ME Disorders (Cholesteatoma) Flashcards

1
Q

what is a cholesteatoma

A

“pseudotumors” that can occupy the external ear canal, ME cavity, or extend through the mastoid bone into the brain cavity

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2
Q

how do cholesteatoma manifest

A

manifest highly aggressive, progressively enlarging, tumor-like characteristics

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3
Q

how do they manifest/fxn like a tumor

A

They are highly erosive and may cause destruction of bone and other tissue
Recently, highly invasive fibroblasts were found in cholesteatoma that are not seen in normal skin, which may explain the aggressive behavior of a cholesteatoma

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4
Q

Cholesteatoma can be

A

congenital or acquired

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5
Q

what is a congenital cholesteatoma

A

Almost always present in children
Median age is ~ 5 years
3:1 male to female ratio
The TM can be normal without a history of perforation, otorrhea, or myringotomy
Most common location is the anterior-superior quadrant
Etiology is controversial

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6
Q

what are acquired cholesteotoma

A

More common than congenital
Often due to chronic or untreated otitis media with effusion or trauma leading to TM perforation
Also occurs as a result of TM retraction in the pars flaccida or posterior-superior quadrant
Previous ear surgery/TM perforation also may be the growth site
Slow growing condition, initially with no symptoms
Usually presents first with a hearing loss

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7
Q

what are iatrogenic cholesteatomas

A

May result because of a blunt knife used during myringotomy
May lead to implantation of squamous epithelium in ME cavity

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8
Q

how do chol grow

A

by forming a keratinized epithelial layer and a fibrous subepithelial layer called a matrix

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9
Q

What forms a keratoma

A

Keratin (dead skin cells and debris) builds up and gets covered by cells

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10
Q

what does a keratoma do

A

evoke inflammatory reaction leading to formation of a cholesteatoma, mostly in the attic area of the ME cavity

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11
Q

how does cholesteatoma result in mastoiditis

A

they will grow, engulf, and erode the ossicles, bones of the tympanic cavity

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12
Q

A cholesteatoma can become

A

secondarily infected producing otorrhea (foul smelling discharge)

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13
Q

iatrogenic

A

something related to surgery procedures

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14
Q

if large enough, can exert pressure on CN VII causing

A

causing facial palsy

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15
Q

what type of tymp would you see with cholesteatomas

A

depends on size, location & how much it has damaged

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16
Q

normal tymp

A

no damage

17
Q

type as

A

cholesteatoma is filling the ME cavity; a stiffness dominated system

18
Q

type ad

A

If ossicular disarticulation has occurred t

19
Q

type b flat with low volume

A

If it has caused TM peroration and is filling up the ME cavity

20
Q

type b high volume

A

If the cholesteatoma is not big enough to fill up the ME cavity and TM perforation is present

21
Q

Auditory sensitivity varies depending on

A

underlying damage

22
Q

Hearing is normal

A

if the ossicular chain is intact and the cholesteatoma only caused TM perforation or no perforatio

23
Q

chl

A

f ossicular disarticulation occurred

24
Q

Mixed hearing loss

A

if goes into the inner ear

25
Q

what are PT complaints of cholesteatoma

A

Foul smelling discharge and often bleeding
Hearing loss verified by an audiologic evaluation
Otalgia, headache, or occasionally mild dizziness

26
Q

is diagnosis difficult of cholesteatoma

A

Usually diagnosis is not difficult because it can be visualized on a microscopic exam of the ear in the physician’s office

27
Q

why ct scan is done

A

To identify potential damage caused by the cholesteatoma, including facial nerve dehiscence and ossicular damage, for better patient counseling
But many otologists do not order a CT scan because it does not change the management

28
Q

what is the primary treatment

A

surgical removal

29
Q

why do they not like bleeding into the surgical site

A

makes it harder to see

30
Q

why are antibiotic steroid drops prescribed prior to surgery

A

decrease inflammation and granulation tissue, which decreases bleeding during surgery

31
Q

surgery can result in

A

HL (tm and ossicles may be removed)
prosthesis
mastoiditis if present requires mastoidectomy

32
Q

what can lead ot recurrences

A

if not all of it is removed
if underlying pathology that led to primary cholesteatoma (ET dysfunction, poor mastoid ventilation) is not corrected a well

33
Q

Patients need to be counseled that surgery can cause complications depending on the size and location of the cholesteatoma, such as

A

Hearing loss (permanent – CHL, mixed, or SNHL)

Facial paralysis

Dizziness

Tinnitus

Intracranial complications such as
meningitis
intracranial absess

Recurrence of the cholesteatoma even after surgery