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36 Transoral Laser Resection forGlottic andSupraglottic Tumours
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disease-specic survival rates of 94% and 96%, respectively [14], and Lucioni etal. achieved disease-specic survival of 100% with 97% laryngeal preservation rates of and local control with laser alone of 97.5% [15].
Similar survival outcomes are demonstrated by retrospec­tive series for T1b tumours treated with transoral laser sur­gery although surgery may be more challenging, and as a type VI cordectomy may be required, the functional result might be worse than treatment with radiotherapy. Taylor etal. describe local control of 95 and 100% laryngeal preser­vation at 2years in a comparative case series from Canada [16], with signicantly improved survival compared to patients in the same series treated with radiotherapy. Lucioni etal. demonstrate disease-specic survival of 97% with 97% laryngeal preservation and local control with laser of 89% [15].
Retrospective data for T2 glottic carcinoma demonstrate local control rates at 5years between 76 and 89% [1720], and 5-year disease-specic survival rates range from 91 to 98% [17, 19, 21]. Laryngeal preservation rates remain high for this group at 90–95% at 5years [17, 22, 23].
Laser excision of supraglottic tumours offers improved functional outcomes when compared to open partial surgery [24] and offers the potential to avoid radiotherapy. Early supraglottic cancers are well suited to transoral laser exci­sion as access is usually good and the resection can be tai­lored to the extent of the tumour. Consequently, adequate resection margins are easier to achieve in the supraglottis, compared to the glottis, without compromising function.
Data describing outcomes after transoral laser surgery for supraglottic cancers is based upon small case series, result­ing in heterogeneity of the data. Cabanillas etal. compared transoral laser to open surgery for supraglottic tumours stage T1–T3, with 80% disease specic survival, 70% local con­trol and 86% laryngeal preservation at 5years [25]. These results were comparable to the patients in the series treated with open surgery. Breda etal. reported disease-specic sur­vival rates of 89% for T1 and 88% for T2in a smaller case series of supraglottic SCC treated with transoral laser [21]. In one of the larger series of patients with supraglottic cancer (45 T1 and 61 T2), Motta etal. demonstrated 5-year local control of 82% and 63% for T1 and T2, respectively, with laryngeal preservation rates of 89% and 85% [26].
Overall, the data for laser laryngeal surgery demonstrates survival outcomes similar to non-surgical treatment, with similar, if not improved laryngeal preservation rates. There are a number of perceived advantages to transoral laser sur­gery for laryngeal carcinomas, including the potential for re­resection in cases of residual or recurrent disease.
If local failure occurs after transoral laser surgery, the options for salvage including further transoral laser surgery, open partial laryngectomy, total laryngectomy or radiother-
apy are all open for consideration. As laser laryngeal surgery is typically a single procedure, many patients consider it more convenient than a course of radiotherapy, and there is a proven cost benet over radiotherapy [27]. These advantages are reected in the UK NICE guidelines [28], which state transoral laser excision should be offered for T1a tumours, with the option of laser surgery or radiotherapy offered for T1b and T2 cases. The change in recommendation for T1a tumours, from the previous guidance of offering either TLM or RT, follows a rigorous cost effectiveness statistical model.
High-quality evidence on voice outcomes following TLM or RT for laryngeal cancer is lacking. Although systematic review data suggests comparable functional outcomes [29], anecdotally many clinicians feel that TLM may result in inferior voice outcomes, particularly if the anterior commis­sure is involved as webbing commonly occurs. The surgeon should consider the site and extent of the tumour resection, as well as the patient’s view on voice quality, when discuss­ing expected post-treatment voice outcomes.
Bulky and locally advanced glottic and supraglottic tumours require larger resection volumes, which can lead to post-operative voice and swallowing impairment. These fac­tors must be openly discussed with the patient. Ultimately, careful selection of the ideal cases for laser excision with detailed preoperative endoscopic assessment by the operat­ing surgeon will provide the best functional and oncological results.
