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Fig. 10.5 Modied and shortened tip of an Endo GIA 30 stapler (top), compared with the original version (bottom)
S. J. Stoeckli et al.
Fig. 10.7 Endoscopic view of the closed stapler in position
Fig. 10.6 Endoscopic view of the open stapler in position
means of a thinner, non-spreadable diverticuloscope (Karl Storz, Tuttlingen, Germany). As the stapler does not pass through this diverticuloscope, the transection of the common wall must be performed with the CO2 laser (Fig.10.9).
Fig. 10.8 Endoscopic view of the transected diverticular bar after removal of the stapler. A minimal residual bar has been transected with the CO2 laser
Fig. 10.9 Endoscopic view through a thinner diverticuloscope, show-
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ing myotomy of the cricopharyngeus muscle with the CO2 laser
10.5 Postoperative Care
It is the authors’ policy to leave the patients on nil per os on the day of surgery, to restrict oral intake to uids for 24h thereafter, and then to introduce soft diet for the next 7days, before returning to normal diet. A feeding tube is not rou­tinely placed. Although this procedure can be done as a day case, the age and comorbidities of most patients, and the risk of complications, result in most patients staying one night in hospital. In particular, after laser myotomy, patients may experience heavy retrosternal chest pain, which may be mistaken for a myocardial infarction. Analgesia is usually necessary for the rst few postoperative days. Success of the procedure is assessed clinically, with no need for routine postoperative barium swallow. Patients should be made aware that recurrence of symptomatic ZD is rare but possible and is amenable to successful endoscopic revision surgery.
References
1. Ludlow A.A case of obstructed deglutition from a preternatural bag formed in the pharynx. Med Obs Inquiries. 1769;3:85–101.
2. Zenker FA, Von Ziemssen H.Dilatations of the esophageus. In: Cyclopaedia of the practice of medicine, vol. 3. London: Low, Marston, Searle & Rivington; 1878. p.46–68.
3. Killian G. Ueber den Mund der Speiseröhre. Z Ohrenheilkd Krankheiten Luftwege. 1908;55:1–41.
4. van Overbeek JJ.Meditation on the pathogenesis of the hypopha­ryngeal (Zenker’s) diverticulum and a report of endoscopic treat­ment in 545 patients. Ann Otol Rhinol Laryngol. 1994;103:178–85.
115
5. Cook IJ, Blumbergs P, Cash K, Jamieson GG, Shearman DJ. Structural abnormalities of the cricopharyngeus muscle in patients with pharyngeal (Zenker’s) diverticulum. J Gastroenterol Hepatol. 1992;7:556–62.
6. Resouly A, Braat J, Jackson A, Evans H. Pharyngeal pouch: link with reux and oesophageal dysmotility. Clin Otolaryngol. 1994;19:241–2.
7. Migliore M, Payne H, Jeyasingham K. Pathophysiologic basis for operation on Zenker’s diverticulum. Ann Thorac Surg. 1994;57:1616–21.
8. Vakil NB, Kahrilas PJ, Dodd WJ, Vanagunas A.Absence of an upper esophageal sphincter response to acid reux. Am J Gastroenterol. 1989;84:606–10.
9. Huang BS, Unni KK, Payne WS. Long-term survival following diverticulectomy for cancer in pharyngoesophageal (Zenker’s) diverticulum. Ann Thorac Surg. 1984;38:207–10.
10. Mosher HP.Webs and pouches of the esophageus, their diagnosis and treatment. Surg Gynecol Obstet. 1917;25:175–87.
11. Dohlman G, Mattsson O. The endoscopic operation for hypo­pharyngeal diverticula. A roentgencinematographic study. Arch Otolaryngol. 1960;71:744–52.
12. van Overbeek JJ, Hoeksema PE.Endoscopic treatment of the hypo­pharyngeal diverticulum: 211 cases. Laryngoscope. 1982;92:88–91.
13. Knegt PP, de Jong PC, van der Schans EJ.Endoscopic treatment of the hypopharyngeal diverticulum with the CO2 laser. Endoscopy. 1985;17:205–6.
14. Collard JM, Otte JB, Kestens PJ.Endoscopic stapling technique of esophagodiverticulostomy for Zenker’s diverticulum. Ann Thorac Surg. 1993;56:573–6.
15. Martin-Hirsch DP, Newbegin CJ.Autosuture GIA gun: a new appli­cation in the treatment of hypopharyngeal diverticula. J Laryngol Otol. 1993;107:723–5.
