Indeterminate cell histiocytosis successfully treated with phototherapy
DOI:
https://doi.org/10.4322/acr.2016.038Keywords:
Histiocytosis, Skin Diseases, PhototherapyAbstract
First described in 1985, intermediate cell histiocytosis is a rare disorder of the cutaneous dendritic cell group with a varied clinical presentation and evolution. The pathologic substrate is constituted by the proliferation of indeterminate cells (ICs) that are immunophenotypically characterized by the positivity of CD1a, CD68, and faint/focal S100, plus the negativity for CD207 (langerin). The authors present the case of a healthy elderly woman who presented generalized dome-shaped reddish cutaneous nodules over her trunk, neck, face, and extremities over a period of 18 months. A laboratory and imaging work-up ruled out internal involvement. The skin biopsy was consistent with IC histiocytosis. The patient was treated with narrowband ultraviolet B phototherapy, which resulted in an excellent short-term outcomeDownloads
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Published
2016-06-11
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Article / Clinical Case Report
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Zerbini, M. C. N., Sotto, M. N., Campos, F. P. F. de, Abdo, A. N. R., Pereira, J., Sanches Junior, J. A., & Martins, J. C. (2016). Indeterminate cell histiocytosis successfully treated with phototherapy. Autopsy and Case Reports, 6(2), 33-38. https://doi.org/10.4322/acr.2016.038