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PRESENTED BY
S.VIGNESH
B.SC (N) III YEAR
SMVNC
 BLOOD BRAIN BARRIER
ACTS AS BOTH A
MECHANICAL BARRIER
MECHANISM AND A
TRANSPORT MECHANISM
 IT PREVENTS HARMFUL
CHEMICAL SUBSTANCES
AND PERMOTS METABOLIC
AND ESSENTIAL MATERIAL
INTO THE BRAIN TISSUES.
NEUROGLIA OR THE GLIA IS THE SUPPORTING CELLS OF THE
NERVOUS SYSTEM. THE NEUROGLIAL CELLS ARE NON EXCITABLE
AND DO NOT TRANSMIT NERVE IMPULSE.SO THESE CELLS ARE
ALSO CALLED NON NEURAL CELLS OR GLIAL CELLS.
1. ASTROCYTES
2. MICROGLIA
3. OLIGODENDROCYTES
4. EPENDYMAL CELLS.
ABNORMAL CELL PROLIFERATION BRAIN
CELLS.
BRAIN CANCER IS A DISEASE OF THE
BRAIN IN WHICH CANCER CELLS
(MALIGNANT CELLS) ARISE IN THE BRAIN
TISSUE.
CANCER CELLS GROW TO FORM A MASS
OF CANCER TISSUE (TUMOR) THAT
INTERFERS WITH BRAIN FUNCTIONS
SUCH AS MUSCLE CONTROL, SENSATION,
MEMORY, AND OTHER NORMAL BODY
FUNCTIONS.
 INCIDENCE OF BRAIN TUMORS IN INDIA IS 3 TO 4 PER
100,000 PERSONS PER YEAR.
 MORE AFFECTED IN MALE
 1.4% OF ALL NEW CANCER PATIENTS PER YEAR
 PRIMARY BRAIN TUMOR
IT ORIGINATES IN YOUR BRAIN. THEY CAN DEVELOP
FROM YOUR
1. BRAIN CELLS
2. MENINGES
3. NERVE CELLS
4. GLANDS
PRIMARY TUMORS CAN BE BENIGN OR NON CANCEROUS. IN
ADULTS, THE MOST COMMON TYPES OF BRAIN TUMOR ARE
GLIOMAS AND MENINGIOMAS.
GLIOMAS ARE TUMORS THAT DEVELOP FROM GLIAL CELLS.
THESE CELLS NORMALLY:
 SUPPORT THE STRUCTURE OF YOUR CENTRAL NERVOUS
SYSTEM.
 PROVIDE NUTRITION TO YOUR CENTRAL NERVOUS SYSTEM.
 CLEAN CELLULAR WASTE.
 BREAK DOWN DEAD NEURON.
 ASTROCYTIC TUMORS SUCH AS ASTROCYTOMAS, WHICH
ORIGINATE IN THE CEREBRUM.
 OLIGODENDROGLIAL TUMORS, WHICH ARE OFTEN FOUND IN
THE FRONTAL TEMPORAL LOBES.
 GLIOBLASTOMAS , WHICH ORIGINATES IN THE SUPPORTIVE
BRAIN TISSUE AND ARE MOST AGGRESSIVE TYPES.
SECONDARY BRAIN TUMORS MAKE UP THE MAJORITY OF BRAIN
CANCERS. THEY START IN ONE PART OF THE BODY AND SPREAD
OR METASTASIZE, TO THE BRAIN. THE FOLLOWING CAN
METASTASIZE TO THE BRAIN:
 LUNG CANCER
 BREAST CANCER
 KIDNEY CANCER
 SKIN CANCER
TNM system to divide cancers into stages.
• STAGE I
• STAGE II
• STAGE III
• STAGE IV
THE TUMOR GROWS SLOWLY AND RARELY SPREAD INTO
NEARBY TISSUES. IT MAY POSSIBLE TO COMPLETELY REMOVE THE
WITH SURGERY.
THE TUMOR GROWS SLOWLY, BUT MAY SPREAD INTO NEARBY
TISSUES OR RECUR.
THE TUMOR GROWS QUICKLY, IS LIKELY TO SPREAD INTO NEARBY
TISSUE AND THE TUMOR CELLS LOOK VERY DIFFERENT FROM
NORMAL CELLS.
THE TUMOR GROWS AND SPREADS VERY QUICKLY, AND THE
TUMOR CELLS DO NOT LIKE NORMAL CELLS.
SECONDARY OR METASTATIC
BRAIN TUMORS, WHICH
HAVE SPREAD TO THE BRAIN
FROM ANOTHER LOCATION
IN THE BODY ARE MUCH
MORE COMMON THAN
PRIMARY BRAIN TUMOR.
THE EXACT CAUSE OF MOST BRAIN CANCER IS UNKNOWN.
