SciELO - Scientific Electronic Library Online

 
vol.38 issue3Lynch syndrome: genetic, clinical and diagnostic aspectsFulminating ischemic hepatitis induced by severe cardiac dysfunction: case report author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

  • Have no cited articlesCited by SciELO

Related links

  • Have no similar articlesSimilars in SciELO

Share


Revista de Gastroenterología del Perú

Print version ISSN 1022-5129

Abstract

MORAN-MARINOS, Cristian; VILCHEZ-CORNEJO, Jennifer  and  QUISPE-COLQUEPISCO, Sarita. Cavernoma complicated with biliopatia secondary to type 1 Gaucher disease: report of a Peruvian case. Rev. gastroenterol. Perú [online]. 2018, vol.38, n.3, pp.280-284. ISSN 1022-5129.

Gaucher disease is an autosomal recessive lysosomal storage disorder characterized by deficiency of beta-glucosidase that would lead to the accumulation of glucosylceramide mainly in cells of the mononuclear phagocytic system causing systemic effectations. We present a patient of twenty years who is suffering from chronic pain in the left hypochondrium with episodes of bleeding for 3 years and sensation of thermal rise, physical examination revealed jaundice and massive splenomegaly, without neurological involvement. Severe osteoporosis, pancytopenia, and the presence of portal vein thrombosis with cavernomatous transformation complicated by portal biliopathy simulating a klatskin tumor, marrow and enzymatic studies were compatible with Gaucher disease, were shown as unexpected findings. he received treatment with imiglucerase, following up. It is a rare case, of great interest, heterogeneity in its clinical manifestations and unpublished by its complication, constituting a challenge to reach its diagnosis of this orphan disease.

Keywords : Gaucher disease; Glucosylceramidase; Histiocytes.

        · abstract in Spanish     · text in Spanish     · Spanish ( pdf )