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RETROGRADE AXONAL TRANSPORT

Retrograde axonal transport is used by what pathologic organisms/toxins?

Herpes
Rabies
Polio
Tetanus toxin
MCC of viral encephalitis?
Coxsackie virus
(late summer early autumn)
MC CNS infection in HIV patients?
Cytomegalovirus

CMV meningitis: common findings- gross and microscopic?
Rx?

Gross: Periventricular calcifications
Micro: Basophilic intranuclear inclusions

Rx: Gamcyclovir and foscarnet
HSV-1 meningitis gross finding?
Hemorrhagic necrosis of temporal lobe
(Herpes= Hemorrhagic)
Difference between bacterial and viral meningitides? (lab values)
GLUCOSE levels DECREASED in Bacterial meningitides
(<40mg/dl)
Viral meningitides associated with decreased CSF glucose?
1. Mumps
2. Herpes
3. Choriomeningitis

Arbovirus encephalitis: Name the virus.
Reservoir? Vector?

1. West nile virus
2. Reservoir- Wild birds(?)
3. Vector- mosquitoes
Lymphochoriomeningitis: Vector? Route of transport?
1. Vector- Mouse
2. Route- Feco-oral contamination with mice feces

Nuchal rigidity and mental status alteration
Post polio syndrome?
1. Occurs 15-30 years after infection.

2. Presents with muscle pain, weakness and fatigue.
Rabies:
Vector animal?
Inclusion bodies? Describe
1. Vector: Raccoon

2. Inclusion bodies- negri bodies
Dark intracytoplasmic eosinophilic bodies.
Rabies:
Viral receptor for entry?
Phases of disease?
1. Receptor-Acetylcholine receptor

2. Phases-
Prodrome- Fever and paresthesias(at site)
Hydrophobia- Pain due to throat muscle spasm while swallowing
Encephalitis- Associated with negri bodies- seizures, coma, death
Rabies: Rx?
1. Wash area with quart. NH4 compound.

2. Passive immunization at site

3. Active immunization with diploid human vaccine
Rabies: Course of virus through body after infection?
1. Replication at site of bite
2. Retrograde axonal transport
3. CNS replication
4. Saliva
Lacunar infarcts?
1. Microinfarcts <1cm
2. Hyaline arteriolosclerosis
3. Pure motor= Post limb of IC
4. Pure sensory= Thalamus
Demyelinating diseases: Name them
(relevant to step1)
1. MS
2. GBS
3. PML: Progressive multifocal leukoencepholopathy
4. CPM- Central Pontine Myelinolysis
5. Metachromatic leukodystrophy
6. Charcot Marie tooth disease
7. Postinfectious encephalitis
Risk factors for meningitis?
1. Undernutrition
2. Otitis media
3. Pneumonia
4. Sickle cell disease
5. Immunodeficiency
6. Craniofacial abnormality
Meningitis affects which meningeal layer?
PIA
Bacterial Meningitides are commonly gram (+ve or -ve)?
+ve
Imaging modality of choice in strokes?
CT with contrast
SAH headache patient description?
1. "Worst headache of life"
2. OCCIPITAL AREA
3. Nuchal rigidity
SAH results from?(cause)
risk factor?
1. Berry aneurysm rupture
2. AV malformations(less common)
3. risk factor: hypertension
Complications of SAH?
1. Hydrocephalus
2. Hemorrhage(recurrence)
3. Permanent neuro deficit
Hydrocephalus in SAH: cause?
Arachnoid granulations blocked
MC site for developing berry aneurysms?
why at that site?
Junction of communicating branches with the main branches
1. ACA-ACA(40%)
2. MCA-PCA(20%)
3. PCA-PCA(8%)

Internal elastic lamina and smooth muscle layer absent at these sites
TE Stroke rx?
1. Thrombolytics within 3 hours
2. Chronic- Antiplatelets, warfarin
Psammoma bodies:
Description?
Disease associations?
Description- Infarction and calcifications of papillary tips

Diseases-
1. Meningioma
2. Papillary ca of thyroid
3. Cystadenocarcinoma of ovaries
4. Renal CC
5. Mesotheliomas
6. Endometrial adenocarcinoma
7. Prolactinoma
8. Somatostatinoma(pancreas)
Creutzfeldt jacob disease: Caused by?
Prion proteins- Proteins devoid of DNA and RNA
Creutzfeldt jacob disease: modalities of spread?
Gross appearance?
1. Corneal transplant
2. Cortical electrodes
3. Infected beef tissue consumption

Gross appearance: "bubble and holes" spongiform cortex
Progressive multifocal Leukoencepholopathy: Etiologic agent?
Papovavirus (JC virus?)occurs in AIDS- <50cells/mm#3
Progressive multifocal Leukoencepholopathy: microscopic findings?
Intranuclear inclusions in oligodendrocytes and neurons
MC demyelinating disease?
MS
MCC of optic neuritis?
MS
MS: Microbial pathogens associated with it?
1. HHV6
2. EBV
3. Chl pneumonia
MS: HLA association(autoimmune)?
HLA-DR2
MS: Autoimmune mechanism type?
Type IV
1. Helper T cells recognize the myelin basic protein as antigen
2. Cytokines from T cells(TNF-A) activate macrophages
3. Macrophages damage myelin sheath and oligodendrocytes
MS: Gross findings?
Microscopic findings?
Demyelinated plaques in white matter of brain

CD4 T cells and microglial cells with phagocytic lipids
MS: Clinical findings?
1. Relapsing and remitting course
2. Optic neuritis- MCC of optic neuritis- blurry vision/loss of vision
3. Sensory dysfunction- Paresthesias, pain/temperature and vibration
4. Motor- UMN- dysfunction
5. Autonomic dysfunction- incontinence, sexual dysfunction, bowel problems
6. SIN- Scanning speech(drunk), Internuclear ophthalmoplegia(MLF demyelination), nystagmus
7. Lhermitte's syndrome- Neck flexion produces an electric shock like pain down the spine
MS: CSF findings?
1. Leukocyte count- CD4+ cells
2. Gamma-globulins
3. MBP- indicates active demyelination/dz
4. High resolution electrophoresis- Oligoclonal bands on Gamma globulin region(indicates demyelination)
MS: Dx? Rx?
1. Spinal tap- CSF examination
2. MRI with gadolinium- MOST SENSITIVE

Rx-
1. Acute relapse- methylpredinisone- high dose steroids
2. Chronic- a. Interferon B
b. Natalizumab
c. Azathioprine
d. Cyclophosphamide
Central Pontine myelinolysis: Cause?
1. Rapid correction of hyponatremia(commonly in alcoholics)
2. Infections- Subacute sclerosing panencephalitis, PML
Causative bacteriae for neonatal meningitis?
1. Group B strept(+ve
2. E.coli(-ve)
3. Listeria monocytogenes(+ve)
Causative bacteria for adult meningitis?
1. S. Pneumoniae
2. N.meningitides
3. M.tb
4. T.pallidum(neurosyphilis)
L.monocytogenes: source?
soft cheese, hot dogs
MC cause of neonatal meningitis?
Group B strept(S.agalactiae)
MC route of spread/source of neonatal meningitis?
Maternal vagina
Streptococcal meningitis: Rx?
1. Empiric: Ampicillin + Cefotaxim
2. Specific: Penicillin/Ampicllin
2nd MC cause of neonatal meningitis?
E.coli
Ecoli meningitis: Rx?
1. Empiric: Ampicillin + Cefotaxime
2. Specific: Ceftazidime + Gentamicin
MC meningitis in pediatric age group? rx?
Neisseria Meningitidis

Ceftriaxone
M.tb meningitis: complications?
Vasculitis--> infarction
Scarring--> hydrocephalus
MCC of adult meningitis? Rx?
S.pneumoniae(or N.meningitides?)
Penicillin G/ Ampicillin
T.pallidum meningitis(neurosyphilis): types?
1. Meningovacuslar: vasculitis causing stroke.
2. General paresis: dementia
3. Tabes dorsalis: Post root ganglia, dorsal columns, argyll robertson pupils(prostitute's pupils)-involvement of pretectal area
Rx neurosyphilis?
Penicillin G
Fungal causes of meningitis?
1. Cryptococcus
2. Mucor
Fungal meningitis/encephalitis associated with immunocompromised patients?
Cryptococcal meningitis.
Stain used for Dx cryptococcal meningitis?
India ink: budding yeasts visible.
2nd MC cause of neonatal meningitis?
E.coli
Ecoli meningitis: Rx?
1. Empiric: Ampicillin + Cefotaxime
2. Specific: Ceftazidime + Gentamicin
MC meningitis in pediatric age group? rx?
Neisseria Meningitidis

Ceftriaxone
M.tb meningitis: complications?
Vasculitis--> infarction
Scarring--> hydrocephalus
MCC of adult meningitis? Rx?
S.pneumoniae(or N.meningitides?)
Penicillin G/ Ampicillin
T.pallidum meningitis(neurosyphilis): types?
1. Meningovacuslar: vasculitis causing stroke.
2. General paresis: dementia
3. Tabes dorsalis: Post root ganglia, dorsal columns, argyll robertson pupils(prostitute's pupils)-involvement of pretectal area
Rx neurosyphilis?
Penicillin G
Fungal causes of meningitis?
1. Cryptococcus
2. Mucor
Fungal meningitis/encephalitis associated with immunocompromised patients?
Cryptococcal meningitis.
Stain used for Dx cryptococcal meningitis?
India ink: budding yeasts visible.
Rx cryptococcal meningitis?
1. Flucanazole (Non AIDS pt)
2. Amphotericin B and flucytosine
Meningitis that commonly occurs in diabetics? source? rx?
1. Mucor sp.
2. Source: frontal sinus
3. rx: Amphotericin B
Meningoencephalitis associated with spread from water? Area of brain affected? rx?
1. Naegleria fowleri meningitis (meningoencephalitis)- protozoal
2. Frontal lobe
3. Amphotericin B
Protozoal CNS infections: name the organisms?
1. Naegleria fowleri(meningoencephalitis)
2. Trypanosoma gambiense/rhodesiense(encephalitis)
Sleeping sickness: causative agent? transmitting agent?
1. Trypanosoma gambiense/ rhodiense(encephalitis)
2. Tsetse fly (Glossina)
Sleeping sickness: Course of organism through the body?
1. Blood/lymphatics
2. Posterior cervical LNs: Winterbottom sign
3. Encephalitis
Trypanosomal encephalitis: clinical finding? (unique)
Somnolescence : hence the name- due to mediators released from organism
MCC death in sleeping sickness?
Starvation
Sleeping sickness: Dx? Rx?
Dx- 1. Characterisitic increase in IgG early in dz
2. Detect organism in blood/ CSF
3. Serology

Rx-
Early stage- Pentamidine
Encephalitis stage- melarsoprol
Most common CNS SOL in AIDS?
Toxoplasma gondii encephalitis
Cysticercosis: causative agent? transmitting agent?
Taenia solium
Pigs
Cysticercosis: Course of organism through body? rx?
Cycle: Patient ingests food containing eggs --> develops into larval form --> invades brain --> calcified cysts --> seizures

Rx: albendazole + dexamethasone
T.gondii encephalitis: part of brain affected? rx?
Parts: Basal ganglia
Rx: pyrimethamine+sulfadiazine+ dexamethasone
Adrenoleukodystrophy: enzyme defect? effect? pattern of inheritance?
Defect involving b-oxidation of fatty acids.(?)

