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A Case of Benign Cephalic Histiocytosis

Benign cephalic histiocytosis (BCH) is a rare non-Langerhans cell histiocytosis of unknown etiology. Clinically, lesions are characterized by small, red-to-yellow papules distributed mainly on the head, face, neck, and shoulders of infants and children. Histopathological specimens show massive histi...

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Detalles Bibliográficos
Autores principales: Kim, Byung Chul, Choi, Woo Jin, Seung, Na Reu, Park, Eun Joo, Cho, Hee Jin, Kim, Kwang Ho, Kim, Kwang Joong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Dermatological Association; The Korean Society for Investigative Dermatology 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3199413/
https://www.ncbi.nlm.nih.gov/pubmed/22028563
http://dx.doi.org/10.5021/ad.2011.23.S1.S16
Descripción
Sumario:Benign cephalic histiocytosis (BCH) is a rare non-Langerhans cell histiocytosis of unknown etiology. Clinically, lesions are characterized by small, red-to-yellow papules distributed mainly on the head, face, neck, and shoulders of infants and children. Histopathological specimens show massive histiocytic infiltration of the superficial dermis. Immunohistochemically, they are positive for CD68, but negative for CD1a and S-100. Two cases have been reported so far in the relevant work published in Korean literature. Herein, we report on an additional case of BCH.