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MSC Neuro 2025 P1

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Inabilitytoplantarflexfootand toes.

Atrophyofposteriorlegmusclesandsolemuscles.

Gaitdisturbance(di icultywalkingontoes).

Peroneal(Fibular)NerveSyndrome

Function:

Motor:dorsiflexion(footextension),toeextension,eversion(turningfoot outward).

Sensory:dorsumoffoot,anterolaterallowerleg.

Clinicalmanifestations:

Footdrop:inabilitytodorsiflexfootand toes.

"Horse'sfoot":foothangsdownandrotatedslightlyinward.

"Cockgait"or"steppagegait":highfootliftingwithtoe-firstfootcontact duringwalking.

Atrophyofanteriorandlaterallegmuscles.

Sensorylossoveranterolateralleganddorsalfoot.

Diagnosis:

Inabilitytodorsiflexfoot,di icultywalkingonheels.

Muscleatrophyofanterolateralleg.

Characteristicgait abnormalities.

TunnelSyndromes(EntrapmentNeuropathies)

Commonatsitesofnervecompression:e.g.,tarsaltunnel(tibial nerve),fibular head(peronealnerve).

Symptoms:pain,paresthesia,weakness innerve distribution.

Conservativetreatmentincludes:

NSAIDsandanalgesics

Physicaltherapy(nerve gliding,strengthening)

Splintingororthotics

Localinjections(steroids,anesthetics)

Avoidanceofpressure/compression triggers

Surgicaldecompressionindicatedifnoimprovementafter3-6monthsof conservativetreatmentorprogressiveneurologicaldeficit.

ConservativeTherapy

Vasculartherapytoimprovenerve perfusion.

AntioxidantsandneurotropicBvitamins.

Physicalmodalities:electricalstimulation,massage, nerve stimulationtechniques.

Rehabilitation:gaittraining, muscle strengthening, orthotics.

SurgicalIndications

Persistentsymptomsrefractorytononinvasivemeasures.

Progressive muscleweakness oratrophy.

Confirmednerveentrapmentonelectrophysiologicstudies.

Traumaticnerveinjuryrequiringdecompressionorrepair.

45.Brachialplexuslesionsyndromes.

BrachialPlexusLesionSyndromes

1.ShoulderPlexopathy Etiology

Injuries duetotrauma, woundsofhealingbones

Prolongeduseofhigh tourniquetduringsurgery

Compressionbetweenclavicleandfirstrib

Shoulderdislocationorfracturesinvolvingshoulder/headregion

ClinicalPresentation

Entireplexuslesion:

Peripheralparalysis/paresisandanesthesiaofshoulderandforearm

Uppertrunklesion(Duchenne-Erbpalsy):

Paralysisandatrophyofproximalarmmuscles:deltoid,biceps, brachialis, brachioradialis,supinator

Lossofshoulderabductionandelbowflexion

Preservedhandandfingermovement

Painandparesthesiaonlateraledgeofshoulderandforearmwithreduced sensation

Lowertrunklesion(Dejerine-Klumpkepalsy):

Paralysisandatrophyofsmallhandmusclesandfinger/handflexors

Preservedshoulderandforearmmovement

Sensorylossonpalmarsurfaceoflittlefingerandulnarsideofotherfingers andforearm

Di erentialDiagnosis

Cervicalosteochondrosis

Humeroscapularperiarthritis(Dupley’ssyndrome)causingpainfullimitationof shouldermovement

Diagnosis

Clinicalexaminationwithneurologicaltestsofmusclestrengthandsensory function

Electromyography(EMG)andnerve conductionstudiestolocalizeandassess severity

Treatment

Conservative:Analgesics,vitaminB complex,C,nicotinic acid, thiocticacid

Anticholinesterasedrugs

Physicaltherapyandmassage,reflexology,physiotherapy

Reconstructivemicrosurgicaloperationsfor traumaticorpersistentnerve damage

46.Bernard-Hornersyndrome,mechanism,topicalvariants.

Bernard-HornerSyndrome(Horner’s Syndrome)

Mechanism

Causedbydamagetothe sympatheticnervoussystempathwaysupplyingthe face andeyeontheipsilateralside.

Sympatheticinnervationoriginatesfromthree-neuronchain:

1.First-orderneuron:fromhypothalamustospinalcordlevelsC8–T2 (ciliospinalcenterofBudge)

2.Second-orderneuron:fromspinalcord,across thorax,tosuperiorcervical ganglion

3.Third-orderneuron:fromsuperiorcervicalganglionalonginternalcarotid arteryintoorbit

Lesionsatanypoint—central, preganglionic,orpostganglionic—causethe syndrome.

ClinicalFeatures

Ptosis:droopingofuppereyelid(duetoparalysisofMüller’smuscle,suppliedby sympatheticnerves;milderthanoculomotornerve palsy).

