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30 ANATOMY OF THE TEMPORAL BONE WITH SURGICAL IMPLICATIONS
Figure 50
This photograph shows the sinus tympani as it lies medial to the facial nerve, separated from the round window niche by the subiculum. Medially lies the ampullated end of the poste­rior canal. The carotid canal is located close to the basal turn of the cochlea (male, age 69yr).
Figure 51
The protympanum is that portion of the middle ear space anterior to a coronal plane passing through the anterior margin of the tympanic annulus. It leads into the eustachian tube. Note the hook end of the cochlear duct and the utric­ular opening into the ampulla of the posterior canal (female, age 68yr).
THE PINNA
Chapter 2
The Pinna and External Auditory Canal
In vernacular parlance, the term “ear” evokes an image of that bilaterally symmetric, cartilage-framed, cranial appendage known as the pinna or auricle. This structure acts to focus and localize sound; otoplasty (surgical correction of lop ears), if not properly done, can increase the error in the lat­ter function from 4° to 20° (1). The pinna normally rests at an angle of 30° to the sagittal plane of the head, while the concha lies at an angle of 90° (⫾15°) to the bony cortex of the mastoid (2). The pinna’s growth parallels overall body growth until approximately nine years of age; in general, the left ear is smaller than the right (2). This text is not concerned with auricular congeni­tal deformities and diseases. Suffice it to say that, due to the multi-component nature of its embryologic development, the pinna manifests a wide variety of configurations. Despite this variability, there are certain relatively constant features that can be recognized in the human ear.
The topography of the visualized pinna is determined almost solely by the contour of its underlying cartilaginous frame. The flange-like pinna has a convex medial surface which attaches to the head at its medial one-third; the lateral surface is concave. The major concavity of the lateral aspect of the pinna is the concha (Fig. 1). Anteriorly, the tragus delimits the concha as it extends over the orifice of the external auditory canal. Superiorly and poste­riorly the concha is bounded by the anthelix and its anterior crus. The infe­rior extent of the concha is determined by the antitragus, which is separated from the anthelix posteriorly by the posterior auricular sulcus, and from the tragus anteriorly by the intertragic incisura. The concha is partitioned at the crus of the helix into a superior cymba concha and an inferior cavum concha; the latter depression points to the meatus of the external auditory canal. Anteroinferiorly, the crus of the helix is separated from the tragus by the anterior incisure. The helix, with its furled edge, sweeps superiorly and pos­teriorly from the crus of the helix to end at the lobule; a projection, the Darwinian or auricular tubercle, occasionally exists at its posterosuperior aspect. There are two additional depressions of note. As it curves antero­superiorly, the anthelix bifurcates into two crura, between which lies a depression known as the triangular fossa. The scaphoid fossa is a trench-like groove separating the helix from the anthelix. Lop ears lack an anthelix, with the consequence that the helix assumes an outstanding position; therefore in a surgical correction an anthelix must be created.
The medial aspect of the pinna is a negative relief model of the lateral aspect. The scaphoid, conchal, and triangular eminences correspond to the respective fossae on the lateral surface. Similarly, depressions of the medial aspect (i.e., the transverse sulcus of the anthelix, the sulcus of the crus of the
31
32 ANATOMY OF THE TEMPORAL BONE WITH SURGICAL IMPLICATIONS
Figure 1
The right auricle (pinna) of the co-author (AJG) showing the principal anatomic features of its lateral surface.
helix, and the fossa of the anthelix) correspond to elevations of the lateral surface of the pinna and are hidden by the cranial attachment of the pinna.
The framework of the pinna consists of elastic cartilage, the contours of which determine its topography; the cartilage measures 0.5 to 2mm in thick­ness (3). It consists of two furled plates of cartilage separated by the termi­nal incisure. The larger plate supports the major bulk of the pinna; the lesser underlies the tragus and is connected to the larger by a narrow isthmus. While the cartilage features much the same topography as the surface of the pinna, there are additional elements which are obscured by its mantle of skin and subcutaneous tissue. Anteriorly, from that portion of the helix just supe­rior to the crus, arises the spine of the helix. Inferiorly, the antitragohelicine fissure separates the tail of the helix (cauda helicis), the posteroinferior ter­minus of the helix, from the antitragus.
CHAPTER 2: THE PINNA AND EXTERNAL AUDITORY CANAL 33
The pinna is attached to the cranium by its skin, cartilage, and a com­plex of muscles and ligaments. There are three extrinsic ligaments and three extrinsic muscles, both sets referred to as superior, anterior, and posterior. The superior ligament links the superior aspect of the bony external auditory canal to the spine of the cartilaginous helix, the anterior ligament connects the zygoma to the helix and the tragus, and the posterior ligament attaches the eminence of the concha to the mastoid process.