16. Baldwin DL, Thoma AG. Endoscopic stapled diverticulotomy: a real advance in the treatment of hypopharyngeal diverticulum. Clin Otolaryngol. 1998;23:244–7.
17. Koay CB, Bates GJ.Endoscopic stapling diverticulotomy for pha­ryngeal pouch. Clin Otolaryngol. 1996;21:371–6.
18. Peracchia A, Bonavina L, Surendra N, Segalin A, Antoniazzi L, Marotta G. Minimally invasive surgery for Zenker diverticu­lum: analysis of results in 95 consecutive patients. Arch Surg. 1998;133:695–700.
19. Cook RD, Huang PC, Richstmeier WJ, Scher RL. Endoscopic staple- assisted esophagodiverticulostomy: an excellent treatment of choice for Zenker’s diverticulum. Laryngoscope. 2000;110:2020–5.
20. Van Eeden S, Lloyd RV, Tranter RM.Comparison of the endoscopic stapling technique with more established procedures for pharyngeal pouches: results and patient satisfaction survey. J Laryngol Otol. 1999;113:237–40.
21. Murer K, Soyka MB, Broglie MA, Huber GF, Stoeckli SJ.Zenker’s diverticulum: outcome of endoscopic surgery is dependent on the intraoperative exposure. Eur Arch Otorhinolaryngol. 2015;272:167–73.
22. Stoeckli SJ, Schmid S. Endoscopic stapler-assisted diverticulo­esophagostomy for Zenker’s diverticulum: patient satisfaction and subjective relief of symptoms. Surgery. 2002;131:158–62.
23. Ishaq S, Sultan H, Siau K, Kuwai T, Mulder CJ, Neumann H. New and emerging techniques for endoscopic treatment of Zenker’s diverticulum: state-of-the-art review. Dig Endosc. 2018;30:449–60.
24. Lau K, Watson MG. Pharyngeal pouch: comparison of surgical treatment with botulinum toxin injection to the cricopharyngeus. J Laryngol Otol. 2019;133(2):125–8. https://doi.org/10.1017/
S0022215119000124. [Epub ahead of print].
25. Shah RN, Slaughter KA, Fedore LW, Huang BY, Deal AM, Buckmire RA.Does residual wall size or technique matter in the treatment of Zenker’s diverticulum? Laryngoscope. 2016;126:2475–9.
Open Approach toPharyngeal Pouch
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andCricopharyngeal Myotomy
JemyJose andR.JamesA.England
11
11.1 Introduction
Pharyngeal pouch (also termed Zenkers diverticulum) refers to a false pulsion diverticulum of the hypopharynx passing most commonly through Killian’s dehiscence [1]. It is most common in the eighth decade. The etiopathogenesis of pha­ryngeal pouch formation remains unclear, although most theories centre on cricopharyngeal dysfunction which could be initially associated with dysphagia and later with aspira­tion and regurgitation as a pouch forms.
Pharyngeal pouches may be treated conservatively. However, when sufciently symptomatic, surgical interven­tion may be required. When required, a number of different techniques are employed. Nationally, the commonest inter­vention involves endoscopic stapling of the pouch. Open pouch surgery provides an alternative feasible option. NICE guidelines in 2003 state that endoscopic stapling allows a more rapid recovery, and requires a shorter stay in hospital (1–2days) than open surgery [2]. A Cochrane review in 2005 failed to nd any suitable trials comparing the efcacy of the two interventions [3]. NICE guidelines in 2015 recommend exible endoscopic management of pharyngeal pouch. This was despite perforation rates of 27% in one of the series quoted [4]. A recent series comparing open pouch surgery with pouch stapling suggests the endoscopic approach is quicker than the open approach. However, it also suggests endoscopic treatment is not possible in 9% of cases and is associated with a 23% recurrent surgery rate. Additionally, if pouch resection is avoided when performing the open approach, inpatient stay is equal when comparing the two methods [5].
J. Jose (*) Department of ENT, Hull University Teaching Hospitals NHS Trust, Castle Hill Hospital, Cottingham, UK e-mail: jemy.jose2@nhs.net
R. J. A. England Department of Otorhinolaryngology, Head and Neck Surgery, Hull and East Yorkshire Hospitals NHS Trust, Hull, UK
11.2 Preop Checklist/Considerations/ Anaesthesia
The procedure is performed under general anaesthesia with oral intubation. The endotracheal tube is normally sited on the right-hand side. There is no documented evidence explaining the left-sided approach, but this is probably to minimize risk to the recurrent laryngeal nerve, because the nerve is more medially placed on the left side than the right. External pouch surgery may be performed on the right side in the same manner, and this is worth bearing in mind in the case of revision surgery.
