From obstructive uropathy to syndromic suspicion: a case of multiglandular primary hyperparathyroidism and pancreatic nodule mimicking multiple endocrine neoplasia type 1
Multiple endocrine neoplasia type 1 (MEN-1) is an autosomal dominant disorder characterized by synchronous or metachronous tumor development within the parathyroid glands, enteropancreatic neuroendocrine framework, and anterior pituitary. A 48-year-old female presented with severe bilateral loin pain and anuria lasting...