The three extrinsic muscles originate from the galea aponeurotica of the scalp. The superior auricular muscle inserts upon the eminence of the tri­angular fossa, the anterior auricular muscle inserts upon the spine of the helix, and the posterior auricular muscle inserts upon the eminence of the cavum concha.
The six intrinsic auricular muscles show great individual variability in their extent of development and are poorly represented in man; four are found on the lateral surface and two on the medial surface. On the lateral surface, the helicis major extends from the spine of the helix to attach tangen­tially to the anterosuperior curve of the helix. The helicis minor hugs the crus of the helix. The tragicus overlies the tragus, and the antitragicus spans the antitragohelicine fissure between the tail of the helix and the inferior aspect of the antitragus. On the medial surface, the transverse auricular muscle links the eminence of the scaphoid fossa and the cavum concha. The oblique auricular muscle connects the eminence of the triangular fossa and the cymba concha.
The skin and subcutaneous tissue reproduce the irregular contours of the cartilaginous frame; the skin of the medial aspect is only loosely attached, while on the lateral surface it is snugly secured by subcutaneous areolar tis­sue. The usual skin adnexal structures are present, including sebaceous and sudoriferous (sweat) glands, and hair. The sebaceous glands are distributed both medially and laterally, especially in the regions of the concha and trian­gular fossa (4). Sudoriferous glands are sparse. A rudimentary type of hair is in abundance over the entirety of the pinna; in elderly male persons, the hairs may be long and large, especially over the tragus and antitragus.
The lobule, the inferior appendage of the pinna, is essentially a fibro­fatty nodule. While the lobule has no known physiologic function, its adi­pose tissue serves as a reservoir for autogenous tissue grafts and its conven­ient anatomical site serves admirably as a tethering base for ornamentation.
THE EXTERNAL AUDITORY CANAL
Normal Anatomy
The external auditory canal is approximately 2.5cm in length and serves as a channel for sound transmission to the middle ear. It also functions to protect the middle and inner ears from foreign bodies and fluctuations in environ­mental temperature (1). Its lateral one-third is bolstered by elastic cartilage oriented in an upward and backward fashion; its anterior aspect is pierced by two or three variably present vertical fissures known as the fissures of Santorini (Fig. 6); these fissures are a potential route for spread of infections or neoplasms between the external auditory canal and the parotid gland.
The medial two-thirds of the external auditory canal is osseous and is oriented in a downward and forward direction. Because of the different angulations of the fibrocartilaginous and bony canal walls, the adult auricle
34 ANATOMY OF THE TEMPORAL BONE WITH SURGICAL IMPLICATIONS
must be pulled upward and posteriorly to achieve alignment during otoscopic examination.
The narrowest portion of the external auditory canal or isthmus is located just medial to the junction of the bony and fibrocartilaginous canals. The inferior tympanic recess is a depression in the inferior aspect of the osseous canal. Because of the angulation of the tympanic membrane, the canal is approximately 6mm longer anteroinferiorly than posterosuperiorly, thus creating an acute angle between the tympanic membrane and anteroinferior
Figure 2
This horizontal section demonstrates the anatomy of the normal osseous external auditory canal (EAC). The ante­rior wall of the canal forms an acute angle with the tympanic membrane. An excessive convexity of the anterior wall can impair otoscopic visualization of the anterior part of the tympanic membrane. Surgically created dehis­cences of the anterior canal wall can result in herniation of the contents of the mandibular fossa into the EAC (female, age 32 yr).
Figure 3
In our collection of temporal bones there are several examples of pneumati­zation of the tympanic bone (male, age 70 yr).
CHAPTER 2: THE PINNA AND EXTERNAL AUDITORY CANAL 35
bony canal wall (Fig. 2). Although the condition is unusual, our collection con­tains several examples of pneumatization of the anterior wall of the external auditory canal (Fig. 3).
The skin of the osseous canal is much thinner than that of the fibrocarti­laginous portion (Fig. 4), measuring about 0.2mm in thickness (3), and is continuous with the skin of the tympanic membrane. The subcutaneous layer has no glands or hair follicles. The bony posterior wall of the external auditory canal, which overlies the mastoid air cells, may be extremely thin (Fig. 4).
The thinness of the skin of the bony external auditory canal has the fol­lowing clinical implications: (1) it is easily traumatized during manipula­tions such as removing cerumen, (2) it is easily torn in the course of surgical procedures such as tympanotomy, and (3) it permits thermal irritation of the periosteum and consequently the formation of exostoses caused by swim­ming in cold water.
The skin of the fibrocartilaginous part of the canal averages 0.5 to 1mm in thickness (3), with an epidermis of four layers (basal, squamous, granular, and cornified) blanketing a true subcutaneous layer. The lateral one-third of the fibrocartilaginous canal is replete with hair follicles, but they are less numerous in the medial part. Both sebaceous and modified apocrine (ceru­minous) glands (Figs. 5–7) develop from the outer root sheath of hair folli­cles; hence their numerical distribution follows a pattern similar to that of the hair follicles. In addition, the modified apocrine glands are found mainly on the superior and inferior walls of the canal. Arrector pili muscles are not found in association with the hair follicles in any portion of the external auditory canal.
