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CENTRAL NERVOUS SYSTEM
TUMORS
CONTENTS
 General information about Central Nervous System tumors
 Symptoms of Central Nervous System tumors
 Stages of Central Nervous System tumors
 Recurrent Central Nervous System Tumors
 Treatment Options
GENERAL INFORMATION ABOUT
CNS TUMORS
 An adult central nervous system tumor is a
disease in which abnormal cells form in the
tissues of the brain and/or spinal cord.
 A tumor that starts in another part of the body and
spreads to the brain is called a metastatic brain
tumor.
 The brain controls many important body
functions.
 The spinal cord connects the brain to nerves in
most parts of the body.
There are different types of brain and spinal cord
tumors.
 Astrocytic Tumors
 Oligodendroglial Tumors
 Mixed Gliomas
 Ependymal Tumors
 Medulloblastomas
 Pineal Parenchymal Tumors
 Meningeal Tumors
 Germ Cell Tumors
 Craniopharyngioma (Grade I)
 Having certain genetic syndromes may increase
the risk of a central nervous system tumor.
 The cause of most adult brain and spinal cord
tumors is not known..
 Tests that examine the brain and spinal cord are
used to diagnose adult brain and spinal cord
tumors.
 A biopsy is also used to diagnose a brain tumor.
 Sometimes a biopsy or surgery cannot be done.
 Certain factors affect prognosis (chance of
recovery) and treatment options.
 The tumors may be either benign (not cancer) or
malignant (cancer):
 Benign brain and spinal cord tumors grow and press
on nearby areas of the brain. They rarely spread into
other tissues and may recur (come back).
 Malignant brain and spinal cord tumors are likely to
grow quickly and spread into other brain tissue.
 When a tumor grows into or presses on an area of
the brain, it may stop that part of the brain from
working the way it should. Both benign and
malignant brain tumors cause signs and symptoms
and need treatment.
W.H.O TUMOR GRADING
SYSTEM
 Grade I (low-grade) — The tumor cells look more like normal
cells under a microscope and grow and spread more slowly
than grade II, III, and IV tumor cells. They rarely spread into
nearby tissues. Grade I brain tumors may be cured if they are
completely removed by surgery.
 Grade II — The tumor cells grow and spread more slowly than
grade III and IV tumor cells. They may spread into nearby
tissue and may recur (come back). Some tumors may become
a higher-grade tumor.
 Grade III — The tumor cells look very different from normal
cells under a microscope and grow more quickly than grade I
and II tumor cells. They are likely to spread into nearby tissue.
 Grade IV (high-grade) — The tumor cells do not look like
normal cells under a microscope and grow and spread very
quickly. There may be areas of dead cells in the tumor. Grade
SIGNS AND SYMPTOMS OF CNS
TUMOR
 The signs and symptoms of adult brain and spinal
cord tumors are not the same in every person.
 Signs and symptoms depend on the following:
 Where the tumor forms in the brain or spinal cord.
 What the affected part of the brain controls.
 The size of the tumor.
BRAIN TUMOR SYMPTOMS
 Morning headache or headache that goes away
after vomiting.
 Seizures.
 Vision, hearing, and speech problems.
 Loss of appetite.
 Frequent nausea and vomiting.
 Changes in personality, mood, ability to focus, or
behavior.
 Loss of balance and trouble walking.
 Weakness.
 Unusual sleepiness or change in activity level.
SPINAL CORD TUMOR
SYMPTOMS
 Back pain or pain that spreads from the back
towards the arms or legs.
 A change in bowel habits or trouble urinating.
 Weakness or numbness in the arms or legs.
 Trouble walking.
DIAGNOSIS OF CNS TUMORS
The following tests and procedures may be used:
 Physical exam and history
 Neurological exams
 Tumor marker test
 Visual field exam
 Gene testing
 CT Scan
STAGES OF CNS TUMORS
 The extent or spread of cancer is usually described
as stages. There is no standard staging system for
brain and spinal cord tumors. Brain tumors that
begin in the brain may spread to other parts of the
brain and spinal cord, but they rarely spread to other
parts of the body. Treatment of primary brain and
spinal cord tumors is based on the following:
 The type of cell in which the tumor began.
 Where the tumor formed in the brain or spinal cord.
 The amount of cancer left after surgery.