Effect:
1. Demyelination
2. Adrenal insufficiency.

Inheritance: XR
Metachromatic leukodystrophy: enzyme defect? fn of enzyme?
Enzyme: ASA
Fn: Hydroxylation of sulfate glycosphingolipids.: accumulation of sulfatides
Metachromatic leukodystrophy: Stain? inheritance pattern?
Alcian blue and PAS
AR
Krabbe's disease: enzyme defect? microscopic appearance?
Enzyme defect: Galactocerebroside b-galactocerbrosidase deficiency

Microscopic appearance: Multinucleated histocytic cells (globoid cells)
Alzheimer's disease: types?
1. Sporadic: Late onset
2. Sporadic: Early onset
3. Familial: Early onset
Trisomy associated with alzheimer's? pathology?
1. Trisomy 21: Down's
2. Chromosome 21 encodes for APP
Alzheimer's disease: Pathology?
1. APP metabolized by sectretase alpha---> inactive fragments(cannot be converted to AB)
APP metabolized by secretes B or gamma --> fragments converted to AB--> increased phosphorylation by GSK(activated by inactivation of wingless integration pathway)
phosphorylated AB protein--> neurotoxicity(induces neuronal apoptosis)--> alzheimer's
2. Tau protein phosphorylation by GSK produces neurofibrillary tangles(visualized by silver stain)- NF have altered structure--> cluster into fibres
NF tangles--> neuronal death
3. Wingless integration pathway defect: required for inhibiting GSK--> increased GSK activity--> hyperphosphorylation
4. Pin 1 enzyme= prolyl isomerase removes phosphate molecules from NF. restoring its original structure--absent in some cases
5. Apolipoprotein gene E: allele epsilon 4 codes for a product that fails to eliminate AB from brain
6. Insulin degrading enzyme- degrades insulin and AB.
in type II DM-- increased insulin levels decreases Insulin degrading enzyme-->more AB deposition

GSK= glycogen synthase kinase
Alzheimer's disease: Role of secretase alpha?
APP--> metabolized into inactive products not convertible to Amyloid. therefore protective
Alzheimer's disease: Role of secretase beta/gamma?
APP--> metabolized into fragments convertible into AB. therefore AD.
Alzheimer's disease: role of Glycogen Synthase Kinase?(GSK)
Hyperphosphorylation of:
1. Amyloid beta protein--> signals neuronal apoptosis
2. Tau proteins-->NF tangles(altered tau protein)-->neuronal death
Normal function of tau protein? Role in Alzheimer's dz?
tau protein: scaffolding - maintains neuron structure

In Alzheimer's dz: increased phosphorylation of tau proteins-->NF tangles--> neuronal toxicity
Alzheimer's disease: role of pin-1 enzyme?
Pin-1 enzyme- aka prolyl isomerase
strips excess phosphate from NF--restoring its original shape and structure
AD: AB protein damages neurons - parts of the cortex involved?
1. Medial temporal lobe
2. Frontal cortex: entorhinal cortex
3. Hippocampus
Wingless integration pathway: Function? role in alzheimer's disease?
Function: neuronal development during embryogenesis and normal functioning
Inhibits GSK
Stains used to detect beta amyloid?
Congo red: apple green birefringence with polarization
Sporadic early onset AD: genetic defect?
apolipoprotein gene E. allelle epsilon 4
chromosome (19?)
codes for product that cannot eliminate AB from brain
Diabetes type associated with Alzheimer's disease?
Type II
Insulin increment reduces insulin degrading enzyme levels also needed for degradation of AB--> accumulates--> Alzheimers Dz
Alzheimer's dz: Gross findings?
1. Cerebral atrophy- frontal, parietal, temporal
2. Ventricular dilation (hydrocephalus ex vacuo)

**Occipital lobe- spared in AD**
Alzheimer's dz: Microscopic findings?
1. NF tangles- silver stain
2. Senile plaques:
Core AB(congo red) surrounded by
Neuronal processes
Microglial cells
Astrocytes
3. Amyloid angiopathy- weakening of vessels--> hemorrhage.
Alzheimer's diz: confirmatory dx?
Post-mortem examination. Senile plaques and NF tangles
Alzheimer's dz: early symptoms?
1. Short term memory loss- hippocampus
2. Loss of smell- entorhinal cortex dysfunction
Common cause of death in Alzheimer's dz pts?
Infections: bronchopneumonia
(lack of hygiene)
Alzheimer's dz: lobe spared?
Occipital lobe
Diseases associated with NF tangles? visualized by (stain)?
1. Alzheimer's dz
2. Huntington's dz
3. Niemann-Pick


Visualized by silver stain
Alzheimer's dz: Rx?
Cholinesterase inhibitors
Memantine- glutamate receptor blockers
Parkinsonism: Causes?
1. Encephalitis
2. Ischemia
3. CO poisoning- necrosis of globus pallidus
4. Wilson's disease
5. MPTP- derived from meperidine
6. Antipsychotics- Phenothiazines
Parkinsonism: Pathophysiology?
Depigmentation and degeneration of neurons: d/t loss of dopamine
Parkinsonism: Microscopic features?
Intracytoplasmic eosinophilic bodies: Lewy bodies.
Parkinsonims: What are Lewy bodies?
Intracytoplasmic eosniophilic bodies
Ubiquinated damaged neurofilaments.
Intracytoplasmic eosinophilic bodies: Associated diseases?
1. Lewy bodies: Parkinson's dz
2. Negri bodies: Rabies
Parkinsonism: Clinical features?
1. Bradykinesia
2. Rigidity: cogwheel
3. Tremors: resting, pill rolling- between thumb and index finger
4. Expressionless face: poker face
5. Shuffling gait
6. Blepharospasm
7. Seborrheic dermatitis.
8. Dementia
Parkinsonism: treatment?
1. Levodopa
2. Carbidopa
3. MAO inhibitors
4. Bromocriptine
5. Pergolide
Parkinsonism: Drugs that worsen disease?
1. Neuroleptics
2. Antiemetics
3. MAO inhibitors
Huntington's dz: inheritance pattern?
AD
Huntington's dz: genetic defect? pathology?
CAG(codes for glutamine) repeats on Chromosome 4(Fab the hunter)

Atrophy of striatal neurons:
1. Caudate,
2. Putamen,
3. Globus pallidus
Huntington's dz: clinical findings?
Chorea
Oculomotor defects
Parkinsonism
Depression
(COPD)
Huntington's dz: Dx?
Genetic testing
CT, MRI- atrophy of caudate and putamen
Friedrich's ataxia: inheritance pattern? genetic defect/pathology?
AR
GAA repeat sequence- frataxin deficiency- impaired mitochondrial Fe homeostasis-->apoptosis
(FFFF)
(Friedrich's ataxia : Frataxin defect Fe homeostasis F*****)
MCC genetic ataxic disorder?
Friedrich's ataxia
Friedrich's ataxia: sites affected?
1. Dorsal root ganglia
2. Dorsal columns
3. Spinocerebellar tracts
4. Corticospinal tracts
5. Large peripheral nerves
Friedrich's ataxia: disease associations?
1. Hypertrophic cardiomyopathy
2. Type I DM
Friedrich's ataxia: clinical findings?
1. Ataxia
2. Loss of vibration and proprioception
3. Loss of deep tendon reflexes-INITIALLY at ANKLES
4. Muscle weakness- L. Extr
Friedrich's ataxia: Dx?
MRI- SC atrophy
Gene testing
Lou Gehrig's dz: (ALS) Genetic defect?
Mutation on chromosome 21: Defective superoxide dismutase 1--> superoxide free radical injury
Lou Gehrig's dz: Clinical findings?
1. UMN signs: (Lower extrm)
2. LMN signs: (Upper extrm)
3. Atrophy of intrinsic muscles of hand
Intact autonomic and sensory functions.
Lou Gehrig's dz: Earliest clinical finding?
Atrophy of intrinsic muscles of hand.
Lou Gehrig's dz: Dx?
Rx?
Electromyography and nerve conduction studies

Riluzole: glutamate antagonist
Lou Gehrig's disease: MCC of death?
Respiratory muscle paralysis
Werdnig Hoffmann dz?
LMN dz in children.
Wilson's dz: inheritance pattern? Pathology?
Autosomal recessive
Defective incorporation of Cu into ceruloplasmin.--> increased free Cu in blood and cirrhosis
Wilson'd dz: structures affected in CNS?
1. **Globus pallidus**
2. Putamen
CNS signs in wilsons dz?
1. Parkinsonism
2. Chorea
3. Dementia
Acute intermittent porphyria: enzyme defect?
Inheritance pattern?
1. Uroporphobilinogen synthase/ porphobilinogen deaminase
Therefore increase in PBG and d-ALA--> neurotoxic

2. Inheritance: AD
Urine color change in acute intermittent porphyria? Reason?
Light exposure produces port wine color. (window sill test)'
PBG--> porphobilin(colored product) on light exposure
Acute intermittent porphyria: compound associated with disease?
Porphobilin
Acute intermittent porphyria: Drugs that worsen dz? how?
Barbiturates
Alcohol
(Drugs that enhance P450) enzyme activity.

ALA: Rate limiting enzyme of heme synthesis
In AIP heme synthesis decreases--> increased activity of ALA synthase--> more porphobilin--> attack precipitated
P450 inducing drugs also induce enhanced ALA synthase activity
AIP: Clinical findings?
1. Painful abdomen- acute abdomen
2. Psychosis
3. Peripheral neuropathy
4. Dementia
(PPPD)
Severe combined degeneration of spinal cord: pathology?
Deficiency of B12--> methyl malonyl coA mutase cannot function--> incorporation of methylmalonic acid--> neuropathy
1. Degeneration of dorsal columns and corticospinal tracts.
2. Dementia
3. Peripheral neuropathy.
CNS conditions associated with dementia?
1. Alzheimer's dz
2. Neurosyphilis
3. Parkinsonism
4. Wilson's dz
5. AIP
6. B12 deficiency
Alcohol abuse: CNS findings?
1. Cortical atrophy
2. Cerebellar atrophy
3. Wernicke-Korsakoff syndrome(thiamine deficiency)- maxillary body hemorrhage
a. Wernicke's: REVERSIBLE- Confusion, ataxia, nystagmus, ophthalmoplegia
b. Korsakoff's: IRREVERSIBLE advanced stage- Amnesia, confabulation, hallucinations
Rx- thiamine supplement
MC primary CNS tumors in adults?
#1. Glioblastoma multiforme(high grade astrocytoma)
#2. Meningioma
#3. Ependymoma
MC primary CNS tumors in children?
#1. Cystic cerebellar astrocytoma
#2. Medullobastoma
#3. Brain stem glioma
Glioblastoma multiforme: GBM: Cell affected?
Astrocyte- high grade
Glioblastoma multiforme: MC site affected.
Corpus callossum
Glioblastoma multiforme: MC organ to get metastasized?
None(Rarely metastasizes)
Glioblastoma multiforme: Gross findings?
1. Hemorrhagic necrosis
2. Multiple areas of necrosis
3. Cystic degeneration

