Lecture 13 Flashcards

(36 cards)

1
Q

what is meningitis

A

it is an inflammatory process, usually caused by infection.
chemical meningitis can occur in response to a nonbacterial irritant in the subarachnoid space

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2
Q

acute pyogenic meningitis (bacterial meningitis)
in what ages ar the most common bacterias

A

bacteria causing
in neonates the most common is escherichia coli and group B strep
in adolescence and in young adults neisseria meningitis is the most common pathogen
in older patients strep pneumonia and listeria monocytogenes are most common

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3
Q

what is aseptic meningitis

A

inflammation of the meninges not caused by bacteria and due to viral infection
symptoms: neck stiffness, fever, change in consciousness, it is less severe
in the CFD we usually find lymphocytosis ( increased lymphocytes) , moderate protein elevation, normal glucose levels.

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4
Q

brain abscess

A

caused by bacterial infections
infection can reach the brain via direct implantation, local spread, hematogenous spread

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5
Q

viral encephalitis

A

infection that affects the brain itself usually accompanied by inflammation of the meninges

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6
Q

Fungal Encephalitis

A

Fungal infections of the brain typically cause granulomas or abscesses in the brain tissue (parenchyma), and are often associated with meningitis. Each fungus tends to show a distinct pattern:

  1. Candida albicans
    Usually causes multiple microabscesses
    May or may not form granulomas
  2. Mucormycosis (Mucorales family)
    Causes rhinocerebral infections (nose/sinuses)
    Classically seen in diabetics with ketoacidosis
    Spreads to the brain via:
    Vascular invasion
    Direct extension through the cribriform plate
  3. Aspergillus fumigatus
    Strong tendency to invade blood vessel walls
    Leads to widespread hemorrhagic infarctions due to thrombosis
  4. Cryptococcus neoformans
    Seen in immunocompromised patients
    Causes meningitis or meningoencephalitis
    May be:
    Fulminant and fatal within 2 weeks
    Or slow and chronic, lasting months to years
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7
Q

what are the signs for meningitis

A

kernels sign –> stiffness of the hamstrings, instability to straighten leg when the hip is flexed to 90 degrees

brudzinskis sign –> supine position, passive flexion of neck, spontaneous flexion of the hips and knees

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8
Q

cysyicercosis

A

consequence of end stage infection by the tape worm Xenia solium.
cysts can be found throughout the body but are mainly common in the brain the the subarachnoid space it can causes seizures

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9
Q

prion disease

A

(TSE) neurodegredation, vacillation and deposition of the abnormal prion protein
symptoms:
- loss of motor control
- dementia
- paralysis
- encephalitis
- wide spread neuronal loss

it can be hereditary spread or infectious via diet, surgical procedure like corneal transplants

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10
Q

creutzfeldt Jakob disease

A

it is rapidly progressive, neurodegenerative disorder, caused by prion protein
we have 3 categories:
- sporadic: individual has no risk factors
- hereditary: family history
- acquired: exposure to brain/ nervous system tissue
symptoms:
personality change, depression, ataxia, insomnia, dementia, involuntary jerky movements

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11
Q

primary disease of myelin

A
  1. multiple sclerosis –> inflammatory and demyelinating disease, progressive, body own immune cells attack the nervous system and the myelin is destroyed, cause is unclear but can be environmental or hereditary. signs: vision impairment, tingling, difficulty walking, memory loss
  2. lysosomal storage disease

3) peroxisomal disorders e.g Zellweger syndrome

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12
Q

metabolic disorders

A

hypoglycaemia: low glucose can cause global hypoxia the highly venerable areas are hippocampal neutrons and spared areas are cerebellar purkinje cells

hyperglycaemia: seen in poorly controlled diabetes mellitus
I can occur in diabetic ketoacidosis and hyperosmolar coma and it can lead to confusion, coma and stupor and it is caused by intracellular dehydration from a high blood sugar

hepatic encephalopathy:
caused by liver dysfunction, accumulation of neurotoxic substances