 The grade of the tumor.
 Treatment of tumors that have spread to the brain
from other parts of the body is based on the number
RECURRENT CNS TUMORS
 A recurrent central nervous system (CNS) tumor
is a tumor that has recurred (come back) after it
has been treated. CNS tumors often recur,
sometimes many years after the first tumor. The
tumor may recur at the same place as the first
tumor or in other parts of the central nervous
system.
TREATMENT OPTIONS
 There are different types of treatment for patients with
adult brain and spinal cord tumors.
 Five types of standard treatment are used:
 Active surveillance
 Surgery
 Radiation therapy
 Chemotherapy
 Targeted therapy
 Supportive care is given to lessen the problems
caused by the disease or its treatment.
 New types of treatment are being tested in clinical
trials.
 Proton beam radiation therapy
 Biologic therapy
ASTROCYTIC TUMORS
 An astrocytic tumor (Astrocytoma) begins in star-
shaped brain cells called astrocytes, which help
keep nerve cells healthy.
 They may occur in many parts of the brain and
sometimes in the spinal cord.
 They can occur at any age and they primarily
occur in males.
 Astrocytic tumors include the following:
 Brain stem glioma (usually high grade): A brain
stem glioma forms in the brain stem, which is the
part of the brain connected to the spinal cord. It is
often a high-grade tumor, which spreads widely
through the brain stem and is hard to cure. Brain
stem gliomas are rare in adults
 Pineal astrocytic tumor (any grade): A pineal
astrocytic tumor forms in tissue around the pineal
gland and may be any grade. The pineal gland is a
tiny organ in the brain that makes melatonin, a
hormone that helps control the sleeping and waking
cycle.
 Pilocytic astrocytoma (grade I): A pilocytic
astrocytoma grows slowly in the brain or spinal cord,
thereby considered benign. It may be in the form of a
cyst filled with fluid and a nodule which is the solid
portion. Most are located in the cerebellum and
rarely spreads into nearby tissues. Therefore, most
symptoms are related to balance or cordination
difficulties. Pilocytic astrocytomas can often be
cured.
 Diffuse astrocytoma (grade II): A diffuse
astrocytoma grows slowly, but often spreads into
nearby tissues. The tumor cells look something like
normal cells. In some cases, a diffuse astrocytoma
can be cured. It is also called a low-grade diffuse
 Anaplastic astrocytoma (grade III): An anaplastic
astrocytoma grows quickly and spreads into nearby
tissues. The tumor cells look different from normal
cells. This type of tumor usually cannot be cured.
This tumor recur more frequently than others
because their tendeny to spread into nearby tissue
makes them difficult to completely remove during
surgery. An anaplastic astrocytoma is also called a
malignant astrocytoma or high-grade astrocytoma.
 Glioblastoma (grade IV): A glioblastoma grows and
spreads very quickly. The tumor cells look very
different from normal cells. This type of tumor usually
cannot be cured. It is also called glioblastoma
multiforme. Approximately 50% of astrocytomas are
gliobastoma
OLIGODENDROGLIAL TUMORS
 An oligodendroglial tumor (Oligodendroglioma) begins
in brain cells called oligodendrocytes, which help
keep nerve cells healthy. An oligodendrocyte is a type
of glial cell. Oligodendrocytes sometimes form tumors
called oligodendrogliomas. Grades of oligodendroglial
tumors include the following:
 Oligodendroglioma (grade II): An oligodendroglioma
grows slowly, but often spreads into nearby tissues.
The tumor cells look something like normal cells. In
some cases, an oligodendroglioma can be cured.
 Anaplastic oligodendroglioma (grade III): An
anaplastic oligodendroglioma grows quickly and
spreads into nearby tissues. The tumor cells look
different from normal cells. This type of tumor usually
cannot be cured.
MIXED GLIOMAS
 A mixed glioma is a brain tumor that has two
types of tumor cells in it — oligodendrocytes and
astrocytes. This type of mixed tumor is called an
oligoastrocytoma.
 Oligoastrocytoma (grade II): An
oligoastrocytoma is a slow-growing tumor. The
tumor cells look something like normal cells. In
some cases, an oligoastrocytoma can be cured.
