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BRAIN TUMOURS 
A brain tumor is a localized intracranial lesion. It occupies space within the skull. These tumors usually 
grow as a spherical mass but can grow diffusely infiltrating tissue. Tumors of the brain can be primary 
arising from tissue in the brain or secondary resulting from metastasis from malignant neoplasm 
elsewhere in the body. 
Brain tumors are generally classified according to tissue from where they originate, if malignant tumor is 
graded according to general cancer staging procedures. 
CLASSIFICATION OF BRAIN TUMORS 
GLIOMAS are a malignant gliomas and most common brain Neoplasm accounting for about 45% of all 
brain tumors. 
ASTROCYTOMA these are the most common type of glaucoma. They arise from supportive tissue glial 
cells and atrocities. Usual location is white matter of frontal and temporal lobes in adult’s lateral and 
cerebella lobes in children. There is mild and moderately malignant grades I and II. 
GLIOBLASTOMA MULTIPOROMEET 
This arises from primitive stem cell (gliobalist) usual location is cerebral usual location are cerebral 
hemispheres. This is highly malignant and invasive and grade iii and IV. 
OIGODENDROGLIOMA 
Arises from glial cells and dendrites usual location is cerebral hemisphere most in frontal lobe, some in 
basal ganglion and cerebellum. Most are benign (encapsulation and calafication) 
EPENDYMOMA 
This arises ependymal epithelium usually occurs in lateral and fourth ventricles in children and young 
adults. They are benign to highly malignant most benign are encapsulated. 
MEDULLOBLASTOMA 
These arise from supportive tissue usually at the posterior fossa, fourth ventricle brain stem in children. 
They are highly malignant and invasive, metastasis to spinal cord and remote areas of the brain. 
2 MENIGIOMA 
Arises from endothelial cells, fibrous tissues elements, transitional cells and angioblasts usual location 
are arachnoids, villi Dura half over convexity of Hemisphere and half at base of hemisphere. They are 
usually benign encapsulation outside brain substance.
3 ACCOUTIC NEUROMA (NEUROFIBROMA) 
They arise from Schwann cells inside auditory meatus on vestibular occurs at the site between the Pons 
and the cerebellum. They are usually benign or low grade malignancy encapsulation 
4. PITUITARY ADENOMA 
Arises from pituitary glandular tissue located at pituitary gland usually benign. 
5 VASCULAR TUMOURS (HEMAGIOBLASTOMA ARTERIO VENOUSE MALFORMATION) 
Arises from over growth of arteries and veins enlarging from vessels. Location is parental cortex near 
middle cerebral vessels. They are benign. 
6 METASTATIC TUMOURS 
These arise due to cancer cells spreading to the brain via circulating system from lungs, breasts ,kidney, 
thyroid and prostate . Usual location is cerebral cortex and they are malignant. 
CASAUSES 
1. Idiopathic 
2. Genetically acquired 
3. Hereditary 
4. Defective immune system 
5. Viruses 
6. Head injury 
PATHOPHYSIOLOGY 
The physiology of brain tumors’ depends on the part of the brain that is affected. Eg 
PITUITARY ADENOMAS 
Functioning pituitary tumors can produce one or more hormones normally produced by anterior 
pituitary. The hormones may cause prolactin secreting pituitary adenomas (prolactinomas) growth 
hormone secreting pituitary adenomas; it produces acnomegally in adults and adrenocortropic 
hormone in female patients whose pituitary gland is secreting excessive quantities of prolactin with 
Amenorrhea or glactorrhea (Excessive or spontaneous flow of milk) male patients with prolactoma 
may present with impotence. 
CLINICAL MANIFESTATION 
Symptoms are generalized as well as specific the tumor location and structure of the brain are 
compressed. 
 Pressure headache (generalized or peri orbital) 

 Nausea and vomiting unrelated to food intake 
 Symptoms of intracranial pressure 
 Visual changes 
 Blurred vision 
 Diplopia (iii,iv,and vi nerve compression) 
 Visual field alteration 
 Enlarged black spots related to papilla edema 
 Seizures 
 Speech difficulty( when the tumor affects language area in dominant hemisphere) 
 Weakness( when tumor affects motor cortex) 
 Alteration in the level of consciousness 
 Personality changes( when tumor affects frontal lobes) 
TUMOUR LOCATION AND ASSOCIATED PRESENTING SYMPTOMS 
CEREBRAL HEMISPHERE 
Frontal lobes (unilateral hemiplagia) : seizures, memory deficit, personality and judgment changes 
,vision disturbances. 