MC site: corpus callossum
Astrocytoma: Common sites of involvement- adults and children
Adults: Frontal lobe
Children: Cerebellum
MC benign tumor in adults?
Meningioma
Meninioma: More common in : Men/women? why?
Women: tumors have estrogen receptor
Meningioma: Sites affected?
1. Parasagittal location
2. Olfactory groove
3. Lesser wing of sphenoid
Meningioma: Disease associations.
1. Neurofibromatosis
2. Radiation exposure
3. New onset seizures
CNS tumor associated with radiation exposure?
Meningioma
Meningioma: Gross features.
Firm mass- Indents surface of brain.
Infiltrates the overlying bone- increases bone density.
Meningioma: Microscopic features?
Psammomma bodies in meningeal cells. (calcified swirling bodies)
Ependymoma: Malignant/ benign? MC sites?
Benign
Adults: Cauda equina
Children: fourth ventricle
Medulloblastoma: Site of origin? Metastasis to?
Cerebellum- External granular cell layer
Fourth ventricle
Oligodendroglioma: Benign/malignant? Common site?
Benign tumor
Frontal lobe tumor- calcified.
CNS lymphoma: Type? Association/s?
Type- Hodgin's lymphoma
Associated with-
AIDS
EBV mediated B cell lymphoma
MC malignancy of brain?
Metastatic
Sites associated with CNS metastasis?
#1. Lungs
#2. Breast
#3. Skin
#4. Kidney
#5. GIT
Peripheral neuropathies.
1. Demyelination related- all

2. DM

3. Toxins-
a. alcohol
b. heavy metals
c. diphtheria

4. Idiopathic Bell's palsy- CN VII
a. Herpes Simplex- MC
b. HIV
c. Sarcoidosis
d. Lyme dz
e. Pregnancy

5. Drugs-
a. Vincristine
b. Hydralazine
c. Phenytoin

6. Vitamins-
a. Thiamine
b. B12
c. Pyridoxine
MCC of all peripheral neuropathies?
DM
Rx of peripheral neuropathies?
1. Antiseizures- Gabapentin, carbamazepine, phenytoin
2. Lidocaine
3. TCAs-
a. Amitriptyline
b. Nortriptyline
MC hereditary peripheral neuropathy? Inheritance pattern?
Charcot Marie Tooth dz
Autosomal dominant
Charcot Marie Tooth dz: MC nerve involved?
Peroneal nerve
Atrophy of lower legs--> inverted bottle appearance
Inverted bottle appearance of legs seen in____?
Charcot Marie Tooth dz
(d/t atrophy of muscles of lower leg)
MC acute peripheral neuropathy?
GBS
MCC of Acute flaccid paralysis?
GBS
GBS: Predominantly motor/sensory?
Motor
GBS: preceding infections?
1. Mycoplasma Pneumonia
2. Campylobacter Jejuni
3. HIV
4. EBV
5. CMV
6. Influenza


1. Mycoplasma Pneumonia
2. Campylobacter Jejuni
3. HIV
4. EBV
5. CMV
6. Influenza

1. Mycoplasma Pneumonia
2. Campylobacter Jejuni
3. HIV
4. EBV
5. CMV
6. Influenza

2 bacterial and 4 viral
GBS: Course of muscle weakness?
**Rapidly progressive ascending motor weakness**
Starts in proximal muscles eventually distal muscles
Areflexia
"Glove stocking" paresthesias/anesthesia
GBS: Common cause of death?
Respiratory failure due to failure of muscles of ventilation
GBS: Dx/ Laboratory findings?
1. Spinal tap- Increased CSF protein- Oligoclonal band on high resolution electrophoresis

2.Electromyography and nerve conduction studies
GBS: Rx?
IVIG
Mechanical ventilation
Diabetes Mellitus(DM): Peripheral neuropathy - reason?
Osmotic damage to Schwann cells
Bell's palsy: Clinical findings- LMN-UMN difference?
LMN- Ipsilateral upper and lower face involvement
UMN- C/l lower face involved and sparing of upper half of face
CNS/PNS: Benign tumors?
Ependymoma
Meningioma
Schwannoma
Schwannoma/neurilemoma: Cranial Nerves generally involved?
1. CN V
2. CN VII
Acoustic neuroma: CN involved- type of tumor? location?
1. Schwannoma
2. Cerebellopontine angle
Acoustic neuroma: features?
1. Located at cerebellopontine angle
2. Encapsulated
3. Unilateral- except those associated with NF-2(B/l)
4. Alternating dark and light areas on microscope
NF-2 associated acoustic neuroma- clinical features?
1. Tinnitus
2. Sensorineural deafness
3. Sensory changes in CN V distribution tumor compression on V
Ulnar nerve injury:
Nerve roots of ulnar n?
Commonly associated fx?
Clinical finding?
1. C8-T1
2. Fx of medial epicondyle of humerus
3. Claw hand- Interosseous muscle affected
Radial nerve injury:
Nerve root?
Associated fx?
Clinical finding?
1. C5-T1
2. Midshaft fx of humerus
3. Wrist drop
Axillary nerve
Nerve root?
Associated fx?
Clinical finding?
1. C5-C6
2. Fx of surgical neck of humerus/anterior dislocation
3. Loss of arm abduction(deltoid muscle paralysis)
Median nerve:
Nerve root?
associated fx?
C6-T1
C6-T1
Associated conditions:
1. Rheumatoid arthritis
2. Pregnancy
3. Overuse of hands
4. Hypothyroidism
5. Amyloidosis
6. Supracondylar fx of humerus
Median nerve compression/ carpal tunnel signs/symtoms?
1. Pain/paresthesias/ numbness over-
a. Thumb
b. Index finger
c. Middle finger
d. Radial side of fourth finger

2. Thenar atrophy- ape hand, difficulty opposing thumb


3. Tinel's sign- Pain produced by tapping median nerve (tap with Tinel's)

4. Phalen's sign- Pain produced by flexion of wrist for 1 minute (Flex with Phanel's)


Dx- nerve conduction studies, EMG
Common peroneal nerve:
nerve roots?
Associated fx?
Clinical findings?
L4-S2
common peripheral neuropathy
lead poisoning
Fx neck of fibula
cast tightness

1. Loss of ankle reflex
2. loss of foot eversion- weakening of peroneus longus and brevis
3. loss of dorsiflexion- weakening of tibialis anterior- foot drop, high stepping/slapping gait
4. loss of toe extension- weakening of extensor digitorum longus and hallucis longus
5. In all EQUINOVARUS deformity
Erb duchene palsy? Nerve roots involved?
C5, C6
"Waiter's tip deformity"
Cerebral edema: types? causes?
1. Intracellular:
a. Dysfunctional Na/K pump(from global hypoxia)
b. Hyponatremia(SIADH)

2. Extracellular:
a. Inflammation: meningitis, encephalitis
b. Metastasis
c. trauma
d. lead poisoning
Head trauma: effect on respiration? how does this help?
Respiratory alKalosis--> vasoConstriction--> decreased vessel permeability

(In aciDosis--> vasoDilation. in acidosis, K channel activity increases--> K moves out--> hyper polarizes cell--> sm relaxation--> vasodilation)
Signs of increased intracranial pressure?
1. Papilledema
2. Headache
3. Projectile vomiting
4. Sinus bradycardia
5. Hypertension
6. Herniation
Pseudotumor cerebri? MC individuals affected/Risk factors?
Vit A excess/ All-trans retinoic acid-(used in rx of AML)
2. hypothyroidism
3. Cushing's disease
4. Isotretinoin
5. Tamoxifen
Pseudotumor cerebri: pathogenesis? clinical findings?
Decreased CSF absorption in the arachnoid granulations
1. Findings in raised ICP
2. Rhythmic sounds in both ears
3. Diplopia
4. Blurry vision
Pseudotumor cerebri: Dx? Rx?
Dx:
1. MRI: flattening of posterior globe
2. CSF pressure> 300mm H2O(normally 70-180 mm go H20)
3. Decreased CSF protein

Rx:
1. Medical:
a. Carbonic anhydrase inhibitor,
b. Systemic corticosteroids
2. Surgical:
a. Lumboperitoneal shunts,
b. Optic nerve sheath fenestration
Cerebral herniation: results as a complication of____?
Complication of raised ICP
Cerebral herniation: Name em. Parts of brain herniating associated and openings.
1. Subfalcine: Cingulate gyrus under falx cerebri
2. Uncal: Medial portion of temporal lobe through tentorium cerebelli
3. Tonsillar: Cerebellar tonsils herniate into foramen magnum
Complications associated with:
Subfalcine
Uncal
Tonsillar herniation.
1. Subfalcine: compression of ACA
2. Uncal: Compression of midbrain(III nerve nuclei--> Eyes deviated down and out+ dilated pupils) and PCA
3. Tonsillar: Cardiorespiratory arrest.
Hydrocephalus: types? respective causes?
Types:
1. Communicating:
a. Increased CSF production: choroid plexus papilloma
b. Defect in reabsorption of CSF- Postmeningitic scarring

2. Non-communicating:
1. Stricture in aqueduct of sylvius--> Paralysis of upward gaze(Parinaud's syndrome)
2. Colloid cyst in the 3rd ventricle
3. Tumor in 4th ventricle- ependymoma, medulloblastoma
4. Scarring at the base of the brain: Tb meningitis
Hydrocephalus: Clinical findings?
1. Signs of raised ICP
2. In children: enlarged head circumference
in adults: no change in size
Hydrocephalus ex-vacuo?
Dilated brain ventricles with reduced brain mass.
Normal pressure hydrocephalus: symptom complex? causes?
Dilated ventricles+ Wide based gait, Urinary incontinence, Dementia
(WWW- wet wobbly whacky)

causes-
1. Idiopathic
2. Secondary:
a. Prior SAH
b. Prior Tumor
c. Prior IC Sx
Normal pressure hydrocephalus: pathogenesis?
Ventriculomegaly
Wide based gait and urinary incontinence: due to sacral motor fibre stretching
Dementia: due to stretching of limbic fibres.
Normal pressure hydrocephalus: Dx? rx?
MRI: ventriculomegaly and sulcal atrophy
Lumbar puncture: Large volume CSF removed--> improved symptoms


Rx:
Ventriculoperitoneal shunt
Ventriculoatrial shunt
Neural tube defects: Pathogenesis?
1. Failure of closure of lateral folds of neural plate
2. Rupture of closed NT.
Serum marker associated with NTD?
Alpha feto protein in serum or amniotic fluid
NTDs: types?
1. Anencephaly
2. Spina bifida occulta
3. Meningocele
4. Meningomyelocele
Anencephaly: Defect? Clinical finding?
Complete absence of brain
Polyhydramnios
Raised AFP levels
Spinca bifida occuta: Defect? clinical finding?
Failure of closure of post vertebral arch
Tuft of hair in skin over L5-S1
Meningocele: Defect? MC location?
Spina bifida with cystic mass containing meninges
Lumbosacral region
Meningomyelocele: defect? MC location?
Spina bifida with cystic mass containing meninges and spinal cord
lumbosacral area
Arnold Chiari malformation: Pathology? hydrocephalus- type?
Herniation of medulla and cerebellar vermis through foramen magnum
Non communicating hydocephalus
Arnold Chiari malformation: Associations? Rx?
1. Syringomyelia
2. Meningomyelocele

Rx: Decompression sx
Dandy waker malformation: defect? hydrocephalus-type? rx?
1. Partial/complete absence of cerebellar vermis
2. Cystic dilation of 4th ventricle
3. Non communicating hydrocephalus

rx- shunt
Syringomyelia: Pathology/ Defect? associations?
Syrinx (fluid filled cavity) within the cervical spinal cord.-->cervical cord enlargement-->cavity expansion causes spinal tract degeneration.
Associated with Arnold- Chiary malformation type II
Obstruction to the outflow to the CSF.
Syringomyelia: clinical findings?
1. Lateral spinothalamic tract: Loss of pain and temperature B/l at the site of lesion--generally cervical(hands involved)

