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NECK SURGERY
LUMP IN THE NECK
The correct diagnosis of a lump in the neck can often be made
with a careful history and examination. The clinical signs of
size, site, shape, consistency, fixation to skin or deep structures,
pulsation, compressibility, transillumination or the presence of
a bruit still remain as important as ever
Diagnosis of a lump in the neck
History
Physical signs
Size
Site
Shape
Surface
Consistency
Fixation: deep/superficial
Pulsatility
Compressibility
Transillumination
Bruit
BRANCHIAL CYST
A branchial cyst, thought to develop from the vestigial remnants
of the second branchial cleft, is usually lined by squamous
epithelium, and contains thick, turbid fluid full of cholesterol
crystals. The cyst usually presents in the upper neck in early or
middle adulthood and is found at the junction of the upper third
and middle third of the sternomastoid muscle at its anterior
border. It is a fluctuant swelling that may transilluminate and is
often soft in its early stages so that it may be difficult to palpate.
Other theories hypothesise that branchial cysts develop from
cystic transformation of cervical lymph nodes
If the cyst becomes infected, it becomes erythematous and
tender and, on occasions, it may be difficult to differentiate from
a tuberculous abscess. Ultrasound and fine-needle aspiration
both aid diagnosis, and treatment is by complete excision, which
is best undertaken when the lesion is quiescent. Although the
anterior aspect of the cyst is easy to dissect, it may pass backwards
and upwards through the bifurcation of the common carotid
artery as far as the pharyngeal constrictors. It passes superficial
to the hypoglossal and glossopharyngeal nerves, but deep to the
posterior belly of the digastric. These structures and the spinal
accessory nerve must be positively identified to avoid damage.
BRANCHIAL FISTULA
A branchial fistula may be unilateral or bilateral and is thought
to represent a persistent second branchial cleft. The external
orifice is nearly always situated in the lower third of the neck
near the anterior border of the sternocleidomastoid, while the
internal orifice is located on the anterior aspect of the posterior
faucial pillar just behind the tonsil. However, the internal
aspect of the tract may end blindly at or close to the lateral
pharyngeal wall, constituting a sinus rather than a fistula. The
tract is lined by ciliated columnar epithelium and, as such, there
may be a small amount of recurrent mucous or mucopurulent
discharge onto the neck. The tract follows the same path as a
branchial cyst and requires complete excision, often by more
than one transverse incision in the neck
CYSTIC HYGROMA
Cystic hygromas usually present in the neonate or in early
infancy, and occasionally may present at birth and be so large
as to obstruct labour. The cysts are filled with clear lymph and
lined by a single layer of epithelium with a mosaic appearance
(Figure 48.54). Swelling usually occurs in the neck and may
involve the parotid, submandibular, tongue and floor of mouth
areas. The swelling may be bilateral and is soft and partially
compressible, visibly increasing in size when the child coughs or
cries. The characteristic that distinguishes it from all other neck
swellings is that it is brilliantly translucent. The cheek, axilla,
groin and mediastinum are other less frequent sites for a cystic
hygroma.
The behaviour of cystic hygromas during infancy is unpredictable.
Sometimes the cyst expands rapidly and occasionally
respiratory difficulty ensues, requiring immediate aspiration
and even, occasionally, a tracheostomy. The cyst may become
infected.
Definitive treatment is complete excision of the cyst at an
early stage. Injection of a sclerosing agent, for example picibanil
(OK-432), may reduce the size of the cyst; however, they are
commonly multicystic and if the injection is extracystic subsequent
surgery may be more difficult.
THYROGLOSSAL DUCT CYSTS
Embryology
The thyroid gland descends early in fetal life from the base of
the tongue towards its position in the lower neck with the isthmus
lying over the second and third tracheal rings. At the time
of its descent, the hyoid bone has not been formed and the track
of the descent of the thyroid gland is variable, passing in front,
through or behind the eventual position of the hyoid body.
Thyroglossal duct cysts represent a persistence of this track and
may therefore be found anywhere in or adjacent to the midline
from the tongue base to the thyroid isthmus. Rarely, a thyroglossal
cyst may contain the only functioning thyroid tissue in the
body.
Clinical features
The cysts almost always arise in the midline but, when they
are
adjacent to the thyroid cartilage, they may lie slightly to one
side of the midline. Classically, the cyst moves upwards on
swallowing
and with tongue protrusion, but this can also occur with
other midline cysts such as dermoid cysts, as it merely
indicates
attachment to the hyoid bone.