The apocrine glands are the ceruminous glands of the ear canal (Fig. 7). They are located in the dermis deep to the sebaceous glands and have three major components (3): (1) a coiled secretory portion, (2) a secretory duct within the dermis, and (3) a terminal funnel. A myoepithelial cell layer is associated with the coiled secretory portion.
Main and Lim (5) detected both apocrine and eccrine modes of secre­tion in these glands. Moreover, they found that these modified apocrine
Figure 4
Surgical enlargement of the external auditory canal (EAC) (canalplasty) is necessarily limited by the thinness of its bony walls, both anteriorly and posteriorly (female, age 67 yr).
36 ANATOMY OF THE TEMPORAL BONE WITH SURGICAL IMPLICATIONS
glands secreted a heterogeneous population of granules as well as secretory vesicles. The exact nature of their secreted product is unclear. They are easily differentiated from the parotid glands which consist principally of serous cells (Fig. 8). The sebaceous glands (Fig. 9) expel the combined prod­ucts of several acini into the hair follicles via short excretory ducts. These sebaceous glands manifest the holocrine mode of secretion; they contain only one type of secretory granule, presumed to consist of squalene and sat­urated fatty acids (5).
Acute circumscribed external otitis is a bacterial infection of a seba­ceous or apocrine gland. It is an extremely painful disorder requiring aggres­sive antibiotic and pain therapy. Acommon cause is swimming in bacterially contaminated water.
Figure 5
This schematic drawing illustrates the adnexae and secretory system of the skin of the external auditory canal. Source: Courtesy of Main and Lim (5).
CHAPTER 2: THE PINNA AND EXTERNAL AUDITORY CANAL 37
Chronic external otitis is a low-grade inflammatory disorder of the skin of the external auditory canal, characterized symptomatically by itching and weeping and also by being exceptionally recalcitrant to treatment. Fibrous tissue proliferation in the subepidermal tissue may lead to stenosis requiring surgical correction.
The ear wax (cerumen) of humans, to a large extent, is the combined product of the sebaceous (lipid-producing) and apocrine (ceruminous)
Figure 6
This photomicrograph shows the anterior wall of the fibrocartilaginous part of the external auditory canal (EAC) of a 3-mo-old infant. The sebaceous (lipid-producing) and apocrine (cerumi­nous) glands are histologically distinct from the glandular tissue of the adjacent parotid gland. The fissures of Santorini in the anterior fibrocartilaginous wall facilitate the spread of bacterial and neo­plastic diseases between the EAC and the parotid gland. Outlined areas A and B are shown in higher magnification in Figures 7 and 8, respectively.
Figure 7
A higher magnification of the outlined area A in Figure 6 showing the cross­sectioned, coiled, secretory portion of apocrine (ceruminous) glands. These are modified sweat glands.
38 ANATOMY OF THE TEMPORAL BONE WITH SURGICAL IMPLICATIONS
Figure 8
A higher magnification of outlined area B in Figure 6 shows the serous cells of the parotid gland.
Figure 9
This photomicrograph of the skin of the fibrocartilaginous part of the external auditory canal (EAC) demonstrates the sebaceous glands. These glands, as well as hair follicles, are most numerous at the meatus of the canal.
CHAPTER 2: THE PINNA AND EXTERNAL AUDITORY CANAL 39
glands; there is also a variable component of desquamated epithelial cells. Impacted cerumen is a common cause of conductive hearing loss.
There are genetically and racially determined differences in the physi­cal characteristics of ear wax; Caucasians and blacks tend to secrete a wet, brown wax, and Orientals a dry, gray wax (6). These differences in appear­ance and consistency seem to be associated with differences in immuno­globulin and lysozyme content (7). The implications of these differences in relation to the role of the external auditory canal in immunocompetence are unknown and possibly irrelevant.
Exostoses
Exostoses are benign bony excrescences of the external auditory canal usually caused by refrigeration periostitis from swimming in cold water (Fig. 10). Histologically, they demonstrate a laminated structure (Figs. 11 and 12) consistent with a periodic growth pattern.
Exostoses remain clinically silent until they become large enough to impair the egress of epithelial debris and water from the canal, in which case there may be an associated external otitis and fluctuating hearing loss. They may also cause a hearing loss by impinging upon the tympanic membrane and/or manubrium. Symptomatic relief is attained by surgical removal and skin grafting of the epithelially denuded areas of the bony walls of the external auditory canal.
Figure 10
This view shows occult (asympto­matic) exostoses of the anterior and posterior walls of the external auditory canal (male, age 75 yr).