2. Corticospinal tract: Atrophy of intrinsic muscles of hands(c- ALS: no sensory loss)
Syringomyelia: Dx? Rx?
Dx: MRI: dilated syrinx
rx: drainage of syrinx
MC phakomatoses?
NF
Neurofibromatosis: types?
Type 1: Peripheral type
Type 2: Central type
Neurofibromatosis type 1: genetic defect? Inheritance pattern?
Chromosome 17: neurofibromin- defective
AD
Neurofibromatosis type 2: genetic defect? Inheritance pattern?
Chromosome 22: merlin - defective
AD
NF-1: Important associations/Clinical findings?
1. Cafe au lait: 100% incidence in children <2yrs
2. Optic glioma: (astrocytoma)
3. Lisch nodules: Hamartomas of the iridae
4. Axillary and inguinal freckling
5. Scoliosis
6. Plexiform neurofibroma
7. Cutaneous/subcut. neurofibromas: DO NOT occur on soles and palms, increase in size with age
8. Pheochromocytoma
9. Wilm's tumor
10. CML
11. Neurodevelopmental problems
NF-2: Important associations/Clinical findings?
1. B/l acoustic neuromas- benign, SN hearing loss
2. Meningiomas
3. Spinal schwannomas
4. Juvenile cataract
NF syndromes: Dx? Rx?
Dx: genetic testing
Rx: Sx
Tuberous sclerosis: Inheritance pattern? Clinical findings?
AD disorder
Clinical findings:
Triad-
1. MR
2. Seizures
3. Ash leaf lesions/angiofibromas
Skin lesions in tuberous sclerosis?
1. Angiofibromas: Adenoma sebaceum
2. Ash leaf lesion: hypo pigmented skin lesions aka shagreen's patch
Tuberous sclerosis: tumors associated?
1. Angiomyolipomas: kidneys
2. Rhabdomyomas
3. Astrocyte proliferation in subependyma
Tumor highly predictive of tuberous sclerosis?
Rhabdomyoma
Sturge Weber syndrome: Inheritance pattern?
1. Sporadic
2. Mosaicism
Sturge Weber syndrome: associations?
Vascular malformation of face- area of distribution of trigeminal nerve.
Ipsilateral AV malformations in meninges.
Cerebral contusions: common sites of involved?
Coup injury: cerebellum
counter coup injury: frontal and temporal lobes
Acute epidural hematoma:
Commonly involved fx?
vessel rupture associated?
complication?
Dx?
rx?
Fx : Temporoparietal bone fx-->
middle meningeal artery rupture(vessel lies between dura and inner table of bone)
complication: raised ICP.--> herniation
dx: CT - hematoma does not cross suture line
rx: burr holes.
Subdural hematoma
Vessel associated?
Pathogenesis?
Causes?
Risk factors?
Clinical findings?
Dx?
Rx?
Venous bleed

Tearing of bridging veins b/w brain and dural sinuses (d/t loss of brain mass--> traction on the veins)

Causes:
1. Blunt trauma
2. Anticoagulation
3. Hemophilia
4. Child abuse- shaken baby syndrome

Risk factors:
1. Elderly
2. Alcoholics

Clinical finidings:
1. Fluctuating levels of consciousness.
2. Herniation
3. Dementia: from chronic blood clot

Dx: CT head

Rx: Burr holes
Global hypoxic injury: causes? complications?
Causes-
1. Cardiac arrest
2. Hypovolemic shock
3. Chronic CO poisoning

** Repeated episodes of hypoglycemia(effect similar to hypoxia)**

Complications-
1. Cerebral atrophy- Apoptosis in areas 3,5,6 of cerebral cortex-->laminar necrosis
2. Watershed infarcts- Jn of ACA and MCA
3. CVA
What are Red neurons?
Apoptotic neurons (from hypoxia)
Amaurosis fugax?
Temporary loss of vision due to embolization to bifurcation of the retinal arteries.
Strokes: peak age group? types?
types-
1. Ischemic- atherosclerotic/embolic
2. Hemorrhagic
3. SAH
4. Lacunar strokes
MC type of stroke?
atherosclerotic
Sites of atherosclerotic strokes?
1. MCA
2. Internal carotid bifurcation
Atherosclerotic strokes: Gross findings? microscopic findings?
1. Pale infarcts: periphery of cortex- wedge shaped
2. Swelling of brain- loss of demarcation of gray and white matter
3. Gliosis- reaction to injury- microglial cells
4. Cystic area- from liquefactive necrosis
Arcus Senilis: identify. location? significance?
Gray opaque ring: Cholesterol deposits in corneal stroma
Cornea- more commonly corneal margin
May indicate hypercholesterolemia if pt<50 yrs and smoker
Common cause of conjunctivitis in neonates?
Causative organisms? Rx?
1. Ophthalmia neonatorum
2. i. N. gonorrhea
ii.C.trachomatis
rx-
N.gonorrhea: ceftriaxone
C.trachomatis: erythromycin
MCC of bacterial conjunctivitis?
S. aureus
Bacterial conjunctivitis: causative bacteriae? Clinical findings? rx?
#1. S.aureus
#2. S.pneumonia
#3. H.Influenza
**pain but no blurry vision**
rx- Gatifloxacin
Viral conjunctivitis: causative viridae?
1. Adenovirus
2. HSV-1
HSV-1 conjunctivitis: complication?
Dendritic ulcers detected by fluorescein stain
Adenovirus clinical findings?
"Pink Eye" (MC viral cause of conjunctivitis?)
Periauricular lymphadenopathy
Allergic conjunctivitis: rx?
rx: antihistaminics, olapatidine-mast cell stabilizer
Acanthamoeba infection: Site? patients affected? rx?
Keratoconjunctivitis- severe
Patients who do not cleanse their contact lenses.
rx: propamidine+ polymyxin/neomycin/gramicidin
Stye: MC organism? Rx?
S.aureus
rx: hot packs + dicloxacillin
Chalazion: ? rx?
Granulomatous inflammation of the meibomian glands in eyelid
self resolving- 2months
rx-intralesional corticosteroid injection/ sx removal
Orbital cellulitis: Source? causative agents?
1. Secondary to sinusitis: ethmoiditis
2. i. S. pneumonia
ii. H.influenza
Orbital cellulitis: clinical findings? rx?
1. Fever,
2. Proptosis
3. Periorbital swelling
4. Ophthalmoplegia
5. <normal retinal examination>
Orbital fx: characteristic finding? complications?
1. Raccoon eyes- edema and ehymosis of eyelids and periorbital region
2. Complications-
i. Prolapse of orbital content maillary sinus- sunken eye
ii. Infraorbital nerve compression
Pterygium? cause? rx?
Raised triangular thickened conjunctiva on nasal side
Exposure to wind/sun/sand
rx- sx removal
Pinguelcula? location? rx?
Conjunctival degeneration.
Location: jn of conjunctiva and cornea- nasal side
rx- none needed
Optic neuritis: Causes? rx?
#1. Multiple sclerosis
#2. Methanol poisoning
rx- corticosteroids
Central retinal artery occlusion: causes?
1. Embolization from ipsilateral carotid and ophthalmic artery
2. Giant cell temporal arteritis
Acanthamoeba infection: Site? patients affected? rx?
Keratoconjunctivitis- severe
Patients who do not cleanse their contact lenses.
rx: propamidine+ polymyxin/neomycin/gramicidin
Stye: MC organism? Rx?
S.aureus
rx: hot packs + dicloxacillin
Chalazion: ? rx?
Granulomatous inflammation of the meibomian glands in eyelid
self resolving- 2months
rx-intralesional corticosteroid injection/ sx removal
Orbital cellulitis: Source? causative agents?
1. Secondary to sinusitis: ethmoiditis
2. i. S. pneumonia
ii. H.influenza
Orbital cellulitis: clinical findings? rx?
1. Fever,
2. Proptosis
3. Periorbital swelling
4. Ophthalmoplegia
5. <normal retinal examination>
Orbital fx: characteristic finding? complications?
1. Raccoon eyes- edema and ehymosis of eyelids and periorbital region
2. Complications-
i. Prolapse of orbital content maillary sinus- sunken eye
ii. Infraorbital nerve compression
Pterygium? cause? rx?
Raised triangular thickened conjunctiva on nasal side
Exposure to wind/sun/sand
rx- sx removal
Pinguelcula? location? rx?
Conjunctival degeneration.
Location: jn of conjunctiva and cornea- nasal side
rx- none needed
Optic neuritis: Causes? rx?
#1. Multiple sclerosis
#2. Methanol poisoning
rx- corticosteroids
Central retinal artery occlusion: causes?
1. Embolization from ipsilateral carotid and ophthalmic artery
2. Giant cell temporal arteritis
Central retinal artery occlusion: clinical findings/ microscopic findings?
1. Sudden complete loss of vision in one eye
2. Pallor of optic disk
3. "Boxcar segmentation" of blood in retinal veins
4. Cherry red macula
Cherry red macula- associated disorders?
1. Tay-Sach's dz
2. Niemann Pick
3. Central retinal artery occlusion
Central retinal art occlusion: rx?
1. acetazolamide
2. carbogen- CO2 + O2
3. hyperbaric O2 therapy
Central vein occlusion: causes? clinical findings/microscopic findings? rx?
1. painless unilateral loss of vision
2. swelling of optic disk
3. engorged retinal veins with hemorrhage- "blood and thunder appearance"
4. rx: laser photocoagulation
Glaucoma- types- mechanism
open angle- reduced outflow rate through canal of schlemm
angle closure- narrowing of anterior chamber
Open angle glauoma- clinical features? rx?
B/l aching eyes.
pathologic cupping of optic disk.
night blindness.
tunnel vision

rx:
1st choice: b-blockers-timolol- decreases rate of flow
2nd: Prostaglandins/ alpha agonists/ pilocarpine/ carbonic anhydrase inhibitors.
3rd: laser trabeculoplasty
Angle closure glaucoma: clinical features? rx?
1. Severe pain
2. Photophobia
3. Blurry vision
4. Pupil fixed and non reactive to light
5. Red eye


rx: pilocarpine +systemic carbonic anhydrase inhibitors(lower pressure): for laser surgery
Optic nerve atrophy: causes?
1. optic neuritis
2. glaucoma
Uveitis: causes? clinical features? rx?
causes-
1. sarcoidosis
2. ulcerative colitis
3. ankylosing spondylitis

clinical findings:
1. pain
2. blurry vision
3. circumcorneal vascular congestion
4. normal iop
5. iris and anterior lens capsule adhesions

rx-
corticosteroids
atropine

*uveal tract inflammation- ciliary boides, iris, choroid
MCC of permanent vision loss in elderly? pathology?
Macular degeneration
Disruption of bruch's membrane in the retina.
Macular degeneration: types? rx?
dry type: thinning of retina and formation of drusen: yellowish white plaque
wet type: retinal vessels hemorrhage-->retinal cell death --> blind spot/distorted central vision.
rx- antiangiogenic- drug that block vascular growth factors. intraocular lens insertion
MCC of blindness in AIDS patients? rx?
Cmv retinitis
CD4 count< 50cells/mm^3
Treatment: Oral, IV. Intraocular ganciclovir or foscarnet.
Cataracts: causes? rx?
1. Age
2. DM
3. Infection- Rubella, CMV
rx: cataract extraction
Malignant tumors of the eye? rx
Retinoblastoma in children: white eye reflex/cat eye reflex
rx: enucleation
Meniere's disease: pathology? clinical findings? rx?
1. Increased endolymph in the inner ear +
2. loss of cochlear hairs

