Literature DB >> 1601012

Progressive cardiac failure following orthotopic liver transplantation for type IV glycogenosis.

E M Sokal1, F Van Hoof, D Alberti, J de Ville de Goyet, T de Barsy, J B Otte.   

Abstract

Orthotopic liver transplantation (OLT) has been proposed to treat patients with type IV glycogenosis because of early progressive cirrhosis. Reports have shown absence of disease progression in other organs after OLT and even regression of cardiac amylopectin infiltration in one case. We describe a 15-month-old child in whom a liver transplant was performed for type IV glycogenosis. There were no clinical signs of extrahepatic disease before OLT. Nine months later, the patient developed progressive cardiac insufficiency and died from cardiac failure. Because of massive amylopectin deposits, decreased myofibrils in cardiac cells, and exclusion of other causes of cardiac failure, death was attributed to amylopectionosis. Our observation contrasts with the Pittsburgh experience and suggests that cardiac amylopectionosis may progress after OLT.

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Year:  1992        PMID: 1601012     DOI: 10.1007/bf01954384

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


  11 in total

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Journal:  Lab Invest       Date:  1956 Jan-Feb       Impact factor: 5.662

2.  Liver transplantation for type IV glycogen storage disease.

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Journal:  N Engl J Med       Date:  1991-01-03       Impact factor: 91.245

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Journal:  Lab Invest       Date:  1979-04       Impact factor: 5.662

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Journal:  Acta Neuropathol       Date:  1971       Impact factor: 17.088

5.  Lack of an alpha-1,4-glucan: alpha-1,4-glucan 6-glycosyl transferase in a case of type IV glycogenosis.

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Journal:  Proc Natl Acad Sci U S A       Date:  1966-08       Impact factor: 11.205

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Journal:  Arch Pathol Lab Med       Date:  1979-03       Impact factor: 5.534

7.  Liver transplantation in children less than 1 year of age.

Authors:  E M Sokal; F Veyckemans; J de Ville de Goyet; D Moulin; N Van Hoorebeeck; D Alberti; J P Buts; J Rahier; L Van Obbergh; P Clapuyt
Journal:  J Pediatr       Date:  1990-08       Impact factor: 4.406

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Journal:  J Biol Chem       Date:  1952-12       Impact factor: 5.157

9.  A new variant of type IV glycogenosis: deficiency of branching enzyme activity without apparent progressive liver disease.

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Journal:  Hepatology       Date:  1988 Mar-Apr       Impact factor: 17.425

10.  Size reduction of the donor liver is a safe way to alleviate the shortage of size-matched organs in pediatric liver transplantation.

Authors:  J B Otte; J de Ville de Goyet; E Sokal; D Alberti; D Moulin; B de Hemptinne; F Veyckemans; L van Obbergh; M Carlier; P Clapuyt
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  8 in total

1.  Living Donor Liver Transplantation in a Korean Child with Glycogen Storage Disease Type IV and a GBE1 Mutation.

Authors:  Hye Ryun Ban; Kyung Mo Kim; Joo Young Jang; Gu-Hwan Kim; Han-Wook You; Kyungeun Kim; Eunsil Yu; Dae Yeon Kim; Ki Hun Kim; Young Joo Lee; Sung Gyu Lee; Young Nyun Park; Hong Koh; Ki Sup Chung
Journal:  Gut Liver       Date:  2009-03-31       Impact factor: 4.519

2.  Glycogenosis type IV: liver transplant at 12 years.

Authors:  A Dhawan; K C Tan; B Portmann; A P Mowat
Journal:  Arch Dis Child       Date:  1994-11       Impact factor: 3.791

Review 3.  Liver transplantation for pediatric inherited metabolic disorders: Considerations for indications, complications, and perioperative management.

Authors:  Kimihiko Oishi; Ronen Arnon; Melissa P Wasserstein; George A Diaz
Journal:  Pediatr Transplant       Date:  2016-06-21

4.  Liver transplantation for inborn errors of liver metabolism.

Authors:  Efienne M Sokal
Journal:  J Inherit Metab Dis       Date:  2006 Apr-Jun       Impact factor: 4.982

Review 5.  Liver transplantation for glycogen storage disease types I, III, and IV.

Authors:  D Matern; T E Starzl; W Arnaout; J Barnard; J S Bynon; A Dhawan; J Emond; E B Haagsma; G Hug; A Lachaux; G P Smit; Y T Chen
Journal:  Eur J Pediatr       Date:  1999-12       Impact factor: 3.183

Review 6.  Quality of life after orthotopic liver transplantation in children. An overview of physical, psychological and social outcome.

Authors:  E M Sokal
Journal:  Eur J Pediatr       Date:  1995-03       Impact factor: 3.183

Review 7.  Response to treatment in hereditary metabolic disease: 1993 survey and 10-year comparison.

Authors:  E Treacy; B Childs; C R Scriver
Journal:  Am J Hum Genet       Date:  1995-02       Impact factor: 11.025

Review 8.  Glycogen storage diseases with liver involvement: a literature review of GSD type 0, IV, VI, IX and XI.

Authors:  Miriam Massese; Francesco Tagliaferri; Carlo Dionisi-Vici; Arianna Maiorana
Journal:  Orphanet J Rare Dis       Date:  2022-06-20       Impact factor: 4.303

  8 in total

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