Fig. 3From: Phenotypic intrafamilial variability including H syndrome and Rosai–Dorfman disease associated with the same c.1088G > A mutation in the SLC29A3 geneH syndrome. The dermis contains a spread fibrosis with an inflammatory perivascular infiltrate (a, HE*40) composed of mainly plasma cells, small histiocytes and lymphocytes (b, HE*200). Basal layer hyperpigmentation in the epidermis was also noted (a, HE*40)Back to article page