Clinical findings:
1. Dizziness
2. vertigo
3. tinnitus
4. sensorineural hearing loss
rx: hydrochlorothiazide + triampterene
MCC of sensorineural hearing loss in elderly? rx?
Presbycusis
degeneration of hair follicles
rx: amplification devices, cochlear implants
MCC of conduction deafness in elderly? rx?
Otosclerosis
fusion of middle ear ossicles
other conduction defects: otitis media, impacted cerumen in middle ear.
rx: antipyrine and benzocaine ear drops.
External otitis. Etiologic agents? rx?
Inflammation of of outer ear canal.
"swimmer's ear"
agents:
1. pseudomonas aeruginosa
2. Staphylococcus aureus
3. Aspergillus
rx: polymyxin b+ neomycin+ hydrocortisone+ selenium sulphide
MCC of malignant otitis externa? rx?
Pseudomonas aeruginosa
Imipenem- cilastin
Spinal nucleus of V: location?
Dorsally and laterally - upper pons
(similar to location of dorsal columns in SC)
Spinal tract of V: location and extent?
Spinal tract of V lies LATERAL to nucleus and
extension from-
-entry point of V nerve
-upto C2
Vascular syndromes associated with spinal nucleus and tract?
Lateral vascular syndrome: lateral pons and medulla
Solitary nucleus: location? CN associated? fn?
Location: upper medulla

CN: VII, IX, X

function: receives visceral afferents:
1. Taste, (VII)
2. Cardiorespiratory, (IX, X)
3. GI sensations (X)
Nucleus ambiguus:
Location?
CN associations?
function?
1. Upper medulla: Dorsal to inferior olive
2. CN IX and X
3. LMN innervation of skeletal muscles of soft palate, larynx, pharynx, upper esophagus
(swallowing and phonation)
Dorsal nucleus of X: location? function?
Location: upper medulla and lateral to XII nucleus in floor of IV ventricle

Function:
Parasympathetic(PREganglionic) nucleus of brain stem-
Supplies smooth muscles and glands of thorax, foregut and midgut
hypoglossal nucleus: location?
near midline- beneath central canal and 4th ventricle
Accessory nucleus: location? function?
location: cervical cord. c2
passes through the foramen magnum ---> cranial cavity ---> exits through jugular foramen.
(intramedullary lesions have no effect on spinal accessory nerve)

fn: supplies trapezius and sternomastoid.
IX, X, XII nerve exits from brain stem: location?
IX, X: Exit between olive and fibers of inferior cerebellar peduncle
XII: Exit between the olive and medullary pyramid.
Abducens nucleus: location? Structure relations?
Lower pons: midline floor of 4th ventricle-
#1. Lateral to MLF
#2. Encircled posteriorly by facial nerve fibers( "internal genu" of facial nerve)
#3. Closely associated with PPRF
Nuclei in the floor of the 4th ventricle?
1. Abducens
2. Hypoglossal
3. Dorsal nucleus of X
Superior olivary nucleus: Location? Function?
Ventral to VII nuclei--

Fn-
B/l auditory impulses from both cochlear nuclei
Sound localization
Vestibular nuclei- Location
Posterior surface of pons- lower
Lateral to abducens nucleus
Extends into the medulla
Cochlear nuclei-location
PM jn lateral to the inferior cerebellar peduncles
Trigeminal nuclei- name em?
1. Sensory
2. Motor
3. Spinal Trigeminal
4. Mesencephalic
Trigeminal nuclei- Motor nucleus: Location? function?
Pons: Medial to main sensory nucleus of trigeminal. At exit point of V
Supply muscles of mastication-
1. Medial and lateral pterygoid
2. Temporalis
3. Masseter
Trigeminal: Sensory nucleus?
Pons: Lateral to motor nucleus. At exit point of V

fn- TACTILE and PRESSURE sense from V1, V2, V3 and DURA
Spinal trigeminal nucleus: location? fn?
Location: Mid pons to C2
Functions- pain temperature by trigeminal nerve
Mesencephalic nucleus : location? function?
At point of entry of 5th nerve.
Extends into MIDBRAIN

fn- proprioceptive input from

1. muscles of mastication- sensory limb of jaw jerk
2. extraocular muscles
3. teeth
V nerve nuclei associated with point of entry of V nerve?
1. Motor
2. Sensory
3. Mesencephalic
Sensory distribution of CN V
ophthalmic: forhead, scalp, cornea, dorsum of nose
maxillary- maxillary skin
mandible- mandibular skin,
external auditory meatus, external tympanic membrane

"onion skin configuration"- pain and temperature(spinal n.):
1: perioral
2: region of the eye
3: between ears and eyes
4: around the ears
Motor fibers of V course through which division of V nerve?
Course of tactile fibers from face?
1st neuron: synapses in main sensory nucleus of V
2nd neuron: crosses midline in vicinity of its cell body--> synapses in thalamus(VPM nucleus)
3rd neuron: thalamus up to somatosensory cortex(join with pain fibers)
Course of pain fibers from face?
1st neuron: enter spinal tract of V--> synapse in spinal nucleus of V
2nd neurons: cross midline in vicinity of CBs--> synapse in thalamus(VPM nucleus)
3rd neurons: thalamus unto somatosensory cortex (join with the tactile fibers)
Complete lesion of trigeminal nerve at entry or exit points.
Complete ipsilateral anesthesia(sensory and spinal tract fibers)
Jaw weakness(motor fibers)
Lateral/caudal pons lesion/lateral medullary lesion?
Ipsilateral loss of pain and temperature(spinal tract of V)
Corticobulbar/ corticonuclear fibers:
CN V- Mastication
CN VII- Facial expression
CN X- Palate, larynx, pharynx
CN XI- Sternomastoid, trapezius
CN XII- Tongue except palatoglossus
Difference between cranial and spinal LMNs?
1. Cranial- B/L corticobulbar(UMN) innervation--exception lower face from VII(U/L)

2. Spinal- U/L corticospinal(UMN) innervation
Hair cells at base of cochlea- sensitive to?
High frequency
Hair cells at apex of cochlea- sensitive to?
Low frequency
Weber's test?
Tuning fork placed on vertex of skull.**
Conductive- Louder in affected ear
Sensorineural- Louder in normal ear

(**bone conduction interferes with air conduction so decreased perception in
normal ear)
Rinne test?
For conductive hearing loss
Place tuning fork on mastoid till no vibrations heard and then place next to the
ear.
Unilateral conductive hearing loss- No air conduction after bone conduction
Conditions causing conuction deafness?
1. Otosclerosis
2. Otits media
3. Impacted cerumen
Presbyucusis?
loss of hair cells in the base of the cochlea-
progressive loss of high frequency sounds
ampular crest
utricle and saccule:fns?
ampular crest- angular acceleration
utricle and saccule- linear acceleration(upright posture)
Endolymph composition? Site of production?
High K+
Low Na+
Striae vascularis
superior olive: function?
(pons)
sound localization.
Lesion above cochlear nucleus?
slight hearing loss in both ears
poor localization-olive, lemniscus, thalamus etc
lesion below cochlear nucleus?
Complete hearing loss in the affected ear
Ion channel myopathies?
Microscopy?
Myotonia- sustained muscle contraction
Episodic hypotonic paralysis
No muscle atrophy

PAS +ve intracytoplasmic vacuoles
Vestibular nuclei:
no?
fn?

Auditory pathway?
. upright posture- source of UMN- vestibulospinal tract- a/gravity muscles-linear
acceleration hair cells
2. vestibulo-ocular reflex- fixation of the eye in response to head turning
endolymph flow stimulate hair cells on side of turning--->
stimulation of cochlear nerve(on side of turning)--->
stimulates cochlear nucleus--->
i. activates MLF to III nucleus on same side---> adduction(same side)
ii. activates MLF to VI nucleus on opp side---> abduction(pop side)
eyes move in opp direction
Vestibular evoked nystagmus
Lesion on one sided--> stimulation of opp side.
therefore
"Slow component"-->
1. Points in direction of lesion
(adduction of opp eye
abduction of same eye)
2. Due to the pathology

"fast component"(corrective phase) -->
1. points to opp side of lesion
2. Due to cortical mediated correction
Caloric test?
Brain stem fun in unconscious pts.
Cold water irrigation--> nystagmus to opp side
Warm water irrigation--> nystagmus to same side
COWS


cool water= mimics lesion
warm water= mimics stimulation
vertigo?
perception of rotation
acute vertigo--> peripheral lesion
chronic vertigo--> central lesion
For conjugate movement to right
cortical gaze center in the frontal eye field: location?
left cortex
Fibres for conjugate gaze: Pathway?
Descend down to brain stem and cross to the opposite side-->
Paramedian pontine reticular formation-->
1. Abducens on same side as PPRF
2. Oculomotor on opp side of PPRF(through the MLF)
Paramedian pontine reitcular formation: location?
Pons: adjacent to VI nucleus.
MLF: Medial longitudanal fasciculus?
Heavily myelinated tracts:
axon fibers to and from III/IV/VI/VIII nerve
Right abducens nerve lesion: Effect?
When patient asked to look right (from looking left position)
Left eye adduction possible
Right eye abduction possible only upto the center:
Reason:
III nerve intact
Superior oblique: weak abduction
Inferior oblique: weak abduction
Right abducens nucleus lesion: Effect?
1. Neither eye can look right.
Since abducens nucleus - very close to the PPRF

2. Compete right side facial paralysis(internal genu of facial nerve)


***PPRF, abducens nucleus and internal genu (VII)ALWAYS involved together***
Left MLF lesion : fn? Commonly involved disease?
Associated with IIIrd nerve function: adduction during conjugate gazing
MS
Failure to adduct eye during gaze
AKA "Internuclear ophthalmoplegia"
Differentiate MLF lesion from pure oculomotor lesion?
In IIIrd nerve palsy:
1. Complete failure of adduction of the eye
2. No dilation of pupil and
3. Ptosis

MLF lesion-
convergence of eye possible. failure of adduction of eye only in conjugate gazing
Left frontal eye field lesion?
1. Inability to move either eyes to right.
Facial muscle weakness-LOWER face- proximity of corticobulbar fibres to the frontal eye field.
UPPER half spared.
Pateint fails to move both eyes to right:
whats the site of the lesion?
A. Right frontal eye field
B. Left frontal eye field
C. Right PPRF
D. Left PPRF
Either Left frontal eye fielder OR right PPRF
Left frontal eye field lesion: Lower 1/2 of face involved only(right-opp side of lesion)
PPRF: entire face involved.(right-same side of the lesion)
Brainstem- supplied by(blood supply)?
Vertebrobasilar system
Basilar artery formed by? location?
Joining of the vertebral arteries.
Pontomedullary junction
Course of basilar artery?
Formed at PM jn--> runs along the medial surface of pons--> bifurcates into
post cerebral arteries at midbrain
Medulla: blood supply?
Medial medulla-
Anterior spinal artery fed by vertebral artery
Lateral medulla-
PICA
Pons- blood supply?
Medial: Basilar artery(paramedian branches)
Lateral-caudal(VII and VIII) - AICA.
Lateral-rostral- superior cerebellar artery
Cerebellar arteries:
Name em.
Structures supplied?
1. Superior- Rostral pons
2. Inferior-
a. Anterior(AICA)- Caudal pons
b. Posterior(PICA)- Lateral medulla
Midbrain-blood supply?
Posterior cerebral artery- medial and lateral
Brain stem lesions- tracts affected with side.
Spinothalamic- C/L
Corticospinal-C/L
Medial lemniscus-C/L
Descending hypothalamic fibres- I/L(horner's)
CN involved: I/L signs/symptoms
Above brain stem level lesion: Effects?
IC/Thalamus/Cortex-
ALL-
C/l signs and symptoms
Lower 1/2 face weakness