36.4 Surgical Technique
Transoral laser resection of glottic and supraglottic tumours may be approached via an en bloc resection approach where the entire tumour is excised, with a surrounding margin. An alternative approach, described by Steiner [4], is to transect the tumour with the laser, to assess depth of invasion and improve manipulation of the tumour (Fig.36.1). This tech­nique relies upon the ability to distinguish normal tissue from tumour when cut into with the laser, as cutting through tumour causes obvious charring when viewed under the microscope. The distinction can easily be observed when cutting cleanly through normal tissue. This enables a more accurate assessment of the depth of invasion and therefore the required depth of resection.
Whilst cutting through a tumour does not adhere to the basic concept of tumour resection, there is no evidence to suggest that transecting a tumour leads to increased risk of local recurrence or metastasis. Proponents of this technique suggest that the risk of an involved deep margin is reduced by the ability to assess tumour depth, and transecting large tumours may facilitate resection by enhancing access to infe­rior components after removal of the tumour bulk.
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Fig. 36.1 (a) Diagram of Steiner method of resecting a glottic tumour. Step 1—transect tumour with laser to assess depth of invasion. (b) Diagram of Steiner method of resecting a glottic tumour. Step 2—Once the tumour is split, excise tumour in two or more pieces
L. Warner et al.
36.4.1 Glottic Resections
tailored to excise more limited lesions. Type II cordectomy is suitable for severe dysplasia and micro-invasive carcinoma
Rigid endoscopes (0° and 30°) should be used to gain a detailed understanding of the 3D anatomy of the tumour prior to resection. Following assessment of the tumour, either an en bloc resection or Steiner method should be decided upon. The European Laryngological Society created a clas-
in situ. With experience, a type II cordectomy can be used for invasive carcinoma. Proponents of hydro-dissection (inject­ing saline into the vocal cord to raise the ligament away from the muscle) claim this can aid carcinoma resection and mini­mise vocal cord deformity.
sication system in 2000 (updated in 2007) aiming to improve standardisation of resection for dysplasia and malignancy of the larynx [30]. Whilst this is a useful frame­work that enables comparison of published outcomes accord­ing to resection type, in practice, the resection area is determined by the location and extent of the tumour.
Described below are the steps involved for laser resection
of glottic cancers, according to the ELS classication.
Type III: Trans-muscular Cordectomy (Fig.36.5)
A trans-muscular cordectomy involves resection of the vocal fold epithelium, the lamina propria, the vocal ligament and the vocalis muscle. The resection extent can encompass the entire vocal fold, or may be targeted to excise a localised lesion with an adequate margin. Partial excision of the false cord may be required to access the entire vocal fold, which does not normally compromise speech or swallowing func-
Type I: Subepithelial Cordectomy (Fig.36.2)
Subepithelial cordectomy is indicated for dysplasia and car­cinoma in situ. The plane for resection is through the super­cial layer of the lamina propria, hence unsuitable for
tion. The majority of T1a lesions without widespread muscu­lar inltration can be successfully resected by type III cordectomy. Fig. 36.6 shows appearances after type III resection.
treatment of invasive carcinoma. Type I cordectomy typi­cally removes the entire epithelium from the length of the vocal fold, from the vocal process to the anterior commis­sure, although the resection can be tailed to the disease and left well short of the anterior commissure to avoid webbing. This technique is well suited to the treatment of dysplastic lesions. Fig.36.3 demonstrates the typical appearance after type I cordectomy for high-grade dysplasia.
Type IV: Total Cordectomy (Fig.36.7)
Total cordectomy excises the entire vocal fold, from the vocal process up to (but not involving) the anterior commis­sure. The deep limit of the resection is the inner perichon­drium of the thyroid cartilage. The attachment of the vocal ligament to the thyroid lamina must be divided anteriorly to complete the resection.
Type II: Subligamental Cordectomy (Fig.36.4)
Subligamental cordectomy excises the vocal fold epithelium, Reinke’s space and the vocal ligament, leaving the vocalis muscle as the deep limit of resection. The resection may encompass the entire length of the vocal cord, or may be
Type Va: Extended Cordectomy Encompassing the Contralateral Vocal Fold (Fig.36.8a)
This is performed in a similar fashion to a type IV cordec­tomy, although includes anterior commissure and may encompass the anterior aspect of the contralateral cord. This
36 Transoral Laser Resection forGlottic andSupraglottic Tumours
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Fig. 36.2 Subepithelial cordectomy
I
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Fig. 36.3 Endoscopic photograph of Type I (subepithelial) Cordectomy for high-grade dysplasia
is indicated for T1b lesions affecting the anterior commis­sure or both anterior vocal folds. This technique is somewhat controversial as resection of the anterior commissure and anterior vocal folds is technically challenging and will fre­quently result in poor vocal outcomes. This procedure is now largely replaced by the type VI cordectomy, outlined below.
