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...

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Detalles Bibliográficos
Autores principales: Adhyaru, Kunal, Menezes, Sherna, Mistry, Pramod K, Nagral, Aabha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Gastroenterology
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

Internet

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

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