We report a case of adrenal pheochromocytoma in a patient with neurofibromatosis type 1 (NF1). A 65-year-old female patient was admitted to our hospital for examination of a right adrenal mass. The adrenal tumor was incidentally discovered by abdominal computed tomography during examination for hypertension in another hospital. She had large multiple neurofibromatous lesions and café-au-lait spots on the trunk. We thought that it was difficult to make a skin incision on normal skin. Serum and urinary catecholamines were markedly increased. Magnetic resonance imaging revealed a solid round tumor 3 cm in diameter, located in the right adrenal gland. Laparoscopic right adrenalectomy was performed. Serum and urinary catecholamines returned to t...
A pheochromocytoma is a tumor of the chromaffin cells of the adrenal gland medulla that produces exc...
BACKGROUND: Neurofibromatosis I may rarely predispose to pheochromocytoma and gastrointestinal strom...
Neurofibromatosis-1 (NF-1) is a genetic neuro-cutaneous disorder that is associated with an increase...
The association of a pheochromocytoma to a neurofibromatosis type 1 is a rare association.We relate ...
Introduction: Pheochromocytomas are rare neuroendocrine tumors that can occur sporadically or, in ab...
BACKGROUND: Neurofibromatosis type 1 is an autosomal dominant condition that has a variety of clinic...
Introduction Composite pheochromocytoma is a rare tumor, occurring in only 3% of pheochromocytomas. ...
Neurofibromatosis type 1 is the most common phakomatoses and is inherited in autosomal dominant fash...
Background: There are 4 prior reports of oncocytic pheochromocytoma of the adrenal. It may histologi...
PHEOCHROMOCYTOMA today cannot be considered an unusually rare tumor, since numerous isolated cases a...
AbstractINTRODUCTIONNeurofibromatosis type 1 is a genetic disease characterized by neoplastic and no...
Pheochromocytoma (PCC) occurs in 4% of pediatric neurofibromatosis type 1 (NF1) patients and is char...
Introduction - Neurofibromatosis type 1 (NF1), known as von Recklinghausen’s disease, is characteri...
Pheochromocytomas are catecholamine-producing neuroendocrine tumours arising from chromaffin cells o...
Abstract Catecholamine-producing tumors may arise in the adrenal medulla (pheochromocytomas) or in e...
A pheochromocytoma is a tumor of the chromaffin cells of the adrenal gland medulla that produces exc...
BACKGROUND: Neurofibromatosis I may rarely predispose to pheochromocytoma and gastrointestinal strom...
Neurofibromatosis-1 (NF-1) is a genetic neuro-cutaneous disorder that is associated with an increase...
The association of a pheochromocytoma to a neurofibromatosis type 1 is a rare association.We relate ...
Introduction: Pheochromocytomas are rare neuroendocrine tumors that can occur sporadically or, in ab...
BACKGROUND: Neurofibromatosis type 1 is an autosomal dominant condition that has a variety of clinic...
Introduction Composite pheochromocytoma is a rare tumor, occurring in only 3% of pheochromocytomas. ...
Neurofibromatosis type 1 is the most common phakomatoses and is inherited in autosomal dominant fash...
Background: There are 4 prior reports of oncocytic pheochromocytoma of the adrenal. It may histologi...
PHEOCHROMOCYTOMA today cannot be considered an unusually rare tumor, since numerous isolated cases a...
AbstractINTRODUCTIONNeurofibromatosis type 1 is a genetic disease characterized by neoplastic and no...
Pheochromocytoma (PCC) occurs in 4% of pediatric neurofibromatosis type 1 (NF1) patients and is char...
Introduction - Neurofibromatosis type 1 (NF1), known as von Recklinghausen’s disease, is characteri...
Pheochromocytomas are catecholamine-producing neuroendocrine tumours arising from chromaffin cells o...
Abstract Catecholamine-producing tumors may arise in the adrenal medulla (pheochromocytomas) or in e...
A pheochromocytoma is a tumor of the chromaffin cells of the adrenal gland medulla that produces exc...
BACKGROUND: Neurofibromatosis I may rarely predispose to pheochromocytoma and gastrointestinal strom...
Neurofibromatosis-1 (NF-1) is a genetic neuro-cutaneous disorder that is associated with an increase...