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[Multiple clustered histiocytofibroma. Apropos of a case with immunohistochemical study]
R Soloeta1, I Yanguas, N Saracíbar
1Service de Dermatologie, Hospital Santiago Apostol, Vitoria, Espagne.
Annales De Dermatologie Et De Venereologie
|January 1, 1994
Abstract:
Multiple clustered dermatofibromas constitute an uncommon entity, of which we have collected seven cases in the literature. We observed the case of a 4-year-old girl, who had dermatofibromas confluent in a central plaque of fibrous aspect, located in the lumbar region. The immunohistochemical study showed positive staining for Factor XIIIa antibody, confirming its origin in the dermal dendrocyte.