Not entirely uncommon is the occurrence of Gianotti-Crosti syndrome in the context of infection with Mollusca contagiosa (Bürgler C et al. 2021). In developed countries, Gianotti-Crosti syndrome is most commonly associated with EBV (Leung AKC et al. 2019). In isolated cases, occurrence has been associated with infections caused by β-hemolytic.. Gianotti-Crosti syndrome (GCS), also known as childhood papular acrodermatitis, is a rare and self-limited disorder that predominantly affects the skin. 1 It consists of a sudden onset of diffuse and symmetrical papular lesions. Its incidence and prevalence are unknown, but it is estimated to be low, despite the disease being probably.

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Gianotti-Crosti syndrome is a relatively common dermatosis that occurs worldwide. The diagnosis is made clinically. Characteristic findings on physical examination. Gianotti-Crosti syndrome is characterized by the acute onset of monomorphous, pink to red-brown papules or papulovesicles that may become confluent (Figure 1).. Gianotti-Crosti syndrome (GCS) is a relatively common dermatosis, seen worldwide, primarily affecting children between 2 and 6 years of age. The classic physical finding is an asymptomatic self-limited papulovesicular exanthem; on rare occasions there are associated systemic signs and symptoms. GCS is usually associated with viral infections or immunization, but the pathogenesis remains a mystery.