Literature DB >> 2126237

False diagnosis of non-A/non-B hepatitis hiding two cases of cystic fibrosis.

M Resti1, C Adami Lami, F Tucci, F Mannelli, M E Rossi, C Azzari, A Vierucci.   

Abstract

We report two cases of children followed for many years with an original diagnosis of non-A/non-B hepatitis. One child developed serious cirrhosis with portal hypertension. Long-term observation of the course of their hepatic disease provided the diagnosis of cystic fibrosis. These cases demonstrate that cystic fibrosis though rarely presenting with initial hepatic signs, can manifest itself with only long-term hepatic symptoms. We therefore strongly recommend analysis of sweat chloride concentration in cases of hepatic disease of unknown origin.

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Year:  1990        PMID: 2126237     DOI: 10.1007/bf02072047

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  14 in total

1.  Clinical observations on the biliary system in cystic fibrosis.

Authors:  J N Isenberg; P R L'Heureux; W J Warwick; H L Sharp
Journal:  Am J Gastroenterol       Date:  1976-02       Impact factor: 10.864

2.  The effects of age on alkaline phosphatase and other serologic liver function tests in normal subjects and patients with cystic fibrosis.

Authors:  J Kattwinkel; L M Taussig; B E Statland; J I Verter
Journal:  J Pediatr       Date:  1973-02       Impact factor: 4.406

3.  Prolonged neonatal jaundice in cystic fibrosis.

Authors:  H B Valman; N E France; P G Wallis
Journal:  Arch Dis Child       Date:  1971-12       Impact factor: 3.791

4.  Common bile duct obstruction causing right upper abdominal pain in cystic fibrosis.

Authors:  M K Patrick; R Howman-Giles; M De Silva; P Van Asperen; J Pitkin; K J Gaskin
Journal:  J Pediatr       Date:  1986-01       Impact factor: 4.406

Review 5.  Gastrointestinal manifestations of cystic fibrosis: a review.

Authors:  R W Park; R J Grand
Journal:  Gastroenterology       Date:  1981-12       Impact factor: 22.682

6.  Additional data on hepatic function tests in cystic fibrosis.

Authors:  J Feigelson; Y Pecau; L Cathelineau; J Navarro
Journal:  Acta Paediatr Scand       Date:  1975-03

7.  Symptomatic hepatic disease in cystic fibrosis: incidence, course, and outcome of portal systemic hunting.

Authors:  R C Stern; D P Stevens; T F Boat; C F Doershuk; R J Izant; L W Matthews
Journal:  Gastroenterology       Date:  1976-05       Impact factor: 22.682

8.  Cystic fibrosis with extensive fat replacement of the liver.

Authors:  R S Wilroy; S E Crawford; W W Johnson
Journal:  J Pediatr       Date:  1966-01       Impact factor: 4.406

9.  Hepatobiliary disease in cystic fibrosis: a survey of current issues and concepts.

Authors:  C C Roy; A M Weber; C L Morin; G Lepage; G Brisson; I Yousef; R Lasalle
Journal:  J Pediatr Gastroenterol Nutr       Date:  1982       Impact factor: 2.839

10.  Morphological findings in the liver of children with cystic fibrosis: a light and electron microscopical study.

Authors:  R Hultcrantz; S Mengarelli; B Strandvik
Journal:  Hepatology       Date:  1986 Sep-Oct       Impact factor: 17.425

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  4 in total

Review 1.  Spectrum of viral infections in patients with cystic fibrosis.

Authors:  H Frickmann; S Jungblut; T O Hirche; U Groß; M Kuhns; A E Zautner
Journal:  Eur J Microbiol Immunol (Bp)       Date:  2012-09-10

2.  Hypertransaminasemia in childhood as a marker of genetic liver disorders.

Authors:  Raffaele Iorio; Angela Sepe; Antonietta Giannattasio; Francesco Cirillo; Angela Vegnente
Journal:  J Gastroenterol       Date:  2005-08       Impact factor: 7.527

Review 3.  Abdominal pain in cystic fibrosis.

Authors:  J M Littlewood
Journal:  J R Soc Med       Date:  1995       Impact factor: 5.344

Review 4.  Persistent hypertransaminasemia in asymptomatic children: a stepwise approach.

Authors:  Pietro Vajro; Sergio Maddaluno; Claudio Veropalumbo
Journal:  World J Gastroenterol       Date:  2013-05-14       Impact factor: 5.742

  4 in total

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