Thyroglossal cysts may become infected and rupture onto the
skin of the neck presenting as a discharging sinus. Although they
often occur in children, they may also present in adults, even as
late as the sixth or seventh decade of life (Figure 48.55).
Treatment
Treatment must include excision of the whole thyroglossal
tract, which involves removal of the body of the hyoid bone and
the suprahyoid tract through the tongue base to the vallecula at
the site of the primitive foramen caecum, together with a core
of tissue on either side. This operation is known as Sistrunk’s
operation and prevents recurrence, most notably from small side
branches of the thyroglossal tract.
TRAUMA TO THE NECK
Wounds above the hyoid bone
The cavity of the mouth or pharynx may have been entered and
the epiglottis may be divided via the pre-epiglottic space. These
wounds require repair with absorbable sutures on a formal basis
under a general anaesthetic. If there is any degree of associated
oedema or bleeding, particularly in relation to the tongue base
or laryngeal inlet, it is advisable to perform a tracheostomy to
avoid any subsequent respiratory distress.
Wounds of the thyroid and cricoid
cartilage
Blunt crushing injuries or severe laceration injuries to the laryngeal
skeleton can cause marked haematoma formation and rapid
loss of the airway. There may be significant disruption of the
laryngeal skeleton. These patients should not have an endotracheal
intubation for any length of time, even if this is the initial
emergency way of protecting the airway. The larynx is a delicate
three-tiered sphincter and the presence of a foreign body in its
lumen after severe disruption gives rise to major fibrosis and loss
of laryngeal function. These injuries are frequently an absolute
indication for a low tracheostomy, following which the larynx
can be carefully explored, damaged cartilages repositioned and
sutured, and the paraglottic space drained.
An indwelling stent of soft sponge shaped to fit the laryngeal
lumen and held by a nylon retaining suture through the neck
may be left in place for approximately 5 days. This stent can
be removed endoscopically after cutting the retaining suture
and, as the laryngeal damage heals, the patient may then be
decannulated.
Division of the trachea
Wounds of the trachea are rare. They should all be formally
explored and, in order to obtain adequate exposure, it is
usually
necessary to divide and ligate the thyroid isthmus. A small
tracheostomy below the wound followed by repair of the
trachea
with a limited number of submucosal sutures is appropriate. In
self-inflicted wounds, the recurrent laryngeal nerves, which lie
protected in the tracheo-oesophageal grooves, are rarely
injured.
Primary repair is rarely possible but may be undertaken at the
time of formal exploration of a major neck wound.
Neurovascular injury
Penetrating wounds of the neck may involve the common carotid
or the external or internal carotid arteries. Major haemorrhagic
shock may occur. Venous air embolism may occur as a result of
damage to one of the major veins, most commonly the internal
jugular. Compression, resuscitation and exploration under general
anaesthetic, with control of vessels above and below the injury,
and primary repair should be undertaken. All cervical nerves are
vulnerable to injury, particularly the vagus and recurrent laryngeal
nerves and cervical sympathetic chain.
Thoracic duct injury
Wounds to the thoracic duct are rare and most often occur in
association with dissection of lymph nodes in the left supraclavicular
fossa. When damage to the duct is not recognised at the
time of operation, chyle may subsequently leak from the wound
in amounts up to 2 litres per day with profound effects on nutrition.
Treatment
Should the damage be recognised during an operation, the
proximal end of the duct must be ligated. Ligation of the duct
is not harmful because there are a number of anastomotic channels
between the lymphatic and venous system in the lower
neck. If undetected, chyle usually starts to discharge from the
neck wound within 24 hours of the operation. On occasion,
firm pressure by a pad to the lower neck may stop the leakage,
but frequently this is unsuccessful and the wound should be reexplored
and the damaged duct ligated.
INFLAMMATORY CONDITIONS OF
THE NECK
Ludwig’s angina
Ludwig described a clinical entity characterised by a brawny
swelling of the submandibular region combined with inflammatory
oedema of the mouth. It is these combined cervical and
intraoral signs that constitute the characteristic feature of the
lesion, as well as the accompanying putrid halitosis.
The infection is often caused by a virulent streptococcal
infection associated with anaerobic organisms and sometimes
with other lesions of the floor of the mouth, such as carcinoma.
The infection encompasses both sides of the mylohyoid muscle
causing oedema and inflammation such that the tongue may
be displaced upwards and backwards, giving rise to dysphagia
and subsequently to painful obstruction of the airway.
