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Familial
cases are diagnosed earlier and are more frequently
bilateral and recurring than sporadic cases. The most
specific and sensitive diagnostic test for the tumor
is the determination of plasma or urinary metanephrines.
The tumor can be located by computed tomography, magnetic
resonance imaging and metaiodobenzylguanidine scintigraphy.
Treatment is resection of the tumor, generally by laparoscopic
surgery.
About 10% of tumors are malignant either at first operation
or during follow-up, malignancy being diagnosed by the
presence of lymph node, visceral or bone metastases.
Recurrences and malignancy are more frequent in cases
with large or extraadrenal tumors. Treatment for malignant
recurrence includes surgery, therapeutic embolization,
chemotherapy and metabolic radiotherapy. Patients, especially
those with familial or extraadrenal tumors, should be
followed-up indefinitely.
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more information on Pheochromocytomas see the links
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