Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Adicionar filtros








Intervalo de ano
1.
Annals of Pediatric Endocrinology & Metabolism ; : 49-52, 2014.
Artigo em Inglês | WPRIM | ID: wpr-158568

RESUMO

Glycogenic hepatopathy (GH) is a rare complication of type 1 diabetes mellitus. We report the case of a 13-year-old diabetic female with poorly controlled blood sugar levels who presented with abdominal pain and distention 1 month in duration. She exhibited tender hepatomegaly, an elevated lipid profile, and elevated serum transaminase levels. Her liver histology was consistent with GH. The pathophysiology and/or underlying genetic background of GH remains unclear. The optimum treatment for GH is optimal glycemic control, and the prognosis is favorable. Clinicians should be aware of the possibility of GH and observe the clinical response to optimal glycemic control prior to invasive investigation.


Assuntos
Adolescente , Feminino , Humanos , Dor Abdominal , Glicemia , Diabetes Mellitus Tipo 1 , Glicogênio , Hepatomegalia , Fígado , Prognóstico
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA