Cargando…
Liver resection for a congenital intrahepatic portosystemic shunt in a child with hyperammonemia and hypermanganesemia: a case report
BACKGROUND: Congenital portosystemic shunt (CPSS) is a rare malformation that leads to hyperammonemia, hypermanganesemia, and various symptoms. CPSSs are divided into intrahepatic and extrahepatic shunts. In patients with persistent CPSS including an intrahepatic portosystemic shunt (IPSS), early in...
Autores principales: | Takama, Yuichi, Nakamura, Tetsuro, Santo, Kenji, Yoneda, Akihiro |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7165232/ https://www.ncbi.nlm.nih.gov/pubmed/32303849 http://dx.doi.org/10.1186/s40792-020-00838-5 |
Ejemplares similares
-
Congenital Portosystemic Shunt Presenting As Hyperammonemia Following Fontan Operation
por: Morneault, Kayla, et al.
Publicado: (2023) -
Asymptomatic Congenital Intrahepatic Portosystemic Shunt
por: Brown, Karen M., et al.
Publicado: (2016) -
Congenital intrahepatic portosystemic venous shunt
por: Kashgari, Amna, et al.
Publicado: (2020) -
Severe Hyperammonemia Due to Fecal Bowel Obstruction With a Congenital Portosystemic Shunt Resulting in Refractory Status Epilepticus and Cerebral Edema
por: Kawakami, Tetsuro, et al.
Publicado: (2023) -
Congenital intrahepatic portosystemic shunts: Imaging findings and endovascular management
por: Chandrasekharan, Rajsekar, et al.
Publicado: (2016)