0113 - Neuro 2/3 Flashcards
(74 cards)
Purpose of the foramina of Luschka and Magendie?
Connect 4th ventricle to the subarachnoid space. Luschka = Lateral. Magendie = Medial.
NPH
Expansion fo ventricles distorts fibers of the CORONA RADIATA -> urinary incontinence, ataxia, cognitive dysfunction
Communicating hydrocephalus
Decreased CSF absorption by arachnoid graduation lead to inc. ICP, papilledema, herniation
Hydrocephalus ex vacuo
Apparent increase of CSF 2/2 atrophy. ICP is normal. (e.g. Alzheimer’s, adv. HIV, Pick)
Noncommunicating hydrocephalus
Due to a structural blockage within the CSF system
How many spinal nerves are there?
31 spinal nerves. “Have the spine of a man walking outside on January 31st.”
Which nerves exit above their corresponding vertebra?
C1-C7.
To what vertebrae does the spinal cord extend to? And where do you do a LP?
Lower border of L1-L2. LP usu. between L3-L4 or L4-L5. Subarachnoid space down to S2.
Dorsal column body organization
Fasciculus gracilis (lower body and legs) are inside. Fasciculus ceunatus (upper body, and arms)
Anterolateral system body organization
Lateral spinothalamic tract. Sacral outside to cervical inside.
Corticospinal tract body organization
Sacral lateral. Cervical medial.
Anterolateral system pathway
Free nerve endings synapse in ipsilateral gray matter and decussates within 2-3 levels in anterior white commisure, ascending CONTRlaterally, synapsing at VPL -> sensory cortex
Dorsal column pathway
Fine touch, vibration, pressure, propioception enter spinal cord and ascend ipsilaterally until it synapses at the nucleus cuneatus (lateral) or gracilis (medial) -> decussates at the MEDULLA and ascends contralaterally up the medial lemniscus -> synapses at VPL -> sensory cortex
Spastic paralysis vs. flaccid paralysis
UMN vs. LMN signs
ALS
Combined UMN and LMN w/ NO sensory, cognitive, or oucular motor deficits. Some etio = defective superoxide dismutase I. Riluozole tx modest (dec. presynaptic glutamate release).
Tabes dorsalis
Tertiary syphilis -> demyelination of dorsal columns and roots -> impaired sensation, propioception, coordination. Charcot joints, Argyll Robertson pupils (small pupils that accommodate but do not react to light). Absent DTRs and POS romberg
Syringomyelia
Syrinx damages anterior white commisure -> b/l loss of pain and temperature
Poliomyelitis
Poliovirus (oropharynx and SI replication before spreading hematogenously to CNS). Destruction of anterior horn cells -> LMN death. Weakness, hypotonia, flaccid paralysis, fasciculations. CSF shows inc. WBCS and slight increased protein w/ NO CSF glucose change.
Spinal muscular atrophy (Werdnig-Hoffmann disease)
Congenital degeneration of anterior horn cells. AR.
Friedreich ataxia
AR GAA on Chromosome 9 (frataxin) -> mt dysf(x). Muscle weakness and loss of DTRs. Staggering, frequent falls,nystagmus, pes caves, hypertrophic cardiomyopathy
Brown-Sequard syndrome
Hemisection. Ipsilateral UMN signs (corticospinal). Ipsilateral dorsal column. Contralateral anterolateral. (pain and temperature). At the level of lesion, loss of all sensation. Above T1, could have Horner’s syndrome
Horner syndrome and its pathway.
Ptosis (superior tarsal m.), Anhidrosis and flushin, Miosis. Hypothalamus to synapse in lateral horn of intermediolateral column of spinal cord (T1) -> superior cervical (sympathetic) ganglion (which is near bifurcate of common carotid) synapse -> sweat glands of face, opthalmic division of trigeminal nerve for pupillary dilator, sweat glands of forehead + smooth muscle of eyelid
C2 vs. C3
Posterior part of skull cap vs. high turtleneck
Spinal cord lvls that would affect erection
S2,3,4