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