Unless
treated, cellulitis may extend beneath the deep fascial layers
of the neck to involve the larynx, causing glottic oedema and
airway compromise.
Antibiotic therapy should be instituted as soon as possible
using intravenous broad-spectrum antibiotics, with additional
anaerobic cover.
In advanced cases when the swelling does not subside rapidly
with such treatment, a curved submental incision may be used to
drain both submandibular triangles. The mylohyoid muscle may
be incised to decompress the floor of the mouth and corrugated
drains placed in the wound, which is then lightly sutured. This
operation may be conducted under local anaesthetic. Rarely, a
tracheostomy may be necessary.
Cervical lymphadenitis
Cervical lymphadenitis is common due to infection or inflammation
in the oral and nasal cavities, pharynx, larynx, ear, scalp
and face.
Acute lymphadenitis
The affected lymph nodes are enlarged and tender, and there
may be varying degrees of general constitutional disturbance
such as pyrexia, anorexia and general malaise. The treatment in
the first instance is directed to the primary focus of infection, for
example tonsillitis or a dental abscess.
Chronic lymphadenitis
Chronic, painless lymphadenopathy may be caused by tuberculosis
in young children or adults, or be secondary to malignant
disease, most commonly from a squamous carcinoma in older
individuals. Lymphoma and/or HIV infection may also present
in the cervical nodes
Tuberculous adenitis
The condition most commonly affects children or young adults,
but can occur at any age. The deep upper cervical nodes are
most commonly affected, but there may be a widespread cervical
lymphadenitis with many matting together. In most cases, the
tubercular bacilli gain entrance through the tonsil of the corresponding
side as the lymphadenopathy. Both bovine and human
tuberculosis may be responsible. In approximately 80 per cent
of patients, the tuberculous process is limited to the clinically
affected group of lymph nodes, but a primary focus in the lungs
must always be suspected.
As renal and pulmonary tuberculosis occasionally coexist,
the urine should be examined carefully. Rarely, the patient may
develop a natural resistance to the infection and the nodes may
be detected at a later date as evidenced by calcification on
radiography.
This can also be seen after appropriate general treatment
of tuberculosis adenitis. If treatment is not instituted, the
caseated node may liquefy and break down with the formation
of a cold abscess in the neck. The pus is initially confined by the
deep cervical fascia, but after weeks or months, this may become
eroded at one point and the pus flows through the small opening
into the space beneath the superficial fascia. The process has
now reached the well-known stage of a ‘collar-stud’ abscess. The
superficial abscess enlarges steadily and, unless suitably treated, a
discharging sinus results.
Investigation
Fine-needle aspirate taken from neck nodes with a suspicion
of
tuberculosis should be tested for the presence of acid-fast
bacilli.
Systemic investigation should not be neglected, with chest x-
ray
and Mantoux testing useful first-line investigations. Depending
on the country of origin, where tuberculosis is diagnosed or
suspected,
the coexistence of other infectious diseases, such as HIV
and malaria, should not be overlooked.
Treatment
The patient should be treated by appropriate chemotherapy,
dependent on the sensitivities derived from the abscess contents.
If an abscess fails to resolve despite appropriate chemotherapy
and general measures, occasionally excision of the abscess and
its surrounding fibrous capsule is necessary, together with the
relevant lymph nodes. If there is active tuberculosis of another
system, for example pulmonary tuberculosis, then removal of
tuberculous lymph nodes in the neck is inappropriate. The
nodes are commonly related to the internal jugular vein,
common
carotid and vagus nerve, and are usually associated with
significant fibrosis making surgery difficult. A portion of the
internal jugular vein may require excision, taking considerable
care to avoid damage to the vagus or the cervical sympathetic
trunk. To facilitate access, the sternocleidomastoid muscle
should be divided, particularly if the disease is adjacent to the
spinal accessory nerve or the hypoglossal nerve. The resected
nodes should be sent for both histology and microbiology.
PRIMARY TUMOURS OF THE NECK
Neurogenic tumours
Chemodectoma (carotid body tumour)
This is a rare tumour that has a higher incidence in areas where
people live at high altitudes because of chronic hypoxia leading
to carotid body hyperplasia. The tumours most commonly
present in the fifth decade and approximately 10 per cent of
patients have a family history. There is an association with
phaeochromocytoma. The tumours arise from the chemoreceptor
cells on the medial side of the carotid bulb and, at this
point, the tumour is adherent to the carotid wall. The cells of
the chemodectoma are not hormonally active and the tumours
are usually benign with only a small number of cases producing
proven metastases.
