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47 Cards in this Set

  • Front
  • Back
CNS Neoplasms

Statistics
2% of all cancer deaths

20% of childhood malignancies

50% primary brain tumors

50% metastatic tumors to the brain
CNS Tumors

Issues to consider
Age of patient

Location of lesion

Radiology results

Gross and Histologic features

Molecular testing

Prognosis and treatment
CNS Tumors

Age and Location
Adults - supratentorial

Children - Infratentorial
Malignant growth

characteristics
Infiltrative

Difficult to remove surgically

Rarely metastasize

Death due to direct impingement on vital centers or herniation
Benign growth

characteristics
curable

may cause death due to inoperability or proximity to vital centers
Origins of CNS Neoplasms
Intrinsic Cells
-Glial Cells
--Astrocytes
--Oligodendroglial cells
--Ependymal
--Microglia

-Neurons

Surrounding Cells
-Vascular Origin
-Meningeal cells

Developmental rests (germ cell tumors

Metastasis (MOST COMMON MALIGNANCY)
Gliomas
From glial cells
-Astrocytes, Oligodendrocytes, Ependymal

-Astrocytoma, Oligodendroglioma, Ependymoma
Grading of Astrocytomas
WHO

I - Pilocytic Astrocytoma
II - Astrocytoma
III - Anaplastic Astrocytoma
IV - Glioblastoma Multiform
Astrocytomas

Pilocytic Astrocytoma
Grade I

20% of pediatric brain tumors

Usually in cerebellum

Indolent (little pain), potential for surgery
Diffuse Astrocytomas
Astrocytoma - II
Anaplastic Astrocytoma - III
Glioblastoma - IV
Astrocytoma
Grade III

Adults, 30-40 yrs

Usually in cerebral hemispheres

Seizures, headache, focal neuro deficits

Median survival: 80 months

50-75% progress to grade III/IV
Anaplastic Astrocytoma
Grade III

Adults, ~40 yrs

Cerebral hemisphere lesion

Progression of lesion = worsening symptoms

Median survival: 30 months
Glioblastoma Multiforme
Grade IV

40-50% of all glial tumors

Older adults, 40-60 yrs

Large mass in cerebral hemisphere

Ring-enhancing lesion

PROGNOSIS BAD: 10 months
Pathogenesis of Grade IV Glioblastoma Multiforme
Develops from Astrocytoma (II)
-Accumulation of genetic hits
"Secondary glioblastoma"

De novo GBM
-Appears with no evidence of previous transformation
"Primary Glioblastoma"
Loss of heterozygosity
Loss of part of chromosome

Can be good or bad prognostic indicator

LOH of 1p and 19q is seen in oligodendrogliomas and indicates good response to chemo
Oligodendroglioma
Middle aged adults, 30-50 yrs

Cerebral white matter lesions

MRI: calcified or cystic

Seizures or other neuro signs may have been present for years

Avg survival: 5-10 yrs
Grading of Oligodendrogliomas
Grade II - favorable
Grade III - anaplastic

LOH in chromosomes 1 & 19 may do better with chemo
Primary CNS Lymphoma
1% of intracranial tumors

Usually in AIDs or elderly/immunocompromised

Large lesion in cerebral hemisphere

Poor Prognosis: avg 18 months

Cannot give surgery, have to do chemo
Medulloblastoma
Primitive neuroectodermal tumor

Bimodal age distribution
-Young children and ~40 yrs

Location
-Children in cerebellar vermis
-Adults in cerebral hemisphere

50% 10 year survival with therapy, kids better (85%)
Meningiomas
Arise from meninges of brain, spinal cord

More common in women

Symptoms are vague, result of brain/SC compression

grows slowly for years

Surgery possible
Metastatic Tumors to the brain
Most common!

Usually carcinomas

Most common from:
-lung, breast, melanoma, kidney, colon, stomach

Often multiple lesions

Can be in meninges
What causes death in brain tumors?
Space occupying lesions
(brain compression, herniation)

Compromise of essential brain functions

Large volume hemorrhage into tumor

Complications of treatment
Pituitary Tumors
Usually benign adenomas

Headache

loss of peripheral vision (optic chiasm compression)

Endocrine disturbances
-growth hormone: acromegaly
-prolactin: milk production
Infectious/inflammatory CNS Disease
Meningitis - meninges

Encephalitis - brain

Myelitis - spinal cord

Abscess - walled-off collection of neutrophils and dead tissue
Acute Bacterial Meningitis
Neonatal - vaginal delivery
-Group B Strep
-E. coli
-Listeria monocytogenes

