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Abstract:

Reticular Histiocytoma (RH) is a rare histiocytic proliferation that shares microscopic similarities with Xanthogranuloma (XG). The condition exists in two clinical forms: the benign solitary form (solitary epithelioid histiocytoma) and the more concerning multicentric form (Multicentric Reticulohistiocytosis). The multicentric variant presents with multiple lesions and is associated with serious systemic issues such as destructive arthritis, autoimmune diseases, and internal malignancy, necessitating a full systemic workup. Microscopically, RH is characterized by large, epithelioid cells featuring dense pink cytoplasm, which helps distinguish it from XG. These histiocytes often display a distinct "two-toned" appearance in the cytoplasm, and their unusual nuclear morphology may require ancillary stains (e.g., Keratin, SOX10) to rule out high-grade mimics like carcinoma.

Reticular Histiocytoma (RH) vs. Xanthogranuloma (XG): Clinical Forms and Key Microscopic Features

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