 Anaplastic oligoastrocytoma (grade III): An
anaplastic oligoastrocytoma grows quickly and
spreads into nearby tissues. The tumor cells look
different from normal cells. This type of tumor has
a worse prognosis than oligoastrocytoma (grade
II
Central nervous system tumors

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Central nervous system tumors

  • 2. CONTENTS  General information about Central Nervous System tumors  Symptoms of Central Nervous System tumors  Stages of Central Nervous System tumors  Recurrent Central Nervous System Tumors  Treatment Options
  • 3. GENERAL INFORMATION ABOUT CNS TUMORS  An adult central nervous system tumor is a disease in which abnormal cells form in the tissues of the brain and/or spinal cord.  A tumor that starts in another part of the body and spreads to the brain is called a metastatic brain tumor.  The brain controls many important body functions.  The spinal cord connects the brain to nerves in most parts of the body.
  • 4. There are different types of brain and spinal cord tumors.  Astrocytic Tumors  Oligodendroglial Tumors  Mixed Gliomas  Ependymal Tumors  Medulloblastomas  Pineal Parenchymal Tumors  Meningeal Tumors  Germ Cell Tumors  Craniopharyngioma (Grade I)
  • 5.  Having certain genetic syndromes may increase the risk of a central nervous system tumor.  The cause of most adult brain and spinal cord tumors is not known..  Tests that examine the brain and spinal cord are used to diagnose adult brain and spinal cord tumors.  A biopsy is also used to diagnose a brain tumor.  Sometimes a biopsy or surgery cannot be done.  Certain factors affect prognosis (chance of recovery) and treatment options.
  • 6.  The tumors may be either benign (not cancer) or malignant (cancer):  Benign brain and spinal cord tumors grow and press on nearby areas of the brain. They rarely spread into other tissues and may recur (come back).  Malignant brain and spinal cord tumors are likely to grow quickly and spread into other brain tissue.  When a tumor grows into or presses on an area of the brain, it may stop that part of the brain from working the way it should. Both benign and malignant brain tumors cause signs and symptoms and need treatment.
  • 7. W.H.O TUMOR GRADING SYSTEM  Grade I (low-grade) — The tumor cells look more like normal cells under a microscope and grow and spread more slowly than grade II, III, and IV tumor cells. They rarely spread into nearby tissues. Grade I brain tumors may be cured if they are completely removed by surgery.  Grade II — The tumor cells grow and spread more slowly than grade III and IV tumor cells. They may spread into nearby tissue and may recur (come back). Some tumors may become a higher-grade tumor.  Grade III — The tumor cells look very different from normal cells under a microscope and grow more quickly than grade I and II tumor cells. They are likely to spread into nearby tissue.  Grade IV (high-grade) — The tumor cells do not look like normal cells under a microscope and grow and spread very quickly. There may be areas of dead cells in the tumor. Grade
  • 8. SIGNS AND SYMPTOMS OF CNS TUMOR  The signs and symptoms of adult brain and spinal cord tumors are not the same in every person.  Signs and symptoms depend on the following:  Where the tumor forms in the brain or spinal cord.  What the affected part of the brain controls.  The size of the tumor.
  • 9. BRAIN TUMOR SYMPTOMS  Morning headache or headache that goes away after vomiting.  Seizures.  Vision, hearing, and speech problems.  Loss of appetite.  Frequent nausea and vomiting.  Changes in personality, mood, ability to focus, or behavior.  Loss of balance and trouble walking.  Weakness.  Unusual sleepiness or change in activity level.
  • 10. SPINAL CORD TUMOR SYMPTOMS  Back pain or pain that spreads from the back towards the arms or legs.  A change in bowel habits or trouble urinating.  Weakness or numbness in the arms or legs.  Trouble walking.
  • 11. DIAGNOSIS OF CNS TUMORS The following tests and procedures may be used:  Physical exam and history  Neurological exams  Tumor marker test  Visual field exam  Gene testing  CT Scan
  • 12. STAGES OF CNS TUMORS  The extent or spread of cancer is usually described as stages. There is no standard staging system for brain and spinal cord tumors. Brain tumors that begin in the brain may spread to other parts of the brain and spinal cord, but they rarely spread to other parts of the body. Treatment of primary brain and spinal cord tumors is based on the following:  The type of cell in which the tumor began.  Where the tumor formed in the brain or spinal cord.  The amount of cancer left after surgery.  The grade of the tumor.  Treatment of tumors that have spread to the brain from other parts of the body is based on the number
  • 13. RECURRENT CNS TUMORS  A recurrent central nervous system (CNS) tumor is a tumor that has recurred (come back) after it has been treated. CNS tumors often recur, sometimes many years after the first tumor. The tumor may recur at the same place as the first tumor or in other parts of the central nervous system.
