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HARRY A. REES, MB, BSc, MRCP

Arch Dermatol. 1964;89(2):277-280.

Abstract
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.

Author Affiliations
PENARTH, ENGLAND

Research Fellow in Cardiology, Llandough Hospital, Penarth.

Footnotes
Patient shown at Meeting of British Association of Dermatology, Cardiff, July, 1958.

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