Benign cephalic histiocytosis: a case report
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Keywords

Benign cephalic histiocytosis, histiocytosis, cutaneous and mucocutaneous histiocytosis, non-Langerhans cell histiocytosis, Langerhans cells histiocitosis cefálica benigna, histiocitosis, histiocitosis cutáneas y mucocutáneas, células de Langerhans

How to Cite

Castillo Botero, A., Alarcón Soldevilla, F., Campoy Carreño, C., García Almazán, L., Torrent García, M., & Ortiz González, A. (2024). Benign cephalic histiocytosis: a case report. Archives of Pathology, 4(1). https://doi.org/10.17811/ap.v4i1.20843

Abstract

Benign cephalic histiocytosis is a rare disease belonging to the cutaneous and mucocutaneous histiocytosis. It is important to recognize this disease to inform the family about its benign prognosis and self-resolving nature. Although no treatment is required, regular follow-up is important to evaluate the progression of the cutaneous lesions. We present the case of a 2-year-old male patient with asymptomatic yellow-orange papules on the face without any accompanying symptoms. A biopsy with histopathological and immunohistochemical analysis was performed, and upon clinical-pathological correlation, the diagnosis of Benign cephalic histiocytosis was established. During the follow-up, stability and involution of the lesions were observed.

https://doi.org/10.17811/ap.v4i1.20843
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