Clinical features
There is often a long history of a slowly enlarging, painless lump
at the carotid bifurcation. About one-third of patients present
with a pharyngeal mass that pushes the tonsil medially and
anteriorly. The mass is firm, rubbery, pulsatile, mobile from side
to side but not up and down, and can sometimes be emptied by
firm pressure, after which it slowly refills in a pulsatile manner.
A bruit may also be present. Swellings in the parapharyngeal
space, which often displace the tonsil medially, should not be
biopsied from within the mouth.
Investigations
When a chemodectoma is suspected, a carotid angiogram
can
be carried out to demonstrate the carotid bifurcation, which
is
usually splayed, and a blush, which outlines the tumour
vessels.
MRI scanning also provides excellent detail in most cases.
This
tumour must not be biopsied and fine-needle aspiration is
also
contraindicated.
Treatment
Because these tumours rarely metastasise and their overall rate
of growth is slow, the need for surgical removal must be considered
carefully as complications of surgery are potentially serious.
The operation is best avoided in elderly patients. Radiotherapy
has no effect. In some cases, it may be possible to dissect the
tumour away from the carotid bifurcation but, at times, when
the tumour is large, it may not be separable from the vessels and
resection will be necessary, such that all appropriate facilities
should be available to establish a bypass while a vein graft is
inserted to restore arterial continuity in the carotid system.
Vagal body tumours
Vagal paragangliomas arise from nests of paraganglionic tissue of
the vagus nerve just below the base of the skull near the jugular
foramen. They may also be found at various sites along the
nerve down to the level of the carotid artery bifurcation
They also present as slowly growing and painless masses in
the anterolateral aspect of the neck, and may also have a long
history, commonly of 2–3 years, before diagnosis. They may
spread into the cranial cavity. Diagnosis is confirmed by CT and
MRI scanning and additional MR angiogram or arteriography if
necessary. Treatment is surgical excision.
Peripheral nerve tumours
Schwannomas are solitary and encapsulated tumours attached
to or surrounded by nerve, although paralysis of the associated
nerve is unusual. The vagus nerve is the most common site.
Neurofibromas also arise from the Schwann cell and may be part
of von Recklinghausen’s syndrome of multiple neurofibromatosis.
Multiple neurofibromatosis is an autosomal dominant,
hereditary disease and the neurofibromata may be present at
birth and often multiply.
Diagnosis requires CT or MRI scanning to differentiate them
from other parapharyngeal tumours but, on occasions, the diagnosis
must wait until excision.
Secondary carcinoma
Metastatic spread of squamous carcinoma to the cervical lymph
nodes is a common occurrence from head and neck primary
cancers. The nasopharynx, tonsil, tongue, pyriform fossa and
supraglottic larynx must be carefully examined by panendoscopy
for the primary growth before considering biopsy or any surgery
on the neck. Investigation is further assisted by ultrasound and
fine-needle aspirate of the neck node.
Management
The management of malignant cervical lymph nodes depends
on the overall treatment regime
If surgery is being used to treat the primary disease and the
cervical nodes are palpable and >3 cm, they may be excised
with the primary lesion.
• If radiotherapy is used initially, as is always the case in
carcinoma of the nasopharynx, then radiotherapy may also
be given to the neck nodes, whatever their stage. In the
case of the tongue, pharynx or larynx, however, if the node
exceeds 3 cm in diameter, then surgery may be necessary
for the neck nodes, even if the primary tumour is treated by
chemoradiation.
• If radiotherapy is used initially with resolution of the primary
tumour, but there is subsequent residual or recurrent nodal
disease, then this situation will require cervical lymph node
dissection.
TYPE OF NECK DISSECTION
Classical radical neck dissection (Crile)
The classic operation involves resection of the cervical lymphatics
and lymph nodes and those structures closely associated:
the internal jugular vein, the accessory nerve, the submandibular
gland and the sternocleidomastoid muscle. These structures
are all removed en bloc and in continuity with the primary disease
if possible. The main disability that follows the operation
is weakness and drooping of the shoulder due to paralysis of the
trapezius muscle as a consequence of excision of the accessory
nerve.
Modified radical neck dissection
In selected cases, one or more of the three following
structures
are preserved: the accessory nerve, the sternocleidomastoid
muscle or the internal jugular vein. Otherwise, all major lymph
node groups and lymphatics are excised. Whichever
structures
are preserved should be clearly noted.
