A Case of Hypokalemic Myopathy Associated with Bartter's Syndrome
Journal of the Korean Neurological Association
;
: 289-294, 1996.
Artigo
em Coreano
| WPRIM
| ID: wpr-93074
ABSTRACT
Bartter's syndrome is characterized by hyperreninemia, hyperaldosteronism, hypokalemic hypochlorenlic alkalosis, normal blood pressure, juxtaglomerular apparatus hyperplasia, general weakness, and muscle weakness. We experienced a case of hypokalemic myopathy associated with Bartter's syndrome in 15 years old male. He had experienced paroxysmal muscle weakness without sensory change and myalgia since 10 years old. Subsequently, he had complaints of progressive muscle weakness, especially proximal muscles. Prominent juxtaglomerular apparatus with cellular proliferation biopsy was seen in the kidney. And there were mild perivascular inflammatory cell infiltration, small degenerating and/or regenerating muscles fibers, and normal muscle fiber distribution without evidence of chronic myopathy in the muscle biopsy. The patient was sucessfully managed with indomethacin and oral potassium chloride.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Cloreto de Potássio
/
Síndrome de Bartter
/
Biópsia
/
Pressão Sanguínea
/
Indometacina
/
Debilidade Muscular
/
Proliferação de Células
/
Alcalose
/
Mialgia
/
Hiperaldosteronismo
Limite:
Adolescente
/
Criança
/
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Journal of the Korean Neurological Association
Ano de publicação:
1996
Tipo de documento:
Artigo
Similares
MEDLINE
...
LILACS
LIS