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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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
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author Scarioti, Vinicius Danieli
de Oliveira, Lucia Tabim
Mattiello, Anye Caroline
Gomes, Nayara dos Santos
author_facet Scarioti, Vinicius Danieli
de Oliveira, Lucia Tabim
Mattiello, Anye Caroline
Gomes, Nayara dos Santos
author_sort Scarioti, Vinicius Danieli
collection PubMed
description 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 procedure to treat the gastrointestinal bleeding. The analysis of the differential diagnosis for chronic liver disease indicated she had a spontaneous splenorenal shunt. Ultrasound-guided biopsy revealed the patient had cirrhosis, as characteristically seen in individuals with ARPKD. She had no symptoms at discharge and was referred for review for a combined transplant.
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spelling pubmed-66994262019-08-26 A teenage patient with autosomal recessive polycystic kidney disease, a splenorenal shunt, and congenital hepatic fibrosis: a case report Scarioti, Vinicius Danieli de Oliveira, Lucia Tabim Mattiello, Anye Caroline Gomes, Nayara dos Santos J Bras Nefrol Case Reports 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 procedure to treat the gastrointestinal bleeding. The analysis of the differential diagnosis for chronic liver disease indicated she had a spontaneous splenorenal shunt. Ultrasound-guided biopsy revealed the patient had cirrhosis, as characteristically seen in individuals with ARPKD. She had no symptoms at discharge and was referred for review for a combined transplant. Sociedade Brasileira de Nefrologia 2018-09-06 2019 /pmc/articles/PMC6699426/ /pubmed/30199558 http://dx.doi.org/10.1590/2175-8239-JBN-2018-0081 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Reports
Scarioti, Vinicius Danieli
de Oliveira, Lucia Tabim
Mattiello, Anye Caroline
Gomes, Nayara dos Santos
A teenage patient with autosomal recessive polycystic kidney disease, a splenorenal shunt, and congenital hepatic fibrosis: a case report
title A teenage patient with autosomal recessive polycystic kidney disease, a splenorenal shunt, and congenital hepatic fibrosis: a case report
title_full A teenage patient with autosomal recessive polycystic kidney disease, a splenorenal shunt, and congenital hepatic fibrosis: a case report
title_fullStr A teenage patient with autosomal recessive polycystic kidney disease, a splenorenal shunt, and congenital hepatic fibrosis: a case report
title_full_unstemmed A teenage patient with autosomal recessive polycystic kidney disease, a splenorenal shunt, and congenital hepatic fibrosis: a case report
title_short A teenage patient with autosomal recessive polycystic kidney disease, a splenorenal shunt, and congenital hepatic fibrosis: a case report
title_sort teenage patient with autosomal recessive polycystic kidney disease, a splenorenal shunt, and congenital hepatic fibrosis: a case report
topic Case Reports
url 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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