  • 14. TREATMENT OPTIONS  There are different types of treatment for patients with adult brain and spinal cord tumors.  Five types of standard treatment are used:  Active surveillance  Surgery  Radiation therapy  Chemotherapy  Targeted therapy  Supportive care is given to lessen the problems caused by the disease or its treatment.  New types of treatment are being tested in clinical trials.  Proton beam radiation therapy  Biologic therapy
  • 15. ASTROCYTIC TUMORS  An astrocytic tumor (Astrocytoma) begins in star- shaped brain cells called astrocytes, which help keep nerve cells healthy.  They may occur in many parts of the brain and sometimes in the spinal cord.  They can occur at any age and they primarily occur in males.  Astrocytic tumors include the following:
  • 16.  Brain stem glioma (usually high grade): A brain stem glioma forms in the brain stem, which is the part of the brain connected to the spinal cord. It is often a high-grade tumor, which spreads widely through the brain stem and is hard to cure. Brain stem gliomas are rare in adults  Pineal astrocytic tumor (any grade): A pineal astrocytic tumor forms in tissue around the pineal gland and may be any grade. The pineal gland is a tiny organ in the brain that makes melatonin, a hormone that helps control the sleeping and waking cycle.
  • 17.  Pilocytic astrocytoma (grade I): A pilocytic astrocytoma grows slowly in the brain or spinal cord, thereby considered benign. It may be in the form of a cyst filled with fluid and a nodule which is the solid portion. Most are located in the cerebellum and rarely spreads into nearby tissues. Therefore, most symptoms are related to balance or cordination difficulties. Pilocytic astrocytomas can often be cured.  Diffuse astrocytoma (grade II): A diffuse astrocytoma grows slowly, but often spreads into nearby tissues. The tumor cells look something like normal cells. In some cases, a diffuse astrocytoma can be cured. It is also called a low-grade diffuse
  • 18.  Anaplastic astrocytoma (grade III): An anaplastic astrocytoma grows quickly and spreads into nearby tissues. The tumor cells look different from normal cells. This type of tumor usually cannot be cured. This tumor recur more frequently than others because their tendeny to spread into nearby tissue makes them difficult to completely remove during surgery. An anaplastic astrocytoma is also called a malignant astrocytoma or high-grade astrocytoma.  Glioblastoma (grade IV): A glioblastoma grows and spreads very quickly. The tumor cells look very different from normal cells. This type of tumor usually cannot be cured. It is also called glioblastoma multiforme. Approximately 50% of astrocytomas are gliobastoma
  • 19.
  • 20. OLIGODENDROGLIAL TUMORS  An oligodendroglial tumor (Oligodendroglioma) begins in brain cells called oligodendrocytes, which help keep nerve cells healthy. An oligodendrocyte is a type of glial cell. Oligodendrocytes sometimes form tumors called oligodendrogliomas. Grades of oligodendroglial tumors include the following:  Oligodendroglioma (grade II): An oligodendroglioma grows slowly, but often spreads into nearby tissues. The tumor cells look something like normal cells. In some cases, an oligodendroglioma can be cured.  Anaplastic oligodendroglioma (grade III): An anaplastic oligodendroglioma grows quickly and spreads into nearby tissues. The tumor cells look different from normal cells. This type of tumor usually cannot be cured.
  • 21. MIXED GLIOMAS  A mixed glioma is a brain tumor that has two types of tumor cells in it — oligodendrocytes and astrocytes. This type of mixed tumor is called an oligoastrocytoma.  Oligoastrocytoma (grade II): An oligoastrocytoma is a slow-growing tumor. The tumor cells look something like normal cells. In some cases, an oligoastrocytoma can be cured.  Anaplastic oligoastrocytoma (grade III): An anaplastic oligoastrocytoma grows quickly and spreads into nearby tissues. The tumor cells look different from normal cells. This type of tumor has a worse prognosis than oligoastrocytoma (grade II