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Adrenal TUMOR
PRESENTED BY:
MR: ABHAY RAJPOOT
ADRENAL GLAND
The adrenal glands are
paired endocrine glands
situated over the medial
aspect of the upper poles of
each kidney. They secrete
steroid and catecholamine
hormones directly into the
blood.
INTRODUCTION
A tumor begins when healthy cells change and grow out of control,
forming a mass. A tumor can be cancerous or benign. A cancerous
tumor is malignant, meaning it can grow and spread to other parts
of the body. A benign tumor means the tumor can grow but will
not spread.
An adrenal gland tumor can sometimes produce too much of a
hormone. When it does, the tumor is called a “functioning tumor.”
An adrenal gland tumor that does not produce hormones is called
a “nonfunctioning tumor.”
DEFINITION
Adrenal cancer is a condition that occurs when abnormal cells
form in or travel to the adrenal glands. Adrenal cancer usually
occurs in the outermost layer of the glands, or the adrenal cortex.
It generally appears as a tumor.
It is catecholamine – secreting neoplasm associated with
hypertension of Chromaffin cells of Adrenal Medulla.
Types of adrenal gland tumors
Benign adenomas
 Benign adenomas are relatively small, usually less than 2 inches
in diameter. Most people with this type of tumor have no
symptoms. These tumors usually occur on only one adrenal
gland, but they can appear on both glands in rare instances.
Adrenal cortical carcinomas
 Adrenal cortical carcinomas are usually much larger than benign
adenomas. If a tumor is more than 2 inches in diameter, it’s
more likely to be cancerous. Sometimes, they can grow large
enough to press on your organs, leading to more symptoms.
They can also sometimes produce hormones that cause
changes in the body.
CAUSES
 Medullary thyroid carcinoma
 Parathyroid Hyperplasia
 Emotional and physical stress.
 General factor
 Increased or Decreased secretion of Hormone.
SIGN AND SYMPTOMS
 Hypertension
 Hypermetabolism
 Hyperglycaemia
 Head ache
 Visual Disturbances
 Nervousness
 Increased blood glucose level
 Abdominal pain
 Polyuria
 High blood pressure (320/200mm.Hg)
 Psychotic Behaviour
 Depression.
 Allergic Reaction
 Emotional Upset.
Staging of Adrenal Carcinoma
The WHO classification of 2004 is based on the McFarlane
Classification & defines four stages:
I stage – Tumor < 5 cm
II stage – Tumor >5 cm
III stage – Locally invasive tumors
IV Stage – Tumor with distant metastasis
DIAGNOSTIC EVALUATION
 History collection
 Physical examination
 Biochemical evaluation
 Morning & midnight plasma cortisol measurement
 Dexamethasone suppression test
 24 hr urinary cortisol measurement
 Serum potassium, plasma aldosterone & plasma renin activity • Abdominal imaging
 CT scan
 MRI scan
 Adrenal vein catheterization
MANAGEMENT
Alpha- Adrenergic Blocking Agents:
-Phentolamine
-Phenoxybenzamine (HCL)
Action- Inhibit the effects of Catecholamines on blood pressure.
Catecholamine Synthesis Inhibitors:
-Metyrosine
Action- Use pre operatively or for long term management of in
operable tumors.
Beta Adrenergic blocking agent:
-Propranolol
- Used for patient with cardiac dysarhythmias or those
not responsive to alpha adrenergic blocking agent.
Cortico- Steroid replacement:
- To prevent adrenal insufficiency
SURGICAL MANAGEMENT
 Unilateral or Bilateral Adrenalectomy
- Removal of one or both adrenal glands
according presence of tumor .
Complication: Metastasis of Tumor
Chemotherapy:
Chemotherapy is a widely used treatment for cancer. The term
chemotherapy refers to the drugs that prevent cancer cells from
dividing and growing. It does this by killing the dividing cells.
Ex.
-Vincristine
-Nethotrexate
SIDE EFFECT
 Hair loss
 Nausea
 Vomiting
 Mouth sores
 Loss of appetite
 Tiredness, easy bruising or bleeding, and an increased
chance of infection.
Radiation therapy
Radiation therapy uses high energy radiation to target cancer
cells. Radiation therapy may be used in the treatment of
leukemia that has spread to the brain, or it may be used to
target the spleen or other areas where leukemia cells have
accumulated.
