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Acute pancreatitis in six non-transplanted uraemic children
Authors:B. Boudailliez  J. L. André  M. Broyer  J. C. Davin  G. Landthaler  J. B. Palcoux
Affiliation:(1) Department of Paediatrics, Renal Unit CHU, F-80030 Amiens Nord, France;(2) Paediatric Nephrology Department of Nancy, F-54511 Candceuvre, France;(3) Paediatric Nephrology Department, Hôpital Necker Enfants, Malades, F-75743 Paris, France;(4) Paediatric Nephrology Department, Hôpital de Bavière, B-4020 Liège, Belgium;(5) Paediatric Nephrology Department, Hôpital Charles Nicolle, F-76038 Rouen, France;(6) Paediatric Nephrology Department, Hôtel Dieu, F-63003 Clermont Ferrand, France;(7) Service de Pediatrie, Hôpital Nord, Place Victor Pauchet, B. P. F-3006, F800300 Amiens Cedex, France
Abstract:
Ten clinical episodes of acute pancreatitis (AP) occurred in six patients (mean age 10 years, range 3–15 years) with chronic renal failure (CRF) during a 9-year period (1977–1986). The underlying cause of CRF was vesicoureteral reflux (2); urethral valves (1); ureterohydronephrosis (1); nephronopthisis (1) and a haemolytic uraemic syndrome which occurred 12 years before (1). In all patients a diagnosis of AP was established both on clinical grounds and with a serum amylase level of >600 IU/1. In 3 patients laparotomy was performed because of suspected appendicitis. All patients required exclusive parentenral feeding (mean duration 25 days) and 2 patients had a partial pancreatectomy. No patient developed pancreatic pseudocysts, 2 patients experienced one relapse (3 and 21 months later) and 1 patient had two relapses and died. Mean duration of follow up was 3 years (range 1–10 years). Possible aetiological factors were: choledochal cyst (1); parotitis without a rise in mumps antibodies (1); familial dyslipidaemia but without AP in other family members (1), and aluminium intoxication with hypercalcaemia and convulsive encephalopathy treated with valproic acid in 1 patient. Severe hyperparathyroidism with radiological signs was absent in all patients. Transplantation had been performed either before AP in 2 patients (1 and 3 years before AP) or had followed AP in 1 patient (7 years after) without occurrence or relapse of AP.This work was presented at the Twenty-First Annual Meeting of European Society for Paediatric Nephrology, 3–5 September 1987, Budapest, Hungary
Keywords:Chronic renal failure  End-stage kidney disease  Children  Pancreatitis  Haemodialysis  Peritoneal dialysis
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