Literature DB >> 3681584

Renal abnormalities in paucity of interlobular bile ducts.

V Tolia1, R S Dubois, F B Watts, E Perrin.   

Abstract

Paucity of interlobular bile ducts is a common histologic characteristic in persistent conjugated hyperbilirubinemia of infancy. It occurs in two forms: the syndromatic and the nonsyndromatic types. The syndromatic form is also called arteriohepatic dysplasia. The nonsyndromatic type of paucity of interlobular bile ducts occurs less frequently and is usually associated with more severe disease and a less favorable prognosis. We present two unusual renal anomalies in association with paucity of interlobular bile ducts. In the first case, juvenile nephronophthisis was diagnosed in a 4-week-old infant with arteriohepatic dysplasia; the patient died from severe renal disease by 2 months of age. The second case presented with severe bilateral hydronephrosis and hydroureter secondary to posterior urethral valves associated with the nonsyndromatic form of paucity of interlobular bile ducts. He, however, improved after corrective surgery of the urethral valves. Other renal abnormalities previously reported in the literature in association with chronic liver disease are also reviewed.

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Year:  1987        PMID: 3681584     DOI: 10.1097/00005176-198711000-00026

Source DB:  PubMed          Journal:  J Pediatr Gastroenterol Nutr        ISSN: 0277-2116            Impact factor:   2.839


  6 in total

Review 1.  Alagille syndrome.

Authors:  I D Krantz; D A Piccoli; N B Spinner
Journal:  J Med Genet       Date:  1997-02       Impact factor: 6.318

Review 2.  Alagille's syndrome associated with cystic renal disease.

Authors:  S R Martin; L Garel; F Alvarez
Journal:  Arch Dis Child       Date:  1996-03       Impact factor: 3.791

3.  Renal anomalies in Alagille syndrome: a disease-defining feature.

Authors:  Binita M Kamath; Gisele Podkameni; Anne L Hutchinson; Laura D Leonard; Jennifer Gerfen; Ian D Krantz; David A Piccoli; Nancy B Spinner; Kathleen M Loomes; Kevin Meyers
Journal:  Am J Med Genet A       Date:  2011-11-21       Impact factor: 2.802

4.  Clinical and pathological characteristics of Alagille syndrome in Chinese children.

Authors:  Jian-She Wang; Xiao-Hong Wang; Qi-Rong Zhu; Zhong-Lin Wang; Xi-Qi Hu; Shan Zheng
Journal:  World J Pediatr       Date:  2008-12-23       Impact factor: 2.764

Review 5.  Renal involvement and the role of Notch signalling in Alagille syndrome.

Authors:  Binita M Kamath; Nancy B Spinner; Norman D Rosenblum
Journal:  Nat Rev Nephrol       Date:  2013-06-11       Impact factor: 28.314

6.  Congenital hepatic fibrosis and its mimics: a clinicopathologic study of 19 cases at a single institution.

Authors:  Irene Y Chen; Christa L Whitney-Miller; Xiaoyan Liao
Journal:  Diagn Pathol       Date:  2021-08-30       Impact factor: 2.644

  6 in total

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