Gianotti-Crosti综合征的流行病学、病因学及Chuh和Zawar诊断标准

A. Chuh, V. Zawar
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引用次数: 2

摘要

gianoti - crosti综合征(GCS)由面部、臀部和四肢伸肌表面突然出现小丘疹或丘疹小囊泡,全身性淋巴结病和急性非黄疸性肝炎组成。大多数早期病例是由乙型肝炎病毒引起的。成年人也可能患有GCS。其他病毒现在可能比乙型肝炎病毒更相关。作者不再需要淋巴结病或肝炎来进行诊断。这种疾病是自限性的。并发症并不常见。GCS研究的纳入和排除标准不统一,导致研究对象的同质性较低。有效的诊断标准将使所有研究中的受试者更加同质,以便进行有效的荟萃分析和系统评价。仅在专业环境中观察到的GCS患者的数据可能存在偏差。在初级保健机构招募受过专门训练的初级保健医生并应用有效和标准化的诊断标准可能是可行的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The epidemiology, etiology and Chuh and Zawar’s diagnostic criteria of Gianotti–Crosti syndrome
Gianotti–Crosti syndrome (GCS) consists of a sudden eruption of small papules or papulovesicles over the face, buttock and extensor surfaces of limbs, generalized lymphadenopathy and acute nonicteric hepatitis in young children. Most early cases were caused by hepatitis B virus. Adults could also suffer from GCS. Other viruses may now be more pertinent than hepatitis B virus. The authors no longer need lymphadenopathy or hepatitis to make a diagnosis. The disease is self-limiting. Complications are uncommon. The inclusion and exclusion criteria of studies in GCS are nonuniform, rendering low homogeneity of study subjects. A validated diagnostic criteria would allow subjects in all studies more homogenous so that valid meta-analyses and systemic reviews can be performed. Data from subjects with GCS seen in specialist settings only might be biased. Recruitment in primary care settings with specifically trained primary care physicians and application of a valid and standardized diagnostic criteria might be c...
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