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Some have attempted to group together SRH, multiple reticulohistiocytomas without extracutaneous involvement and MR as part of a disease spectrum under the rubric reticulohistiocytoma cutis (4). Recent studies have provided evidence that at least the very ends of the spectrum, SRH and MR, show different clinical, histopathological as well as immunophenotypical features and therefore might better be considered different entities (1,4). The principal distinguishing histological and immunophenotypical features of SRH and MR are summarized in Table 1.

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