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This is a presentation that I gave to first year PA students
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Tumors of the Brain and Spine
Joe Hlavin PA-C, MSTexas Brain and Spine Institute
Bryan, [email protected]
Introduction/Bio
US Navy – Corpsman – 1984 to 1989Cuyahoga Comm College – 1991 – surgical PA
◦Went right into private practice neurosurgery22 years of neurosurgery experienceBS in Education – BGSUMS in Organizational Learning – TAMUPhD Student - Organizational Design - TAMUDesigner & director of the TAMHSC/TBSI Postgraduate PA Residency in Neurosurgery
Objectives• For this lecture:
• Review of the normal brain and spine anatomy and physiology, including CT and MRI
• Review neurological exam
• Discuss selected intracranial and intraspinal lesions
• Provide current treatment schemes
• Discuss reasoning for treatment decisions
• Case studies
AnatomyQuidi Vidi Bay, Newfoundland
The Brainsome A&P
• Lobes - Supertentorial
• Frontal
• Temporal
• Parietal
• Occipital
• Cerebellum - Subtentorial
UT student????
the brain A&P• Frontal
• Reasoning, planning, “personality”
• Frontal eye fields – Brodman 8
• Visual attention
• Motor strip
• Temporal
• Speech – dominant
• Memory – non-dominant
• High Sz region
PERSONALITYPLANNINGREASONING
MOTORSENSORY
SPEECHHEARING
SPEECH
MEMORYSMELL
VISIONPROCESSING
FRONTAL
PARIETAL
TEMPORAL
OCCIPITAL
CEREBELLUM
TENTORIUM
the brain A&P• Parietal
• Sensory
• Proprioception
• Calculia, graphesthesia, left/right – dominant
• Occipital
• Visual cortex – processing/understanding
• End point of the ocular tracts
• Cerebellum
• Coordination, balance
PERSONALITYPLANNINGREASONING
MOTORSENSORY
SPEECHHEARING
SPEECH
MEMORYSMELL
VISIONPROCESSING
FRONTAL
PARIETAL
TEMPORAL
OCCIPITAL
CEREBELLUM
TENTORIUM
writing
Important – DominantInvolves 3 lobes
Spinal Cord
• Anatomy
• Tracts
• Ascending
• sensory
• Descending
• Motor
Spinal Cord
• Understanding the medullary component
• Simply – relay station for input and output of transmissions
• Important to know:
• Medial to lateral IS:
• Cervical to Sacral
Spinal Cord
• Focusing for function
• Keys
• Ascending – sensory
• Lesions are not as easily identified due to subjective nature
• Descending – motor
• Easier to find level due to objectiveness of the exam
StudiesSt. John’s Bay – The Narrows
CT
• Usually the first study performed• Fast• Easy• Least expensive• Consists of 60 to 70 – 5mm slices• Can be done with dye
MRIpreferred for brain and a
must for spine• Most detailed
• Used with Gadolinium (“dye”)
• No radiation
• But
• Expensive
• Tight space
• Takes more time
• Cannot do with some implanted devices
Lesions
Lesion Types
Lesion Types• Benign
• Non-aggressive but can be devastating based on size and location
• Meningioma is most common – ARISE FROM?
• less common
• Neuromas – acoustic
• Dermoid
• Pituitary adenomas
Lesion types•Metastatic
• The primary cancer: lung, breast, colon, kidney, or skin (melanoma), but can originate in any part of the body
Malignant lesionsGlial tumors
• World Health Organization grading (WHO) scale ASTROCYTOMAS, I – VI
• Grade – I – e.g. Pilocytic and Subependymomas
• Grade – II – low grade astrocytoma and oligodendrocytoma
• Grade – III – medium, anaplastic astrocytoma
• Grade – VI – high, Glioblastoma Multiforme (GBM)
Examples
• Four different astrocytic lesions, four different looks
Sub-ependymoma Oligodendroglioma
Anaplastic astrocytoma
GBM – grade VI
Cerebellar Lesions
• Very similar to CEREBRAL lesions
• Have increased risks with compression of essential component of CSF drainage
• Primarily noted in children, e.g. medulloblastoma, PNET (prim. neuroecto. Tumor)
• Will present in adults as astrocytoma and cystic
• Common area for metastatic seeding
Describing Studies
General Descriptionsfor Brain and Spinal Lesions
• For the brain
• Extra-axial
• Intra-axial
• For the spinal cord
• Extra-dural vs. Intra-dural
• Extra-medullary vs. Intra-medullar
• For both
• Non-enhancing vs. enhancing (MRI)
General Descriptionsfor Brain and Spinal Lesions
• Location, location, location
• For the brain
• What lobe? Size? Edema? Shift? Obstructive?
