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