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13
Q

list of toxins that can effect the bairn

A

metals such as:
- lead ( diffuse encephalopathy)
- arsenic and mercury

  • organophosphates in pesticides
  • environmental polluters such as carbon monoxide
  • ethanol In high doses can lead to cerebellar dysfunction
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14
Q

alzheimers

A

degenerative brain disorders –> progressive memory loss, impaired thinking, disorientation and changes in personality and mood, degeneration of brain neurone esp in the cerebral cortex and presence of neurofibrillary tangles and plaques containing beta amyloid cells

attacks the nerves and the brain and neurotransmitters, causes plaques and bindles

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15
Q

frontotemporal dementia

A

deterioration of personality. prominent frontal and temporal lobe
- neuronal loss and gilosis, ballooned tumors

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16
Q

Parkinson’s disease

A

chronic and progressive disorder of the CNS, it is a motor disorder
direct loss of cells In the substantial nigra
these cells produce dopamine, loss of dopamine can cause the neuron’s in the brain to fire out of control, so the person can not control their movement

most cases are idiopathic and caused by Brian trauma/ viral inflammation/ poisoning by manganese/ intoxication with MPTP

17
Q

Huntington’s

A

inherited, faulty gene on chromosome 4 (IT-15) located in exon 1 –> uninterrupted polyglutamine stretch within the N terminus of the Huntington molecule (CAG)
symptoms: uncontrolled jerky movements, disorganised gait, impaired chewing and swallowing

18
Q

ALS (amyotrophic lateral sclerosis)

A

neurodegenerative disease of upper and lower motor neurone of Brain and spinal cord

first mutation was discovered in the SOD1 gene on chromosome 21

19
Q

giolomas and astrocytoma

A

gliomas: tumors of the Brain parenchyma
main types of gliomas:
Astrocytomas – resemble astrocytes
Oligodendrogliomas – resemble oligodendrocytes
Ependymomas – resemble ependymal cells

Astrocytomas are tumors that arise from astrocytes, a type of glial cell in the brain.
There are several types, each with distinct histologic features, locations, and clinical behavior.

20
Q

adult primary brain tumors

A

1) Glioblastoma is the most aggressive and most common type of primary malignant brain tumor in adults. commonly occurs in the cerebral hemispheres (especially frontal and temporal lobes) Can cross the corpus callosum, producing a classic “butterfly glioma” appearance on imaging

2) Oligodendrogliomas are primary brain tumors that arise from oligodendrocytes, the cells responsible for producing myelin in the central nervous system.commonly found in the cerebral hemispheres, especially the frontal lobes

3) Meningiomas are typically benign, slow-growing tumors that arise from the meninges, specifically the arachnoid cap cells of the dura mater.

4) Hemangioblastomas are rare, benign vascular tumors of the central nervous system, arising from blood vessel-forming cells (endothelial precursors or stromal cells). Most commonly in the cerebellum
Also found in the brainstem, spinal cord, and sometimes retina

5) pituitary adenoma can be silent or hyper functioning, primary adenoma generally refers to a benign tumor that arises from glandular epithelial tissue.

21
Q

childhood brain tumours

A
  1. pilocytic astrocytoma: found in posterior fossa, benign, sciatic appearance with mural nodule
  2. medullloblastoma: common malignant brain tumor involves cerebellum and can compress the 4th ventricle causing hydrocephalus
  3. ependymoma: found in the 4th ventricle can cause hydrocephalus
  4. craniopharyngioma: classification is common, associated with high recurrence rate
  5. pineal gland tumors: more common in males, parinaud syndrome
22
Q
  1. primary CNS lymphoma
  2. primary brain germ cell tumors
  3. meningiomas
A
  1. diffuse large B cell lymphoma and is associated with EBV and can occur anywhere in the CNS esp periventricular
  2. occurs along the midline in the pineal region or the supra cellar region
  3. usually benign, from arachnid meningothelial cells
23
Q

what is conjunctivitis

A

Conjunctivitis (Pink Eye)
Definition: Inflammation of the conjunctiva (the membrane covering the white of the eye and inner eyelid)
Can be acute or chronic

Causes:
Most commonly viral or bacterial
Includes gonococcal and chlamydial infections
Transmission:
Spread by direct contact, such as:
Fingers
Towels
Handkerchiefs
Can spread to the other eye or to other people

