Ear Reconstruction Flashcards
Ear molding should be in the first month only
F Timely ear molding less than 3 months of age, ideally less
than I month of age is a powerful option for miscellaneous
ear anomalies to obviate the need for surgery
Blood supply to the ear ?
vascular supply comes from the
superficial temporal anteriorly and posterior auricular vessels posteriorly.
The sensory supply to the auricle
The sensory supply to the auricle is mainly derived from the
inferiorly coursing greater auricular nerve ( C2-CJ
the neve supply to the upper portion of the ear?
Upper portions of
the auricle are supplied by lesser occipital (C2-C3) and auriculotemporal nerves (V3) (tragus and crus helicis)
Nerve supply to the the concha
is supplied by a branch of vagal nerve
what is Arnold nerve?
Arnold nerve (CN 7,9,10) 1s
an auricular branch of the vagus nerve that receives contributions from
the facial nerve and glossopharyngeal nerve. Arnold’s nerve supplies the posterior inferior external auditory canal and meatus, and inferior conchal bowl.
Lymphatic drainage of the ear?
correlates with six embryonic hillocks. The tragus, root of the helix, and superior helix arise from first branchial
arch (anterior hillocks 1-3) and drain into parotid nodes.
The antihelix, antitragus, and lobule arise from second branchial arch (posterior hillocks 4-6) and drain into cervical nodes.
When auricle starts to protrude
The auricle begins to protrude from the developing face at approximately 3 to 4 months of gestation
The auricle arises
from which branchial arch?
The auricle arises
from two branchial arches: mandibular branchial arch (first) and
hyoid branchial arch (second)
how much the normal ear size ?
The vertical height of an adult auricle is approximately 55 to
65 mm. Width is approximately 50% to 55% of its length
auricle is normally located approximately 10 mm behind the sideburn
auricle is normally located approximately 20 mm behind the sideburn
What is cryptosia ?
in which upper pole of ear
cartilage is buried underneath the scalp The superior auriculocephalic sulcus is absent but can be demonstrated when you pull up the helical pole
The common cartilage deformity in cryptotia?
A common cartilage deformity associated with cryptotia is helix-scapha adhesion, which may be addressed by cartilage
remodeling techniques.
Type of stahl ears
Type I: Obtuse-angled bifurcation of antihelix; looks as though
superior crus is missing
Type 2: Trifurcation of antihelix
Type 3: Broad superior crus and broad third crus (protruded
scaphoid fossa)
Ear molding is not benefit in Stahl ear ?
Ear molding may work well if ear molding is started in early
infancy.
what is Constricted Ear?
helix and
scapha fossa are hooded, and crura of antihelix is flattened
the surgical tech of (group 1,2A Tanzer classification
The musgrave technique is a useful method to expand the helix.
When superior crus is deficient, partial helix plus superior crus frame from rib cartilage5 can normalize the deformity
The features of Tanzer group 2B group
Has both skin and cartilage defects in the
upper one-third of the auricle. The loss of folding may
involve anti helical crura, and hooding is more pronounced.
The height of the ear is sharply reduced
Park tech in the reconstruction of ear deformity of class 2B Tanzer involve 6 rib as a cartilage graft
F Grotting flap (postauricular
flap) for skin defect and 8 th rib for cartilage defect
What are the option of management of Tanzer group 3
Brent recommends treating severe constricted ear as if it is a
form of microtia, when the construction is severe enough to
produce a height difference of 1.5 cm.
Nagata recommends treating severe constricted ear as a concha-type microtia, to replace the defective framework with a full rib cartilage
framework
surgical molding is possible in hypo plastic and non hypoplastic ear
F If ear deformities are not hypoplastic, nonsurgical correction is easy and reliable
Stahl ear protruding ears and cryptotia respond responds
well to the nonsurgical correction
Stahl ear responds
well to the nonsurgical correction only during the neonatal period,
whereas protruding ears and cryptotia respond until approximately
6 months of age (Matsuo)
Most agree that if ear molding is started after 1 months of age, the response tends to be poor
F Most agree that if ear
molding is started after 3 months of age, the response tends to be
poor
What is the most congenital ear anomaly that responds poorly to molding?
Helix-antihelix adhesion responds poorly to the ear molding
treatment and may not be an indication of the ear molding
the most common complication of molding ?
Skin
irritation is probably the most frequent complication, possibly due
to tape or adhesive.
Percentage of unilateral microtia
80% to 90% of microtia is unilateral, and 10% to
20% is bilateral
common syndrome associated with microtia
is hemifacial microsomia and Treacher-Collins syndrome
Treacher-Collins syndrome, inherited in an autosomal
dominant fashion, often presents with bilateral microtia
Isolated microtia rarely run
in families
T
Nagata’s classification
Anotia: Absence of auricular tissue
Lobule type: Vestige ear with lobule, without concha, acoustic
meatus, and tragus
Concha type: Vestige ear with lobule, concha, acoustic meatus,
and tragus
Small concha type: Vestige lobule with small indentation of concha (need lobule-type construction)
Atypical microtia: Cases do not fall into previous categories
Hoe many patients with microtia have associated anomalies
About 20% to 60% of children with microtia have associated anomalies or an identifiable syndrome; therefore, individuals with microtia should be examined for other dysmorphic features
Always need genetic counseling with microtia
F If there is
family history of the syndrome, genetic counseling may be necessary
Moderate defect Cartilage Construct for Constricted Ear, how ?
Floating rib (Park)
Hemifacial microsomia is often associated with difficult airway for intubation t f
T
partial facial paralysis is frequent
finding in microtia
T
Percentage of cholesteatoma in microtia?
cholesteatoma (squaipous epithelium
trapped in the middle ear), present in 4% to 7% of atresia
In bilateral microtia, som times we need to use of bone-conductive hearing aid .
F In bilateral microtia, early and conscientious use of bone-conductive hearing aid is imperative for hearing and speech development