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Transjugular Intrahepatic Portosystemic Shunt for Refractory Ascites in Gaucher Disease
Gaucher disease is rare, inherited lysosomal storage disorder that leads to the excessive accumulation of certain lipids, especially within the bone marrow, liver, and spleen. We present a case of a 30-year-old man with Gaucher disease who underwent a splenectomy at the age of eight for severe cytop...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Cureus
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079779/ https://www.ncbi.nlm.nih.gov/pubmed/35535294 http://dx.doi.org/10.7759/cureus.23941 |