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PAROTID GLAND
Embryology
Because, for all practical purposes, the neck does not exist in embryos, a
discussion about the embryogenesis of the neck is impossible. To understand
the embryology of this region, one must study the embryology of each of the
organs contained there, specifically, the pharyngeal apparatus and its derivatives,
such as the thyroid, parathyroid, and thymus. Pouches, clefts, and arches de-
velop and disappear. The esophagus and vessels are elongated while other
embryologic entities, such as the diaphragm, descend.
Early in the 6th week of gestation, solid epithelial buds of ectodermal origin
form the wall of the primitive mouth and invaginate into the surrounding
mesenchyme. A groove that later becomes a tunnel develops. The future parotid
gland is formed in the blind end of the tunnel by proliferation, budding length,
and extensive branching. The end of the solid ducts forms the secretory acini.
The mesenchyme is responsible for the genesis of the capsule and the connective
parotid tissue. Later in fetal life, the solid epithelial buds and acini become
hollow. All of the salivary glands have a similar embryogenesis.A close associa-
tion between the facial nerve and the parotid ductules begins early in the fetal
period. They practically embrace each other in a way described best by McKen-
zie6 as “A creeper weaving itself into the meshes of a trellis-work fence.”
Anatomy
Because the parotid gland is located behind the lower jaw and the base of
the cranium, it cannot be palpated under normal conditions. Also, at birth,
From the Department of Surgery, Emory University School of Medicine; and the Winship
Clinic, Atlanta, Georgia
-
VOLUME 80 NUMBER 1 FEBRUARY 2000 261
262 CARLSON
Figure 1. The parotid gland covers the ascending ramus of the mandible.
Figure 2. Deep lobe parotid tumors may extend into the parapharyngeal space and present
in the mouth.
(5) cervical. The temporal and zygomatic branches share the motor supply of
the orbicularis oculi, and the temporal branch alone supplies the forehead
musculature. The cervical branch supplies the platysma, and the remaining
buccal and mandibular branches share the supply of the remaining facial mus-
cles. The primary division is constant, but considerable variation exists in the
origins, inter-relationships, and distribution of the peripheral branches (see Fig.
3). The pattern of branching is especially variable, and rami often communicate
between branches, sometimes within the gland but more often in front of its
anterior border.' The presence of these communicating rami explains the occur-
rence of unexpectedly mild paralysis following the division of a branch.
The facial nerve runs within the substance of the gland, but within the
gland, the facial nerve is superficial, the veins are deeper, and the arterial
branches are deepest. Traditionally, the path of the nerve has been used to
separate the parotid gland into superficial and deep lobes, but no true facial
planes separate the two lobes. In 1956, two important but controversial articles
in the literature discussed the unilobar formationloand bilobar formation' of the
parotid gland. Both types have been found, but they were not well defined or
separated (John E. Skandalakis, MD, personal communication, 1996). Tumors
generally develop superficial or deep to the plane of the nerve, hence the
distinction of superficial and deep lobe tumors. In some cases, tumors arise in
the plane of the nerve, separating the branches.
Parotidectomy requires precise identification of the facial nerve. The main
trunk is constantly found between the base of the styloid process and the
mastoid process. The tail of the parotid gland must be separated from the
sternocleidomastoid muscle. Lateral traction of the muscle exposes the digastric
muscle, which is followed to its insertion on the mastoid tip. The nerve lies
THE SALIVARY GLANDS 265
Figure 3. The facial nerve has considerable variation in the distribution of peripheral
branches. It has a constant location anterior to the attachment of the digastric muscles as
it exits the stylomastoid foramen.
between the insertion of the muscle and the styloid process (see Fig. 3). In
difficult cases, the nerve can be found by removing the mastoid tip with an
osteotome, which exposes the nerve in the descending portion of the facial canal
as it exits through the stylomastoid foramen. If the tumor mass overlies the
main nerve trunk, physicians can identify the posterior facial vein as it enters
the gland. The marginal mandibular nerve can be seen crossing superficial to it
and can be followed to the main trunk.
The external carotid artery enters the inferior surface of the gland and
divides into the maxillary and superficial temporal arteries at the junction
between the middle and upper thirds of the gland. The superficial temporal
artery gives off the transverse facial artery to supply the face before continuing
upward to emerge from the upper border of the gland. The maxillary artery
passes forward and slightly upward behind the condylar neck in the part of the
gland lying deep to it. The artery emerges from the gland and passes into the
infratemporal fossa.
266 CARLSON
The venous drainage of the area varies, but the superficial temporal vein
typically enters the superior surface and receives the internal maxillary vein to
become the posterior facial vein. Within the gland, it divides into a posterior
branch, which joins the posterior auricular vein to form the external jugular
vein. The anterior branch emerges from the gland to join the common facial
vein. The facial nerve is superficial to the vessels, the artery is deep, and the
veins lie between them.