24
Q

red eye

A

without vision loss: allergic, bacterial and viral conjunctivitis

with vision loss: acute anterior uveitis, acute angle closure glaucoma, corneal ulcer

signsL severe eye pain, severe photophobia, reduced visual activity,

25
gonococcal conjunctivitis
acquired through contact with infected genital secretions, causes the copious prudent discharge
26
dry eyes ( keratoconjunctivitis sick)
Patient Complaints Mild to moderate: Dryness Redness Foreign body sensation (feeling like something is in the eye) Severe cases: Persistent, intense discomfort Photophobia (sensitivity to light) Difficulty moving the eyelids Excessive mucus secretion Examination Findings Marked conjunctival redness Loss of the normal shiny appearance (luster) of the conjunctiva and cornea Presence of epithelial keratitis (damage to the surface cells of the cornea), which may progress to: Ulceration (open sores on the cornea) Mucous strands visible on the eye surface
27
CORNEAL ABRASIONS
Clinical Features Severe eye pain Photophobia (light sensitivity) Often a history of eye trauma, commonly from: Fingernail Piece of paper Contact lens use Examination Measure visual acuity Examine cornea and conjunctiva carefully with light and magnification (loupe) Check for foreign body presence or corneal injury
28
UVEITIS
Uveitis is usually immunologic but can also occur due to infective or neoplastic pathology. Types- acute or chronic -anterior, intermediate or posterior (sluggish pupil) -granulomatous or non-granulomatous (b/gradual loss of vision, no pain/redness, recurrent)
29
NORMAL ANTERIOR SEGMENT & PUPIL & PAINLESS SUDDEN LOSS OF VISION
Retinal detachment Vitreous haemorrhage Venous occlusions Arterial occlusions PCA territory stroke
30
glaucoma
A group of eye diseases characterized by optic nerve damage usually caused by increased intraocular pressure (IOP), leading to progressive, irreversible vision loss. - Primary Open-Angle Glaucoma (POAG) Most common form Gradual blockage of the trabecular meshwork Slow, painless loss of peripheral vision (tunnel vision) - Primary Angle-Closure Glaucoma (PACG) Sudden closure of the anterior chamber angle Rapid increase in IOP Symptoms: severe eye pain, headache, nausea, vomiting, blurred vision, halos around lights Ophthalmic emergency Secondary Glaucoma Due to other eye conditions or injuries (e.g., trauma, inflammation, tumors, steroid use) -Congenital Glaucoma Present at birth due to developmental abnormalities of the anterior chamber angle
31
OCULOMOTOR PALSIES
Complaints- the recent onset of diplopia /squinting/drooping of the eyelid Examination- VA, pupil reaction, eom , ptosis Medical officers role -Any patient with recent-onset isolated third nerve palsy, particularly if there is pupillary involvement or pain, must be referred emergently for dysfunction or other neurologic abnormalities.
32
PROPTOSIS –FORWARD PROTRUSION OF EYE
omplaints- forward protrusion of the eye, diplopia, foreign body sensation, grittiness Causes- hyperthyroidism, orbital tumors, pseudotumor orbit Examination- proptosis, conjunctival congestion, and chemosis Criteria for referral -Moderate to severe grave’s disease -Decreased vision -Recent onset diplopia
33
retinal detachment
Separation of the neurosensory retina from the underlying retinal pigment epithelium (RPE), leading to vision loss if not promptly treated. Types - Rhegmatogenous (most common) Due to a retinal tear or break allowing fluid to accumulate under the retina Tractional Caused by fibrous or scar tissue pulling the retina away - Exudative (serous) aka nonrhegmatogenous Caused by fluid accumulation beneath the retina without a tear (e.g., inflammation, tumors)
34
otitis externa
inflammation of the external auditory canal, associated with water exposure, malignant otitis externa: infection causing osteomyelitis, may lead to cranial nerve palsies
35
otitis media
inflammation of the middle ear can b e due to haemophilus influenzae, step pneumoniae, maraxella catarrhalis and is associated with eusthian tube dysfunction. mastitis - infection of the mastoid process of the temporal bone
36
causes of hearing loss
presbycubis: aging related progressive hearing loss sue to destruction of hair cells at the cochlear base