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Pheochromocytoma is curable in 90% of cases, yet its diagnosis and localization are among the most challenging problems in clinical medicine. Although only 10% of these tumors are malignant, others may be lethal because of excessive circulating catecholamines. The clinical hallmark of pheochromocytoma is hypertension, but some patients are normotensive and may even be hypotensive.
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Nuzhet O. Atuk (1983) studied this question.
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