 FAMILY HISTORY
 AGE
 RACE(AFRICAN AND AMERICAN)
 CHEMICAL EXPOSURE
 EXPOSURE TO RADIATION
due to etiological factors
growth of tumor
increased ICP in adjacent organ in CSF
obstructive hydrocephalus
tumor generator to blood vessels
dustrupting normal blood brain barrier
IN FRONTAL LOBE:
Personality changes
Memory loss
Visual disturbance
unilateral hemiplegia
IN TEMPORAL LOBE
- seizure
-dysphagia
 IN PARIETAL LOBE:
sensory imaprement
speech disturbance
 IN OCCIPITAL LOBE:
visual disturbance
hearing hallucination
nystagmus
diplopia
 IN CEREBELUM:
 IMPAIRED EQULIBIRIUM
 IMPAIRED COORDINATION
 IN PITUTARY:
nipple discharge
lack of menstrual cycle
gynecomastia
obesity
low bp
 Blurred Vision
 Head ache
 Vomiting
 Confusion
 Clumsiness
 Dizziness
 Difficulty in reading and writing
 hand tremors
 Muscle weakness
 History collection
 Physical examination
 Neurological examination
 CT
 MRI
 Computerised assested stereotact biopsy(3 dimention)
 Angiography
 Brain mapping
 Positron emission tomography(PET)
 Electro encephalogram(EEG)
 Pharmacologic therapy
1. Corticosteroids(dexamethasone &
prednisome 4 to 24 mg per day)
2. Osmotic diuretic(mannitol)
3. Antiseizure drugs(phenytoin)
4. Anticoagulant
5. Antineoplasm(vincristine,camustine)
6. Antiemetic(ondansetron)
7. Antianalgesic(morphine)
Chemotherapy
the effectiveness of chemotherapy has been
limited by difficulty getting drugs across the
blood brain barrier, tumor cell heterogeneity
and tumor cell resistance. A group of
chemotherapeutic drugs called the
NITROSOUREAS
(Procarbazine and temozolomide and
methotrexate)
 RADIATION THERAPY
STEREOTACTIC
RADIOSURGERY
 CRANIOTOMY
 ENDONASAL ENDOSCOPY
 NEUROENDOSCOPY
 SHUNT
 PLACEMENT OF OMMAYA RESERVOIR
 Position for head ache(upright position)and pain
medication
 Assess neurological examination
 Monitor ICP level
 Monitor vital signs
 Assess electrolytes abnormalities
 Protect for injury
 Assess eye moment & pupillary size
Brain heriniation
Death
Metastasis
Brain cancer(Tumor)
Brain cancer(Tumor)
Brain cancer(Tumor)
Brain cancer(Tumor)
Brain cancer(Tumor)

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Brain cancer(Tumor)

  • 2.
  • 3.
  • 4.  BLOOD BRAIN BARRIER ACTS AS BOTH A MECHANICAL BARRIER MECHANISM AND A TRANSPORT MECHANISM  IT PREVENTS HARMFUL CHEMICAL SUBSTANCES AND PERMOTS METABOLIC AND ESSENTIAL MATERIAL INTO THE BRAIN TISSUES.
  • 5.
  • 6.
  • 7. NEUROGLIA OR THE GLIA IS THE SUPPORTING CELLS OF THE NERVOUS SYSTEM. THE NEUROGLIAL CELLS ARE NON EXCITABLE AND DO NOT TRANSMIT NERVE IMPULSE.SO THESE CELLS ARE ALSO CALLED NON NEURAL CELLS OR GLIAL CELLS. 1. ASTROCYTES 2. MICROGLIA 3. OLIGODENDROCYTES 4. EPENDYMAL CELLS.
  • 8. ABNORMAL CELL PROLIFERATION BRAIN CELLS. BRAIN CANCER IS A DISEASE OF THE BRAIN IN WHICH CANCER CELLS (MALIGNANT CELLS) ARISE IN THE BRAIN TISSUE.
  • 9. CANCER CELLS GROW TO FORM A MASS OF CANCER TISSUE (TUMOR) THAT INTERFERS WITH BRAIN FUNCTIONS SUCH AS MUSCLE CONTROL, SENSATION, MEMORY, AND OTHER NORMAL BODY FUNCTIONS.
  • 10.  INCIDENCE OF BRAIN TUMORS IN INDIA IS 3 TO 4 PER 100,000 PERSONS PER YEAR.  MORE AFFECTED IN MALE  1.4% OF ALL NEW CANCER PATIENTS PER YEAR
  • 11.  PRIMARY BRAIN TUMOR IT ORIGINATES IN YOUR BRAIN. THEY CAN DEVELOP FROM YOUR 1. BRAIN CELLS 2. MENINGES 3. NERVE CELLS 4. GLANDS PRIMARY TUMORS CAN BE BENIGN OR NON CANCEROUS. IN ADULTS, THE MOST COMMON TYPES OF BRAIN TUMOR ARE GLIOMAS AND MENINGIOMAS.
