pheochromocytomas การใช้

• Thus, the clinical presentation may resemble pheochromocytoma or Kawasaki disease.
• People with this condition have paragangliomas, pheochromocytomas, or both.
• Adrenal pheochromocytomas are usually benign while extraadrenal ones are more malignant.
• Pheochromocytomas are tumors of the adrenal medulla that arise from chromaffin cells.
• Other rare tumors may be dangerous to biopsy, such as pheochromocytoma.
• Pheochromocytoma linked to MEN II can be caused by RET oncogene mutations.
• Occasionally pheochromocytoma or primary hyperparathyroidism may be the initial diagnosis.
• HVA presence supports a diagnosis of neuroblastoma and malignant pheochromocytoma.
• It is a marker for catecholamine-secreting tumors such as pheochromocytoma.
• Patients experiencing symptoms associated with pheochromocytoma should be aware that it is rare.
• Chromaffin paragangliomas are issued from chromaffin cells, and are known as pheochromocytomas.
• Surgery, especially adrenal laparoscopy, is the most common treatment for small pheochromocytomas.
• A pheochromocytoma can also cause resistant arterial hypertension.
• The patient with pheochromocytoma is invariably volume depleted.
• Extra-adrenal tumors account for around 10 % of all cases of pheochromocytoma.
• The same condition is often called familial pheochromocytoma.
• Pheochromocytoma may occur in patients with MEN 2 and MEN 3 ( MEN 2B ).
• Both syndromes are characterized by pheochromocytoma as well as thyroid cancer ( thyroid medullary carcinoma ).
• Therefore, it is usually advised to " salt load " pheochromocytoma patients before their surgery.
• Other disorders that can cause high blood pressure include thyrotoxicosis, pheochromocytoma, and drug misuse.