Spinothalamic fibers and descending hypothalamic fibers go together.
lesion of one produces another in brain stem.
medial lemniscus system- course across the brain stem?
medially in medulla
laterally in the mid brain
Nuclei lined across-
medially to laterally along floor of 4th ventricle,

Location of nuclei in upper medulla.
hypoglossal-dorsal nucleus of X- solitary nucleus-vestibular nucleus
medial lemniscus- medially

nucleus ambiguus- dorsal to the inferior olive

CS tract dorsal to medial lemniscus

CN IX and X- exit between inferior olive and pyramids

CN XII- exits between the inferior olive and inferior cerebellar peduncle

spinothalamic and hypothalamic tracts anterolaterally next to olive

spinal trigeminal tract and nucleus adjacent to inferior cerebellar nucleus
Medial medullary syndrome: cause? effect?
Cause- Anterior spinal artery occlusion
effect-
pyramids- C/l spastic paralysis
medial lemniscus- C/l loss of tactile, vibration, proprioception
hypoglossal- I/l flaccid paralysis--> tongue deviation on protrusion
towards the side of the lesion
Lateral medullary syndromes(Wallenberg syndrome): cause? effect?
Cause: PICA

Effect:
1. Spinothalamic tract- C/l loss of pain and temperature
2. Descending hypothalamic fibers: I/L horner's syndrome
3. CN IX, X- Hoarseness, weak vocal cords, dysarthria, dysphagia
4. Spinal nucleus and tract- I/L loss of pain and temperature of face
5. Vestibular nucleus- N/V and vertigo
6. Cerebellar peduncle- I/L ataxia
Medial caudal pontine syndrome: Cause? Effect?
Cause: Basilar artery(paramedian branches)
Effect:
1. Corticospinal- C/l spastic paralysis
2. Medial lemniscus- C/l loss of pressure/vibration
3. CN VI: strabismus- internal/medial
Lateral pontine syndromes: Cause? Effect?
AICA
1. Spinothalamic tract: C/l pain and temperature- limbs/trunk
2. Descending hypothalamic fibres- I/L horner
3. Spinal nuclei and tract- I/L pain and temperature- face
4. VII- I/l facial muscle paralysis(LMN)
5. VIII- I/l hearing loss
Pontocerebellar angle syndrome: cause? effect?
Cause: Acoustic neuroma
Effect:
Affects CN VIII
Compression of V, VII(LMN)

ABSENCE OF LONG TRACT LESIONS
Medial midbrain syndrome.
Corticospinal tract: C/l spastic lesion
Corticobulbar tract: C/l lower face weakness(UMN)
III nerve lesion: I/L external strabismus, dilated pupils and ptosis
Dorsal midbrain sydrome.
Pineal gland tumor: directly above superior colliculus and pretectal area
1. Disruption of vertical conjugate gaze
2. Diminished pupillary light reflex(pretectal area compression)
3. Elevated ICP- non communicating
Reticular nuclei: name em.(Reticular formation)
1. Raphe nuclei
2. Locus ceruleus
3. Periaqueductal gray
Raphe nucleus:
Location?
Function?
Location- Midline of brain stem- extends from medulla to midbrain
Function- serotonin(dorsal raphe nucleus)
Locus ceruleus: function?
Synthesize norepeinephrine.
(associated with arousal/ sleep wake cycle)
Periacqueductal gray:
location?
function?
Collection of nuclei surrounding cerebral aqueduct
Opioid receptors in periaqueductal gray- collaterals to spinothalamic tract-help suppress painful stimuli
Cerebellum: parts? function?
Midline vermis: axial and proximal
Intermediate hemisphere: distal
lateral hemisphere: motor planning
flocculonodular lobe: balance and smooth conjugate gaze of eye muscles.
Vermis/intermediate zone: function? input from?
Ongoing motor smooth execution of axial and proximal muscles.
input: proprioceptive inputs from muscle spindles and golgi tendon organs.
Input to cerebellum from spinal cord thru ___cerebellar peduncle/s
Inferior and Middle
(IIM- Input inferior and middle)
Output from cerebellum to spinal cord thru___cerebellar peduncle
Superior.

(OS)
Lateral hemisphere:input from? function?
Input:
1. Cerebrum
2. Inferior olive: error detection
function: motor planning
Flocculonodular lobe: input from? function?
Input : Vestibular nucleus.(VIII)
function: balance and eye movements
Cerebellar cortex layers?
Molecular layer:
Outer layer-
cells:
basket cells
stellate cells
parallel fibers(axons of granule cells)


Purkinje cell layer:
Middle- most important cell layer
cells: purkinje cells

Granular cell layer:
innermost layer
cells:
Golgi cells
Granule cells
Glomerulus= Granule cell+ golgi cell axons+ glial capsule
granule cells= the only excitatory cells in cerebellum
The only excitatory cells in cerebellum ____
Granule cells
The only cells whose axons leave the cerebellum____
Purkinje cells
Purkinje cell: function and location?
Cerebellar middle layer- purkinje layer
function-
all inputs to cerebellum influence firing of purkinje cells
Only axons of purkinje cells leave the cerebellum.(longest axons in the CNS)----> influence deep Cerebellar nuclei(cerebellar medulla)
All(except granule cells) outputs of cerebellum are: excitatory/inhibitory?
Inhibitory
All input to cerebellum are: excitatory/inhibitory?
Excitatory
Inputs to cerebellum:
fibers?
associated tracts?
Target and function?
Mossy fibers:
Vestibulocerebellar--->Granule cells(excitatory- glutamate)---> purkinje cells
Spinocerebellar--->Granule cells(excitatory- glutamate)
fn: balance, smooth coordination

Climbing fibers:

Olivocerebellar--->Purkinje cells(excitatory)
(inf. olives)
fn: error detection
Spinocerebellar and Vestibulocerebellar circuit system through cerebellar cortex?
Mossy fibers---> Granule cells---> Parallel fibers (axons of granule cells)--->Purkinje cells---> CB cells
Olivocerebellar circuit system through cerebellar cortex?
Climbing fibers---> Purkinje fibers--->CB cells
Cerebellum cell types? Target? Transmitter? function?
Cerebellum cell types? Target? Transmitter? function?
Purkinje cells-CB nuclei-GABA-Inhibitory
Granule cells-Purkinje cells-glutamate-Excitatory
Stellate cells-Purkinje cells- GABA- Inhibitory
Basket cells- Purkinje cells-GABA-Inhibitory
Golgi cells-Granule cells-GABA-Inhibitory
Deep CB nuclei? associated cerebellar parts?
Fastigial: Vermis
Interposed: Globose+ Emboliform: Paravermis/intermediate
Dentate: Lateral
Basal ganglia: Fn?
1. Initiation
2. Suppression of unwaned movements
3. Gross motor
Structural organization across horizontal section (CT head)
Caudate- striatum
Putamen-striatum
separated by ant limb of internal capsule
An
External, internal globus pallidus(medial to putamen therefore lateral to the IC)

Caudate- ant limb of IC-globus pallidus and putamen

Substantia nigra
subthalamic nucleus
Basal ganglia circuit?
Cerebral cortex(motor)--> VL thalamus--> direct/indirect basal ganglia
DIRECT basal ganglia pathway?
Effect?
DIRECT
Cortical excitation(glutamate)
striatum(CAUDATE/ Putamen)(GABA)
Globus pallidus-Internal(GABA)
Thalamus(VA/VL)
Motor cortex-->initiation of movement

Direct: Drives movement
INDIRECT basal ganglia pathway?
Effect?
Cortical excitation(glutamate)
Striatum(GABA)
Globus pallidus-External(GABA)
Subthalamic nucleus(Glutamate)
Globus pallidus- Internal(GABA)
Thalamus(VA/VL)
Motor cortex-->inhibition of movement

Indirect: Inhibits movement
Dopaine: site of formation? receptors? fn?
Dopamine-
dopaminergic neurons- substantia nigra
Stimulate
D1- Direct(GABA)
D2-Supress indirect pathway

Dopaminergic drive the direct pathway.
Dopaminergics drive movement.
Cholinergic transmission: Role in basal ganglia functioning?
Striatum
Stimulate-->indirect--> inhibition
Diseases of basal ganglia?
Parkinson's: pathology
Direct basal ganglia pathway--loss of dopaminergic neurons-b/l
So motor cortex active--loss of dopaminergic.
therefore decreased direct pathway activity
increased indirect pathway activity

Tremor at rest


Huntington's disease: Part of motor system affected?
Associated with defective indirect pathway
loss of GABA neurons in indirect pathway.
Overactive motor cortex.
Hemiballism: Part of motor system affected? symptoms?
Subthalamic nucleus- indirect structure
Wild flinging of movements
U/L problem--> C/L effect
associated with hypertension
Tourette's dz: part of motor system affected?
Indirect basal ganglia phenomenon
Associated with
OCD
ADHD
Rx- antipsychotics
Wilson's dz: associated tremors?
Wing beating tremor- upper limb tremors associated with intention
Intentional tremors: lesion in ___(part of CNS)
Cerebellum
Eyeball layers? fn?
Outer-
Sclera-
Attachment site for ocular movement muscles
Corneal sensory fibers
Autonomic sensory fibers

Middle- Choroid- Blood supply to retina

Inner-Retinal fibers
Refractive areas of the eye?
Cornea- Non adjustable
Lens- Adjustable
Posterior chamber- associated fn?
Ciliary bodies: epithelium produce aqueous humor
Drainage of aqeous
canals of schlemm at angle of anterior chamber
Parasympathetic and symathetic nerve supply to the eyes.
Parasympathetics-
III innervate ciliary muscle- sphincter- constrictor

sympathetic- dilator -radial muscles

cornea supplied by by V1 of trigeminal
Light reflex pathway?
Retina-->CN II-->
b/l to midbrain nuclei(adjacent to sup.colliculi) pretectal nuclei-->
b/l Edinger Westphal nuclei III nerve nucleus(parasympathetic-pregang)-->
III nerve--->
Ciliary ganglion(parasympathetic- postgang)-->
pupillary sphincter ms-->miosis

Afferent: CN II (Pretectal)
Efferent: CN III (Edinger westphal and ciliary ganglion)
Parasympathetic controlled muscles of the eye? Receptor? fn?
Pupillary sphincter
Ciliary muscles

Receptors:
Radial: alpha receptors
Ciliary: beta receptors

Fn:
Radial: mydriasis
Ciliary body epithelium: aqueous humor secretion
Accommodation convergence reaction: components?
Accommodation
Convergence
Miosis
Accommodation convergence: Pathway involved?Parasympathetics-->
Parasympathetics-->
Ciliary contraction-->
Suspensory ligament relaxation-->
Increased convexity of lens-->
Increased RI of the lens-->
Near object focus
Convergence: Involved muscles?
Skeletal muscle axons(III)-->
Medial recti
Argyll Robertson pupil?
Associated dzs?
Lesion site?
Diminished light reflex
Accommodation reaction preserved

Associated dzs -
1.Tabes dorsalis
2. Diabetes
Marcus gunn pupil?
associated dz?
associated test?
Diminished pupillary light reflex.

