Summary
The clinical features of eight cases of multicentric reticulohistiocytosis are presented. Although minor variations do occur, the disease is generally a well delineated and homogenous entity. Treatment is discussed briefly but, with the possible exception of cyclophosphamide, has proved relatively ineffective. Emphasis is given to the relationship between multicentric reticulohistiocytosis and malignant disease, which has now been reported in eighteen of seventy‐four cases.