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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...
Autores principales: | Scarioti, Vinicius Danieli, de Oliveira, Lucia Tabim, Mattiello, Anye Caroline, Gomes, Nayara dos Santos |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Nefrologia
2018
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Materias: | |
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 |
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