Chapter 31 - Otology anatomy, embryology, radiology Flashcards
Where outer, middle and inner ear structures come from embryologically
Outer and middle: 1/2 arches, 1 pouch/groove
Inner ear: bilateral otic placodes
Detection of angular and linear acceleration
Semicircular canals- angular
Utricle, saccule- linear (horiz, vert, respectively)
Pathway of auditory information to brain
Hair cells Auditory nerve Cochlear nucleus Superior olivary complex (crossover here) lateral lemniscus inferior colliculi medial geniculate body auditory cortex (Upper Temporal Lobe/Heschl)
Cochlea basilar membrane vs apex
BM: thick, stiff, narrow, for high frequencies
Apex: thin, flexible, wide for low frequencies
Anatomy of ear canal
Lateral third cartilaginous, hair follicles, cerumen/sebaceous
Medial 2/3 osseus
Length and resonance frequency of EAC
2.5cm adults
3-4kHz
6 Hillocks of His
Mesenchyme buds surrounding dorsal end of 1st branchial cleft. 1-3 mandibular (1st) arch, 4-6 from hyoid (2nd) arch
1- tragus
2-3- helix
4-5- antihelix
6- antitragus
Function of auricle
Collect, direct sound toward TM
Shape creates small high-pitched frequency resonances helping you localize sound vertically
From which branchial structure does the EAC develop?
1st branchial groove
Treacher-Collins
ALso called mandibulofacial dysostosis AD, complete penetrance, variable expression down-slanting palperal fissures auricular malformations (tag, stenosis, atresia) ossicular abnormalities malar hypoplasia, mandibular hypoplasia flat nasal bridge cleft palate dental
Goldenhar syndrome (Oculo-Auriculo-Verteral Synd)
1/2 arch malformation
Unilateral craniofracial malf
hemifacial microsomia, eye, strabismus, anotia, tags, atresia
Scoliosis
Branchio-oto-renal syndrome
AD Hypoplastic/absent kidneys pit/tag middle ear malformation branchial cleft cyst/fistula
CHARGE
Coloboma Heart Atresia choana Retard growth/develop Genital (hypogonad) ear (low set, lop ears, asymmetric pinnae)
DiGeorge sequence
22q11 deletion
Hypoplasia thymus/parathyroid
Cardiovascular
Low ears, micrognathia, hypertelorism, short philtrum, cleft palate, choanal atresia
Crouzon syndrome
AD
Craniosynostosis
exophthalmos, hypotelorism, strabismus, beak-shaped nose, hypoplastic maxilla, low ears, atresia/stenosis canal
Middle ear anatomy: what it contains, and is continuous with
1-2cm^3
ossciles, stapedius, tensor tympani, chorda
continuous with mastoid air cells via antrum, nasopharynx via ET
1st branchial arch: ossicles
head/neck malleus
body incus
2nd arch: ossicles
long process malleus, incus
stapes
Where does stapes footplate derive from
2nd arch and otic capsule
Embryology of annulus
NCC-origin, mesenchyme, ossifies during 3rd month gestation
Embyrology of TM
outer ectoderm
middle mesoderm
inner endoderm
Stapedius and tensor tympani
CN VII, V3
contracts with high intensity sound, especially low frequency
Stiffen ossicular chain to decrease sound transmission
Protect cochlea from damage
reduce intensity of low-frequency background noise to preserve higher frequency speech info
Four sections of temporal bone
squamous
petrous
tympanic
mastoid
Describe course of CN VII through T bone
Exit IAC
Labyrinthine- superior to cochlea, angle forward just sup/lat to cochlea to reach geniculate ganglion, then posterior/inferior turn (first genu)
Tympanic- extend down from genu posteriorly, laterally along medial wall of tympanic cavity, above oval window, below lateral SCC, reach pyramidal eminence, then drop sharp inferior for second genu
Mastoid- after genu, downward in posterior wall of tympanic cavity, anterior wall of mastoid, exit SMF