FRONTAL LOBES 
Bilateral symptoms associated with frontal lobes and ataxic gait aphasia (motor dysfunction) 
PARIETAL LOBES 
Speech disturbance if tumor is in dominant hemisphere, inability to write. Inability to replace pictures, 
loss of right –left discrimination, seizures. 
OCCIPITAL LOBE 
Visual disturbances, blindness, headache and seizures 
TEMPORAL LOBE 
Complex or partial seizures with automatic behavior, hallucination. 
METASTATIC TUMORS 
Headache, nausea or vomiting because of intracranial pressure other symptoms depends on location of 
tumor. 
THALAMUS SELLAR TUMORS UMOUR 
Headache, nausea or vomiting and diabetes inapedus may occur. 
FOUTH VENTRICLE AND CEREBELLAR TUMORS
Headache, nausea and papilloedema, mystagamus, occur from intra cranial pressure, ataxic gait and 
changes in coordination. 
CEREBRELLOPONTINE TUMOUR 
Tinnitus and vertigo deafness. 
BRAINSTEM TUMOURS 
Headache, upon awakening, drowsness, vomiting, ataxic gait, facial muscle, dysphagia, dysaithria, 
crossed eyes or other visual changes. 
MANAGEMENT 
INVESTIGATIONS 
HISTORY TAKING and physical exams. History taking of the illness and the manner in which the 
symptoms involved are important in diagnosis. This will help to provide data and location. Assess the 
level of consciousness, motor abilities, and sensory perception. 
CT SCAN 
This is done to check the number, size and density of the lesions and the extent of secondary cerebral 
edema. 
SKULL X-RAYS 
This is done to detect fractures, bones erosion, calcification and abnormal vascularity. 
MAGNETIC RESONANCE IMAGING (MRI) 
This is where internal body parts are visualized by means of magnetic energy. This is used to detect 
tumors in the brain stem and pituitary regions where bones interfere with CT scan. 
CEREBRAL ANGIOGRAPHY 
This involves the injection of contrast medium into the cerebral arterial circulation which assists in 
determining etiology of strokes, seizures, headaches and motor weakness. It is used to visualize the 
cerebral blood vessels and can localize most cerebral tumors. 
ELECTROENCEPHALOGRAM (EEC) 
This is used to detect abnormal brain waves in regions occupied by a tumor and is used to evaluate 
temporal lobe seizures and assists in ruling out other disorders. 
CYTOLOGIC STUDIES OF CSF 
Is done to detect malignant cells because tumors of the CNS are capable of shedding cells into CSF.
DRUG THERAPY 
I. Phenytoin ( Dilantin ) used to prevent seizures. 
Dose: as per doctor’s order 
Nursing implication: assess for gingiral hyperplasia. Administer drug on schedule and assess for signs of 
toxicity and rash. 
II. Dexamethasone used to reduce cerebral edema 
Dose: as per doctor’s order 
Nursing implication: monitor for blood glucose. Taper dosage after long term therapy 
III. Laxatives / stool softeners are used to prevent constipation. 
Dose: as per doctor’s order 
Nursing implication: Monitor fecal impaction and instruct patients not to strain. 
IV. Ranitidine or fomatidine used to decrease gastric acid secretion 
Dose: As per doctors’ order. 
SURGICAL MANAGEMENT 
INTRACRANIAL SURGERY 
Indications 
1. Intracranial infections caused by bacteria. 
2. Hydrocephalus due to overproduction of CSF, obstruction to flow defective reabsorption. 
3. Intracranial tumors due to benign or malignant growth of cell growth. 
4. Intracranial bleeding due to rapture of cerebral blood vessels because of trauma or 
cardiovascular accident. (CVA) 
5. Artenovenouse malformations due to congenital tangle arteries. 
6. The surgical removal tumors which is called craniotomies. 
NURSING CARE 
PRE OPERATIVE CARE 
Collection of baseline data of neurological and physiological states and recording. 