Type Vb: Extended Cordectomy Encompassing the Arytenoid (Fig.36.8b)
This is similar to a total cordectomy, also excising the ipsilat­eral arytenoid cartilage. Type Vb cordectomy is indicated for posterior glottic lesions; however, vocal fold mobility may be compromised by arytenoid resection, resulting in poor
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Fig. 36.4 Subligamental cordectomy
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II
Fig. 36.5 Trans-muscular cordectomy
III
36 Transoral Laser Resection forGlottic andSupraglottic Tumours
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Fig. 36.6 Endoscopic photograph of trans-muscular (type III) cordectomy for T1a glottic SCC
Fig. 36.7 Total cordectomy.
The false cord may also be excised for access
IV
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Fig. 36.8 (a) Extended cordectomy including anterior commissure and contralateral anterior vocal cord. (b) Extended cordectomy with excision of ipsilateral arytenoid. (c) Extended cordectomy with excision of ventricular fold. (d) Extended cordectomy with subglottic excision
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V (A) V (C)
V (B) V (D)
functional outcomes. Posterior glottic tumours can be chal­lenging to excise well. If tackled with TLM, the resection should be radical in the initial attempt. A partial arytenoidec-
tomy can be performed. Genuine involved margins with TLM resections are more frequent when excising tumours off the arytenoid.
36 Transoral Laser Resection forGlottic andSupraglottic Tumours
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Fig. 36.9 Anterior commissure resection
VI
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Type Vc: Extended Cordectomy Encompassing the Ventricular Fold (Fig.36.8c)
This is an extension of a total cordectomy, encompassing the laryngeal ventricle and false vocal fold. This is indicated for tumours within the laryngeal ventricle, or T2 lesions with inltration of the ventricle or false cord.
Type Vd: Extended Cordectomy Encompassing the Subglottis (Fig.36.8d)
This is a total cordectomy with inferior extension onto the subglottic mucosa, exposing the inner perichondrium of the cricoid cartilage. This is indicated for T2 glottic carcinomas with limited subglottic extension.
Type VI: Cordectomy for Anterior Commissure Carcinoma (Fig.36.9)
This approach is indicated for anterior commissure tumours. The anterior commissurectomy encompasses the anterior commissure and anterior aspects of both vocal folds. To gain adequate access part of the false cords may be removed. The resection begins at the epiglottic petiole, superior to the attach­ment of the vocal ligaments and continues through the liga­ments, detaching them from the thyroid lamina. If cartilage invasion is suspected, cartilage may be excised with the speci­men. The subglottic mucosa or cricothyroid membrane may also need to be resected if required for adequate clearance.
Tumours of the infra-hyoid epiglottis are more challeng­ing to excise transorally as pre-epiglottic space extension may be present even if not detected on staging imaging. If pre-epiglottic space involvement is suspected, the pre­epiglottic fat pad must be divided, approached via the val­lecula to ensure adequate exposure and visualisation of the anterior limit of the tumour. To achieve this, the medial glosso-epiglottic fold is divided, and the suprahyoid epiglot­tis is transected in the sagittal plane. This exposes the pre­epiglottic fat and the laryngeal surface of the epiglottis. Resection of an ipsilateral arytenoid may also be performed, but to avoid signicant aspiration and laryngeal incompe­tence, bilateral arytenoidectomy should not be undertaken.
All resected specimens should be assessed for adequacy of margins, and further marginal biopsies can be taken if there is any uncertainty. Specimens must be orientated for accurate histopathological assessment. Glottic resection specimens may be too small to pin to a board and can be mounted with tissue glue onto a piece of desiccated cucum­ber with a triangular cut out to represent the glottic inlet. Thorough description, ideally with operative photographs and diagrams on the pathology form, will assist the patholo­gist in comprehending the area resected, plus the location of any extramarginal tissue specimens.
