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6.2 Case Presentations
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laser treatments and reported successful results although disease regression postoperatively could not be assessed routinely in all subjects [22]. Centric et al. also reported the use of ofce-based PDL in 33 patients, 8 of whom had RRP, but reported the need for surgical intervention in the operating room in 81% of their study group (33 patients) [23]. Hamdan et al. reported the successful use of the blue laser (wavelength 445 nm) in a case of RRP that had complete regression of the lesion at 6 weeks follow-up [24]. Several other cases have been also treated with similar outcome. Miller etal. in their cohort of 29 patients with vocal fold lesions, 48% of whom had RRP, reported a signicant decrease in VHI-10 score after therapy [25].
Intralesional injections have gained popular­ity as an adjuvant therapy in patients with rapid growth of the RRP and need for frequent surgi­cal interventions [26, 27]. The most common injected drug with promising long-term results is cidofovir. Intralesional cidofovir injection has been shown to increase the interval between recurrences and to decrease the total number of surgical interventions needed. The drug is used at a concentration that varies between 2.5 mg and 15 mg/ml with a total dose that ranges between 5.6 and 143mg per injection [28, 29]. The carcinogenic effect of cidofovir adjuvant therapy remains controversial with no clear con­sensus on the association between intralesional injections and increased risk of dysplasia or malignant transformation [30, 31]. Although Moore etal found no difference in pre-cidofovir and post-cidofovir dysplasia in 17 patients with an average of 4.6 injections per patient and data for an average of 19.3 months before the rst cidofovir injection and an average of 45 months follow-up after the rst injection [32]. They concluded that cidofovir does not increase dys­plasia risk over the time period studied. Other less used treatment modalities include vascular endothelial growth factor inhibitors (VEGF), bevacizumab, indol-3- carbinol, HPV vaccina­tion, and others. The benecial role of vaccina­tion in patients with active disease remains controversial [33, 34].
6.2 Case Presentations
6.2.1 Case 1: Right Vocal Fold RRP
A 63-year-old man presented to the Voice Clinic (ALH) with hoarseness and throat irritation of a few months’ duration. The patient was a heavy smoker but denied any history of reux, allergy, or voice abuse. His Voice Handicap Index-10 score on presentation was 6, and perceptual eval­uation of his voice revealed grade 1 dysphonia with no breathiness, strain, or asthenia. On laryn­geal examination, he had a right papillomatous lesion extending from the vocal process to the mid-third of the membranous vocal fold (Fig. 6.1). The patient underwent biopsy of the lesion using the transnasal exible endoscope with a working channel, and 3 soft tissue speci­men measuring 0.4 × 0.2 × 0.2cm in aggregate were submitted for pathologic examination. Histologic examination revealed squamous pap­illoma, negative for dysplasia and malignancy. The patient underwent ofce-based blue laser therapy for right vocal fold papilloma using the 400nm glass ber (power 10 W, pulse pause 40 ms, interpole 300 ms). The laser was used in con­tact and non-contact modes. The cup forceps was used to remove the necrotic tissues after laser sur­gery (Fig.6.2, Video 6.1). Four months following the surgery, the patient had no symptoms, and
Fig. 6.1 An endoscopic view of the larynx showing a papillomatous lesion involving the right vocal process through the mid-third vocal fold musculomembranous portion
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Fig. 6.2 An image of the blue laser glass ber directed to the site of the lesion (non-contact mode). (Video 6.1 Blue laser therapy of a right vocal fold papillomatous lesion. The laser is used in non-contact mode) (▶ https://doi.org/10.1007/000- anf)
6 Blue Laser Therapy ofRecurrent Respiratory Papillomatosis
patient was a known smoker but denied a history of reux disease or allergy. The VHI-10 score on presentation was 15. On perceptual evaluation, he had grade 3 dysphonia, grade 3 roughness, and grade 2 breathiness with grade 2 strain. Laryngeal examination showed a papillomatous lesion involving the entire right true vocal fold includ­ing the vocal process and extending to the ante­rior commissure (Fig.6.4). The patient also had a solitary lesion on the laryngeal surface of the epi­glottis. He underwent two blue laser therapy sessions in an ofce setting using non-contact mode and contact mode (Fig. 6.5, Video 6.2).
Fig. 6.3 Laryngeal examination 4 months following blue laser therapy showing complete regression of the lesion
complete regression of the lesion was seen on laryngeal examination (Fig.6.3).