11.2.1 Indications
1. Cricopharyngeal muscle hypertrophy/stricture/spasm
causing dysphagia
2. Pharyngeal pouch of any size
11.2.2 Surgical Technique withTips
1. Pharyngoscopy is performed in order to identify the
pouch. If access is difcult, a short oesophagoscope may be used. An oesophageal bougie of appropriate size is used to dilate the cricopharyngeal segment that is always found anterior to the neck of the pouch. The authors pre­fer to leave the bougie in situ for the duration of the pro­cedure, because this facilitates cricopharyngeal myotomy (it helps when dividing the muscle bres from the outside as it provides a rm surface on which to cut). Insertion of a roll of BIPP pack into the pouch is another technique that may help identication of the pouch during dissec­tion in the neck; this is often not feasible, however, because the BIPP may fall out of the pouch and into the oesophagus.
© Springer Nature Switzerland AG 2024 R. Simo et al. (eds.), Atlas of Head and Neck Surgery, Springer Surgery Atlas Series,
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Oesophagus
Thyropharyngeus
dissected
(divided)
Cavotid sheath
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J. Jose and R. J. A. England
2. The patient is then positioned for the open procedure using a cushion/sandbag under the shoulder and a head ring in order to achieve exion of cervical vertebrae and extension at the atlanto-occipital joint. The patient’s head is rotated to the right in the majority of cases.
3. A J-shaped incision is made along the anterior border of the sternocleidomastoid muscle from the level of hyoid bone curving medially down to 1cm below the cricoid cartilage. The incision is deepened through platysma and deep cervical fascia. The sternocleidomastoid mus­cle is lateralized with a retractor to identify the carotid sheath. The omohyoid muscle is divided. The middle thyroid vein when seen is ligated and divided. The carotid sheath is then retracted laterally to demonstrate the prevertebral fascia. In this manner, the midline struc-
Fig. 11.1 Exposing the pouch after dividing the omohyoid muscle
Cricopharyngeus
tures have been separated from the carotid sheath. The laryngeal skeleton is then rotated away from the sur­geon, whereby the posterolateral aspect of the inferior constrictor bres and the pouch come into view (Fig.11.1). Rotation is crucial, as it protects the recur­rent laryngeal nerve from damage by ensuring the approach is posterolateral and behind the nerve. The pouch is separated from the remaining hypopharyngeal and esophageal mucosa to identify its neck. If the neck of the pouch can thus be identied easily, then a myot­omy may be performed at this stage. If the neck is not obvious, as is often the case, then a vertical myotomy is performed starting in the oesophageal musculature and extending up through the cricopharyngeus (Fig.11.2). This is best performed using a 15 blade gently running
Thyroid cartilage
Cricoid cartilage
Fig. 11.2 Isolating the pouch away from carotid sheath structures
Pouch
out
Pouch
Omohyoid
Sternocleidomastoid
left intact
Neck of
11 Open Approach toPharyngeal Pouch andCricopharyngeal Myotomy
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(b) It does not physiologically add any benet to the pro-
4. At this juncture, pharyngoscopy is performed again
the sac
Cricoid cartilage
Mucosa
Trachea
5. A nasogastric tube is then inserted if there is any doubt
6. Finally, closure of platysma with soluble sutures and skin
11.2.3 Postoperative Care
1. Monitor temperature, pulse, and blood pressure hourly
Fig. 11.3 A cricopharyngeal myotomy
the knife over the muscle bres, which are kept under tension by retraction and the oesophageal bougie. Once oesophageal mucosa is visible, it is often possible to extend the myotomy by opening them perpendicular to the mucosal surface to separate muscle from mucosa and extending the incision cranially. If this is not possi­ble, then the myotomy is extended using the scalpel to expose the oesophageal mucosa. This myotomy is then continued upward until it blends with the cricopharyn­geus and, further up, with the thyropharyngeus. In this manner, a generous myotomy 3–4cm long is performed (Fig.11.3).
Some authors suggest excising the pouch mucosa using a stapling device or excision with primary suture. We do not believe this to be necessary in most cases, because of the following reasons:
(a) It creates a stula that needs to heal in patients who
are often elderly and frail.
