Abstract

Many clinical and laboratory-based studies have been reported for skin rashes which may be due to viral infections, namely pityriasis rosea (PR), Gianotti-Crosti syndrome (GCS), asymmetric periflexural exanthem/unilateral laterothoracic exanthem (APE/ULE), papular-purpuric gloves and socks syndrome (PPGSS), and eruptive pseudo-angiomatosis (EP). Eruptive hypomelanosis (EH) is a newly discovered paraviral rash. Novel tools are now available to investigate the epidemiology of these rashes. To retrieve epidemiological data of these exanthema and analyze whether such substantiates or refutes infectious etiologies. We searched for articles published over the last 60 years and indexed by PubMed database. We then analyzed them for universality, demography, concurrent patients, temporal and spatial-temporal clustering, mini-epidemics, epidemics, and other clinical and geographical associations. Based on our criteria, we selected 55, 60, 29, 36, 20, and 4 articles for PR, GCS, APE/ULE, PPGSS, EP, and EH respectively. Universality or multiple-continental reports are found for all exanthema except EH. The ages of patients are compatible with infectious causes for PR, GCS, APE/ULE, and EH. Concurrent patients are reported for all. Significant patient clustering is demonstrated for PR and GCS. Mini-epidemics and epidemics have been reported for GCS, EP, and EH. The current epidemiological data supports, to a moderate extent, that PR, GCS, and APE could be caused by infectious agents. Support for PPGSS is marginal. Epidemiological evidences for infectious origins for EP and EH are inadequate. There might be growing epidemiological evidence to substantiate or to refute our findings in the future.

Highlights

  • Contributions: AC, original conceptualization of the systematic review, devising the methodology, data collection, data interpretation, drafting the Antonio Chuh,[1] Vijay Zawar,[2] first version, writing the final version; VZ, sys-Gabriel F

  • Kong and Prince of Wales Hospital, Shatin, Hong Kong; 2Department of ly Dermatology, Godavari Foundation n Medical College and Research Center, DUPMCJ, India; 3Department of o Dermatology, Mayo Clinic College of e Medicine, Rochester, MN, USA; s 4Department of Dermatology, University u Hospital Zürich, Zürich, Switzerland cial Abstract er Many clinical and laboratory-based studies have been reported for skin rashes which may m be due to viral infections, namely pityriasis rosea (PR), Gianotti-Crosti syndrome (GCS), m asymmetric periflexural exanthem/unilateral o laterothoracic exanthem (APE/ULE), papularc purpuric gloves and socks syndrome (PPGSS), and eruptive pseudo-angiomatosis (EP)

  • Employing regression analyses with bootstrapped simulations, we have previously reported on the detection of spatial-temporal clustering for children with GCS (P=0.044).[82]

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Summary

Introduction

Contributions: AC, original conceptualization of the systematic review, devising the methodology, data collection, data interpretation, drafting the Antonio Chuh,[1] Vijay Zawar,[2] first version, writing the final version; VZ, sys-Gabriel F. The etiologies of several exanthema includ- tematic literature search, data interpretation, Albert Lee[1] ing pityriasis rosea (PR), Gianotti-Crosti syndrome (GCS), asymmetric periflexural exaninputs on clinical aspects, drafting the first version, writing the final version, as corresponding. Kong and Prince of Wales Hospital, Shatin, Hong Kong; 2Department of ly Dermatology, Godavari Foundation n Medical College and Research Center, DUPMCJ, India; 3Department of o Dermatology, Mayo Clinic College of e Medicine, Rochester, MN, USA; s 4Department of Dermatology, University u Hospital Zürich, Zürich, Switzerland cial Abstract er Many clinical and laboratory-based studies have been reported for skin rashes which may m be due to viral infections, namely pityriasis rosea (PR), Gianotti-Crosti syndrome (GCS), m asymmetric periflexural exanthem/unilateral o laterothoracic exanthem (APE/ULE), papularc purpuric gloves and socks syndrome (PPGSS), and eruptive pseudo-angiomatosis (EP). Virological tools such as real-time PCR, virus load, reverse-transcriptase PCR, and antibody avidities are much advanced today

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