Download - Brain Tumor
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NEUROLOGIC SYMPTOMSNEUROLOGIC SYMPTOMS– BRAIN TUMORS– BRAIN TUMORS
INTP - PPO, PHO, IAP.P2 – 27 slides
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Topic IncludesTopic Includes
Clinical history Presentation / signs Diagnosis Classification Treatment overview Management of common tumors
INTP - PPO, PHO, IAP.P2 – 2/27
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Pediatric Brain Pediatric Brain TumorsTumors
Commonest Solid Tumors Symptoms mimic other conditions Delay in diagnosis possible High index of suspicion necessary Long term survivors more than 60%
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Clinical Summary: 06 year, female child Complaints – Headache, vomiting Unsteadiness of gait / difficulty in
walking/ swaying visual deterioration
Case –1
Clinical signs
No cranial nerve palsy
No sensory / Motor deficit
Conscious / cooperative
Reflexes (N)
Rhomberg’s sign absent
Bilateral papillodema (+)
Broad based gait
Falls on either side (Lt) > (Rt)
(Lt) cerebellar signs positive
INTP - PPO, PHO, IAP.P2 – 4/27
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Case – 2Clinical summary: 07 year male child complaints difficulty in
swallowing/speech weakness (Rt) side of body, double vision, altered sensorium.
Case – 3Clinical summary: 14 year male child, complaints headache,
seizures, memory loss
Possible diagnosis: Brain tumor/neoplasmINTP - PPO, PHO, IAP.P2 – 5/27
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Normal Anatomy Normal Anatomy of Brain (MRI)of Brain (MRI)
Supratentorial compartment: Cerebral hemispheres Basal ganglia Thalamic nuclei Lateral ventricles Hypothalamus Corpus callosum
Infratentorial compartment: Cerebellum Brain stem (MB/P/MO) 4th ventricle
Sagittal
AxialINTP - PPO, PHO, IAP.P2 – 6/27
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Clinical SymptomsClinical Symptoms Location / age Non localised / raised intracranial pressure Localised
Nonlocalised Tumor mass Blockage of CSF pathways
Weight loss, listlessness, irritability, decreased appetite, lethargy / withdrawn behaviour, headache, vomiting, double vision.
INTP - PPO, PHO, IAP.P2 – 7/27
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Clinical SymptomsClinical Symptoms
Infratentorial tumors Symptoms of ICP Imbalance / Swaying Diplopia, swallowing
difficulty
Intrinsic brain tumors Diplopia, swallowing and
breathing difficulty, weakness limbs, swaying ICP
Supratentorial tumors
Weakness of limbs, loss of sensation, abnormal vision, learning difficulty, memory loss,
Deep midline tumors
Obesity, visual complaints, growth abnormalities.
Localised
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Clinical Signs
Non-localisedPapillodema, head circumference, malaligned eyes, cranial nerve palsy (6th)
LocalisedInfratentorial tumorsAtaxia, defects in co-ordination, nystagmus, abnormal speech.Intrinsic brain tumorsCranial neuropathy, long tract signs, ataxia.Supratentorial tumors Hemiparesis, hemisensory, visual field abnormalities, cognitive/learning difficulties, seizures.Deep midline tumorsEndocrinopathies, visual acuity and visual, field abnormalities, Parinaud’s syndrome.