2. If observations are normal, clear uids are allowed over-
References
1. Siddiq MA, Sood S, Strachan D.Pharyngeal pouch (Zenker’s diver-
2. National Institute for Health and Care Excellence (NICE).
3. Sen P, Lowe DA, Farnan T. Surgical interventions for pharyngeal
4. National Institute for Health and Care Excellence (NICE). Flexible
5. Agalato E, Jose J, England RJ.Is pharyngeal pouch stapling supe-
119
cedure, because, once the tight cricopharyngeal sphincter muscle bres are divided completely, the pouch stops being a sump.
(BIPP pack removed if inserted) and the scope is inserted into the oesophagus to conrm that the cricopharyngeal bar is no longer present. If the bar is persistent, then return to the neck to divide more muscle bres that have been missed towards the neck of the pouch.
about the integrity of the pharyngoesophageal mucosa.
by clips or sutures is performed.
for 4 h and observe for evidence of backpain, surgical emphysema, tachycardia, and pyrexia, which are features of a perforated oesophagus.
night and normal feeding allowed the following morning followed by discharge.
ticulum). Postgrad Med J. 2001;77(910):506–11.
Endoscopic stapling of pharyngeal pouch: interventional proce­dures guidance [IPG22]. overview 2003.
pouch. Cochrane Database Syst Rev. 2005;(3):CD004459.
endoscopic treatment of a pharyngeal pouch: interventional proce­dures guidance [IPG513]; 2015.
rior to open pharyngeal pouch repair? An analysis of a single institu­tion’s series. J Laryngol Otol. 2016;130(9):873–7.
Part V
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Neck Dissection
Radical andModified Radical Neck
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Dissection
AnthonyBrianPowellMorlandt andAnilD’Cruz
12
12.1 Introduction
The lymphatic basins draining the head and neck contain approximately 300 lymph nodes, 40% of the body’s total, invested within a network of brofatty tissue. Considered the most important prognostic indicator in head and neck epithe­lioid carcinomas, regional lymph node metastasis decreases survival by greater than 50% when compared with localized disease. Radical neck dissection, rst described in 1905, was once performed in conjunction with excision of nearly all primary head and neck cancers. In the current era, however, selective neck dissection with preservation of the internal jugular vein, sternocleidomastoid muscle, and spinal acces­sory nerve is recommended prophylactically for all but the most thin, supercial mucosal head and neck cancers.
12.2 Indications forSurgery
12.2.1 Selective Neck Dissection
A modied radical or selective neck dissection is performed in an elective or therapeutic fashion to remove all lymph nodes from at-risk cervical echelons. In patients with oral tongue tumours deeper than 2–3mm, a survival benet has been seen following selective neck dissection. The selective neck dissection, when performed by an experienced surgeon, involves minimal morbidity and scarring, and can be per­formed on an outpatient basis in some units. In the salvage setting, isolated nodal recurrences have been shown to
A. B. P. Morlandt (*) Section of Oral Oncology, Department of Oral and Maxillofacial Surgery, University of Alabama at Birmingham, Birmingham, AL, USA e-mail: morlandt@uab.edu
A. D’Cruz Department of Head and Neck Surgery, Tata Memorial Hospital, Mumbai, Maharashtra, India
decrease disease-specic survival by 54%. Sentinel lymph node biopsy, though accepted for treatment of the N0 neck in patients with head and neck melanoma, has not supplanted the selective neck dissection as the standard of care for early­stage oral cavity or oropharyngeal tumours.
12.2.2 Radical Neck Dissection
The radical neck dissection is carried out for therapeutic pur­poses when bulky nodal disease precludes preservation of the internal jugular vein, sternocleidomastoid muscle, or spi­nal accessory nerve.
12.2.3 Microvascular Free Flap Access
In some cases, such as sarcoma, low-grade salivary gland malignancy, or early-stage squamous cell carcinoma of the oral cavity, a low risk of occult metastasis may preclude elec­tive neck dissection. In these instances, to provide access to the blood-supplying artery and recipient vein used for micro­vascular anastomosis, the surgeon may be inclined to per­form a limited neck dissection, with removal of the submandibular gland and lymph node–bearing brofatty tis­sue, on approach to the vessels.
12.3 Surgical Technique withTips
Positioning: The operation is performed in the supine posi­tion, with a shoulder roll oriented vertically between the scapulae or horizontally at the level of C7. In one of the authors’ units, we position the patient’s head 180° from the anaesthesia machine to provide adequate space for the sur­geon’s team and any additional equipment needed (endo­scope, navigation, etc.).