Knowledge of the lymphatics of the parotid gland is important in evaluating
skin cancers of the head. Preauricular lymph nodes in the superficial fascia drain
the temporal scalp, upper face, and anterior pinna. Lymph nodes within the
parotid substance drain the gland, nasopharynx, palate, middle ear, and external
auditory meatus. These lymphatics drain into the internal jugular and spinal
accessory nodes.
The parotid gland is innervated by sympathetic and parasympathetic fibers.
The function of the sympathetic fibers is most likely vasoconstriction, and the
function of the parasympathetic fibers (IX nerve) is most likely secretory.
The greater auricular nerve emerges from the posterior border of the sterno-
cleidomastoid muscle at Erb's point (Fig. 4). It crosses the midportion of the
muscle approximately 6.5 cm beneath the external auditory r n e a t u ~ It
. ~travels
parallel and superior to the external jugular vein to supply sensation to the ear
and preauricular region. It passes on the surface of the parotid gland and can
be preserved unless invaded by tumor by retracting it posteriorly. If the nerve
must be sacrificed, it is preserved in saline solution for possible use as a nerve
Cervical v.
Figure 4. Erb's point (circle) is an important landmark in the posterior triangle. n = nerve;
v = vein.
THE SALIVARY GLANDS 267
graft. Loss of the branches to the ear can cause disturbing numbness of the
lobule, making earrings difficult to wear and, in some cases, causing frostbite.
The auriculotemporal nerve is a branch of the mandibular division of the
trigeminal nerve. It traverses the upper part of the parotid gland and emerges
from the superior surface with the superficial temporal vessels. It carries sensory
fibers from the trigeminal and secretory fibers from the glossopharyngeal nerve
by the otic ganglion.
Frey's syndrome is localized sweating and flushing during the mastication
of food. It is a common disorder that occurs in 35% to 60% of patients after
parotidectomy with facial nerve dis~ection.~,The syndrome usually presents
several months after surgery and has varying degrees of severity. It may result
from aberrant regeneration of nerve fibers from postganglionic secretomotor
parasympathetic innervation to the parotid gland occurring through the severed
axon sheaths of the postganglionic sympathetic fibers that supply the sweat
glands of the skin. Most affected patients do not seek treatment.
Surgical Applications
Preoperative Preparation
The history and physical examination are often diagnostic of parotid masses.
A slow-growing mass that has been present for many years is most likely a
pleomorphic adenoma. Facial nerve paralysis usually indicates a malignant
process. CT scanning can be useful in equivocal cases when a deep lobe tumor
or malignancy is suspected.
Fine-needle aspiration cytology is useful in cases in which malignancy is
suspected. It aids in preoperative counseling regarding the risk for nerve injury
but should not determine operability.
Figure 5. Incision for a parotidectomy curves around the ear and proceeds down the neck
in a transverse skin crease. (From Carlson GW: Lateral neck. In Wood WC, Skandalakis
JE (eds): Anatomic Basis of Tumor Surgery. St. Louis, Quality Medical Publishing, 1999, p
128; with permission.)
Figure 6. Surgical exposure of the parotid gland. (From Carlson GW: Lateral neck. In
Wood WC, Skandalakis JE (eds): Anatomic Basis of Tumor Surgery. St. Louis, Quality
Medical Publishing, 1999, p 129; with permission.)
is followed to its insertion on the mastoid tip. The nerve lies between the
insertion of the muscle and the styloid process (see Fig. 3). In difficult cases, the
nerve can be found by removing the mastoid tip with an osteotome, which
exposes the nerve in the descending portion of the facial canal as it exits through
the stylomastoid foramen. If the tumor mass overlies the main nerve trunk, an
optional approach is to identify the posterior facial vein as it enters the gland.
The marginal mandibular nerve crosses superficial to it and can be followed to
the main trunk. Approximately 1.0 cm to 1.5 cm from the stylomastoid foramen,
the nerve divides into the upper zygomaticofacial and lower cervicofacial divi-
sions at the pes anserinus.
Tumor Resection
Resection of a parotid mass should be considered an attack on the tumor,
not the gland. Most tumors of the parotid gland arise in the superficial portion.
The underlying nerve usually limits the removal of tumors in this portion
unless it is sacrificed. A pleomorphic adenoma has a well-defined capsule, but
enucleation results in an unacceptable recurrence rate. When nerve branches
disappear into the tumor, malignancy should be suspected. Nerve resection is
270 CARLSON
indicated when the nerves are clinically involved. The greater auricular nerve
can be used as a nerve graft. A total parotidectomy is typically performed to
treat malignant neoplasms.
