| 1. | Thus, the clinical presentation may resemble pheochromocytoma or Kawasaki disease.
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| 2. | People with this condition have paragangliomas, pheochromocytomas, or both.
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| 3. | Adrenal pheochromocytomas are usually benign while extraadrenal ones are more malignant.
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| 4. | Pheochromocytomas are tumors of the adrenal medulla that arise from chromaffin cells.
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| 5. | Other rare tumors may be dangerous to biopsy, such as pheochromocytoma.
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| 6. | Pheochromocytoma linked to MEN II can be caused by RET oncogene mutations.
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| 7. | Occasionally pheochromocytoma or primary hyperparathyroidism may be the initial diagnosis.
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| 8. | HVA presence supports a diagnosis of neuroblastoma and malignant pheochromocytoma.
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| 9. | It is a marker for catecholamine-secreting tumors such as pheochromocytoma.
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| 10. | Patients experiencing symptoms associated with pheochromocytoma should be aware that it is rare.
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