• For spinal cord
• What level? Size? Syrinx?
• Lesion consistency
• Heterogenous vs. homogenous
• Ring enhancing (w/ cyst) vs. diffuse enhancement
PA circa 1989
examples
More Examples
Neurological Exam
Neuro Exam
•Tenets of the approach to the NS patient
• DO NOT BELIEVE ANYONE ELSES EXAM –
• DO YOUR OWN
• LOOK at the studies yourself, NOT just the report
• SEE the patient as MORE THAN the studies
Neuro exam
• The mental status
• “normal” or “Sleeping” is not a good descriptor. Use:
• Awake/alert/talking
• Less than alert – obtunded
• Unresponsive – comatose, stupor
• In this case, give the Glasgow Coma Scale as descriptor
Neuro exam• Glasgow Coma Scale
• Eyes – 4, spontaneous, 3, to voice, 2, to pain, 1, none
• Motor – 6, obeys, 5, localizes, 4, w/drawls, 3, flexion response, 2, extension to pain, 1, none
• verbal – 5, oriented, 4, confused, 3, inappropriate words, 2, incomprehensible words, 1, none
• PEARL – if pt is brought in by EMS – GET THE GCS NOTED AT THE SCENE
• Remember, everything has a GCS – even a rock has a GCS of 3
Neuro exam• Cranial nerves
• LOOK AT THE EYEs
• Symmetry – light response, movements, gaze pref
• LOOK AT THE FACE
• Symmetry – right = left, pay attention to motor
• LOOK IN THE MOUTH
• Symmetry – tongue and pharynx
Neuro exam• Motor exam
• Abbreviated evaluation
• Look for: (KEEP IN MIND – Right cortex = left body)
• Right vs. left strength – if equal then
• Check individual groups – start with upper extremities
• Keep level of any deficit in mind
• example: bilateral weakness from biceps down = C6 level
Neuro exam
• Reflexes
• Know the difference between UMN and LMN reflex changes
Neuro exam• Upper motor neuron reflexes
• Cranial nerve reflexes are considered normal and loss of reflex is concerning – e.g. pupillary response
• Primitive Reflexes – found in newborns, but can present in patients with neurological disease due to loss of blunting of reflexes.
• Hyper-reflexia and ankle clonus – unsustained/sustained
• Babinski Reflex – blunted by myelination of SC
• Hoffman Reflex – blunted also
Neuro exam• Lower motor neuron reflexes
• Spinal reflexes
• Relay station in the medullary cord
• E.g. knee jerk, triceps jerk
• Loss: indicative of root irritation/compression, e.g. HNP, tumor
• May be associated with motor group deficit
Neuro exam
• Cerebellar exam
• Coordination
• Rapid movements
• Finger-to-nose
• KEEP IN MIND – RIGHT cerebellum = RIGHT body
• Docusates twice – once at peduncle and then medulla
Treatment
Treatment
• Initial treatment plan – generally speaking
• Dependent on the patient presentation and clinical status
• Steroids – Decadron
• H2 blocker du jour
• Admission to hospital for continued treatment, w/u, and neurosurgical consultation (UNLESS THAT IS YOU)
Treatment• The treatment is based on clinical exam, age,
comorbidities, and patient’s/family’s wishes – KNOWING risk/complications and outcomes.
• Benign lesions can be followed, treated with surgical decompression (if clinically warranted), and/or radio-surgical techniques, e.g. Gamma knife, Linear accelerator, etc.
Treatment• Metastatic Lesions
• Based on original lesion, location, and clinical picture
• Surgical resection for symptomatic lesions AND diagnosis
• Also based on surgical safety
• Some metastatic lesions are very hemorrhagic – risk outweighs reward
Treatment - Survival• Astrocytomas
• Grade I – surgery based on clinical picture, location, and risk but considered benign and can be followed with serial MRIs for growth. Stereotactic bx can also be considered or even total resection
• Survival is quite acceptable and may have complete remission after surgical removal
• Grade II – Same as above but consider the incidence of conversion to more aggressive lesion.
• Can consider serial MRIs, bx, surgical resection. Survival based on diagnosis
Treatment - Survival
• Astrocytomas
• Grade III – these are considered malignant and are likely to convert to higher grade. Clinic picture likely to require surgical intervention.
• Gross total resection, radiation therapy, possible include chemotherapy – Tamodar
• Survival is tenuous based on lesion type, resection, and response to treatment
Treatment - Survival• Astrocytomas
• Grade VI – most aggressive, Glioblastoma Multiforme, high mitotic changes, low percentage of overall cancers in the US but very devastating.