Selective neck dissection
In this type of dissection, one or more of the major lymph
node
groups is preserved along with the sternocleidomastoid
muscle,
accessory nerve and internal jugular vein. In these
circumstances,
the exact groups of nodes excised must be documented.
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Neck surgery

  • 2. LUMP IN THE NECK The correct diagnosis of a lump in the neck can often be made with a careful history and examination. The clinical signs of size, site, shape, consistency, fixation to skin or deep structures, pulsation, compressibility, transillumination or the presence of a bruit still remain as important as ever Diagnosis of a lump in the neck History Physical signs Size Site Shape Surface Consistency Fixation: deep/superficial Pulsatility Compressibility Transillumination Bruit
  • 3. BRANCHIAL CYST A branchial cyst, thought to develop from the vestigial remnants of the second branchial cleft, is usually lined by squamous epithelium, and contains thick, turbid fluid full of cholesterol crystals. The cyst usually presents in the upper neck in early or middle adulthood and is found at the junction of the upper third and middle third of the sternomastoid muscle at its anterior border. It is a fluctuant swelling that may transilluminate and is often soft in its early stages so that it may be difficult to palpate. Other theories hypothesise that branchial cysts develop from cystic transformation of cervical lymph nodes
  • 4. If the cyst becomes infected, it becomes erythematous and tender and, on occasions, it may be difficult to differentiate from a tuberculous abscess. Ultrasound and fine-needle aspiration both aid diagnosis, and treatment is by complete excision, which is best undertaken when the lesion is quiescent. Although the anterior aspect of the cyst is easy to dissect, it may pass backwards and upwards through the bifurcation of the common carotid artery as far as the pharyngeal constrictors. It passes superficial to the hypoglossal and glossopharyngeal nerves, but deep to the posterior belly of the digastric. These structures and the spinal accessory nerve must be positively identified to avoid damage.
  • 5. BRANCHIAL FISTULA A branchial fistula may be unilateral or bilateral and is thought to represent a persistent second branchial cleft. The external orifice is nearly always situated in the lower third of the neck near the anterior border of the sternocleidomastoid, while the internal orifice is located on the anterior aspect of the posterior faucial pillar just behind the tonsil. However, the internal aspect of the tract may end blindly at or close to the lateral pharyngeal wall, constituting a sinus rather than a fistula. The tract is lined by ciliated columnar epithelium and, as such, there may be a small amount of recurrent mucous or mucopurulent discharge onto the neck. The tract follows the same path as a branchial cyst and requires complete excision, often by more than one transverse incision in the neck
  • 6.
  • 7.
  • 8. CYSTIC HYGROMA Cystic hygromas usually present in the neonate or in early infancy, and occasionally may present at birth and be so large as to obstruct labour. The cysts are filled with clear lymph and lined by a single layer of epithelium with a mosaic appearance (Figure 48.54). Swelling usually occurs in the neck and may involve the parotid, submandibular, tongue and floor of mouth areas. The swelling may be bilateral and is soft and partially compressible, visibly increasing in size when the child coughs or
  • 9. cries. The characteristic that distinguishes it from all other neck swellings is that it is brilliantly translucent. The cheek, axilla, groin and mediastinum are other less frequent sites for a cystic hygroma. The behaviour of cystic hygromas during infancy is unpredictable. Sometimes the cyst expands rapidly and occasionally respiratory difficulty ensues, requiring immediate aspiration and even, occasionally, a tracheostomy. The cyst may become infected. Definitive treatment is complete excision of the cyst at an early stage. Injection of a sclerosing agent, for example picibanil (OK-432), may reduce the size of the cyst; however, they are commonly multicystic and if the injection is extracystic subsequent surgery may be more difficult.
  • 10.
  • 11. THYROGLOSSAL DUCT CYSTS Embryology The thyroid gland descends early in fetal life from the base of the tongue towards its position in the lower neck with the isthmus lying over the second and third tracheal rings. At the time of its descent, the hyoid bone has not been formed and the track of the descent of the thyroid gland is variable, passing in front, through or behind the eventual position of the hyoid body. Thyroglossal duct cysts represent a persistence of this track and may therefore be found anywhere in or adjacent to the midline from the tongue base to the thyroid isthmus. Rarely, a thyroglossal cyst may contain the only functioning thyroid tissue in the body.
  • 12. Clinical features The cysts almost always arise in the midline but, when they are adjacent to the thyroid cartilage, they may lie slightly to one side of the midline. Classically, the cyst moves upwards on swallowing and with tongue protrusion, but this can also occur with other midline cysts such as dermoid cysts, as it merely indicates attachment to the hyoid bone.