© Springer Nature Switzerland AG 2024 R. Simo et al. (eds.), Atlas of Head and Neck Surgery, Springer Surgery Atlas Series,
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Incision: For selective neck dissection, the incision is designed in a curvilinear fashion and extends from the ster­nocleidomastoid muscle towards the midline. In patients with a thin neck and lax skin, a short-scar incision (4–5cm) improves cosmesis. A radical neck dissection requires unre­stricted access to level V, so a posterior releasing incision is often used. A popular design is the “inverted wine glass”– shaped Schobinger modication.
Flap elevation: The wound is deepened through the sub­cutaneous tissues and platysma muscle, and subplatysmal aps are elevated to the inferior border of the mandible supe­riorly and to the clavicle inferiorly (Fig.12.1). In the radical neck dissection, care must be exercised when raising the posterior skin aps to avoid injuring the spinal accessory nerve, which runs immediately deep to the dermis in this region. Skin hooks or Lahey clamps are used to provide skin retraction during ap elevation. Maintaining a plane above the external and anterior jugular veins and greater auricular nerve is key to avoid injuring these structures inadvertently.
The operation then proceeds generally in the anterior to posterior direction, starting in level Ia with elevation of the brofatty node-bearing tissues off of the anterior bellies of the digastric muscles bilaterally, the mandibular symphysis superiorly, and, on the deep aspect, the mylohyoid muscle. The submental vessels are clipped and divided, and the spec­imen is retracted inferiorly towards the hyoid bone. The anterior jugular veins are a potentially troublesome source of bleeding if entered during sharp elevation of the specimen off of the infrahyoid muscles.
Next, inferior to the antegonial notch, the supercial layer of deep cervical fascia is incised to expose the submandibu­lar gland and provide access to the anterior facial vein and facial artery; the marginal mandibular branch of the facial nerve may be visualized coursing through the fascia. The “Hayes Martin” manoeuvre involves ligating and dividing the facial vessels, then superiorly retracting the ligature to protect the facial nerve, positioned superiorly and supercially.
Level Ib is then cleared by skeletonizing the lateral sur­face of the mylohyoid muscle. Lying on the muscle are numerous ranine veins, which should be controlled prior to dividing, lest they retract into the muscle and continue to bleed during the procedure or even after the patient is sitting upright in the recovery suite. An appendiceal or Army-Navy retractor retracts the mylohyoid muscle superomedially to expose the submandibular ganglion and submandibular duct, both of which are clipped and divided. The lingual nerve may be seen coursing under the mylohyoid muscle (Fig. 12.2), and when the ganglion is divided, it typically retracts towards the oor of the mouth. Deep to the digastric posterior belly, the hypoglossal nerve may be encountered and should be protected from injury. After dividing the sub­mandibular duct and ganglion, the gland and remaining specimen are retracted inferiorly, where the facial artery is once again encountered and divided.
Tip: If microvascular reconstruction is planned, an addi­tional 1–3cm of length may be gained by freeing the facial artery from the medial aspect of the gland until the rst major branch point is encountered. This manoeuvre, which is often necessary when upper or midface reconstruction is planned, may obviate the need for vein grafting to augment the pedi­cle length.
Fig. 12.1 Subplatysmal aps
Fig. 12.2 Lingual nerve is seen in level Ib, with the submandibular
ganglion connecting the nerve with the submandibular gland (retracted inferiorly in Allis clamps)
12 Radical andModied Radical Neck Dissection
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Dissection is then carried posteriorly across the tail of the parotid gland, where the retromandibular vein is ligated and divided. When clinically free of disease, judicious removal of the parotid gland is advised, as signicant facial oedema may follow.
Attention is then directed to the midline, where dissection proceeds along a broad front, from level Ia superiorly to the inferior edge of the omohyoid muscle inferiorly. The supe­rior thyroid and superior laryngeal arteries are preserved, as is the common facial vein (also an important option for microvascular reconstruction).
Next, the carotid artery is exposed by incising the carotid sheath vertically along its length. The vagus nerve and inter­nal jugular vein (IJV) are now seen, and care must be exercised to include the nodes posterior to the vein in the specimen.
One of several techniques may be then used to skeletonize the IJV.The surgeon may dissect sharply with a #10 or #15 blade or Metzenbaum scissors, or may choose to bluntly separate the vein from its fascial sheath with Kittner dissect­ing sponges or a plain gauze pad, using digital pressure. Regardless of the method used, the four to six tributary veins draining into the IJV must be carefully identied and ligated before proceeding to the next step in the operation. Failure to recognize disruption of one of these small veins may result in signicant postoperative haemorrhage, and the weight of the large IJV may occlude and obscure bleeding during the operation.