Encourage patients’ family to verbalize their fears. 
Explain procedures to be done and why
Give pre operative medication to allay anxiety and for them to understand. 
Shave the head in readiness for the operation.prepare the family and patient on the appearance of the 
patient after surgery, head dressings, edema and ecchymosis of the face and possible decrease in 
mental status. 
POST OPERATIVE CARE 
OBSERVATIONS 
Assess neurological status including ability to move, level for orientation and alertness of the patients 
pupils. 
Assess degree and character of drainage, amount and bleeding should be minimized. 
Initial head dressing should be reinforced as necessary; often incision is left open to air after first several 
days. 
Observe for signs of postural hypertension. 
PROMOTE MOBILITY 
Two hourly turning either side to promote mobility and prevent pressure sore formation. 
If supratentional surgery is done, the head of bed is kept elevated at 30 degrees. 
Encourage early ambulation to prevent complication of bed rest .eg hypostatic pneumonia and deep 
vein thrombosis. 
Raise head end of the bed gradual and encourage patient to sit on edge of bed before standing to 
prevent further injury. 
PROMOTE DECREASED INTRA CRANIAL PRESSURE 
Space nursing activities to allow patients to rest between them. Encourage patient to avoid progressive 
coughing and vomiting. 
Do suctioning only when necessary and the gently and cautiously. 
PROTECT SAFETY OF THE PATIENT 
Use soft hand restraints if necessary to prevent injury. Use mittens as alternative to restraints, change 
mitt fourth hourly and provide range of motion exercises to hands at this time. Cut nails short to prevent 
self injury. 
PROMOTE ELECTROLYTE BALANCE
Perform accurate intake and output with measurement of specific gravity to prevent overload. Do 
frequent testing for blood glucose to prevent blood glucose in balance. Have patient resume oral diet as 
quick as possible to maintain good electrolyte balance. Assess for difficult in swallowing or absence of 
gag reflex before stating oral diet. Monitor electrolytes for presence of abnormality. 
PROMOTE COMFORT 
Medication for comfort with codeine sulphate or non-carcotic analgesic to relieve pain. Ice cap for 
headache may help. 
COMPLICATIONS 
1. Hydrocephalus- due to obstruction of normal flow cerebral spinal fluid. 
2. Respiratory failure- can result from edema in the brain stem, inability to protect the airway and 
the cough and gag reflex. 
3. Cerebral spinal fluid leak – due to opening into the Dura matter. 
4. Corneal abrasion is due to trauma or surgery in the seventh cervical nerve.

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Brain tumours

  • 1. BRAIN TUMOURS A brain tumor is a localized intracranial lesion. It occupies space within the skull. These tumors usually grow as a spherical mass but can grow diffusely infiltrating tissue. Tumors of the brain can be primary arising from tissue in the brain or secondary resulting from metastasis from malignant neoplasm elsewhere in the body. Brain tumors are generally classified according to tissue from where they originate, if malignant tumor is graded according to general cancer staging procedures. CLASSIFICATION OF BRAIN TUMORS GLIOMAS are a malignant gliomas and most common brain Neoplasm accounting for about 45% of all brain tumors. ASTROCYTOMA these are the most common type of glaucoma. They arise from supportive tissue glial cells and atrocities. Usual location is white matter of frontal and temporal lobes in adult’s lateral and cerebella lobes in children. There is mild and moderately malignant grades I and II. GLIOBLASTOMA MULTIPOROMEET This arises from primitive stem cell (gliobalist) usual location is cerebral usual location are cerebral hemispheres. This is highly malignant and invasive and grade iii and IV. OIGODENDROGLIOMA Arises from glial cells and dendrites usual location is cerebral hemisphere most in frontal lobe, some in basal ganglion and cerebellum. Most are benign (encapsulation and calafication) EPENDYMOMA This arises ependymal epithelium usually occurs in lateral and fourth ventricles in children and young adults. They are benign to highly malignant most benign are encapsulated. MEDULLOBLASTOMA These arise from supportive tissue usually at the posterior fossa, fourth ventricle brain stem in children. They are highly malignant and invasive, metastasis to spinal cord and remote areas of the brain. 2 MENIGIOMA Arises from endothelial cells, fibrous tissues elements, transitional cells and angioblasts usual location are arachnoids, villi Dura half over convexity of Hemisphere and half at base of hemisphere. They are usually benign encapsulation outside brain substance.
