Cargando…
Obstructive jaundice in a patient with polycystic liver disease complicated with polycystic kidney and polycystic lung: A case report
RATIONALE: Polycystic liver disease (PLD) is an autosomal-dominant disorder that is commonly associated with autosomal-dominant polycystic kidney disease (PKD) but rarely complicated with polycystic lung. Here, we report the first case of severe obstructive jaundice caused by multiple liver cysts in...
Autores principales: | Zhang, Liling, Gan, Linwang, Liu, Qi, Li, Ying, Lin, Jiaru, Ou, Santao |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220720/ https://www.ncbi.nlm.nih.gov/pubmed/32243367 http://dx.doi.org/10.1097/MD.0000000000019511 |
Ejemplares similares
-
Hyperaldosteronism and cardiovascular risk in patients with autosomal dominant polycystic kidney disease
por: Lai, Silvia, et al.
Publicado: (2016) -
Autosomal dominant polycystic kidney disease combined with hypertrophic cardiomyopathy: A case report
por: Shen, Yingjing, et al.
Publicado: (2017) -
Renal volume and cardiovascular risk assessment in normotensive autosomal dominant polycystic kidney disease patients
por: Sans, Laia, et al.
Publicado: (2016) -
Comprehensive analysis of mutations of renal cell carcinoma in an autosomal dominant polycystic kidney disease patient
por: Shim, Kwang Eon, et al.
Publicado: (2020) -
Fatal outcome of autosomal recessive polycystic kidney disease in neonates with recessive PKHD1 mutations
por: Jung, Jiwon, et al.
Publicado: (2020)