SciELO - Scientific Electronic Library Online

 
vol.19 número6Acromegalia. A propósito de un casoÍleo biliar: una causa infrecuente de oclusión intestinal. Presentación de un caso clínico índice de autoresíndice de materiabúsqueda de artículos
Home Pagelista alfabética de revistas  

Servicios Personalizados

Articulo

Indicadores

  • No hay articulos citadosCitado por SciELO

Links relacionados

  • No hay articulos similaresSimilares en SciELO

Compartir


MediSur

versión On-line ISSN 1727-897X

Resumen

SARDINAS PONCE, Raysy; GUERRA LEAL, Obel Alcides  y  VERDECIA, Servando Roig. Giant splenomegaly due to Gaucher disease. Medisur [online]. 2021, vol.19, n.6, pp. 1021-1027.  Epub 30-Dic-2021. ISSN 1727-897X.

Gaucher disease is the most common disease of the lysosomal storage diseases group comprised within innate errors of metabolism. There is glucocerebrosides accumulation in different organs and as a consequence, the development of symptoms and multisystemic signs that are established in a chronic and progressive way, such as: visceromegaly, bone destruction and peripheral cytopenias. A 43-years-old male patient is presented with a diagnosis of this disease since childhood, who developed giant splenomegaly with hypersplenism, for which he required splenectomy, obtaining good results with surgical treatment.

Palabras clave : Gaucher´s disease; splenomegaly; splenectomy.

        · resumen en Español     · texto en Español     · Español ( pdf )