A teenage patient with autosomal recessive polycystic kidney disease, a splenorenal shunt, and congenital hepatic fibrosis: a case report

A 16-year-old female patient previously diagnosed with autosomal recessive polycystic kidney disease (ARPKD) presented with acute bilateral pneumonia, upper gastrointestinal bleeding caused by ruptured esophageal varices, ascites, and lower limb edema. She required intensive care and an endoscopic p...

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Detalles Bibliográficos
Autores principales: Scarioti, Vinicius Danieli, de Oliveira, Lucia Tabim, Mattiello, Anye Caroline, Gomes, Nayara dos Santos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Nefrologia 2018
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6699426/
https://www.ncbi.nlm.nih.gov/pubmed/30199558
http://dx.doi.org/10.1590/2175-8239-JBN-2018-0081

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6699426/
https://www.ncbi.nlm.nih.gov/pubmed/30199558
http://dx.doi.org/10.1590/2175-8239-JBN-2018-0081

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