  • 13. Thyroglossal cysts may become infected and rupture onto the skin of the neck presenting as a discharging sinus. Although they often occur in children, they may also present in adults, even as late as the sixth or seventh decade of life (Figure 48.55). Treatment Treatment must include excision of the whole thyroglossal tract, which involves removal of the body of the hyoid bone and the suprahyoid tract through the tongue base to the vallecula at the site of the primitive foramen caecum, together with a core of tissue on either side. This operation is known as Sistrunk’s operation and prevents recurrence, most notably from small side branches of the thyroglossal tract.
  • 14.
  • 15. TRAUMA TO THE NECK Wounds above the hyoid bone The cavity of the mouth or pharynx may have been entered and the epiglottis may be divided via the pre-epiglottic space. These wounds require repair with absorbable sutures on a formal basis under a general anaesthetic. If there is any degree of associated oedema or bleeding, particularly in relation to the tongue base or laryngeal inlet, it is advisable to perform a tracheostomy to avoid any subsequent respiratory distress.
  • 16. Wounds of the thyroid and cricoid cartilage Blunt crushing injuries or severe laceration injuries to the laryngeal skeleton can cause marked haematoma formation and rapid loss of the airway. There may be significant disruption of the laryngeal skeleton. These patients should not have an endotracheal intubation for any length of time, even if this is the initial emergency way of protecting the airway. The larynx is a delicate three-tiered sphincter and the presence of a foreign body in its lumen after severe disruption gives rise to major fibrosis and loss of laryngeal function. These injuries are frequently an absolute indication for a low tracheostomy, following which the larynx can be carefully explored, damaged cartilages repositioned and sutured, and the paraglottic space drained.
  • 17. An indwelling stent of soft sponge shaped to fit the laryngeal lumen and held by a nylon retaining suture through the neck may be left in place for approximately 5 days. This stent can be removed endoscopically after cutting the retaining suture and, as the laryngeal damage heals, the patient may then be decannulated.
  • 18. Division of the trachea Wounds of the trachea are rare. They should all be formally explored and, in order to obtain adequate exposure, it is usually necessary to divide and ligate the thyroid isthmus. A small tracheostomy below the wound followed by repair of the trachea with a limited number of submucosal sutures is appropriate. In self-inflicted wounds, the recurrent laryngeal nerves, which lie protected in the tracheo-oesophageal grooves, are rarely injured. Primary repair is rarely possible but may be undertaken at the time of formal exploration of a major neck wound.
  • 19. Neurovascular injury Penetrating wounds of the neck may involve the common carotid or the external or internal carotid arteries. Major haemorrhagic shock may occur. Venous air embolism may occur as a result of damage to one of the major veins, most commonly the internal jugular. Compression, resuscitation and exploration under general anaesthetic, with control of vessels above and below the injury, and primary repair should be undertaken. All cervical nerves are vulnerable to injury, particularly the vagus and recurrent laryngeal nerves and cervical sympathetic chain.
  • 20. Thoracic duct injury Wounds to the thoracic duct are rare and most often occur in association with dissection of lymph nodes in the left supraclavicular fossa. When damage to the duct is not recognised at the time of operation, chyle may subsequently leak from the wound in amounts up to 2 litres per day with profound effects on nutrition.
  • 21. Treatment Should the damage be recognised during an operation, the proximal end of the duct must be ligated. Ligation of the duct is not harmful because there are a number of anastomotic channels between the lymphatic and venous system in the lower neck. If undetected, chyle usually starts to discharge from the neck wound within 24 hours of the operation. On occasion, firm pressure by a pad to the lower neck may stop the leakage, but frequently this is unsuccessful and the wound should be reexplored and the damaged duct ligated.
  • 22. INFLAMMATORY CONDITIONS OF THE NECK Ludwig’s angina Ludwig described a clinical entity characterised by a brawny swelling of the submandibular region combined with inflammatory oedema of the mouth. It is these combined cervical and intraoral signs that constitute the characteristic feature of the lesion, as well as the accompanying putrid halitosis. The infection is often caused by a virulent streptococcal infection associated with anaerobic organisms and sometimes with other lesions of the floor of the mouth, such as carcinoma. The infection encompasses both sides of the mylohyoid muscle causing oedema and inflammation such that the tongue may be displaced upwards and backwards, giving rise to dysphagia and subsequently to painful obstruction of the airway.
