Hyperaminotransferasemia –in daily practice of a paediatrician and general practitione

Authors

  • Anna Płoskoń Z Klinicznego Oddziału Dziecięcego, Szpitala Wojewódzkiego nr 2 w Rzeszowie
  • Monika Lonc Z Klinicznego Oddziału Dziecięcego, Szpitala Wojewódzkiego nr 2 w Rzeszowie

Keywords:

hyperaminotransferasemia, children, differential diagnosis, liver diseases, muscular diseases

Abstract

Hyperaminotransferasemia — elevated liver enzymes, is one of the most frequently observed abnormali-ties in the lab studies. It is present in many various diseases such as: liver or neuro-muscular disorders, in-born errors of metabolism, drug side effects and many others. Therefore differential diagnosis remains a difficult problem in the daily practice of many specialists, but first and foremost of a general practitioner and paediatrician. While diagnosing a patient with elevated liver enzymes a cilnicist must firstly think of the most frequent diseases, secondly of more rare disorders. It is believed that following aspects should be con-sidered in the diagnosis: clinical symptoms, duration, complementary lab tests, imaging. Only appropriate differential diagnosis should lead to a truthful diagnosis and adequate treatment.

Downloads

Download data is not yet available.

References

G. Herold, Medycyna Wewnętrzna, PZWL 2001, 4: 550–612

J. Socha, Pediatria pod red W. Kubickiej i W. Kawalec, PZWL 2003, 12: 384–390

S. Pawelski, S. Maj, Normy i diagnostyka chorób, PZWL 1993, 8: 506–512

A. Dobrzyńska, J. Ryżko, Pediatria, Urban & Partner 2004, 10: 355–368

J. Socha, Choroby wątroby i dróg żółciowych u dzieci, PZWL 1994, 2–6: 20–180

T. Zalewski, Choroby przewodu pokarmowego u dzieci, PZWL 1995, 19: 316–347

H. H. Sukerek, Autoimmune Chronic Active Hepatitis, 2006, www.emedicine.com

Krawitt EL: Autoimmune hepatitis, N Engl J Med 2006 Jan 5; 354

D. Bogdanos, D.Vergani, (2004), Overlap syndromes from pediatrics to adulthood, Journal of Gastroenterology and Hepatology 19 (7): 284–S286

J. Pawłowska, Postępy w hepatologii dziecięcej w 2006 r, Med. Prakt, Pediatr., 2007, 7: 88–90

Adams LA, Lymp JF, St Sauver J, et al., The natural history of nonalcoholic fatty liver disease: a population–based cohort study, Gastroenterology. Jul 2005; 129: 113–121

Ong JP, Younossi ZM., Approach to the diagnosis and treatment of nonalcoholic fatty liver disease, Clin Liver Dis. Nov 2005; 9(4):617–34

Brunt EM., Sem. In Liver Disease 2001; 21:195–212

J. Zschocke, G. Hoffman, Vademeceum Metabolicum, Podręcznik pediatrii metabolicznej, Milupa 2004; 1: 22–40

Ala A, Walker AP, Ashkan K, Dooley JS, Schilsky ML., Wilson's disease, Lancet. Feb 3 2007, 369:397–408

EuroWilson Project. EuroWilson. Living with Wilson's, available at: www.eurowilson.com

D. E. Johnston, Special Considerations in Interpreting Liver Function Tests (American Family Physician Apr. 1999; 59(8): 2223–30

Published

2008-03-30

How to Cite

Płoskoń, A., & Lonc, M. (2008). Hyperaminotransferasemia –in daily practice of a paediatrician and general practitione. European Journal of Clinical and Experimental Medicine, 6(1), 77–83. Retrieved from https://journals.ur.edu.pl/ejcem/article/view/13285