Literature DB >> 3958471

Hepatobiliary fibropolycystic diseases. A clinical and histological review of 51 patients.

J A Summerfield, Y Nagafuchi, S Sherlock, J Cadafalch, P J Scheuer.   

Abstract

The clinical, radiological and hepatic histological features of 51 patients with hepatobiliary fibropolycystic disease were reviewed. Many of the patients had more than one of the diseases; the combination of both congenital hepatic fibrosis (CHF) and Caroli's disease was most striking. Twelve patients with CHF (50% male) presented at 6 +/- 2 years of age (mean +/- SEM) with hepatosplenomegaly or variceal bleeding. Their main problems were recurrent variceal bleeds and renal disease. Polycystic kidneys and renal stones were present in 79% and chronic renal failure in 30%. Six of the 8 patients with Caroli's disease were male (75%) and presented later (aged 37 +/- 8 years) with hepatomegaly or cholangitis. Recurrent cholangitis developed in most (7/8) and 2 had polycystic kidneys. Twelve patients had a combination of CHF and Caroli's disease presenting with hepatosplenomegaly, bleeding or cholangitis. As in Caroli's disease, most (83%) were male, but the age of presentation (15 +/- 4 years), and the incidence of polycystic kidneys (42%) and renal failure (8%) was intermediate between CHF and Caroli's disease. In these patients, bleeds always predated cholangitis. Histologically, acute cholangitis was superimposed on the changes of CHF. Adult polycystic liver disease (10 patients) presented later (43 +/- 3 years) in females (90%) with pain, a mass or incidentally; polycystic kidneys were present in 33%. Microhamartomas (10 patients), which were usually incidental findings, were diagnosed latest (50 +/- 6 years). Three choledochal cysts were seen. The hazard of cancer in these diseases was reflected by 2 bile duct cancers and 1 pancreatic cancer (incidence 6%). This study has confirmed that hepatobiliary fibropolycystic diseases form part of a family and are often associated together. However, the diseases are of greatly differing severity and the prognosis in an individual patient is determined by the fibropolycystic diseases present.

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Year:  1986        PMID: 3958471     DOI: 10.1016/s0168-8278(86)80073-3

Source DB:  PubMed          Journal:  J Hepatol        ISSN: 0168-8278            Impact factor:   25.083


  35 in total

1.  Congenital hepatic fibrosis leading to cirrhosis and hepatocellular carcinoma: a case report.

Authors:  Mohammad Reza Ghadir; Mohammad Bagheri; Amir Hossein Ghanooni
Journal:  J Med Case Rep       Date:  2011-04-22

2.  Caroli's disease in three siblings.

Authors:  K Yoshizawa; K Kiyosawa; K Yabu; S Usuda; S Shimizu; Y Fujimori; K Mukawa; E Tanaka; T Sodeyama; S Furuta
Journal:  Gastroenterol Jpn       Date:  1992-12

3.  Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: summary statement of a first National Institutes of Health/Office of Rare Diseases conference.

Authors:  Meral Gunay-Aygun; Ellis D Avner; Robert L Bacallao; Peter L Choyke; Joseph T Flynn; Gregory G Germino; Lisa Guay-Woodford; Peter Harris; Theo Heller; Julie Ingelfinger; Frederick Kaskel; Robert Kleta; Nicholas F LaRusso; Parvathi Mohan; Gregory J Pazour; Benjamin L Shneider; Vicente E Torres; Patricia Wilson; Colleen Zak; Jing Zhou; William A Gahl
Journal:  J Pediatr       Date:  2006-08       Impact factor: 4.406

Review 4.  Liver and kidney disease in ciliopathies.

Authors:  Meral Gunay-Aygun
Journal:  Am J Med Genet C Semin Med Genet       Date:  2009-11-15       Impact factor: 3.908

5.  Neonatal presentation of Caroli's disease.

Authors:  F Keane; N Hadzić; M L Wilkinson; S Qureshi; C Reid; A J Baker; G Mieli-Vergani
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  1997-09       Impact factor: 5.747

6.  Hepatobiliary cystadenocarcinoma of the liver with features of ductal plate malformations.

Authors:  Tadashi Terada
Journal:  J Gastrointest Cancer       Date:  2015-06

Review 7.  Large-duct cholangiopathies: aetiology, diagnosis and treatment.

Authors:  Shyam Menon; Andrew Holt
Journal:  Frontline Gastroenterol       Date:  2019-01-04

Review 8.  Pathology of Fibropolycystic Liver Diseases.

Authors:  Jason Lewis
Journal:  Clin Liver Dis (Hoboken)       Date:  2021-05-01

9.  A Retrospective Case Control Study of Ductal Plate Malformation-like Features in Consecutive 200 Autopsies.

Authors:  Tadashi Terada
Journal:  Pathol Oncol Res       Date:  2017-02-24       Impact factor: 3.201

10.  Pleuropulmonary blastoma in a child with autosomal-recessive polycystic kidney disease.

Authors:  Jeffrey Traubici; Gino R Somers; Simon C Ling; Rachel J Pearl; Paul C Nathan
Journal:  Pediatr Radiol       Date:  2011-07-01
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