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1.
Article in English | IMSEAR | ID: sea-42434

ABSTRACT

Mesangial proliferative glomerulonephritis (MesPGN) is the most common histopathological finding of primary nephrotic syndrome in Thai children. Prediction of glomerular morphology is possible by the clinical characteristics: the age at onset older than 6 years old, occurring mostly in males, with or without hematuria, no hypertension, normal serum creatinine level, response to initial corticosteroid therapy but frequent relapses. Epidemiological study pertaining to associated environmental factors and immunological response of Thai children is needed.


Subject(s)
Adolescent , Child , Child, Preschool , Female , Glomerulonephritis/pathology , Glomerulonephritis, Membranoproliferative/pathology , Humans , Infant , Male , Nephrotic Syndrome/pathology
6.
Southeast Asian J Trop Med Public Health ; 1975 Dec; 6(4): 592-8
Article in English | IMSEAR | ID: sea-35631

ABSTRACT

A total of 240 cases of a bleeding syndrome in infants due to prothrombin complex deficiency of unknown aetiology were reviewed. The majority of patients were breast fed, aged 1-2 months and the syndrome was more prevalent in males. Clinical manifestations consisted of bleeding, pallor and mild hepatomegaly in the majority of cases. Mild fever, diarrhoea, jaundice, and upper respiratory tract infection were associated in a few patients. Acute onset, short course and a high rate of intracranial bleeding (65%), particularly subdural and subarachnoid, were observed. The haemostatic defects appeared to be a marked reduction in factor II, VII, IX, and X. Complete blood counts remained relatively normal, with the exception of some changes (anaemia, leukocytosis), in response to the acute bleeding. Liver chemistry was normal or slightly impaired. No specific pathological changes were noted at autopsy, there were mild changes of liver cells, such as rare focal necrosis of liver cells, the proliferation of Kupffer cells, extramedullary haemopoeisis and mild cholestasis. Clinical improvement and correction of hemostatic defects were noted after vitamin K therapy alone or with fresh blood transfusion. Mortality rates were high in infants with intracranial bleeding (40-55%), while the overall mortality rate was 25%. The pathogenesis and the possibility of prevention of the syndrome were discussed.


Subject(s)
Blood Coagulation/drug effects , Blood Coagulation Factors/analysis , Breast Feeding , Cerebral Hemorrhage/epidemiology , Female , Gastrointestinal Hemorrhage/epidemiology , Hemorrhage/drug therapy , Humans , Hypoprothrombinemias/drug therapy , Infant , Infant, Newborn , Liver/pathology , Male , Purpura/epidemiology , Thailand , Vitamin K/therapeutic use
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