HIGH BLOOD PRESSURE SYMPTOMS CAUSES DIET & TREATMENT

Dr.Armughan Riaz
M.B.B.S, Dip Card
Consultant Cardiologist

 

Pheochromocytoma Symptoms Diagnosis Treatment

Pheochromocytoma signs symptoms diagnosis investigations treatment and management. Pheochromocytoma is a rare tumor of Adrenal glands

Pheochromocytoma Symptoms Diagnosis Treatment

 Pheochromocytomais an important cause of secondary Hypertension. We have adnenal gland located at upper portion of each kidney. It is devided into adrenal cortex and adrenal medulla. Pheochromocytoma is a tumor of Adrenal Medulla. Normal function of adrenal medulla is to produce epinephrine or adrenaline. Which is responsible for controlling blood pressure and to help cope with stressful situations.

Symptoms of Pheochromocytoma


So majority of symptoms of pheochromocytoma are due to excess secreation of adrenaline from adrenal medulla. Most patients of pheochromocytoma have recurrent episodes of headache, sweating and a feeling of high anxiety. The following symptoms are listed from the most common to the least common
Headaches (severe)
sweating Episodes (generalized)
heart palpitatios (tachycardia and palpitations)
Anxiety
nervousness (feelings of impending death)
tremors
Pain in the lower chest or upper abdomen
Nausea (with or without nausea)
Weight loss
Heat intolerance

These symptoms may come by situations which causes pressure over tumor like physical activity, exercise, defecation, anesthesia, or change in body position.

Who should be examined for Pheochromocytoma
Those who have uncontrolled hypertension
Those who have age between 40 and 60
Those who are already taking 4 antihypertensive drugs but blood pressure is not controlable.
Those who have episodes of above symptoms


Causes of Pheochromocytoma


Cause of pheochromocytoma is unknown, however some forms of this tumor runs in families like,
a-Multiple endocrine neoplasia, type II (MEN-II). In addition to a pheochromocytoma, people with MEN-II also have thyroid cancer. Other forms of MEN-II include pheochromocytoma with thyroid cancer and hyperparathyroidism (MEN-IIA), and pheochromocytoma with thyroid cancer and tumors of nerves in the eyes lips, mouth and digestive tract (MEN-IIB).
b-Neurofibromatosis 1 (NF1). Pheochromocytomas can occur in a small percentage of people with NF1, a syndrome that includes multiple tumors in the skin (neurofibromas), pigmented skin spots, tumors of the optic nerve of the eye, and bone diseases.
c-Von Hippel-Lindau (VHL) disease. People with this rare multisystem disorder are at high risk of pheochromocytoma brain eye and kidney tumors.

Most pheochromocytomas are benign tumors and they dont spread to other parts of body however some forms do show metastasis (spread) to other parts of body like lungs, bones and brains. Usually only one gland is involved however this tumor can be present in both adrenal glands.


Investigations of Pheochromocytoma

Blood and Urine tests: We perform blood and urine tests to diagnose pheochromocytoma. 24 hr urine collection is tested for epinephrine, norepinephrine and dopamine. This test is called VMA. Idea is just to check level of epinephrine and its metabolites in urine. If these are detected in urine in excess quantity, then tumor is diagnosed.

Abdominal scan.
Now you have diagnosed tumor by blood and urine tests, after that to find out location of tumor, do Ultrasound, CT scan of abdomen.

Complications:
If high blood pressure remained uncontrolled it may lead to complications of heart failure, infarction, cerebrovascular accident, vision damage and kidney failure.

Treatment of Pheochromocytoma


First treatment is to control high blood pressure with medication like Alpha Blockers and Beta Blockers. When epinephrine is secreated by this tumor it acts on alpha and beta receptors present on heart and blood vessels, result is vasoconstriction and increase heart rate. Now if if we take drugs like alpha blocker and beta blocker, epinephrine will be blocked by these drugs to act on these receptors so result is vasodilation and slow heart rate. Common Alpha blockers are Prazosin (Minipress), Terazosin (Hytrin) Phenoxybenzamine( Dibenzaline). Common Beta Blockers are Atenolol(Tenormin), Carvedilol(Carveda), Metoprolol(Mepressor), Inderal.

Treatment of choice for this tumor is Surgery. After removal of this gland by surgery, blood pressure becomes normal with a day. There are two types of surgeries. General and Laproscopic surgery. However Surgery is not an option for those tumors which show metastasis to other parts of body. For that we use chemotherapy and radiations.

Whenever you have high blood pressure with any symptom, don't ignore it, you may be the patient of Pheochromocytoma. Always contact your Doctor.

 



Your Comments
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Suzamara from LOCNtQSh
Toprol-XL (metoprolol) for Mitral Valve Prolapse: I was diagnosed with mitarl valve prolapse syndrome my senior year in college, resulting in a medical discharge from the Army rather than commissioning as an officer. I was blacking out, fainting, and my activity tolerance dropped dramatically as the condition progressed. Metoprolol was prescribed for me to help regulate my heart rate it worked great for that. I didn't feel the palpitations and heart racing with minimal activity. Downside was that my blood pressure was already low so being on this medication made my blood pressure drop even lower. Doctors eventually put me on MIDODRINE which constricts my blood vessels causing an increase in blood pressure. The combination works great!GD Star Ratingloading...
Posted at 9:51:am 06/02/12
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