A teenage patient with autosomal recessive polycystic kidney disease, a splenorenal shunt, and congenital hepatic fibrosis: a case report.
J Bras Nefrol
; 41(2): 300-303, 2019.
Article
em En, Pt
| MEDLINE
| ID: mdl-30199558
ABSTRACT
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.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Anastomose Arteriovenosa
/
Rim Policístico Autossômico Recessivo
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Doença de Caroli
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Cirrose Hepática
Idioma:
En
/
Pt
Ano de publicação:
2019
Tipo de documento:
Article