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Bone marrow involvement and obstructive jaundice in Farber lipogranulomatosis: clinical and autopsy report of a new case.

Authors :
Nowaczyk MJ
Feigenbaum A
Silver MM
Callahan J
Levin A
Jay V
Source :
Journal of inherited metabolic disease [J Inherit Metab Dis] 1996; Vol. 19 (5), pp. 655-60.
Publication Year :
1996

Abstract

We report a case of Farber lipogranulomatosis in a girl with hepatosplenomegaly, macular cherry-red spot, and subcutaneous nodules who developed liver dysfunction with jaundice and ascites, and myelophthisic anaemia because of infiltration of bone marrow with storage cells. Acid ceramidase assay confirmed the diagnosis. We conclude that the bone marrow dysfunction and cherry-red spot are features of type IV Farber lipogranulomatosis that have not been previously recognized, and should be added to the clinical phenotypic description.

Details

Language :
English
ISSN :
0141-8955
Volume :
19
Issue :
5
Database :
MEDLINE
Journal :
Journal of inherited metabolic disease
Publication Type :
Academic Journal
Accession number :
8892023
Full Text :
https://doi.org/10.1007/BF01799842