Swinging light test:
normal eye-- pupils constrict normally
swing light immediately in affected eye--> dilation of both pupils
associated dz: MS
Horner's syndrome?
Lesion of oculosympathetic fibers:
T1- superior cervical ganglion
syndrome-peripheral
descending- central
ptosis, miosis and hemianhidrosis
Ipsilateral
Adie pupil?
Poor light reflex
Good accommodation
lesion of ciliary ganglia
suppressed knee jerks/muscle streth reflex
Transtentoral herniation: eye effect?
Uncal herniation--> compression of IIIrd nerve- "Down and out"
miosis- 1st sign.(since parasympathetic fibers are the outermost hence affected 1st)
ptosis
Retina: layers?
Ganglion layer
Inner nuclear layer
Outer nuclear layer

Outer segments associated with pigment epithelium
Site of detachment of retina?
Outer segments are embedded in pigmented epithelium-->ultimately the retina degenerates due to lack of nutrients
Pigmented epithelia: fn?
pigmented epithelia--> transport glucose and vit a to outer segment of rods and cones
Rods- distribution? function?
Distributed across the retina except the fovea


Fn-
Motion sensitive
Night vision
Optic pathway
3 Neuron pathway:
#1. Photoreceptors-->BIPOLAR CELLS(inner nuclear layer)
#2. Ganglion cell layer(optic nerve)--->
lateral geniculate body
Pretectal area(light reflex)
suprachiasmatic nucleus(hypothalamus)
#3.
2nd optic neurons cross midline: unique features?
1. Only 60% cross midlines @ optic chiasm(nasal nerve optic retina)
Temporal DO NOT.
NASAL NERVES CARRY TEMPORAL information
THEREFORE TEMPORAL HEMIFIELD INFO CROSS.
2. Cross above the level of their cell bodies
Optic tract? Projecting nuclei?
Remixed optic nerves:
temporal retina+ nasal retina from opp eye

Nuclei:
Geniculate body
Pretectal area

Photoreceptors-->
Bipolar cells-->
Ganglion cells-->
Optic nerves-->
Optic chiasm-->
Optic tracts-->
Lateral geniculate body-->
Optic radiations-->
Prim visual cortex= Cuneal gyrus + Lingual gyrus
Lesion ahead of optic chiasm:
Associated conditions?
effect?
associated conditions:
1. Optic neuritis(MS)
2. Central retinal artery occlusion
3. Internal carotid artery aneurysm

effect:
Complete monocular ipsilateral anopsia
Lesion at optic chasm?
associated with?
effect?
1. May affect only temporal fibers
associated lesion-
Medially expanding aneurysm of internal carotid artery.


effect-
IPSILATERAL
MONOCULAR
NASAL hemianopsia

OR

2. AT chiasm
Affect only nasal fibers


Effect-
BINOCULAR
BITEMPORAL(heteronymous)

Associated lesions-
1. adenoma- superior quadrantanopsia
2. craniopharyngioma- inferior quadrantanopsia
Adenoma: associated visual field changes?
1. Bitemporal
2. Superior quadrant
3. Quadrantanopsia
(aDenoma comes from Down)
Craniopharyngioma: associated visual field changes?
1. Bitemporal
2. Inferior
3. Quadrantanopsia
(Craniopharyngioma comes from the Ceiling)
Lesions Past the chiasm:
Standard features-
monocular/binocular?
homonymous/heteronymous?
features:
BINOCULAR
HOMONYOUS
MCA occlusion: visual structures affected?
Optic tracts
Optic radiations
PCA occlusion: visual structures affected?
Primary visual cortex
Optic tract lesions: features?
C/L Homonymous hemianopsia
Lateral geniculate body lesion: features?
C/L Homonymous hemianopsia
Optic radiations' lesions: features?
#1. Meyer's loops: C/L homonymous sup quad hemianopsia
#2. Non Meyer's loops: C/L homonymous inf quad hemianopsia
Meyer's loop?
associated lesions?
Associated cerebral lobe?
Target?
Meyer's loops fibers - lower retinal fibers traversing laterally
(as meyer's loop)- carry superior visual info

Associated lobe:
Temporal lobe

Associated lesion:
1. MCA infarct
2. Temporal lobe tumor

Target:
Lingual gyrus
Lingual gyrus:
Location?
Function?
Location: Occipital lobe: prim visual cortex
Function: SUPERIOR VISUAL FIELD info processing
Cuneus gyrus:
Location?
Function?
Location: Occipital lobe: prim visual cortex
Function: INFERIOR VISUAL FIELD info processing
Non meyer's loop lesion:
effect?
target?
effect: C/L Homonymous inf quadrantanopsia
target: Cuneus gyrus
Complete lesions of optic tract and optic radiations have the same effect: ?
differentiating factor?
C/L homonymous hemianopsia:

Optic tract lesion will have slightly diminished pupillary light reflex
Optic radiation lesion: no effect on pupillary light reflex.
Primary visual cortex:
effect?
cause?
effect:
C/L Homonymous hemianopsia
Macular sparing
Macular sparing in primary visual cortex lesion: cause?
Cause of prim visual cortex lesion: PCA infarct
Macular vision area in cortex is supplied by collaterals from MCA
(in addition to PCA)

cause:
PCA infarct
Diencephalon: components?
Thalamus
Hypothalamus
Epithalamus: pineal gland
Subthalamus
Mammillary bodies: fn?
Associated with memory consolidation
sites of degeneration from korsakoff psychosis
Thalamic nuclei: Name em.
VPL
VPM
VA
VL
MGB
LGB
Ant
MD
VPL: Input? Output?
Input: Sensory from body and limbs(Limbs=vpL)
Spinothalamic and Medial lemniscus
Output: Somatosensory cortex
vPm or vPl= Pain(sensory)
VPM: Input? Output?
Input: Sensory relay from face(Makeup=vpM) and taste

Output: Somatosensory cortex
vPm or vPl= Pain(sensory)
VA: Input? Output?
Input: Motor info from BG(Globus pallidus, substantia nigra)
Output: Primary motor cortex
VL: Input? Output
Input: Motor info from BG(GP), cerebellum(Dentate nucleus)
Output: Primary motor cortex: brodmann area 4
LGB:Input? Output?
Input: Visual info from optic tracts
Output: Visual cortex
(L= Light)
MGB: Input? Output?
Input: Auditory info from inferior colliculus
Output: Auditory cortex
(M= Music)
AN: Input? Output?
Input: Mammillary nucleus.(short memory processing into long term): "Mammillothalamic tracts"
Output: Cingulate gyrus(part of PAPEZ circuit)
Papez circuit?
Mammillar bodies--> Mammillothalamic tract-->Anterior nuclear group thalamus--> Ant limb of internal capsule--> Cingulate gyrus--> Hippocampus-->fornix-->Mammillary bodies
MD: fn? stimulation associated with?
Input: amygdala, prefrontal cortex and temporal cortex
Output: Prefrontal cortex and cingulate gyrus
Medial-dorsal nucleus.
Involved in memory- damaged in Wernicke- Korsakoff syndrome
Stimulation produces savage behavior
Pulvinar: fn?
Integrate somatic visual and auditory input
Midline/intralaminar:Input? Output? fn?
Input:
Reticular formation
Spinothalamic tract

Output:
Cingular gyrus

fn
Associated painful stimulus should be avoided in the future
Limbic system: fn?
5 Fs:
Feeding
Feeling
Fleeing
Fighting
Fornicating
Ventral nuclear group:
lesion associated with isolated lacunar stroke?
Thalamic pain syndrome:
1. loss of position and vibration sense
2. Increased C/l pain-burning aching resistant to analgesic medications
Hypothalamus:
location?
1. Collection of nuclei in the wall of the 3rd ventricle
2. Above the optic chasm
3. Above the pituitary
The only grossly visible part of the hypothalamus?
1. Mammillary bodies.
2. Posterior lobe of the hypothalamus
Gross structures closely associated with location of hypothalamus?
1. Optic chiasm
2. Posterior pituitary
3. Mammillary bodies.
Preoptic area:
Derived from ___?
function?
Effect of pre-optic lesions?
Telencephalon

Fn:
sex hormone RELEASE FACTOR production(estrogen/androgen)

Effect:
Before puberty: arrest of sexual development
After puberty: Impotence and Amenorrhea
Anterior region:
Location?
Nuclei?
fn?
effect of lesion?
Location-
Directly above the optic chiasm

Nuclei:
1. Paraventricular
2. Supraoptic
3. Suprachiasmatic

Function:
Paraventricular and supraoptic
1. ADH
2. Oxytocin production and release into post pituitary(neurohypophysis)

lesion--> diabetes insipidus
polyuria
polydipsia
Suprachiasmatic: fn?
1. Circadian rhythm---> influences pineal gland
(Visual input from retina)
supraChiasmatic= Circadian)
Post pituitary contain____
Axons of paraventricular and supraoptic nuclei
Anterior pituitary derived from? cell types in pituitary?
From Rathke's pouch
Dorsal outgrowth of oral ectoderm.

cell types-
Acidophils
Basophils
Arcuate nuclei:
location?
fn?
Location:
hypothalamus- directly above the infundibulum

fn: control release of anterior pituitary hormones.
thru releasing and inhibitory factors--->hypophyseal-portal veins-->secondary capillary plexus in ant pituitary
Ventromedial nucleus: VM nucleus;
location?
Fn?
Location: tuberal region of hypothalamus
fn: Satiety center: lesions--> obesity
(VM= Vomit..you are full so you vomit.)
Feeding center: location?
Lateral hypothalamus
lesions--> aphagia
Posterior region:
nuclei/structures?
respective fns?
Mammillary bodies- part of limbic system: memory consolidation

Anterior hypothalamic zone:
Senses body-temp elevation-->mediates heat dissipation response
lesion-->hyperthermia

Posterior hypothalamic zone
Senses body-temp drop-->mediates heat conserving response.
lesion-->poikilothermy
Hyperthermia: associated hypothalamic lesion?
Posterior hypothalamic zone
Diencephalic structures associated with thiamin deficiency?
1. DM nucleus of thalamus
2. Mammillary bodies
Epithalamus? location? fn?
Pineal gland : melatonin release(increased during darkness-->sleep)-
plays a role in -
growth/development
circadian rhythm
habenular nucleus(fn:?)

location: above posterior commissure
pinealocytes: fn?
synthesis :
melatonin
serotonin
cholecystokinin

melatonin production control

through light across the retinal-suprachiasmatic-pineal pathway
light inhibits-->melatonin
darkness stimulate-->melatonin
Pineal tumor-effect?
Parinuad syndrome:
Compression of
superior colliculus- vertical conjugate gaze impaired
midbrain- pupillary light reflex(pretectal area)
Subthalamus: fn? lesion effect?
Movement inhibition(indirect basal ganglia pathway)
lesion: hemiballismus--- C/l flinging movements of extremities
Primary motor cortex: location? Area no __?
Precentral gyrus
Area 4
Primary somatosensory cortex: location?
Postcentral gyrus
(poStCentral: SomatoSensory)
Homunulus orientation across the cortical surface?
Laterally head (near lateral sulcus) --->medially legs/feet
Primary visual cortex: location? divisions?
Location: Medial surface of occipital lobe
division: (by calcarine sulcus)
1. Cuneus gyrus: Superiorly situated: Non meyer's loop info: Inferior visual field info
2. Lingual gyrus: Inferiorly situated- meyer's loops: Superior visual field info
Area of brain associated with watershed infarct?
Cause?
Effect?
Area: Jn of ACA and MCA
Cause: Hypotension
Effect:
1. Weakness of trunk musculature.
2. B/L loss of pain and temperature in trunk
"Person in a barrel syndrome"
Cortical cell layers?
1. Molecular layer
2. External granular layer(well developed in sensory cortices)
3. External pyramidal layer(well developed in motor cortices)
4. Internal granular layer(well developed in sensory cortices)
5. Internal pyramidal layer(well developed in motor cortices)
6. Multiform layer