36.5 Post-operative Care
36.4.2 Supraglottic Resection
Suprahyoid supraglottic tumours are ideal for transoral laser resection, particularly those on a free edge of the epiglottis, on the lingual surface or tumours of the ventricle or aryepi­glottic fold. En bloc tumour excision is normally feasible for such lesions as access is typically good; however, bulk­ier lesions can be transected to enable access to inferior aspects.
Although uncommon, post-operative airway compromise is a potential risk of transoral laser surgery. This mandates a period of observation for signs of airway obstruction in the immediate post-operative period, although most patients undergoing limited laser laryngeal surgery may be safely managed on a day case basis.
Intravenous dexamethasone is administered on induction of anaesthesia, with repeated doses post-op if required. Nebulised adrenaline (5 mL of 1/1000) should be given if
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signs of airway compromise are observed. Analgesic require­ments are minimal, and simple analgesics or small doses of oral morphine solution normally sufce.
Glottic resections rarely compromise swallowing func­tion, in the absence of pretreatment dysphagia. However, all patients undergoing supraglottic resections should be assessed preoperatively and post-operatively by a head and neck speech and language therapist as these patients may be at risk of aspiration.
Resective pathology should be discussed in a head and neck multidisciplinary team meeting for cases of invasive carcinoma. The technique of TLM resection frequently leads to laser coagulation at tumour margins, which can compro­mise pathological assessment of tumour clearance. Separate marginal/patient-side biopsies at time of the TLM resection can provide additional condence on tumour clearance. Cases where margins are close or involved warrant further microscopic assessment, potentially with repeated resection to ensure clearance, at approximately 6 weeks post­operatively [31]. Regular follow-up with breoptic laryngos­copy is indicated in all cases, ideally with serial endoscopic pictures for case notes to allow comparison. Narrow band imaging is benecial in endoscopic surveillance and should be utilised where available.
References
1. Duncavage J, Ossoff R.Laser application in the tracheobronchial tree. Otolaryngol Clin N Am. 1990;23:67–75.
2. Polanyi T, Bredemeier H, Davis T. A CO2 laser for surgical research. Med Biol Eng. 1970;8:541–8.
3. Vaughan CW, Strong MS, Jako GJ.Larygneal carcinoma: transoral treatment utilizing the CO2 laser. Am J Surg. 1978;163:490–3.
4. Steiner W, Vogt P, Ambrosch P, Kron M.Transoral carbon dioxide laser microsurgery for recurrent glottic carcinoma after radiother­apy. Head Neck. 2004;26:477–84.
5. Canis M, Ihler F, Martin A, Wolff HA, Matthias C, Steiner W.Organ preservation in T4a laryngeal cancer: is transoral laser microsur­gery an option? Eur Arch Otorhinolaryngol. 2013;270:2719–27.
6. Canis M, Ihler F, Martin A, Wolff HA, Matthias C, Steiner W.Results of 226 patients with T3 laryngeal carcinoma after treat­ment with transoral laser microsurgery. Head Neck. 2014;36:652–9.
7. Omi T, Numano K.The role of the CO2 laser and fractional CO2 laser in dermatology. Laser Ther. 2014;23:49–60.
8. Ahmed F, Kinshuck AJ, Harrison M, O’Brien D, Lancaster J, Roland NJ, etal. Laser safety in head and neck cancer surgery. Eur Arch Otorhinolaryngol. 2010;267:1779–84.
9. English J, Norris A, Bedforth N.Anaesthesia for airway surgery. Contin Educ Anaesth Crit Care Pain. 2006;6(1):28–31. https://doi.
org/10.1093/bjaceaccp/mki060.
10. Hemantkumar I. Anesthesia for laser surgery of the airway. Int J Otorhinolaryngol Clin. 2017;9:1–5.
11. O’Hara J, Markey A, Homer JJ. Transoral laser surgery versus radiotherapy for tumour stage 1a or 1b glottic squamous cell car­cinoma: systematic review of local control outcomes. J Laryngol Otol. 2013;127:732–8.