At this point, the specimen is laid upon the great vessels and attention is directed to the lateral edge of the sternoclei­domastoid (SCM) muscle. The fascia overlying the muscle is grasped with Allis clamps and lifted off the muscle, includ­ing any external jugular lymph nodes associated with the vein. The external jugular vein and greater auricular nerve should be carefully protected, again preserving the length of this vein for the microsurgeon. As the SCM is unwrapped medially, many vessels must be clipped as they enter the muscle. With a Green or similar retractor, the SCM is then held laterally and dissection continues towards the deep cer­vical fascia (Fig.12.3).
Radical Neck Dissection Modication: The IJV is double­suture ligated and divided superiorly at the skull base and inferiorly just above the clavicle. A transxion suture pro­vides additional safety.
At the junction of the upper third and lower two-thirds of the SCM muscle, the spinal accessory nerve is found pierc­ing the muscle on its course from the skull base to the trape­zius muscle. Judicious mobilization of the nerve is recommended, as even minor trauma may result in postop­erative shoulder weakness and pain. A nerve hook is then used to gently lift the nerve, so that the contents of level IIb may be elevated off of the splenius capitus muscle and brought under the nerve, in continuity with the remainder of
125
Fig. 12.3 Specimen out
the specimen. Occasionally, the occipital artery is seen coursing laterally through the submuscular recess of level IIb.
With two Army-Navy retractors oriented at right angles to one another—one under the SCM and one under the poste­rior belly of the digastric muscle—the specimen is then brought off of the deep cervical fascia using monopolar cau­tery. The phrenic nerve runs immediately deep to this fascia, so dissection should proceed in a more supercial plane. To aid with orientation, the surgeon maintains the plane of dis­section above the cervical nerve rootlets. A vein retractor is used to protect the great vessels medial to the specimen. With the omohyoid muscle retracted inferiorly towards the clavicle, the inferior boundary of the dissection is dened at the lower edge of level IV. Here, the transverse cervical artery and vein are seen and should be protected. At times, a high-riding subclavian vein is seen in this location. On the left side of the neck, the thoracic duct also resides in this location and should be checked for injury by asking the anaesthetist to perform a Valsalva manoeuvre (Fig.12.4).
Radical Neck Dissection Modication: The SCM is divided, and the spinal accessory nerve may be sacriced as well during this step if bulky disease is present. The cervical nerve rootlets are also divided and included with the specimen.
The specimen is then delivered intact, oriented with sutures or tags for the pathologist, and submitted for perma­nent section histology. The neck wound should then be irri­gated with warm saline and closed over suction drains.
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Fig. 12.4 (a) Thoracic duct injury is seen deep in level IV, with clear, instead of white, chyle egress in the fasting surgical patient. (b) Repaired thoracic duct injury and no chyle seen on Valsalva manoeuvre
12.4 Nomenclature andClassication
12.5 Complications andPostoperative
Management
The rst widely adopted classication system was presented in 1991 by the American Society of Head and Neck Surgery and was later revised in 2002 and 2008 (Robbins etal.). In 2011, Ferlito etal. proposed an updated, concise classica­tion schema based on three designations:
1. Symbol ND with laterality indicated
2. Specic lymphatic levels removed (Ia/b, IIa/b, III, IV, Va/b, VI, and VII)
3. Specic nonlymphatic structures removed (e.g. SCM, IJV, CN XII, skin, ECA)
For example a selective neck dissection including removal of levels I through IV with preservation of the SCM, IJV, and CN XI would be designated as “ND (R) (Ia, Ib, IIa, IIb, III, IV).” Outdated terms such as “supraomohyoid” or “antero­lateral neck dissection, ” among others, have been largely replaced by the more descriptive terms above.
12.5.1 Neurologic Injury
Risk of injury to CN VII (marginal mandibular branch), X, XI, and XII and the phrenic nerve accompanies the modied and radical neck dissection operations, though permanent dysfunction is rare. The brachial plexus theoretically may be injured low in level IV if the deep fascia is violated. Dividing the cervical nerve rootlets is associated with temporary inci­sional numbness, which may extend to the earlobe or supra­clavicular skin, though this often presents nothing more than a nuisance to the patient.
12.5.2 Vascular Injury
If the great vessels of the neck are entered during surgery, the vessel wall should be repaired rapidly using nonabsorbable