  • 23. Unless treated, cellulitis may extend beneath the deep fascial layers of the neck to involve the larynx, causing glottic oedema and airway compromise. Antibiotic therapy should be instituted as soon as possible using intravenous broad-spectrum antibiotics, with additional anaerobic cover. In advanced cases when the swelling does not subside rapidly with such treatment, a curved submental incision may be used to drain both submandibular triangles. The mylohyoid muscle may be incised to decompress the floor of the mouth and corrugated drains placed in the wound, which is then lightly sutured. This operation may be conducted under local anaesthetic. Rarely, a tracheostomy may be necessary.
  • 24. Cervical lymphadenitis Cervical lymphadenitis is common due to infection or inflammation in the oral and nasal cavities, pharynx, larynx, ear, scalp and face. Acute lymphadenitis The affected lymph nodes are enlarged and tender, and there may be varying degrees of general constitutional disturbance such as pyrexia, anorexia and general malaise. The treatment in the first instance is directed to the primary focus of infection, for example tonsillitis or a dental abscess. Chronic lymphadenitis Chronic, painless lymphadenopathy may be caused by tuberculosis in young children or adults, or be secondary to malignant disease, most commonly from a squamous carcinoma in older individuals. Lymphoma and/or HIV infection may also present in the cervical nodes
  • 25. Tuberculous adenitis The condition most commonly affects children or young adults, but can occur at any age. The deep upper cervical nodes are most commonly affected, but there may be a widespread cervical lymphadenitis with many matting together. In most cases, the tubercular bacilli gain entrance through the tonsil of the corresponding side as the lymphadenopathy. Both bovine and human tuberculosis may be responsible. In approximately 80 per cent of patients, the tuberculous process is limited to the clinically affected group of lymph nodes, but a primary focus in the lungs must always be suspected.
  • 26. As renal and pulmonary tuberculosis occasionally coexist, the urine should be examined carefully. Rarely, the patient may develop a natural resistance to the infection and the nodes may be detected at a later date as evidenced by calcification on radiography. This can also be seen after appropriate general treatment of tuberculosis adenitis. If treatment is not instituted, the caseated node may liquefy and break down with the formation of a cold abscess in the neck. The pus is initially confined by the deep cervical fascia, but after weeks or months, this may become eroded at one point and the pus flows through the small opening into the space beneath the superficial fascia. The process has now reached the well-known stage of a ‘collar-stud’ abscess. The superficial abscess enlarges steadily and, unless suitably treated, a discharging sinus results.
  • 27. Investigation Fine-needle aspirate taken from neck nodes with a suspicion of tuberculosis should be tested for the presence of acid-fast bacilli. Systemic investigation should not be neglected, with chest x- ray and Mantoux testing useful first-line investigations. Depending on the country of origin, where tuberculosis is diagnosed or suspected, the coexistence of other infectious diseases, such as HIV and malaria, should not be overlooked.
  • 28. Treatment The patient should be treated by appropriate chemotherapy, dependent on the sensitivities derived from the abscess contents. If an abscess fails to resolve despite appropriate chemotherapy and general measures, occasionally excision of the abscess and its surrounding fibrous capsule is necessary, together with the relevant lymph nodes. If there is active tuberculosis of another system, for example pulmonary tuberculosis, then removal of tuberculous lymph nodes in the neck is inappropriate. The nodes are commonly related to the internal jugular vein,
  • 29. common carotid and vagus nerve, and are usually associated with significant fibrosis making surgery difficult. A portion of the internal jugular vein may require excision, taking considerable care to avoid damage to the vagus or the cervical sympathetic trunk. To facilitate access, the sternocleidomastoid muscle should be divided, particularly if the disease is adjacent to the spinal accessory nerve or the hypoglossal nerve. The resected nodes should be sent for both histology and microbiology.
  • 30. PRIMARY TUMOURS OF THE NECK Neurogenic tumours Chemodectoma (carotid body tumour) This is a rare tumour that has a higher incidence in areas where people live at high altitudes because of chronic hypoxia leading to carotid body hyperplasia. The tumours most commonly present in the fifth decade and approximately 10 per cent of patients have a family history. There is an association with phaeochromocytoma. The tumours arise from the chemoreceptor cells on the medial side of the carotid bulb and, at this point, the tumour is adherent to the carotid wall. The cells of the chemodectoma are not hormonally active and the tumours are usually benign with only a small number of cases producing proven metastases.