Adrenal tumor

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Adrenal tumor

  • 2. ADRENAL GLAND The adrenal glands are paired endocrine glands situated over the medial aspect of the upper poles of each kidney. They secrete steroid and catecholamine hormones directly into the blood.
  • 3. INTRODUCTION A tumor begins when healthy cells change and grow out of control, forming a mass. A tumor can be cancerous or benign. A cancerous tumor is malignant, meaning it can grow and spread to other parts of the body. A benign tumor means the tumor can grow but will not spread. An adrenal gland tumor can sometimes produce too much of a hormone. When it does, the tumor is called a “functioning tumor.” An adrenal gland tumor that does not produce hormones is called a “nonfunctioning tumor.”
  • 4.
  • 5. DEFINITION Adrenal cancer is a condition that occurs when abnormal cells form in or travel to the adrenal glands. Adrenal cancer usually occurs in the outermost layer of the glands, or the adrenal cortex. It generally appears as a tumor. It is catecholamine – secreting neoplasm associated with hypertension of Chromaffin cells of Adrenal Medulla.
  • 6. Types of adrenal gland tumors Benign adenomas  Benign adenomas are relatively small, usually less than 2 inches in diameter. Most people with this type of tumor have no symptoms. These tumors usually occur on only one adrenal gland, but they can appear on both glands in rare instances. Adrenal cortical carcinomas  Adrenal cortical carcinomas are usually much larger than benign adenomas. If a tumor is more than 2 inches in diameter, it’s more likely to be cancerous. Sometimes, they can grow large enough to press on your organs, leading to more symptoms. They can also sometimes produce hormones that cause changes in the body.
  • 7. CAUSES  Medullary thyroid carcinoma  Parathyroid Hyperplasia  Emotional and physical stress.  General factor  Increased or Decreased secretion of Hormone.
  • 8. SIGN AND SYMPTOMS  Hypertension  Hypermetabolism  Hyperglycaemia  Head ache  Visual Disturbances  Nervousness  Increased blood glucose level  Abdominal pain  Polyuria  High blood pressure (320/200mm.Hg)  Psychotic Behaviour  Depression.  Allergic Reaction  Emotional Upset.
  • 9. Staging of Adrenal Carcinoma The WHO classification of 2004 is based on the McFarlane Classification & defines four stages: I stage – Tumor < 5 cm II stage – Tumor >5 cm III stage – Locally invasive tumors IV Stage – Tumor with distant metastasis
  • 10. DIAGNOSTIC EVALUATION  History collection  Physical examination  Biochemical evaluation  Morning & midnight plasma cortisol measurement  Dexamethasone suppression test  24 hr urinary cortisol measurement  Serum potassium, plasma aldosterone & plasma renin activity • Abdominal imaging  CT scan  MRI scan  Adrenal vein catheterization
  • 11. MANAGEMENT Alpha- Adrenergic Blocking Agents: -Phentolamine -Phenoxybenzamine (HCL) Action- Inhibit the effects of Catecholamines on blood pressure. Catecholamine Synthesis Inhibitors: -Metyrosine Action- Use pre operatively or for long term management of in operable tumors.
  • 12. Beta Adrenergic blocking agent: -Propranolol - Used for patient with cardiac dysarhythmias or those not responsive to alpha adrenergic blocking agent. Cortico- Steroid replacement: - To prevent adrenal insufficiency
  • 13. SURGICAL MANAGEMENT  Unilateral or Bilateral Adrenalectomy - Removal of one or both adrenal glands according presence of tumor . Complication: Metastasis of Tumor
  • 14. Chemotherapy: Chemotherapy is a widely used treatment for cancer. The term chemotherapy refers to the drugs that prevent cancer cells from dividing and growing. It does this by killing the dividing cells. Ex. -Vincristine -Nethotrexate
  • 15.
  • 16. SIDE EFFECT  Hair loss  Nausea  Vomiting  Mouth sores  Loss of appetite  Tiredness, easy bruising or bleeding, and an increased chance of infection.
  • 17. Radiation therapy Radiation therapy uses high energy radiation to target cancer cells. Radiation therapy may be used in the treatment of leukemia that has spread to the brain, or it may be used to target the spleen or other areas where leukemia cells have accumulated.