Gianotti-Crosti syndrome: a case report

Authors

  • José de Jesús Méndez Castro Facultad de Medicina, Universidad Popular Autónoma del Estado de Puebla Author
  • Juan Manuel Méndez Castro Facultad de Medicina, Benemérita Universidad Autónoma de Puebla Author
  • Beatriz Sarai Muñoz Delgado Facultad de Medicina, Universidad Popular Autónoma del Estado de Puebla Author
  • Karime Esquerra Cazares Facultad de Medicina, Universidad Autónoma de Guadalajara Author
  • Paulina Cruz Fuentes Facultad de Medicina, Universidad Autónoma de Tamaulipas Author
  • Martin Yudovich Virsub Baylor College of Medicine, Texas Children’s Hospital Author

DOI:

https://doi.org/10.62954/tg4c2471

Keywords:

Gianotti-Crosti, Dermatology, Pediatrics, Maculopapular erythema

Abstract

Gianotti-Crosti syndrome is a rare, benign, and self-limiting exanthem frequently seen in children under six years old. The objective of this study is to describe an unusual case in a pediatric patient. A 16-year-old adolescent presented with multiple acral, papulovesicular, erythematous, and pruritic lesions, with no other symptoms. Laboratory tests suggested an uncomplicated viral etiology, supporting the clinical diagnosis. Treatment included loratadine 10 mg/day and a moisturizing cream. Recognizing this disease is important, as it is often misdiagnosed and improperly treated.

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Published

2025-06-11

How to Cite

Gianotti-Crosti syndrome: a case report. (2025). Revista Mexicana De Investigación Médica, 1(2), 25-29. https://doi.org/10.62954/tg4c2471