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Biomedical subjects

D Hébert

Publications and source records attributed to D Hébert.

28 records · Page 2Linked to original sources

Pulmonary thrombo-embolism in the nephrotic syndrome.

The case of a 10.5-year-old boy who had complete right main pulmonary artery thromboembolism complicating steroid-resistant nephrotic syndrome is presented. Despite the massive nature of the lesion clinical symptoms were relatively minor. The thromboembolism was successfully treated with intrapulmonary artery streptokinase. The case highlights the discrepancy that may be found between the clinical and pathological findings in pulmonary thromboembolism in the nephrotic syndrome of childhood.

Child↗

Post-transplantation outcome of patients with hemolytic-uremic syndrome: update.

The outcome of renal transplantation in patients with hemolytic-uremic syndrome (HUS) is variable in reported cases. An update of the previously published series of patients from the University of Minnesota is reported. Seventeen patients with HUS received a renal transplant. Seven patients had recurrent HUS based on strict clinical and histological features and in 4 of these patients grafts were loss from recurrent HUS, with 1 patient losing three successive grafts. Three patients had histological features consistent with HUS but lacked some of the clinical features. Seven patients had no evidence of recurrent HUS post transplantation. The incidence of recurrence of HUS post transplantation in this updated report remains high (7/17 patients). There was no difference in the allografts used (living-related donor grafts were more common in all groups) or in the immunosuppression in the different groups of patients; only 1 patient with recurrent HUS received cyclosporine. The published cases of transplantation in patients with HUS show a variable recurrence rate of 0-25% in different centers with a poor graft outcome in patients with recurrence; a higher incidence of early chronic vascular rejection with decreased graft survival is also reported in patients without recurrence. Patients with HUS post renal transplant are at a variable risk of recurrence of HUS or decreased graft survival, and the factors responsible for this outcome are not known.

Adolescent↗

The rare phenotype En(a-) in a French-Canadian family.

A French-Canadian En(a-) propositus, whose red cells are phenotypically like the three previously reported, differs in the mode of reaction of this antibody which is apparently not immune. His consaguineous parents and 2 of this 4 sibs are heterozygous EnaEn, the other 2 being EnaEna. Sialic acid levels and the MN glycoprotein content of the red cells of the family and the PAS-straned patterns of the red cell membranes of the propositus confirm the serological findings.

Adult↗