Case for diagnosis. Multinucleated cell angiohistiocytoma

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Abstract

Multinucleate cell angiohistiocytoma is a rare idiopathic benign fibrohistiocytic and vascular proliferation usually presenting as multiple asymptomatic papules, red to violaceous in colour, primarily located on the extremities of middle-aged females. This entity is probably underdiagnosed due to the lack of recognition by clinicians and pathologists. We describe a patient with a multinucleate cell angiohistiocytoma of the face, a less frequent localization, in order to increase awareness of this entity and elucidate its clinical, histopathological, and immunohistochemistry features.

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Rato, M. P. G. S., Parente, J., Monteiro, A. F., & Aranha, J. (2018). Case for diagnosis. Multinucleated cell angiohistiocytoma. Anais Brasileiros de Dermatologia, 93(2), 291–293. https://doi.org/10.1590/abd1806-4841.20186821

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