  • 31. Clinical features There is often a long history of a slowly enlarging, painless lump at the carotid bifurcation. About one-third of patients present with a pharyngeal mass that pushes the tonsil medially and anteriorly. The mass is firm, rubbery, pulsatile, mobile from side to side but not up and down, and can sometimes be emptied by firm pressure, after which it slowly refills in a pulsatile manner. A bruit may also be present. Swellings in the parapharyngeal space, which often displace the tonsil medially, should not be biopsied from within the mouth.
  • 32. Investigations When a chemodectoma is suspected, a carotid angiogram can be carried out to demonstrate the carotid bifurcation, which is usually splayed, and a blush, which outlines the tumour vessels. MRI scanning also provides excellent detail in most cases. This tumour must not be biopsied and fine-needle aspiration is also contraindicated.
  • 33. Treatment Because these tumours rarely metastasise and their overall rate of growth is slow, the need for surgical removal must be considered carefully as complications of surgery are potentially serious. The operation is best avoided in elderly patients. Radiotherapy has no effect. In some cases, it may be possible to dissect the tumour away from the carotid bifurcation but, at times, when the tumour is large, it may not be separable from the vessels and resection will be necessary, such that all appropriate facilities should be available to establish a bypass while a vein graft is inserted to restore arterial continuity in the carotid system.
  • 34. Vagal body tumours Vagal paragangliomas arise from nests of paraganglionic tissue of the vagus nerve just below the base of the skull near the jugular foramen. They may also be found at various sites along the nerve down to the level of the carotid artery bifurcation They also present as slowly growing and painless masses in the anterolateral aspect of the neck, and may also have a long history, commonly of 2–3 years, before diagnosis. They may spread into the cranial cavity. Diagnosis is confirmed by CT and MRI scanning and additional MR angiogram or arteriography if necessary. Treatment is surgical excision.
  • 35. Peripheral nerve tumours Schwannomas are solitary and encapsulated tumours attached to or surrounded by nerve, although paralysis of the associated nerve is unusual. The vagus nerve is the most common site. Neurofibromas also arise from the Schwann cell and may be part of von Recklinghausen’s syndrome of multiple neurofibromatosis. Multiple neurofibromatosis is an autosomal dominant, hereditary disease and the neurofibromata may be present at birth and often multiply. Diagnosis requires CT or MRI scanning to differentiate them from other parapharyngeal tumours but, on occasions, the diagnosis must wait until excision.
  • 36. Secondary carcinoma Metastatic spread of squamous carcinoma to the cervical lymph nodes is a common occurrence from head and neck primary cancers. The nasopharynx, tonsil, tongue, pyriform fossa and supraglottic larynx must be carefully examined by panendoscopy for the primary growth before considering biopsy or any surgery on the neck. Investigation is further assisted by ultrasound and fine-needle aspirate of the neck node.
  • 37. Management The management of malignant cervical lymph nodes depends on the overall treatment regime If surgery is being used to treat the primary disease and the cervical nodes are palpable and >3 cm, they may be excised with the primary lesion. • If radiotherapy is used initially, as is always the case in carcinoma of the nasopharynx, then radiotherapy may also be given to the neck nodes, whatever their stage. In the case of the tongue, pharynx or larynx, however, if the node exceeds 3 cm in diameter, then surgery may be necessary for the neck nodes, even if the primary tumour is treated by chemoradiation. • If radiotherapy is used initially with resolution of the primary tumour, but there is subsequent residual or recurrent nodal disease, then this situation will require cervical lymph node dissection.
  • 38. TYPE OF NECK DISSECTION Classical radical neck dissection (Crile) The classic operation involves resection of the cervical lymphatics and lymph nodes and those structures closely associated: the internal jugular vein, the accessory nerve, the submandibular gland and the sternocleidomastoid muscle. These structures are all removed en bloc and in continuity with the primary disease if possible. The main disability that follows the operation is weakness and drooping of the shoulder due to paralysis of the trapezius muscle as a consequence of excision of the accessory nerve.
  • 39. Modified radical neck dissection In selected cases, one or more of the three following structures are preserved: the accessory nerve, the sternocleidomastoid muscle or the internal jugular vein. Otherwise, all major lymph node groups and lymphatics are excised. Whichever structures are preserved should be clearly noted.
  • 40. Selective neck dissection In this type of dissection, one or more of the major lymph node groups is preserved along with the sternocleidomastoid muscle, accessory nerve and internal jugular vein. In these circumstances, the exact groups of nodes excised must be documented.