Miosis:constrictedpupildue tounopposedparasympatheticactivity.

Enophthalmos:apparentsinkingofeye into orbit(due toparalysisoforbital muscles).

Anhidrosis:lossofsweatingontheipsilateral faceorbodydependingonlesionsite.

Vasodilationandhyperemia:reddeningofconjunctivaduetoloss ofsympathetic vasoconstriction.

Heterochromia: (lightiriscolorona ectedside)seenincongenitalorlong-standing casesinchildren.

Decreasedciliospinalreflex.

Visualadaptationtodimlightimpaireddue topersistentmiosis.

VariantsbyLesionSite

 

LesionLocation

Features

CommonCauses

 

 

Stroke,tumor,

First-order

Ipsilateralhemibody

syringomyelia,lateral

(central)

anhidrosis,miosis,ptosis

medullarysyndrome

LesionLocation

Features

CommonCauses

 

Ipsilateralfaceanhidrosis;

 

 

morecommon;

Pancoasttumor,cervical

Second-order

associatedwith thoracic

rib,trauma,thoracic

(preganglionic)

lesions

surgery

 

Minimalorabsentfacial

Carotiddissection,cluster

Third-order

anhidrosis(branchhas

headache,cavernous

(postganglionic)

left)

sinus pathology

Diagnosis

Oxymetazolinetest(Amphetaminetest): assessesintegrityofsympatheticpathway.

Sluggishpupillaryreactiontolightanddilation.

Imaging: CT/MRIofneck, chest,brain tolocalizecause.

Biomicroscopy:conjunctivalvesselinjection,irispigmentation.

Treatment

Treatunderlyingcause(tumor,dissection,etc.).

Symptomatic:neurostimulation,surgicalcorrectionforptosis ifneeded.

47.Meningealsyndrome(Meningism):manifestations,diagnosis.

MeningealSyndrome

Manifestations

Generalcerebralsymptoms:

Intense headache(di useorlocalized:forehead,occiput)

Vomiting(sudden,oftenwithoutnausea,unrelatedtofoodintake)

Fever

Photophobia(sensitivitytolight)andphonophobia(sensitivitytosound)

Inseverecases: psychomotoragitation,delirium,hallucinations,seizures,lethargy, stupor,coma

Actual meningealsymptoms(reflectmeningealirritation):

Necksti ness: inabilitytopassivelyflextheneck duetomusclerigidity(notjust pain)

Meningealposture:patientliesonsidewithheadthrownbackandlegsflexed ("pointingdog"posture)

Kernig’ssign:unabletostraightenkneewhenhipisflexed→painor resistance

Brudzinski’ssigns:

Upper:passive neckflexioncausesinvoluntaryleg andarmflexion

Lower:passiveextensionofone legcauses involuntaryflexion ofopposite leg

Buccal:pressurebelow zygomaticarchescausesshoulderraisingand forearmflexion

Shoulder:passiverotationofheadcausescontralateralshoulderandarm flexion

Levinson’ssign:active neckflexioncausesmouthopening

Gordon’ssign:calfmusclecompressionproduces extensortoeresponse

Lesage’ssign(children):whenliftedbyarmpits,legsflexand remainflexed

Bikele’ssign(infants): resistancetoarmextension

Diagnosis

Historyandexamination: Identifyheadache,fever,necksti ness,associated symptoms

Lumbarpuncture:

MeasureCSFpressure

Analyzeappearance(color,clarity)

Cellcount(pleocytosisininfection)

Protein,glucose levels

Microbiological studies (Gramstain,culture,PCR)

Imaging(CT/MRI):toexclude masslesionorelevatedintracranialpressure beforeLP

Clinicaltests:PositiveKernig’sandBrudzinski’ssignssupportmeningealirritation diagnosis

48.Intracranialhypertensionsyndrome,characteristics. Leartificial correction.

IntracranialHypertensionSyndromeisaconditioncharacterizedbyanincreaseinpressure withintheskull,a ectingbraintissue,cerebrospinalfluid(CSF),andbloodvessels uniformly.

Aspect

Cause

SymptomsinAdults

Symptomsin

Children/Newborns

Signs

Diagnosis

MedicalCorrection

Details

Increasedintracranialpressure(ICP)duetobrain pathology(tumors,trauma,hemorrhage, encephalitis),cerebraledema,orsystemiccauses (heartfailure,COPD,hypercapnia)

Intenseheadache(worseinmorning/night),vomiting withoutnausea,nausea,visualdisturbances(blurred vision,diplopia,papilledema),drowsiness,irritability, seizures,hypertension,bradycardia,respiratory irregularity

Vomiting, prolongedcrying,developmentaldelay, bulgingfontanel, 'settingsun'eyes(downward gaze withsclerashowingabovepupils),poorlightreflex

Papilledemawithoptic nerveswelling,hemorrhages onfundus,pupillarychanges,cranialnervepalsies (esp.VI),muscleparesis,increasedBP,bradycardia, abnormalpulse

