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Bone marrow involvement and obstructive jaundice in Farber lipogranulomatosis: clinical and autopsy report of a new case.
- 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.
- Subjects :
- Acid Ceramidase
Amidohydrolases deficiency
Anemia, Myelophthisic etiology
Bone Marrow pathology
Ceramidases
Cholestasis etiology
Conjunctiva pathology
Female
Hepatomegaly etiology
Humans
Infant
Liver pathology
Lysosomal Storage Diseases diagnosis
Lysosomal Storage Diseases enzymology
Phenotype
Splenomegaly etiology
Lysosomal Storage Diseases etiology
Subjects
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