1/2. Small intestinal infarction: a fatal complication of systemic oxalosis.Primary hyperoxaluria is a rare genetic disorder characterised by calcium oxalate nephrolithiasis and nephrocalcinosis leading to renal failure, often with extra-renal oxalate deposition (systemic oxalosis). Although ischaemic complications of crystal deposition in vessel walls are well recognised clinically, these usually take the form of peripheral limb or cutaneous ischaemia. This paper documents the first reported case of fatal intestinal infarction in a 49 year old woman with systemic oxalosis and advocates its consideration in the differential diagnosis of an acute abdomen in such patients.- - - - - - - - - - ranking = 1keywords = nephrocalcinosis (Clic here for more details about this article) |
2/2. Primary hyperparathyroidism: an unusual cause of pancreatitis in adolescence.We present the case of an adolescent with hypercalcemia secondary to unrecognized hyperparathyroidism, which lead to complications such as pancreatitis, diabetes mellitus, and nephrocalcinosis. Although hypercalcemia is not common in the pediatric age, its early recognition and intervention are crucial for the prevention of highly morbid complications.- - - - - - - - - - ranking = 1keywords = nephrocalcinosis (Clic here for more details about this article) |