Introduction Composite pheochromocytoma is a rare tumor, occurring in only 3% of pheochromocytomas. We report case composite with neurofibromatosis type 1. Case presentation A 42-year-old man was referred to our department for further evaluation an incidentally detected right adrenal tumor. He patient at another hospital The serum and urinary catecholamine levels exceeded the normal range. Abdo...

Pheochromocytoma in elderly people is a very rare disease and surgical removal the only cure. Here we present an 81-year-old gentleman with multiple co morbidities left adrenal incidentaloma. He was diagnosed to have pheochromocytoma biochemical evaluation. underwent laparoscopic adrenalectomy after prolonged preparation alpha beta blockers. This second oldest patient histo-pathological diagnos...

Pheochromocytomas are rare tumours originating in chromaffin cells, representing 0.1–1% of all secondary hypertension cases.1 A case pheochromocytoma a 34 year old male presenting with unusual symptoms abdominal discomfort and vomiting is presented. He has been generally well the past but started feeling excessively tired for last 4 years had dyspepsia off on. On presentation his blood pressure...

Pheochromocytoma (PC) is a tumor of chromaffin cells the sympathetic-adrenal system that produces large amount catecholamines (adrenaline, norepinephrine, dopamine). There are no reliable data in literature on frequency cardiac manifestations pheochromocytoma, which associated with rarity this pathology. This case demonstrates development catecholamine-induced cardiomyopathy, proceeding under g...

summary: pheochromocytoma is an adrenal tumor characterized by symptoms of hypertension, headache, increased sweating, and tachycardia .in one third of patients, the tumor is discovered incidentally during radiological evaluation of the abdomen. in this article a case of bilateral pheochromocytoma is reported. the patient, a twelve years old boy, referred with complaints of headache, flushing, ...

a case of pheochromocytoma of the bladder is presented with a r eview of the literature. we discuss general management principles of bladder pheochromocytoma. successful diagnosis and treatment of this lesion requires a high index of suspicion based upon the patient's symptom complex, allowing preoperative preparation prior to surgical treatment.

Introduction: Pheochromocytoma is an exceptional cause of Cushings syndrome. We report the very case a composite pheochromocytoma-ganglioneuroma with ectopic secretion adrenocorticotrophic hormone, two rare histological entities grouped into one, in patient complex clinical feature. Case Report: This 62-year-old consulting for polyarthralgia and low back pain whom physical examination found The...

Abstract Background Pheochromocytoma is a rare tumor originating from the adrenal medulla, and surgical removal main treatment. We report case of large size pheochromocytoma that was removed laparoscopically without preoperative blockade alfa adrenergic receptors. Case presentation A 58-y-old woman referred to our center with incidentally found 7 cm right mass. She did not have any history hype...

Chromaffin granule transmitters such as chromogranin A and catecholamines have been used in the diagnosis of pheochromocytoma, but the diagnostic and prognostic value of chromogranin A have not been explored in malignant pheochromocytoma. We evaluated these transmitters in patients with pheochromocytoma (n=27), both benign (n=13) and malignant (n=14). Patients with benign pheochromocytoma were ...