Pheochromocytoma Associated with Renal Agenesis:A Case Report and Review of Literature- Juniper Publishers
Journal of Surgery - JuniperPublishers Pheochromocytomas are neuroendocrine tumors developed at the expense of cells derived from the neural crest. They occur sporadically in 50-55% of cases, but they can be familial in 5 to 10% of cases and then be isolated or integrated into an inherited syndrome of multiple neuroendocrinopathy. The properly operated pheochromocytoma is radically and definitively cured as long as it is benign and sporadic. Renal anomalies have been reported rarely in this disease. Here we report a rare case of pheochromocytoma associated with renal agenesis. Patient was a female presented with headache and hypertension. In radiologic examinations, an adrenal mass was detected in the right side, with no renal tissue on that side. It was reported an adrenal pheochromocytoma in histopathology. Renal agenesis confirmed during surgery. All of the patient’s symptoms alleviated after the resection of tumor. Considering association of renal abnormali...