  • 2. 3 ACCOUTIC NEUROMA (NEUROFIBROMA) They arise from Schwann cells inside auditory meatus on vestibular occurs at the site between the Pons and the cerebellum. They are usually benign or low grade malignancy encapsulation 4. PITUITARY ADENOMA Arises from pituitary glandular tissue located at pituitary gland usually benign. 5 VASCULAR TUMOURS (HEMAGIOBLASTOMA ARTERIO VENOUSE MALFORMATION) Arises from over growth of arteries and veins enlarging from vessels. Location is parental cortex near middle cerebral vessels. They are benign. 6 METASTATIC TUMOURS These arise due to cancer cells spreading to the brain via circulating system from lungs, breasts ,kidney, thyroid and prostate . Usual location is cerebral cortex and they are malignant. CASAUSES 1. Idiopathic 2. Genetically acquired 3. Hereditary 4. Defective immune system 5. Viruses 6. Head injury PATHOPHYSIOLOGY The physiology of brain tumors’ depends on the part of the brain that is affected. Eg PITUITARY ADENOMAS Functioning pituitary tumors can produce one or more hormones normally produced by anterior pituitary. The hormones may cause prolactin secreting pituitary adenomas (prolactinomas) growth hormone secreting pituitary adenomas; it produces acnomegally in adults and adrenocortropic hormone in female patients whose pituitary gland is secreting excessive quantities of prolactin with Amenorrhea or glactorrhea (Excessive or spontaneous flow of milk) male patients with prolactoma may present with impotence. CLINICAL MANIFESTATION Symptoms are generalized as well as specific the tumor location and structure of the brain are compressed.  Pressure headache (generalized or peri orbital) 
  • 3.  Nausea and vomiting unrelated to food intake  Symptoms of intracranial pressure  Visual changes  Blurred vision  Diplopia (iii,iv,and vi nerve compression)  Visual field alteration  Enlarged black spots related to papilla edema  Seizures  Speech difficulty( when the tumor affects language area in dominant hemisphere)  Weakness( when tumor affects motor cortex)  Alteration in the level of consciousness  Personality changes( when tumor affects frontal lobes) TUMOUR LOCATION AND ASSOCIATED PRESENTING SYMPTOMS CEREBRAL HEMISPHERE Frontal lobes (unilateral hemiplagia) : seizures, memory deficit, personality and judgment changes ,vision disturbances. FRONTAL LOBES Bilateral symptoms associated with frontal lobes and ataxic gait aphasia (motor dysfunction) PARIETAL LOBES Speech disturbance if tumor is in dominant hemisphere, inability to write. Inability to replace pictures, loss of right –left discrimination, seizures. OCCIPITAL LOBE Visual disturbances, blindness, headache and seizures TEMPORAL LOBE Complex or partial seizures with automatic behavior, hallucination. METASTATIC TUMORS Headache, nausea or vomiting because of intracranial pressure other symptoms depends on location of tumor. THALAMUS SELLAR TUMORS UMOUR Headache, nausea or vomiting and diabetes inapedus may occur. FOUTH VENTRICLE AND CEREBELLAR TUMORS
  • 4. Headache, nausea and papilloedema, mystagamus, occur from intra cranial pressure, ataxic gait and changes in coordination. CEREBRELLOPONTINE TUMOUR Tinnitus and vertigo deafness. BRAINSTEM TUMOURS Headache, upon awakening, drowsness, vomiting, ataxic gait, facial muscle, dysphagia, dysaithria, crossed eyes or other visual changes. MANAGEMENT INVESTIGATIONS HISTORY TAKING and physical exams. History taking of the illness and the manner in which the symptoms involved are important in diagnosis. This will help to provide data and location. Assess the level of consciousness, motor abilities, and sensory perception. CT SCAN This is done to check the number, size and density of the lesions and the extent of secondary cerebral edema. SKULL X-RAYS This is done to detect fractures, bones erosion, calcification and abnormal vascularity. MAGNETIC RESONANCE IMAGING (MRI) This is where internal body parts are visualized by means of magnetic energy. This is used to detect tumors in the brain stem and pituitary regions where bones interfere with CT scan. CEREBRAL ANGIOGRAPHY This involves the injection of contrast medium into the cerebral arterial circulation which assists in determining etiology of strokes, seizures, headaches and motor weakness. It is used to visualize the cerebral blood vessels and can localize most cerebral tumors. ELECTROENCEPHALOGRAM (EEC) This is used to detect abnormal brain waves in regions occupied by a tumor and is used to evaluate temporal lobe seizures and assists in ruling out other disorders. CYTOLOGIC STUDIES OF CSF Is done to detect malignant cells because tumors of the CNS are capable of shedding cells into CSF.
