The world literature on sclerosing lipogranuloma is reviewed and a further case described. The patient in this report has clinical features of sclerosing lipogranuloma and Weber-Christian disease, but the distinctive histological appearances of the former. The skin involvement and lymph node enlargement produced a diagnostic problem. Chemical examination of the fat was normal and should be carried out in every case to exclude exogenous granulomata.
REES HA. Sclerosing Lipogranuloma. Arch Dermatol. 1964;89(2):277–280. doi:10.1001/archderm.1964.01590260115022
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