| Literature DB >> 26847548 |
Giacomo Gotti1, Antonio Marseglia1, Costantino De Giacomo2, Maria Iascone3, Aurelio Sonzogni1, Lorenzo D'Antiga1.
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.Entities:
Keywords: gaucher disease; lysosomal storage disease; neonatal hepatitis
Mesh:
Year: 2016 PMID: 26847548 DOI: 10.3109/15513815.2015.1130762
Source DB: PubMed Journal: Fetal Pediatr Pathol ISSN: 1551-3815 Impact factor: 0.958