• Best quality of life, ~ one (1) year, is w/ gross total resection, radiation, and Tamodar
• Other treatments have been, or are being, studied:
• Gene therapy
• Immunotherapy
• Novel delivery methods
Case Studies
• 22 y/o WM presents to the ER with focal RUE seizures
• No prior history – very healthy
• Student at local university
• Exam – mild “drift” of the RUE and ? Mild weakness, no UMN findings, gait not tested
• Next step?
Case 1Describe
What’s next?
Case 1
• Notify the NS service – UNLESS that’s you
• Admit to the hospital
• Start steroids
• Start Dilantin
• Order MRI w/ GAD
Case 1
Is this extra-axial, intra-axial, infiltrative, edematous?
Describe
Case 1
• Next treatment course?
• Surgery?
• Watch?
• Medicine?
• Other studies?
Case 1
• What we did:
• Continued the steroids and Dilantin
• Family discussion and surgical planning as outpatient
• Craniotomy for biopsy and debulking
• Initial postoperative course was uneventful
• Awaited final diagnosis
Case 1
• Final Diagnosis
• Glioblastoma Multiforme
• High grade lesion – aggressive
• Oncology and radiation therapy involved
• Family made one trip to MD Anderson for second opinion
• Started treatment – We will be following up this month
Case 2
• 30 y/o female presented to outlying clinic with progressive thoracic pain – ONLY
• No significant PMHx
• Exam was essentially normal
• What would be your initial study if conservative medical treatment failed?
Case 2
Describe this MRI of the
Thoracic spine w/ Gadolinium:Level?Extra-dural?intra-dural?extra-medullary?Intra-medullary?Enhancing?
Case 2
• Treatment
• Surgical resection?
• Medications?
• Radiation?
• Watch?
Case 2
• What we did:
• Surgical discussion with patient and husband
• Remember that patient’s only problem was pain
• Thoracic laminectomy for partial resection and biopsy
• Steroid treatment in post op phase
• Stable post op exam w/ minor sensory changes
Case 2
• Final diagnosis
• Ependymoma – Grade II
• High likelihood of future neurological dysfunction
• Completed radiation treatment and first post radiation MRI was stable – exam also stable
• Due for f/u with new MRI of the Tspine
Case 3
• 63 y/o BM presented after struck in the head and pelvis by a toolbox
• w/u by ER and trauma service was, initially, just the abd and pelvis
• Head CT done as inpatient to complete work up
• No neurological complaints or exam findings
Case 3
Describe
Case 3
DescribeExtra or intra axial?Enhancing?Heterogeneous or homogenous?Location?Mass effect?
Case 3
• Treatment?
• Steroids?
• Surgery?
• Medications?
• Watch?
Case 3
• This is what we did:
• Discharged from hospital after recovery from pelvic injury
• Took to surgery for craniotomy and excision of the tumor
• Excellent postoperative course with discharge w/ in 3 days to home – no loss of function
Case 3
• Diagnosis
• Meningioma – benign lesion – total resection with attachment to the dura upon entry
• No need for aggressive post op treatment
• Follow up MRI in 6 months
• Return to normal activity
Case 4 – Last one
• 50 y/o WF well known to our practice with multiple intracranial CAVERNOMAs
• In 2008, developed new symptoms of neck and arm pain that progressed to gait instability
• Her exam fits with parasthesias and UMN findings in extremities
• What is the next step? Medications, studies?
Case 4
MRI - Hem W/ Gad w/o Gad
Case 4
Describe:Location?Extradural/intradural?Extramedullary/intra-medullary?Levels/location?
Case 4
• Treatment?
• Surgery?
• watch?
• Medications?
• Steroids?
• Immobilize?
Case 4
• What we did:
• Surgical decompression
• Steroids – short term
• PT
• F/U w/ serial MRIs
• Last study in Sept. 2012 – stable
• Very mild neurologic sequelae
Wrap up
Wrap up
• Tumor types of the CNS are numerous but are categorized for description, correlation to clinical picture, and treatment strategies
• Current imaging techniques are quite useful in identifying and predicting CNS lesions
• Take the time to gather a history, obtain your own exam, and look at the actual studies (use the radiology report as reference)
Wrap up
• The clinical picture of the patient upon presentation coupled with the studies is paramount to the development of a treatment strategy
• Studies and new treatments of aggressive CNS lesions, e.g. GBMs, remain at the forefront of cancer research
• Finally, all of you should endeavor to be neurosurgical PAs
Questions?