Childhood
-Haemophilus influenzae (vaccine now)
-Strep pneumoniae
-Neisseria meningitis

Adolescence
-Neisseria meningitidis

Adult
-Strep pneumoniae
-Gram-negative bacteria
Causes of Bacterial Meningitis
Hematogenous Spread

Shunt infections

Traumatic injury

Mastoiditis, sinusitis
SX of meningitis
Babies
fever, crying, unresponsiveness

Adults
fever, headache, stiff neck, rash

Changes in CSF by lumbar puncture
-Lots of neutrophils
-Culture may grow bacteria

High morbidity and mortality if untreated
DX of meningitis
Kernigs sign
pain with combined hip flx/knee ext

Brudzinski's sign
flx neck produces flx knees
Brain Abscess facts
50% spread from sinus, middle ear, dental infections

25% hematogenous spread

due to bacteria, AFB, fungus

20% mortality

50% of survivors have persistent deficits
Viral infections

Aseptic Meningitis
Usually self limiting

Acute - Echovirus & Coxsackie virus (late usmjmer), arthropod borne

Subacute - mesales (winter, spring)
Viral infections

Parenchymal infection with tissue destruction
Acute - HSV, CMV, rabies

Subacute - SSPE (measles), PML (JC virus)
Herpes Simplex Virus (HSV)
Most common sporadic, non epidemic viral encephalitis

Adults - HSV-1 spread through retrograde axonal transport

Neonates - HSV-2 acquired through delivery, mucous membranes (eyes, mouth)

with no tx progresses rapidly and is usually fatal

SX can include phantom smells
HIV/AIDS
HiV infects macrophages and T-cells which import virus into brain

Direct infection of CNS by HIV
-neuro deterioration, dementia

Opportunistic infections

CNS lymphoma
Alzheimers Disease
Most common cause of dementia

50-60 yrs

memory, personality, disorientation

steadily progressive, death in 3-12 yrs

Down's Syndrom ppl at greater risk

Pathogenesis multifactorial and complex

Gross appearance of brain
-Cortical atrophy
-Enlarged (appearance of) ventricles
Histopathology of Alzheimers
Senile plaques - extracellular w/pink amyloid core

Neurofibrillary tangles - intraeuronal cytoplasmic filament collections

Amyloid angiopathy (sometimes)

*All of this is only observable after death*
Seizure
def: finite event resulting from paroxysmal excessive discharge of cerebral neurons

Transcient impairment, loss of consciousness

Many causes

Children - constitutional
Adults - acquired over time
Types of seizures

Partial Seizures
Local onset in cortex

Focal EEG abnormality

Simple parital
-No consciousness loss, just one hemisphere

Complex Partial
-Alteration/loss of consciousness, both hemispheres
Types of seizures

Generalized Seizures
Onset not localized in brain

Diffuse EEG abnormalities

Generalized absence
-person just stares off into space (petit mal)

Generalized tonic-clonic
-Tonic generalized rigidity
-Clonic generalized jerking
-Loss of consciousness, BB control
-Post-ictal tiredness
(grand mal)
Seizures in childhood
Febrile seizures

Hypoglycemia, hypocalcemia

Epilepsy

Intracranial lesions
Seizures in adults
Epilepsy

Trauma

Stroke

Hypozia

Drugs

Intracranial lesions
Tx of seizures
look for cause

anti-epileptic drugs
Prognosis of epilepsy
75% remission rate in children where it is idiopathic

major lifestyle impact

Death can occur if the seizures don't stop, or they choke on food or drown in bath
Near-drowning
def: surviving 24+ hours after hypoxemia and acidosis from fluid immersion

Dry drowning - 15%, little fluid inhalation

Wet drowning - 85%, fluid aspiration

Recurrence of respiratory distress
Drowning stats
Major cause of accidental death
-#2 in children less than 15yrs
-#3 in all ages

80% male

risk factors
-epilepsy, trauma, retardation

50% involved with alcohol
Complications of near drowning
Prolonged anoxia/hypoxia
-Brain most affect
-Cold may decrease oxygen requirements = less damage

Acute lung injury from aspiration
Prognosis of near drowning
20% of pt have permanent sequelae

Many also have CNS traumatic injuries

Many ultimately die
Key associations for headache
Worse headache of life
=subarachnoid hemorrhage
=possible ruptured aneurysm

Fever and stiff neck
=meningitis or meningoencephalitis

New onset seizure in older adult
=intracranial lesion

Papilledema
=brain is swelling (no lumbar punctures!)