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Pheochromocytoma
Group 5
BMDC05
SIMAD University
Introduction
 Pheochromocytoma (PCC) is a rare tumor that
usually grows in the adrenal glands, above the
kidneys.
 PPC is catecholamine-secreting tumor, typically of
the adrenal medulla or extraadrenal paraganglion
tissue.
 It’s also known as an adrenal paraganglioma or a
chromaffin cell tumor.
 It’s most common in adults ages 30 to 50, but
people of all ages can have it. Children make up
about 10% of all cases.
 Adrenal glands make hormones that control things
like metabolism and blood pressure.
 A pheochromocytoma also releases hormones, at
much higher levels than usual. These extra
hormones cause high blood pressure, which can
damage heart, brain, lungs, and kidneys.
 About 10% to 15% of these tumors are cancerous,
and they can spread to other parts of the body. But
most pheochromocytoma tumors are benign,
meaning they’re not cancerous.
Causes
 The primary cause of pheochromacytoma is idiopathic in
origin.
 People who inherit PCC from their parents may also
develop associated genetic conditions. These conditions
include:
 Von Hippel-Lindau disease, a condition where cysts and
tumors grow in the central nervous system, kidneys,
adrenal glands, or other areas of the body, most are non-
cancerous
 Neurofibromatosis type 1, the development of tumors on
the skin and optic nerves
 Multiple endocrine neoplasia type 2 (MEN2), a form of
thyroid cancer that develops in conjunction with PCC
Pheochromocytoma Symptoms
 Some people with these tumors have high blood
pressure all the time. For others, it goes up and
down.
 But most people have at least one other symptom,
including:
 Constipation
 Dizziness when standing
 Tremors
 Shortness of breath
 Pale skin
 Fast or uneven heartbeat (heart palpitations)
 Severe headache
 Unusual sweating
 Weight loss
 Weakness
 Anxiety attacks
Pheochromocytoma Triggers
 Some people’s attacks are set off by things like:
 Pressure on the tumor
 Medications, especially anesthesia or beta-
blockers
 Emotional stress
 Physical activity
 Childbirth
 Surgery
 Foods with a lot of the amino acid tyramine, such
as red wine, chocolate, or cheese
Pheochromocytoma
Complications
 PCC can lead to life-threatening conditions,
including:
 Disease of your heart muscle (cardiomyopathy)
 Heart muscle inflammation(myocarditis)
 Bleeding in your brain
 Fluid buildup in your lungs (pulmonary edema)
 Stroke
 Heart attack
 Kidney failure
 Nerve damage in your eyes
Pheochromocytoma Diagnosis
 Blood or urine tests to look for high levels of
hormones
 An MRI (magnetic resonance imaging) scan, which
uses powerful magnets and radio waves to make
images of organs and tissues to check for a tumor
 A CT scan, which puts together several X-rays taken
from different angles to spot a tumor
 M-iodobenzylguanidine (MIBG) imaging, a scanning
technology that can detect tiny amounts of an
injected radioactive compound taken up by
pheochromocytomas or paragangliomas
Treatment
 The primary treatment for pheochromocytoma is
surgery to remove the tumor
 Preoperative preparations
 Alpha blockers. These drugs keep smaller arteries
and veins open and relaxed, improving blood flow
and decreasing blood pressure.
 Alpha blockers include
 phenoxybenzamine,
 doxazosin (Cardura)
 prazosin
 Beta blockers. These drugs cause the heart to beat
more slowly and with less force. They also help keep
blood vessels open and relaxed.
 Beta blockers include:
 atenolol .
 metoprolol .
 propranolol .
 High-salt diet. Alpha and beta blockers widen the blood
vessels, causing the amount of fluid within the blood
vessels to be low.
 A high-salt diet will draw more fluid inside the blood
vessels, preventing the development of low blood
pressure during and after surgery.
Thank You
Group 5

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Pheochromocytoma

  • 2. Introduction  Pheochromocytoma (PCC) is a rare tumor that usually grows in the adrenal glands, above the kidneys.  PPC is catecholamine-secreting tumor, typically of the adrenal medulla or extraadrenal paraganglion tissue.  It’s also known as an adrenal paraganglioma or a chromaffin cell tumor.  It’s most common in adults ages 30 to 50, but people of all ages can have it. Children make up about 10% of all cases.
  • 3.  Adrenal glands make hormones that control things like metabolism and blood pressure.  A pheochromocytoma also releases hormones, at much higher levels than usual. These extra hormones cause high blood pressure, which can damage heart, brain, lungs, and kidneys.  About 10% to 15% of these tumors are cancerous, and they can spread to other parts of the body. But most pheochromocytoma tumors are benign, meaning they’re not cancerous.
  • 4. Causes  The primary cause of pheochromacytoma is idiopathic in origin.  People who inherit PCC from their parents may also develop associated genetic conditions. These conditions include:  Von Hippel-Lindau disease, a condition where cysts and tumors grow in the central nervous system, kidneys, adrenal glands, or other areas of the body, most are non- cancerous  Neurofibromatosis type 1, the development of tumors on the skin and optic nerves  Multiple endocrine neoplasia type 2 (MEN2), a form of thyroid cancer that develops in conjunction with PCC
  • 5. Pheochromocytoma Symptoms  Some people with these tumors have high blood pressure all the time. For others, it goes up and down.  But most people have at least one other symptom, including:  Constipation  Dizziness when standing  Tremors  Shortness of breath  Pale skin
  • 6.  Fast or uneven heartbeat (heart palpitations)  Severe headache  Unusual sweating  Weight loss  Weakness  Anxiety attacks
  • 7. Pheochromocytoma Triggers  Some people’s attacks are set off by things like:  Pressure on the tumor  Medications, especially anesthesia or beta- blockers  Emotional stress  Physical activity  Childbirth  Surgery  Foods with a lot of the amino acid tyramine, such as red wine, chocolate, or cheese
  • 8. Pheochromocytoma Complications  PCC can lead to life-threatening conditions, including:  Disease of your heart muscle (cardiomyopathy)  Heart muscle inflammation(myocarditis)  Bleeding in your brain  Fluid buildup in your lungs (pulmonary edema)  Stroke  Heart attack  Kidney failure  Nerve damage in your eyes
  • 9. Pheochromocytoma Diagnosis  Blood or urine tests to look for high levels of hormones  An MRI (magnetic resonance imaging) scan, which uses powerful magnets and radio waves to make images of organs and tissues to check for a tumor  A CT scan, which puts together several X-rays taken from different angles to spot a tumor  M-iodobenzylguanidine (MIBG) imaging, a scanning technology that can detect tiny amounts of an injected radioactive compound taken up by pheochromocytomas or paragangliomas
  • 10. Treatment  The primary treatment for pheochromocytoma is surgery to remove the tumor  Preoperative preparations  Alpha blockers. These drugs keep smaller arteries and veins open and relaxed, improving blood flow and decreasing blood pressure.  Alpha blockers include  phenoxybenzamine,  doxazosin (Cardura)  prazosin
  • 11.  Beta blockers. These drugs cause the heart to beat more slowly and with less force. They also help keep blood vessels open and relaxed.  Beta blockers include:  atenolol .  metoprolol .  propranolol .  High-salt diet. Alpha and beta blockers widen the blood vessels, causing the amount of fluid within the blood vessels to be low.  A high-salt diet will draw more fluid inside the blood vessels, preventing the development of low blood pressure during and after surgery.