Neonatal ascites in autosomal recessive polycystic kidney disease (ARPKD)

被引：0

作者：

Ling, Galina ^{[1
]}

Landau, Daniel ^{[2
]}

Bergmann, Carsten ^{[4
,5
,6
]}

Maor, Esther ^{[3
]}

Yerushalmi, Baruch ^{[1
]}

机构：

[1] Soroka Univ, Med Ctr, Pediat Gastroenterol Unit, IL-84101 Beer Sheva, Israel

[2] Soroka Univ, Med Ctr, Pediat Nephrol Unit, IL-84101 Beer Sheva, Israel

[3] Soroka Univ, Med Ctr, Pediat Pathol Unit, IL-84101 Beer Sheva, Israel

[4] Univ Med Ctr, Dept Nephrol, Freiburg, Germany

[5] Univ Med Ctr, Clin Res Ctr, Freiburg, Germany

[6] Bioscientia, Ctr Human Genet, Ingelheim, Germany

来源：

CLINICAL NEPHROLOGY | 2015年 / 83卷 / 05期

关键词：

neonate; ascites; SAAG; congenital hepatic fibrosis; ARPKD; CONGENITAL HEPATIC-FIBROSIS; DIAGNOSIS; PKHD1;

D O I：

10.5414/CN108345

中图分类号：

R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

1002 ; 100201 ;

摘要：

Background: Neonatal ascites is a rare entity, which is usually biliary, urinary, or chylous. Congenital hepatic fibrosis as part of the manifestations of autosomal recessive polycystic kidney disease (ARPKD) is usually a histological adjunct to the diagnosis of this mainly clinically renal entity in the neonatal period. Case-diagnosis: We describe a rare case of severe ascites in a new-born child complicating ARPKD, which was later confirmed by clinical, histological, and genetic studies. Conclusion: ARPKD should be considered in differential diagnosis of neonatal ascites.

引用

页码：297 / 300

页数：4

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