  • 5. DRUG THERAPY I. Phenytoin ( Dilantin ) used to prevent seizures. Dose: as per doctor’s order Nursing implication: assess for gingiral hyperplasia. Administer drug on schedule and assess for signs of toxicity and rash. II. Dexamethasone used to reduce cerebral edema Dose: as per doctor’s order Nursing implication: monitor for blood glucose. Taper dosage after long term therapy III. Laxatives / stool softeners are used to prevent constipation. Dose: as per doctor’s order Nursing implication: Monitor fecal impaction and instruct patients not to strain. IV. Ranitidine or fomatidine used to decrease gastric acid secretion Dose: As per doctors’ order. SURGICAL MANAGEMENT INTRACRANIAL SURGERY Indications 1. Intracranial infections caused by bacteria. 2. Hydrocephalus due to overproduction of CSF, obstruction to flow defective reabsorption. 3. Intracranial tumors due to benign or malignant growth of cell growth. 4. Intracranial bleeding due to rapture of cerebral blood vessels because of trauma or cardiovascular accident. (CVA) 5. Artenovenouse malformations due to congenital tangle arteries. 6. The surgical removal tumors which is called craniotomies. NURSING CARE PRE OPERATIVE CARE Collection of baseline data of neurological and physiological states and recording. Encourage patients’ family to verbalize their fears. Explain procedures to be done and why
  • 6. Give pre operative medication to allay anxiety and for them to understand. Shave the head in readiness for the operation.prepare the family and patient on the appearance of the patient after surgery, head dressings, edema and ecchymosis of the face and possible decrease in mental status. POST OPERATIVE CARE OBSERVATIONS Assess neurological status including ability to move, level for orientation and alertness of the patients pupils. Assess degree and character of drainage, amount and bleeding should be minimized. Initial head dressing should be reinforced as necessary; often incision is left open to air after first several days. Observe for signs of postural hypertension. PROMOTE MOBILITY Two hourly turning either side to promote mobility and prevent pressure sore formation. If supratentional surgery is done, the head of bed is kept elevated at 30 degrees. Encourage early ambulation to prevent complication of bed rest .eg hypostatic pneumonia and deep vein thrombosis. Raise head end of the bed gradual and encourage patient to sit on edge of bed before standing to prevent further injury. PROMOTE DECREASED INTRA CRANIAL PRESSURE Space nursing activities to allow patients to rest between them. Encourage patient to avoid progressive coughing and vomiting. Do suctioning only when necessary and the gently and cautiously. PROTECT SAFETY OF THE PATIENT Use soft hand restraints if necessary to prevent injury. Use mittens as alternative to restraints, change mitt fourth hourly and provide range of motion exercises to hands at this time. Cut nails short to prevent self injury. PROMOTE ELECTROLYTE BALANCE
  • 7. Perform accurate intake and output with measurement of specific gravity to prevent overload. Do frequent testing for blood glucose to prevent blood glucose in balance. Have patient resume oral diet as quick as possible to maintain good electrolyte balance. Assess for difficult in swallowing or absence of gag reflex before stating oral diet. Monitor electrolytes for presence of abnormality. PROMOTE COMFORT Medication for comfort with codeine sulphate or non-carcotic analgesic to relieve pain. Ice cap for headache may help. COMPLICATIONS 1. Hydrocephalus- due to obstruction of normal flow cerebral spinal fluid. 2. Respiratory failure- can result from edema in the brain stem, inability to protect the airway and the cough and gag reflex. 3. Cerebral spinal fluid leak – due to opening into the Dura matter. 4. Corneal abrasion is due to trauma or surgery in the seventh cervical nerve.