12. Warner L, Lee K, Homer J. Transoral laser microsurgery ver­sus radiotherapy for T2 glottic squamous cell carcinoma: a sys-
tematic review of local control outcomes. Clin Otolaryngol. 2017;42:629–36.
13. Canis M, Ihler F, Martin A, Matthias C, Steiner W.Transoral laser microsurgery for T1a glottic cancer: review of 404 cases. Head Neck. 2015;37:889–95.
14. Lester SE, Rigby MH, Taylor SM. Transoral laser microsurgery outcomes with early glottic cancer: the Dalhousie University expe­rience. J Laryngol Otol. 2011;125:509–12.
15. Lucioni M, Marioni G, Bertolin A, Giacomelli L, Rizzotto G.Glottic laser surgery: outcomes according to 2007 ELS classi­cation. Eur Arch Otorhinolaryngol. 2011;268:1771–8.
16. Taylor SM, Kerr P, Fung K, Aneeshkumar MK, Wilke D, Jiang Y, etal. Treatment of T1b glottic SCC: laser vs. radiation—a Canadian multicenter study. J Otolaryngol Head Neck Surg. 2013;42:22.
17. Peretti G, Piazza C, Cocco D, De Benedetto L, Del Bon F, Redaelli De Zinis LO, Nicolai P. Transoral CO(2) laser treatment for T(is)-T(3) glottic cancer: the University of Brescia experience on 595 patients. Head Neck. 2010;32:977–83.
18. Fang TJ, Courey MS, Liao CT, Yen TC, Li HY.Frozen margin analysis as a prognosis predictor in early glottic cancer by laser cordectomy. Laryngoscope. 2013;123:1490–5.
19. Mantsopoulos K, Psychogios G, Koch M, Zenk J, Waldfahrer F, Iro H. Comparison of different surgical approaches in T2 glottic cancer. Head Neck. 2012;34:73–7.
20. Rödel RM, Steiner W, Müller RM, Kron M, Matthias C.Endoscopic laser surgery of early glottic cancer: involvement of the anterior commissure. Head Neck. 2009;31:583–92.
21. Breda E, Catarino R, Monteiro E.Transoral laser microsurgery for laryngeal carcinoma: survival analysis in a hospital-based popula­tion. Head Neck. 2015;37:1181–6.
22. Lee HS, Chun BG, Kim SW, Kim ST, Oh JH, Hong JC, Lee KD.Transoral laser microsurgery for early glottic cancer as one­stage single-modality therapy. Laryngoscope. 2013;123:2670–4.
23. Hoffmann C, Cornu N, Hans S, Sadoughi B, Badoual C, Brasnu D.Early glottic cancer involving the anterior commissure treated by transoral laser cordectomy. Laryngoscope. 2016;126:1817–22.
24. Rudert HH, Werner JA, Hoft S. Transoral carbon dioxide laser resection of supraglottic carcinoma. Ann Otol Rhinol Laryngol. 1999;108:819–27.
25. Cabanillas R, Rodrigo JP, Llorente JL, Suárez C.Oncologic out­comes of transoral laser surgery of supraglottic carcinoma com­pared with a transcervical approach. Head Neck. 2008;30:750–5.
26. Motta G, Esposito E, Testa D, Iovine R, Motta S.CO2 laser treat­ment of supraglottic cancer. Head Neck. 2004;26:442–6.
27. Higgins KM. What treatment for early-stage glottic carcinoma among adult patients: CO2 endolaryngeal laser excision versus standard fractionated external beam radiation is superior in terms of cost utility? Laryngoscope. 2011;121:116–34.
28. National Institute for Health and Care Excellence. 2016. Cancer of the upper aerodigestive tract: assessment and management in people aged 16 and over (NICE Guideline NG36). https://www.
nice.org.uk/guidance/ng36/chapter/Recommendations. Accessed 3
Dec 2018.
29. Spielmann P, Majumdar S, Morton R.Quality of life and functional outcomes in the management of early glottic carcinoma: a system­atic review of studies comparing radiotherapy and transoral laser microsurgery. Clin Otolaryngol. 2010;35:373–82.
