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GEN ; 63(4): 288-291, dic. 2009. ilus, graf
Artigo em Espanhol | LILACS | ID: lil-664445

RESUMO

The congenital liver cysts may be unique, multiple or diffusely distributed in the liver parenchyma ("polycystic liver"). In polycystic liver, the number, size cysts may be associated with polycystic kidney, with the severity of renal disease, which affects the prognosis. The pain and progressive increase in the abdominal cavity, associated with the growth of cysts worsen the quality of life coming to incapacitate the patient. Medical treatment consists of conservative amendments to the diet, AIN, use of antihypertensive and diuretics if developed hypertension. Others include the use of percutaneous drainage led by ultrasound, fenestration, partial hepatectomy and eventually liver transplantation and / or liver-kidney. The following case is a patient of 39-year-old female, with polycystic kidney and liver who does not respond to conservative medical treatment; presenting diffuse persistent abdominal pain, breathlessness on moderate efforts to limit the activity of daily living and incapacity to work, who was practiced remove the wall and fenestration of liver cysts with satisfactory postoperative evolution and improvement of the quality of life.

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