During dissection, the individual nerve branches are dissected with a fine
mosquito clamp. The overlying parotid mass is divided with a no. 12 knife blade
(Fig. 7). Hemostasis is controlled with the bipolar cautery device. Lesions deep
to the facial nerve necessitate removal of the superficial parotid tissue first. The
remaining tissue can then be carefully dissected out between nerve branches.
SUBMAXILLARY GLAND
The submandibular salivary gland is the site of approximately 10% to 15%
of salivary neoplasms. Approximately 30% to 55% of these tumors are malignant,
with adenoid cystic carcinoma being the most common type of cancer. Most
neoplasms are asymptomatic, but if a patient shows evidence of neural involve-
ment, such as marginal mandibular or hypoglossal paresis or loss of sensation,
an aggressive malignant neoplasm is probable. Bimanual examination through
the mouth allows assessment of possible extension under the mylohyoid muscle.
Anatomy
The submaxillary gland and associated lymph nodes fill the triangle over-
lapping the digastric muscles and extending upward deep to the mandible5(Fig.
8). Differentiating the gland from the lymph nodes may be difficult. The gland
sends a prolongation of tissue with the submaxillary, or Wharton’s, duct under
the mylohyoid muscle (Fig. 9). The duct opens into the mouth on the side of the
frenulum of the tongue. Superficial to the gland, the facial vein crosses the
submaxillary triangle to reach the anterior border of the mandible. The facial
artery enters the triangle under the posterior belly of the digastric and stylohyoid
muscles. It ascends to emerge above or through the upper border of the gland.
Figure 7. Individual facial nerve branches are dissected with a fine mosquito clamp, and
the overlying parotid gland is divided with a No. 12 knife blade. (From Carlson GW: Lateral
neck. In Wood WC, Skandalakis JE (eds): Anatomic Basis of Tumor Surgery. St. Louis,
Quality Medical Publishing, 1999, p 130; with permission.)
THE SALIVARY GLANDS 271
Figure 8. The contents of the submaxillary triangle just deep to the platysma muscle. a =
artery; v = vein; n = nerve.
The marginal mandibular branch of the facial nerve courses through the triangle
beneath the platysma muscle. It is the only important structure encountered
above the digastric muscle in a submaxillary dissection. The course of the nerve
varies, and this nerve commonly has multiple branches. Dingman and Grabb2
found the nerve to be located above the anterior ramus of the mandible in 81%
of cadaver dissections. In the author’s experience, the nerve loops below the
Figure 9. The superficial portion of the submaxillary salivary gland has been removed to
reveal structures deep in the triangle. m = muscle.
272 CARLSON
Surgical Applications
Figure 10. The entire submaxillary gland is removed to show the floor of the triangle. m =
muscle; n = nerve; br = branch; CN VII = facial nerve.
THE SALIVARY GLANDS 273
References
1. Davis RA, Anson BJ, Budinger JM, et al: Surgical anatomy of the facial nerve and
parotid gland based upon a study of 350 cervicofacial halves. Surg Gynecol Obstet
102:385, 1956
2. Dingman RO, Grabb WC: Surgical anatomy of the mandibular ramus of the facial
nerve based on dissection of 100 facial halves. Plast Reconstr Surg 29:266, 1962
3. Gordon AB, Fiddian R V Frey’s syndrome after parotid surgery. Am J Surg 132:54, 1976
4. Hays LL, Novack AJ, Worsham JC: The Frey syndrome: A simple, effective treatment.
Otolaryngol Head Neck Surg 90:419, 1982
5. Johns ME, Kaplan MJ: Surgical therapy of tumors of the salivary glands. In Thawley
SE, Panje WR (eds): Comprehensive Management of Head and Neck Tumors. Philadel-
phia, WB Saunders, 1987, p 1104
6. McKenzie J: The first arch syndrome. Dev Med Child Neurol 8:56, 1966
7. McKinney P, Katrana DJ: Prevention of injury to the great auricular nerve during
rhytidectomy. Plast Reconstr Surg 66:675, 1980
8. Skandalakis JE, Gray SW, Rowe JS Jr: Surgical anatomy of the submandibular triangle.
Am Surg 45:590, 1979
9. Skandalakis JE, Gray SW, Rowe JS Jr: The neck. In Anatomical Complications in
General Surgery. New York, McGraw-Hill, 1983, pp 3-17
10. Winsten J, Ward GE: The parotid gland: An anatomic study. Surgery 40:585, 1956
Address reprint requests to
Grant W. Carlson, MD
Winship Clinic
13658 Clifton Road
Atlanta, GA 30322