pheochromocytoma वाक्य
उदाहरण वाक्य
मोबाइल
- 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.
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