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Article
November 1977

Atypical Multicentric Reticulohistiocytosis With Paraproteinemia

Author Affiliations

From the Department of Dermatology, Slade Hospital, Headington (Drs Vickers, Ryan, and Rendall), and the Department of Pathology, Radcliffe Infirmary (Drs Robb-Smith and Vanhegan), Oxford, England; and the Department of Dermatology, Gloucester Royal Hospital, Gloucester, England (Dr Bowers).

Arch Dermatol. 1977;113(11):1576-1582. doi:10.1001/archderm.1977.01640110096017
Abstract

• Two women had multiple subcutaneous nodules that showed features of multicentric reticulohistiocytosis (MR). Neither had joint symptoms. Both had a raised erythrocyte sedimentation rate, an immunoglobulin G paraproteinemia, and raised levels of nonhepatic serum alkaline phosphatase. The skin lesions have been followed up, using light and electron microscopy, immunoperoxidase, and histochemical methods. The material in the giant cells stained positively for γ heavy chain determinants: the light chain type in each case was that of the paraprotein. An attempt to reproduce the skin lesions in one patient by intradermal injection of her paraprotein failed.

(Arch Dermatol 113:1576-1582, 1977)

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