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Biomedical subjects

M Foulard

Publications and source records attributed to M Foulard.

35 records · Page 2Linked to original sources

Berger's disease in children. Natural history and outcome.

The clinical course and outcome of 91 children less than 15 years of age at onset and followed for at least 1 year have been retrospectively analyzed. The course has been characterized by recurrent macroscopic hematuria in 74 patients, by proteinuria-microscopic hematuria and a single episode of macroscopic hematuria occurring either at onset or a few months later in 8, by proteinuria-microscopic hematuria in 7, and by proteinuria only in 1. Lastly, one patient showed rapidly progressive renal failure. Four groups were identified by light microscopy: minimal glomerular changes (26), focal and segmental glomerulonephritis (41), pure mesangial proliferation (3) and proliferative glomerulonephritis with crescents (21). A good correlation was found between the glomerular lesions observed by light microscopy and the outcome. In this series we have not observed a dramatic clinical deterioration suggesting a transformation from one histologic type to another, as reported by others. None of the 70 patients belonging to the first three groups has impaired renal function but two with focal and segmental glomerulonephritis have developed hypertension. Although the clinical course is benign, many patients have, at the last observation, an abnormal urinalysis characterized by microscopic hematuria and/or mild proteinuria; the proteinuria is over 1 g/24 h in six patients with focal and segmental glomerulonephritis. Ten patients remained in clinical remission for several years, but mesangial IgA deposits were still present in the only patient who had a repeat biopsy while in remission. In contrast, none of the patients with proliferative glomerulonephritis with crescents has had a prolonged remission. Six patients developed terminal renal failure 0.7, 0.11, 2, 4, 8 and 10 years after onset. Two additional patients are in moderate chronic renal failure with hypertension 10 and 12 years after onset. Most children show a persistent nephropathy, (in five proteinuria is over 1 g/24 h), and two of them have developed hypertension. Therapeutic trials using drugs with side-effects should, therefore, be used only in this group of patients.

Adolescent↗

[Comparison of left ventricular function in children hemodialyzed with bicarbonate and acetate. An echocardiographic study].

Left ventricular function before and after hemodialysis with acetate (A) and hemodialysis with bicarbonate (B) was investigated in 8 children on regular dialysis treatment. The decrease in left ventricular volume overload is similar in A and B. There is a significant increase in shortening fraction (B: 9,7 +/- 16,1%; p less than 0,05. A: 7,8 +/- 10,9%; p less than 0,05), in velocity of circumferential fiber shortening (Vcf) (B: 30,6 +/- 16,5%; p less than 0,0005. A: 23,5 +/- 16,6%; p less than 0,0025) and in corrected Vcf (B: 19,3 +/- 16,4%; p less than 0,0025. A: 13,6 +/- 11,4%; p less than 0,005). The ratio of pre-ejection period with the left ventricular ejection time (PEP/LVET) is increased significatively only after hemodialysis with bicarbonate. This difference may be due to a better left ventricular function in hemodialysis with bicarbonate than with acetate.

Acetates↗

[Echocardiographic findings in children with chronic renal failure ].

Echocardiographic examinations were carried out in 2 groups of children with chronic renal failure. Group 1 consisted of 9 children who were not treated with hemodialysis. Group 2 consisted of 9 children undergoing chronic hemodialysis. Results in both groups were compared with a control group of 35 normal children. No difference was found between normal children and group 1 children. Group 2 children presented with a moderate myocardial hypertrophy and dilatation of the left atrium. Indices of contractility were also decreased. Comparison before and after hemodialysis showed no change in cardiac function.

Adolescent↗

[Cerebral abscess due to abnormal caval return].

A case of abnormal venous return is reported. It was discovered during investigation of a cerebral abscess. There was a persisting and unique left superior vena cava, draining in the left atrium. No other cardiac malformation was present. This abnormality is rare as only 2 other cases have been reported. It should be suspected in children presenting with cyanosis, clubbing of the fingers and left ventricular hypertrophy on electrocardiography.

Brain↗