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Progress in Pediatrics
April 1949

RETICULOGRANULOMA: Report of a Case of Eosinophilic Granuloma of Bone Associated with Nonlipid Reticulosis of Skin and Oral Mucosa Under the Clinical Picture of Hand-Schüller-Christian Disease

Author Affiliations

From the Laboratory of Dermopathology of Monroe Hospital, Monroe, Mich., and the Department of Dermatology, Wayne University Medical College, Detroit, (Dr. Pinkus) and the Marshfield Clinic and St. Joseph's Hospital, Marshfield, Wis. (Dr. Copps, Dr. Custer and Dr. Epstein).

Am J Dis Child. 1949;77(4):503-519. doi:10.1001/archpedi.1949.02030040515008

ONE OF the most interesting recent developments in the field of pathology is the concept, first advanced by Farber and Green,1 that "eosinophilic granuloma of bone" is the mildest form of a group of reticuloendothelial diseases. Other members of this group of "peculiar inflammatory histiocytosis" (Jaffe and Lichtenstein2) are Hand-Schüller-Christian and Letterer-Siwe diseases. If this concept is correct, it was to be expected that cases of eosinophilic granuloma would be observed in which other organs besides the bones are affected.

The first case of this kind was published by Curtis and Cawley.3 Their patient was a 2 year old girl who had cutaneous manifestations of specific character, in addition to multiple involvement of bones. The case which forms the basis of our report was seen at the Marshfield Clinic in January 1946 and was diagnosed clinically as Schüller-Christian disease. Tissue sections of the bone lesion, however, were

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