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Pediatric Brain TumorsPediatric Brain TumorsDiagnosisDiagnosis
ImagingCT scan (plain + contrast)
MRI with Contrast (Gd) MRI preferred sensitivityresolution three planer views
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Pediatric Brain TumorsPediatric Brain Tumors
Posterior fossa neoplasm – MedulloblastomaINTP - PPO, PHO, IAP.P2 – 11/27
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Intrinsic pontine glioma
Pediatric Brain TumorsPediatric Brain Tumors
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Pediatric Brain TumorsPediatric Brain Tumors
Supratentorial tumors – Astrocytoma & ependymoma
Pinealoblastoma & craniopharyngioma INTP - PPO, PHO, IAP.P2 – 13/27
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Histologic: Craniotomy / Tumor resection CT/MRI / STB Exception Pontine glioma
Pediatric Brain TumorsPediatric Brain TumorsDiagnosisDiagnosis
Classification: Histology Location – Differs from adult brain neoplasms
Low grade Infratentorial
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Common Brain TumorsCommon Brain Tumors
Location Percentage
Infratentorial 45-60
Supratentorial Hemispheric
Midline – Suprasellular / Pineal region
25-40
15-20
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Medulloblastoma undifferentiated, barophilic round to oral nuclei with minimal perceptible cytoplasm
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Distribution of common brain tumors in children Distribution of common brain tumors in children – location and histologic appearance– location and histologic appearance
Infra-tentorial % of all brain tumors
PNET (Medulloblastoma) 20-25
Low grade astrocytoma cerebellar
12-18
Ependynoma 4-8
Malignant glioma, brain stem 3-6
Other 2-5
Total 45-60INTP - PPO, PHO, IAP.P2 – 17/27
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Supratentorial % of all brain tumors
Low grade astrocytoma 8-20
Malignant glioma 6-12
Ependymoma 2-5
Mixed glioma 1-5
Ganglioglioma 1-5
Oligodendroglioma 1-2
Chorioid plexus tumor 1-2
PNET 1-2
Meningioma 0.5-2
Other 1-3
Total 25-40
Distribution of common brain tumors in children Distribution of common brain tumors in children – location and histologic appearance– location and histologic appearance
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Supratentorial midline % of all brain tumors
Suprasellar
Craniopharyngioma 6-9
Low grade glioma, chasmatic hypothalamic 4-8
Germ cell tumor 1-2
Pituitary adenoma 0.5-2.5
Pineal region
Low grade glioma 1-2
Germ cell tumor 0.5-2
Pineal parenchymal tumor 0.5-2
Total 15-20
Distribution of common brain tumors in children Distribution of common brain tumors in children – location and histologic appearance– location and histologic appearance
INTP - PPO, PHO, IAP.P2 – 19/27
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Staging Work upStaging Work up
Dissemination extraneurally rare – staging work up seldom indicated
Spinal MRI/CSF cytology – mandatory Medulloblastoma, PF ependymoma, Germ cell tumor
Blood / CSF - FP, Hcg – Germ cell tumors
INTP - PPO, PHO, IAP.P2 – 20/27
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TreatmentTreatment General principlesGeneral principles
Surgery Diagnosis Tumor burden is decreased/reduced CT/MRI Guided STB Open biopsy / extensive microsurgical
resectionINTP - PPO, PHO, IAP.P2 – 21/27
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Problem Associated tumors Peri / intraoperative Management
Postop management
Odema Large tumors small tumors in critical areas
Corticosteroids Dexona
0.1mg/kg Q6h
Corticosteroids tapered
Obstructive hydrocephalus
Intra and periventricular tumors
External ventricular drain placement or VP shunt
Closure or permanent
Seizures Tumors of cerebral hemispheres
Anticonvulsant phenytoin
Stopped in follow-up
Hypothalamic Pituitary hormonal insufficiency
Tumors close to hypothalamus
Endocrine Evaluation, Steroids fluid and electrolyte balance
Hormone replacement
Perioperative ManagementPerioperative Management
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Radiotherapy High energy machines Volume – Craniospinal irradiation, localised
irradiation Dose – 50-60 Gy / 24-36 Gy, 180-200 Gy / # STRS/STRT – Interstitial brachytherapy /
conformal and intensity modulated treatment Delay/defer irradiation for children younger than
3 years
TreatmentTreatment General principlesGeneral principles
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Useful and standard
Medulloblastoma, malignant astrocytomas, optic pathway / hypothalamic gliomas, malignant tumors in children less than 3 years of age.
Upfront CT / neo-adjuvant CT, HD CT - BMT
Useful drugs: CCNU/VCR/Prednisalone, Procarbazine, Carboplatinum, Vincristine, Temozolamide
TreatmentTreatment General principlesGeneral principles
ChemotherapyChemotherapy
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Infratentorial TumorsInfratentorial Tumors
High risk M1
>1.5 cms residual tumor <3 years RT + CT
Standard risk RT ?CT
Medulloblastoma Sx Adjuvant Treatment
Cerebellar Astrocytoma Ependymomas Brain stem glioma
Sx alone ?RT (adjuvant) Sx Adjuvant RT RT alone
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Supratentorial TumorsSupratentorial TumorsHemispheric tumors:
Gliomas: Low grade: Sx alone
High grade: Sx RT + CT (adjuvant)
Ependymomas: Sx RT (adjuvant)
Optic pathway/ Sx CT RT
Hypothalamic
Gliomas Craniopharyngioma Sx RT Pineal region tumors Individualized
treatment
Midline Supratentorial Tumors
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