Benign Cephalic Histiocytosis: The face of a rare pathology

Authors

  • Gladys Castillo Soto Universidad Tecnológica Equinoccial https://orcid.org/0000-0001-5648-4014
  • Carla Verdugo Morales Universidad Tecnológica Equinoccial
  • Juan Freire Londoño Universidad Tecnológica Equinoccial
  • Fernando Montalvo Zumárraga Universidad Tecnológica Equinoccial
  • Cecilia Moyano Vega CEPI Center
  • Santiago Palacios Álvarez CEPI Center

DOI:

https://doi.org/10.63787/6.2.2024.32-37

Keywords:

cephalic histiocytosis, non-Langerhans cells

Abstract

Benign cephalic histiocytosis (BCH) is a rare dermatological disease that primarily affects infants and young children, characterized by the appearance of multiple asymptomatic, flat, erythematous-yellow papules, often in the cephalic region. We present the case of a 1 year and 3 months old male patient with asymptomatic brown papules on the face. Following clinical-pathological correlation, a diagnosis of benign cephalic histiocytosis was established. During follow-up, stability and involution of the lesions were observed.

Published

2026-07-17

How to Cite

Castillo Soto, G., Verdugo Morales, C., Freire Londoño, J., Montalvo Zumárraga, F., Moyano Vega, C., & Palacios Álvarez, S. (2026). Benign Cephalic Histiocytosis: The face of a rare pathology. Revista Dermatologica Centro Úraga, 6(2), 32–37. https://doi.org/10.63787/6.2.2024.32-37