30. Remacle M, Van Haverbeke C, Eckel H, Bradley P, Chevalier D, Djukic V, etal. Proposal for revision of the European laryngologi­cal society classication of endoscopic cordectomies. Eur Arch Otorhinolaryngol. 2007;264:499–504.
31. Bradley PJ, Mackenzie K, Wight R, Pracy P, Paleri V, ENT-UK Head & Neck Group. Consensus statement on management in the UK: transoral laser assisted microsurgical resection of early glottic cancer. Clin Otolaryngol. 2009;34:367–73.
Part XV
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Laryngeal Surgery: Open Approaches
Total Laryngectomy
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HansEdmundEckel andMiquelQuer
37
37.1 Introduction
Total laryngectomy for the treatment of laryngeal cancer was rst performed in Vienna in 1873 by Theodor Billroth. It became the rst standardised major procedure in head and neck oncological surgery and still has a place in the era of chemo-radiation. Advanced laryngeal and hypopharyngeal cancer is the main indication for performing total laryngec­tomy. The aim of the operation is the removal of the entire larynx from the tongue base down to the cervical trachea. The procedure generally requires general anaesthesia with intubation of the airway and post-operative monitoring of the patient at an intermediate care unit. If total laryngectomy is done for previously untreated cancer of the larynx or hypo­pharynx, a unilateral or bilateral neck dissection will invari­ably be an integral part of the surgical concept, and postoperative (chemo-) radiotherapy will usually be recom­mended after surgery. In hypopharyngeal cancer, a partial or total pharyngectomy is included in the procedure, frequently together with a unilateral or subtotal thyroidectomy. The operation results in a complete separation of the alimentary tract from the airway and requires a permanent tracheos­tomy. Post-operatively, the patient will depend on a nasogas­tric feeding tube or intravenous alimentation for a couple of days, before an oral diet can be resumed. Major complica­tions include wound infection, wound dehiscence, pharyngo­cutaneous stula and secondary bleeding. Although nonsurgical organ-preservation protocols have now replaced total laryngectomy for the treatment of many moderately advanced tumours, it is still the standard of care for most
H. E. Eckel (*) Department of Oto-Rhino-Laryngology, Klinikum Klagenfurt am Wörthersee, Klagenfurt am Wörthersee, Austria e-mail: hans.eckel@kabeg.at
M. Quer Department of Otorhinolaryngology–Head and Neck Surgery, Hospital de la Santa Creu I Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain e-mail: mquer@santpau.cat
high-volume tumours and for those with gross cartilage inl­tration. In spite of the deleterious impact on quality of life, it is the only viable option for recurrent disease after initial nonsurgical treatment and for chronic aspiration in patients with a nonfunctioning larynx [1].
37.2 Indications
Current indications for total laryngectomy are essentially the following ones [2]:
• Advanced laryngeal and hypopharyngeal malignant
tumours (mostly squamous cell carcinoma) [3]
• Recurrent laryngeal and hypopharyngeal cancer after
failed radiation or chemo-radiation therapy [4]
• Severe and not otherwise manageable chronic aspiration
in a nonfunctioning larynx (resulting from nonsurgical or surgical organ-preservation approaches to laryngeal can­cer or from neurological disorders) [5, 6]
Prior to advising and scheduling total laryngectomy, alter­native approaches to the disease need to be discussed in an institutional tumour board. Relevant alternatives to total lar­yngectomy include partial laryngectomy (open or via a tran­soral route), radiotherapy and chemo-radiation. For recurrent primary cancer, the best supportive care and/or chemotherapy alone need to be discussed. For chronic aspiration, simple tra­cheostomy and provision of an inatable cannula, laryngo­tracheal separation or closure of the larynx may be considered. Because total laryngectomy is essentially not reversible, the indication should be checked meticulously, and alternatives should be considered with the patient.
Prior to discussing the indications for total laryngectomy, a thorough preoperative assessment is required, which will include a general medical assessment, basic laboratory stud­ies and pulmonary function tests. The latter are particularly important in patients with a longstanding history of smoking
© Springer Nature Switzerland AG 2024 R. Simo et al. (eds.), Atlas of Head and Neck Surgery, Springer Surgery Atlas Series,
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