  • 12. GLIOMAS ARE TUMORS THAT DEVELOP FROM GLIAL CELLS. THESE CELLS NORMALLY:  SUPPORT THE STRUCTURE OF YOUR CENTRAL NERVOUS SYSTEM.  PROVIDE NUTRITION TO YOUR CENTRAL NERVOUS SYSTEM.  CLEAN CELLULAR WASTE.  BREAK DOWN DEAD NEURON.
  • 13.  ASTROCYTIC TUMORS SUCH AS ASTROCYTOMAS, WHICH ORIGINATE IN THE CEREBRUM.  OLIGODENDROGLIAL TUMORS, WHICH ARE OFTEN FOUND IN THE FRONTAL TEMPORAL LOBES.  GLIOBLASTOMAS , WHICH ORIGINATES IN THE SUPPORTIVE BRAIN TISSUE AND ARE MOST AGGRESSIVE TYPES.
  • 14.
  • 15. SECONDARY BRAIN TUMORS MAKE UP THE MAJORITY OF BRAIN CANCERS. THEY START IN ONE PART OF THE BODY AND SPREAD OR METASTASIZE, TO THE BRAIN. THE FOLLOWING CAN METASTASIZE TO THE BRAIN:  LUNG CANCER  BREAST CANCER  KIDNEY CANCER  SKIN CANCER
  • 16. TNM system to divide cancers into stages. • STAGE I • STAGE II • STAGE III • STAGE IV
  • 17. THE TUMOR GROWS SLOWLY AND RARELY SPREAD INTO NEARBY TISSUES. IT MAY POSSIBLE TO COMPLETELY REMOVE THE WITH SURGERY.
  • 18. THE TUMOR GROWS SLOWLY, BUT MAY SPREAD INTO NEARBY TISSUES OR RECUR.
  • 19. THE TUMOR GROWS QUICKLY, IS LIKELY TO SPREAD INTO NEARBY TISSUE AND THE TUMOR CELLS LOOK VERY DIFFERENT FROM NORMAL CELLS.
  • 20. THE TUMOR GROWS AND SPREADS VERY QUICKLY, AND THE TUMOR CELLS DO NOT LIKE NORMAL CELLS.
  • 21. SECONDARY OR METASTATIC BRAIN TUMORS, WHICH HAVE SPREAD TO THE BRAIN FROM ANOTHER LOCATION IN THE BODY ARE MUCH MORE COMMON THAN PRIMARY BRAIN TUMOR.
  • 22. THE EXACT CAUSE OF MOST BRAIN CANCER IS UNKNOWN.
  • 23.  FAMILY HISTORY  AGE  RACE(AFRICAN AND AMERICAN)  CHEMICAL EXPOSURE  EXPOSURE TO RADIATION
  • 24. due to etiological factors growth of tumor increased ICP in adjacent organ in CSF obstructive hydrocephalus tumor generator to blood vessels dustrupting normal blood brain barrier
  • 25. IN FRONTAL LOBE: Personality changes Memory loss Visual disturbance unilateral hemiplegia IN TEMPORAL LOBE - seizure -dysphagia
  • 26.  IN PARIETAL LOBE: sensory imaprement speech disturbance  IN OCCIPITAL LOBE: visual disturbance hearing hallucination nystagmus diplopia
  • 27.  IN CEREBELUM:  IMPAIRED EQULIBIRIUM  IMPAIRED COORDINATION  IN PITUTARY: nipple discharge lack of menstrual cycle gynecomastia obesity low bp
  • 28.  Blurred Vision  Head ache  Vomiting  Confusion  Clumsiness  Dizziness  Difficulty in reading and writing  hand tremors  Muscle weakness
  • 29.  History collection  Physical examination  Neurological examination  CT  MRI  Computerised assested stereotact biopsy(3 dimention)  Angiography  Brain mapping  Positron emission tomography(PET)  Electro encephalogram(EEG)
  • 30.  Pharmacologic therapy 1. Corticosteroids(dexamethasone & prednisome 4 to 24 mg per day) 2. Osmotic diuretic(mannitol) 3. Antiseizure drugs(phenytoin) 4. Anticoagulant 5. Antineoplasm(vincristine,camustine) 6. Antiemetic(ondansetron) 7. Antianalgesic(morphine)
  • 31. Chemotherapy the effectiveness of chemotherapy has been limited by difficulty getting drugs across the blood brain barrier, tumor cell heterogeneity and tumor cell resistance. A group of chemotherapeutic drugs called the NITROSOUREAS (Procarbazine and temozolomide and methotrexate)
  • 34.  ENDONASAL ENDOSCOPY  NEUROENDOSCOPY  SHUNT  PLACEMENT OF OMMAYA RESERVOIR
  • 35.  Position for head ache(upright position)and pain medication  Assess neurological examination  Monitor ICP level  Monitor vital signs  Assess electrolytes abnormalities  Protect for injury  Assess eye moment & pupillary size