Layer 2, 4 well developed in sensory cortices:
site of synapsis of thalamic relay nuclei

Layer 3, 5 well developed in motor cortices
UMN cell bodies--->from corticospinal/bulbar= aka Betz cells
Structures supplied by posterior circulation--->
1. Brain stem
2. Cerebellum
3. Medial cerebral hemisphere
4. Inferior cerebral hemisphere
MCA- cortical structures supplied?
Lateral aspect- upper half of body and face
ACA- cortical structures supplied
Medial aspect- lower half of body
Internal carotid aneurysms
Site?
Effects?
Site:
Before it branches off into MCA and PCA

Effects:
1. Medially expanding:
Compress temporal fibers of Optic nerve- Nasal hemianopsia

2. Laterally expanding:
Cavernous sinus
Compression of Abducens nerve- Internal strabismus
Margins of cortex supplied by?
either-
ACA
PCA

NOT MCA
Dominant hemisphere- left/right? blood supply?
Left hemisphere-
since it contains the language centers:
Broca's area
Wernicke's area
(both on lateral surface)

Blood supply-
Left MCA
Corpus callosum : blood supply?
MCA except Splenium- PCA
Cerebral artery most commonly associated with emboli?
MCA
Lacunar infarcts: cause? site? effect?
hypertension
penetrating branches of ACA/MCA-
basal ganglia/diencephalon/IC
Berry aneurysm: associated dzs?
1. Marfan's dz
2. ED type IV
3. ADPKD
4. Htn
5. Smoking
Brodman areas?
Primary motor area: 4
Primary somatosensory area: 3,1,2
Primary visual cortex: 17
Oral comprehension: 22 (Wernicke's)
Written comprehension: 39 (Angular)
Auditory complex: 41 and 42
Visual field/voluntary c/l horizontal gaze: 8
Motor speech area: 44, 45
Premotor areas: fn? brodman no? input from? lesion effect?
Motor planning
area 6

input: basal ganglia, cerebellum

lesion effect:
Apraxia
No weakness
Somatosensory association area: location? fn? lesion effect?
Location:
Parietal lobe: lateral aspect
Posterior to area 3,1,2.
fn: Integration of sensory systems

Lesion effect:
Astereognosia
No loss of touch /pressure sense
Astereognosia and apraxia more common in _____(lt/rt) hemisphere damage?
Lt hemisphere damage
Frontal eye field: location: brodman no?
Frontal lobe: lateral aspect
Anterior to area 6
Brodman no :Area 8
Primary auditory complex: location? B no? lesion effect?
location: Superior bank of temporal lobe under lateral sulcus
B no: 41 and 42
Lesion effect:
1. B/L slight diminution of sound
2. Poor sound localization
Visual cortex: location? brodman no?
Location: Medial aspect of occipital lobe
Brodman no: 17
Language centers? location? blood supply?
Broca's:
44 and 45 (motor speech areas)
Location:
Lateral aspect of frontal lobe
Anterior to premotor cortex

Wernicke's:
22(oral comprehension)
loaction
left temporal lobe- lateral
Posterior to prim auditory complex

Angular gyrus:
39(written comprehension)
location:
lateral aspect of parietal lobe-adjacent to visual association cortex
Aphasia: name em
Common features?
1. Broca's
2. Wernicke's
3. Gerstmann's
4. Conduction


Agraphia
Broca's aphasia: site? symptoms?
Reduced use of words- use of monosyllable words
aware and frustrated
lesion may extend into adjacent primary motor areas:
c/l spastic limb weakness
Wernicke's aphasia site?symptoms?
fluent aphasia.
no comprehension
verbal output- n
misuse words- "ford salad"
paraphasic speech
unaware and not concerned by deficit
area 22
Gerstmann's syndrome: site? symptoms?
Lesion in area 39: angular gyrus

Symptoms
1. Agraphia- cannot write
2. Alexia- cannot understand written material
3. Acalculia
4. Finger agnosia
5. Right-left disorientation
6. Unaware of defect



Spoken language understood
Conduction aphasia: site? defect?
Defect in fiber bundles that connect language centers
"Arcuate fasciculus"

1. Paraphrasing
2. Word finding pauses
3. Cannot repeat words/execute command-disconnect
4. Pt aware of deficit-- Frustrated
Arcuate fasciculus? fn?
Fibers connecting language centers in frontal/temporal/parietal lobes
Comprehension-response.
Non dominant lesion (Right parietal lobe lesion)dominant lobe?
test?
Lesion: U/L neglect on C/L half of the body: left sided
No visual defect but fail to recognize
No somatosensory defect

Test: bisect line or write numbers on a clock face--cram now in right side
Visual agnosia: lobe involved?
Temporal lobe- inability to recognize visual patterns
Prosopagnosia? lesion location?
Inability to recognize faces
lesion sites:
1. Area 20 and 21 of temporal lobe
2. adjacent occipital lobe
typically temporal lobe infarct

typical symptom: when person speaks, pt recognizes the individual.
Disconnect syndrome: site? fn?
Transcortical apraxia
Alexia without agraphia
Transcortical apraxia? lesion site?
Motor deficit of left arm on verbal command

Vascular occlusion of corpus callossum branches of ACA.
(4/5ths of corpus callosum)

verbal interpretation intact

but information transmission across the corpus callossum from dominant hemisphere to right hemisphere fails to travel.

No motor weakness.

Right arm movement executed successfully on command. (no disconnect problem between wernicke's area and prim motor
cortex on left.
Alexia without agraphia. Cause? lesion site?
Cause: Occlusion of the left PCA
Left PCA supplies:
1. L.Visual cortex: right
Lesion site:
Splenium of corpus callosum
Can write but cannot comprehend written material.
Internal capsule blood supply?
associated tracts?
Anterior limb-
medial striate branches
thalmocortical
rostral part of frontal lobes.

Genu-
lenticulostriate branches of MCA
corticobulbar fibers

Posterior limb:
Lenticulostriate branches of MCA
Corticospinal(entire homunculus)
Somatosensory: Thalamocortical projections
effect: C/L spastic paralysis
C/L anesthesia
Thalamic nuclei associated with thalamocortical projections?
VPL
VPM
Structures supplied by Anterior spinal artery? deficit stroke?
Ant 2/3rd of spinal cord:
All affected except dorsal columns
compare with ALS(limited to motor problems)
PICA: structure supplied? Deficit after stroke?
Dorsolateral medulla - wallenberg syndromes
Vertebrobasilar system:?
Pontine arteries
AICA
Superior cerebellar
Labyrinthine
Basilar artery: structures supplied? Lesion effect?
Medial aspect of pons
Medial pontine syndrome(CST+ CN VI)
AICA: Structures supplied? Lesion effect?
Inferior cerebellum cerbellar nuclei
Lateral pontine syndrome:(STT, DHF, CN VII, CN VIII)
Structures supplied by Anterior spinal artery? deficit stroke?
Ant 2/3rd of spinal cord:
All affected except dorsal columns
compare with ALS(limited to motor problems)
PICA: structure supplied? Deficit after stroke?
Dorsolateral medulla - wallenberg syndromes
Vertebrobasilar system:?
Pontine arteries
AICA
Superior cerebellar
Labyrinthine
Basilar artery: structures supplied? Lesion effect?
Medial aspect of pons
Medial pontine syndrome(CST+ CN VI)
AICA: Structures supplied? Lesion effect?
Inferior cerebellum cerbellar nuclei
Lateral pontine syndrome:(STT, DHF, CN VII, CN VIII)
Superior cerebellar art: structures supplied? lesion effect?
Cerebellum and sup peduncle
Rostral and lateral pons= (STT DHF, V)
Labyrinthine artery:structures supplied? lesion effect?
Inner ear
Sensorineural hearing loss
PCA:structures supplied? lesion effect?
Midbrain
thalamus
occipital lobe


C/L hemianopsia with macular sparing
Alexia without agraphia.(splenium of corpus callosum)
Internal carotid branches? lesion effect of each branch?
Ophthalmic artery
Post comm artery
Ant comm artery
Middle Cerebral artery
Posterior cerebral artery

Lesions of respective branches of int carotid.

Ophthal artery- retina- blindness(monocular)

Post communicating artery=
2nd most common aneurysm

Ant cerebral artery=
C/l spastic paralysis of LL

Ant communicating artery:
MC site for developing aneurysm-
B/l temporal inf homonyous quadrant anopsia.

Middle cerebral artery:
upper half of motor homunculus.
1. C/l anesthesia;
2. Gaze palsy= Unable to gaze away from lesion site
3. Aphasia(l)
4. Dysprosodias®
5. Gerstmann synd(L)
6. Hemineglect®
Frontal lobe: functions?
1. Primary motor cortex/premotor cortex: C/l spastic paresis
2. Frontal eye fields: Eyes deviate to ipsilateral side
3. Broca speech: Expressive, non fluent aphasia(l), motor dysprosodia(monotone- no emotions attached) (r)
4. Prefrontal cortex:
Prefrontal cortex: lesion?
1. Poor judgement
2. Difficulty concentrating
3. Apathy
4. Inappropriate behavior
Parietal lobe: fns? lesions
1. Primary somatosensory cortex: C/l hemihypesthesia
2. Superior parietal lobule: C/l astereognosis/apraxia
3. Inferior parietal lobule- area 39(gerstmann syndrome: alexia/dyscalculia/dysgraphia/finger agnosia/CL hemianopia
unilateral neglect(r)
Temporal lobe: fns/lesions?
1. Primray auditory cortex: B/L diminished hearing
2. Wernicke's: Fleutn aphasia(l), sensory dysprosodia®: emotional content of speech not understood
3. Hippocampus: B/l lesions--> consolidation of short term--> long term memory
4. Amygdala: Kluver Bucy syndrome
5. Olfactory bulb, tract: Anopsia
6. Meyer loop: "Pie in the sky"
Occipital lobe : fns/lesions?
Visual: C/l hemianopsia with macular sparing
Limbic system: fn?
Memory consolidation
Emotional response center
Visceral fns- mainly smell
Sex drive
Behavior
Unique feature: Olfactory system
I. Reaches-
1. temporal lobe
2. amygdala
without thalamic relay

II: Primary olfactory neurons are replaced continuously: 30-120 days.

III. Do NOT form any sensory ganglia
Fx of cribriform plate associated with? (lesions)?
1. Anosmia
2. CSF rhinorrhea
Fns:
Hippocampus
Amygdala
fornix?
hipp: memory consolidation

amyg: emotional content to memory

Fornix: Connects hippocampus to the mammillary bodies
loops over diencephalon
Kluver bucy syndrome: cause?
1. hypotension
2. b/l lesion in amygdala and hippocampus
3. placidity
4. Visual agnosia
5. Hyper metamorphosis
6. Increased oral exploration
7. Hyper/hyposexual
8. Anterograde amnesia