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Neonatal Jaundice with Splenomegaly: Not a Common Pick.

Authors :
Gotti, Giacomo
Marseglia, Antonio
De Giacomo, Costantino
Iascone, Maria
Sonzogni, Aurelio
D’Antiga, Lorenzo
Source :
Fetal & Pediatric Pathology. Apr2017, Vol. 36 Issue 2, p108-111. 4p.
Publication Year :
2017

Abstract

The most common conditions causing cholestatic jaundice in infants are biliary atresia, neonatal hepatitis, and Alagille syndrome. In these disorders, the clinical presentation includes jaundice, pale stools, dark urine and hepatomegaly. Splenomegaly is not an early feature since it is due to portal hypertension, a later event. The finding of cholestatic jaundice and a large spleen usually raises the suspicion of Niemann-Pick type C disease (NP-C), a lysosomal storage disorder. We present and discuss here a case of an infant with liver disease and splenomegaly that were not ascribed to NP-C, but to Gaucher disease type 2. Liver biopsy, enzymatic studies and whole exome sequencing allowed to make the diagnosis. Although rare, Gaucher disease can cause neonatal hepatitis. A prompt recognition is advocated. [ABSTRACT FROM PUBLISHER]

Details

Language :
English
ISSN :
15513815
Volume :
36
Issue :
2
Database :
Academic Search Index
Journal :
Fetal & Pediatric Pathology
Publication Type :
Academic Journal
Accession number :
121270046
Full Text :
https://doi.org/10.3109/15513815.2015.1130762