inflammatory and systemic antihistamines did not lead to any improvement. The patient was hospitalized in the pediatric department at the place of residence, where the diagnosis “Henoch-Schonlein purpura, mixed type” was established according to the results of physical, laboratory (double increase of ALT and AST, ESR up to 166 mm/h, IgM to EBV), and ultrasound (mesenteric lymph nodes hyperplasia) studies. Systemic glucocorticosteroids have led to improvement, however, few days after the end of the treatment there was relapse of rash and arthralgia. Thus, the girl was administrated to clinical diagnostic center. Patient’s general condition was satisfactory at the time of examination. There were numerous erythematous annular urticarial and macular elements (3–12 cm) on the skin of face, body and limbs. Some foci, as well as some resolved rashes had blue spots with indistinct boundaries that disappeared after compression. Mucous membranes, nails and hair were intact. Subjective symptoms — slight burning around rashes, at palpation — low-intensity pain in the left radiocarpal joint. Blood tests: C-reactive protein concentration increased up to 12 mg/L, ESR up to 26 mm/h, IgG to EBV up to 47.7. Conclusion. During differential diagnosis we should consider the possibility of SSLR development in all pediatric patients with annular rashes associated with arthralgia and/or arthritis, fever, history of drug use (most often beta-lactam antibiotics), recent vaccination or manifestations of viral infection, especially in case of cyanotic spots after rashes resolution and non-specific laboratory parameters.
与eb病毒相关的血清病样反应:临床病例
背景。环状皮肤病是以皮疹为主要临床表现的一类疾病。这种表现模式给诊断带来困难。病例罕见诊断环状皮肤病提出:由eb病毒(EBV)引发的血清病样反应(SSLR)。临床病例描述。患者D, 8岁女孩,住院前3周出现腹痛,随后出现大量多形态皮疹(红斑、荨麻疹成分),关节肿胀和疼痛。用非甾体抗炎药和全身抗组胺药进行自我治疗没有任何改善。患者在住院地儿科住院,根据体格检查、实验室检查(ALT和AST双增高,ESR达166 mm/h, IgM至EBV)和超声检查(肠系膜淋巴结增生)确定诊断为“Henoch-Schonlein紫癜,混合型”。全身糖皮质激素已导致改善,然而,几天后治疗结束有复发皮疹和关节痛。因此,该女孩被送往临床诊断中心。检查时病人的一般情况令人满意。面部、全身及四肢皮肤可见大量红斑性环状荨麻疹及黄斑成分(3 ~ 12 cm)。部分病灶及已消退的皮疹有边界不清的蓝点,压缩后消失。粘膜、指甲和毛发完好无损。主观症状-皮疹周围轻微灼烧,触诊-左桡腕关节低强度疼痛。血液检查:c -反应蛋白浓度升高至12 mg/L,血沉可达26 mm/h, IgG对EBV升高至47.7。结论。在鉴别诊断时,我们应考虑所有伴有关节痛和/或关节炎、发烧、药物使用史(最常见的是β -内酰胺类抗生素)、最近接种疫苗或病毒感染表现的儿科环形皮疹患者发生SSLR的可能性,特别是在皮疹消退后出现紫斑和非特异性实验室参数的情况下。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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