Clinicalexam,fundoscopy(papilledema),imaging (CT/MRI),lumbarpuncturewithICP measurement andCSFanalysis

-Maintainairway,oxygenation

-Elevatehead15-30°toimprovevenousdrainage

-Restrictfluidsto~1.5L/day;avoidfreewater(e.g., 5%glucose)

-Managebloodpressure, fever,seizures,agitation

-Avoidvasodilators

-Osmoticdiuretics(mannitol),loopdiuretics

Aspect

Details

 

(furosemide)

 

-Corticosteroids (fortumors)

 

-Mechanicalventilationandhyperventilation(acute

 

cases)

 

-Surgicalintervention(ventriculardrainage)if

 

indicated

 

Long-term ICP monitoringcriticalforsevere cases;

Prognosis/

outcomedependsoncause andpromptnessof

Monitoring

treatment

49.Dislocationbrainsyndromes. Clinicalcharacteristics.

BrainDislocationSyndrome

Pathogenesis

Braindoesnot fullyoccupyskull;subarachnoidspacesandcisternsallow displacement.

Increasedintracranialpressureorfocal lesionscausedisplacement(dislocation)of brainstructures throughnaturalduralfoldsorskullopenings (foramina).

Brainherniationisanalogoustoahernia; criticalcomplicationsarise whenbrain tissueispinched(infringed)compressingbloodvesselsanddisruptingcirculation.

Typesofherniation:Protrusion→Wedging→Infringement(increasedseverity).

Dislocations:lateral(transverse)oraxial(longitudinal)(alongbrainstemaxis).

TypesofDislocationSyndromes(clinicallysignificantones)

No.

DislocationType

Location&Description

 

 

Causescingulategyrus herniation,

 

Displacementofcerebral

compressesanteriorcerebralartery,

 

hemispheresunder

leadstolateralventricledeformation

1

falciformprocess

andedema

No.

DislocationType

Location&Description

 

 

Temporallobe herniatesthrough

 

Temporotentorial

tentorialnotch,compressingmidbrain

2

Displacement

andcranialnerves(IIIpalsy)

 

 

Cerebellartonsilsherniatethrough

 

Cerebellar-tentorial

foramenmagnum,compressingmedulla

3

Displacement

andupperspinalcord(life-threatening)

 

Displacementofpons

Ponsdisplacedintointerpeduncular

4

throughcerebellarforamen

cistern

 

Fillingofmiddle&side

 

5

cisternsaroundpons

Compressionofbrainstemstructures

 

Displacementofposterior

 

 

corpuscallosumdorsalinto

Seenwithhydrocephalus,severebrain

6

cistern

swelling

 

Displacementoffrontal gyri

 

7

intochiasmaticcistern

Causesvisualdisturbances

 

 

Braintissue bulgesthroughskulldefect

8

Externaldislocation

(fromtrauma)

ClinicalFeatures

Dependonlocation,size,speedofherniation

Earlysigns:headache, consciousnessalteration,oculomotor palsy(dilatedpupil), hemiplegia

Ipsilateralpupildilation(due tothirdnervecompression)with medialrectuspalsy

Hemiparesisipsilateraltolesion(Kernohan'snotchphenomenon)

ElevatedICPsigns:vomiting,bradycardia,hypertension

Alteredrespiratorypatterns;comainadvancedcases

Cerebellartonsilherniation→respiratoryandcardiovascularfailure →death

Diagnostics

Imaging: CT,MRItoconfirmherniationtype and plansurgical intervention

Echoencephalographycandetectlateraldisplacementsbutnotaxial

Lumbarpuncture iscontraindicatedduetoriskofprecipitatingherniation

Treatment

Addressunderlyingcause (tumor,hemorrhage,edema)urgently

Medicaltherapy:barbiturateanesthesia,controlledhypothermia,controlled hyperventilation,corticosteroids(tumors)

Surgicaldecompression(decompressivecraniotomy,ventriculardrainage)

Earlyinterventioncriticaltopreventfatalbrainstemdamage

50.Examinationofcerebrospinalfluid,thecompositionofcerebrospinalfluidinnormal andpathologicalconditions. Cerebrospinalfluiddynamicssamples.

CerebrospinalFluid (CSF)Study

NormalCSFCharacteristics

Volume:~150 mltotal,renewed~6times/day

Appearance:Clear,colorless

Pressure:80–120mmH2O

Protein:~0.3g/L(15-40 mg/dL)

Cells:1–5/mm³,mostlyleukocytes

Glucose:2.7–3.7mmol/L(~2/3of bloodglucose)

Chlorides:~110mmol/L

Functions:Nutrientsupply,wasteremoval,neurotransmittertransport,bactericidal activity

CSFCollectionMethods

Lumbarpuncture:Mostcommon, betweenL3-L4

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