6.2.2 Case 2: Right Vocal Fold RRP
A 68-year-old male smoker presented to the Voice Clinic (ALH) with a history of persistent dysphonia following several surgeries performed over the last 2 years for recurrent respiratory pap­illomatosis. Medical history was positive for dia­betes mellitus type 2 and dyslipidemia. The
Fig. 6.4 An endoscopic view of the larynx showing an exophytic papillomatous lesion involving the right vocal fold and extending to the anterior commissure
Fig. 6.5 An image of the in-ofce surgery showing the blue laser used in a non-contact mode on the superior sur­face of the vocal fold. Note blanching of the lesion. (Video
6.2 Blue laser therapy of a right vocal fold papillomatous lesion. Note blanching of the lesion toward the end of treatment) (▶ https://doi.org/10.1007/000- ane)
6.2 Case Presentations
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Toward the end of the procedure, a cup forceps was used to remove the necrotic tissue from the surgical bed (Fig.6.6). Following laser therapy,
0.1–0.2 cc of cidofovir (15 mg/ml) was injected at the site of the surgery (Fig.6.7). Three months later, the patient underwent another procedure using the same technique (Video 6.3). On his last follow- up, 6 weeks after the second procedure, the patient had marked improvement in his voice quality, and laryngeal examination showed almost complete regression of his laryngeal lesion (Fig.6.8). His VHI-10 score dropped to 0, and perceptual evaluation revealed a normal
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Fig. 6.8 Laryngeal examination 6 weeks after the last surgical intervention showing almost complete regression of the lesion
voice. His fundamental frequency increased from
179.5 Hz to 215.8 Hz, his jitter and shimmer dropped from 1.68 and 7.08, respectively, to
0.453 and 2.78, respectively.
Fig. 6.6 An image showing cup forceps used to clean the debris of the surgical bed following blue laser therapy. (Video 6.3 Blue laser therapy of a papillomatous lesion of the lower lip of the right vocal fold) (▶ https://doi.org/10.1007/000- and)
Fig. 6.7 Image showing tip of a 25-G needle directed toward the surgical bed for injection of 0.1–0.2 Cidofovir (15 mg/ml)
6.2.3 Case 3: Laryngeal RRP
A 53-year-old male patient presented to the Voice Clinic (ALH) with a history of hoarseness associ­ated with shortness of breath that was worsening over time. The patient had known recurrent respi­ratory papillomatosis (RRP) for which he had undergone multiple microlaryngeal surgeries in another hospital using cold steel instruments and carbon dioxide laser. Laryngeal biopsy done pre­viously showed human papilloma virus (HPV) 6 and 11. On presentation the patient had grade 3 dysphonia, grade 3 roughness, and grade 2 breathiness and strain. His VHI-10 score was 19. His dyspnea index score was 8. Acoustic analysis was performed and showed fundamental fre­quency of 165.4 Hz, shimmer percent of 13.14%, jitter percent of 11.86%, noise-to-harmonic ratio of 1.27, voice turbulence index of 0.804, and maximum phonation time of 10.2 s. Laryngeal examination showed papillomatous lesions occu­pying the entire laryngeal surface of the epiglottis, and extending to the aryepiglottic folds, vocal
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6 Blue Laser Therapy ofRecurrent Respiratory Papillomatosis
folds, and subglottic region resulting in narrow­ing of the airway. The patient was advised to undergo serial ofce-based blue laser therapy to widen the glottic opening and facilitate future surgical intervention in the operating room under general anesthesia. The patient and the surgeon reached that consensus given the history of dif­culty intubation that the patient reported and which had led to abortion of the surgery that had been in another hospital prior to his referral. The patient underwent biopsy of the lesion using the transnasal exible endoscope with a working channel, and a soft tissue lesion measuring
0.2 cm was submitted for pathologic examina­tion. Results showed squamous papilloma. This was followed by blue laser therapy which was used in contact and non-contact modes (power 10, pulse duration 400 ms, and pulse pause 300 ms) (Figs.6.9 and 6.10).
On follow-up one month later, the patient reported marked improvement in his voice quality and breathing. Laryngeal examination showed regression in the size of the lesion, mainly poste­riorly where the surgery had been performed. The patient was advised to undergo another blue laser therapy session in addition to intralesion cidofo­vir injection. On follow-up, the patient had improvement in his glottic aperture which allowed intubation for microlaryngeal surgery under suspension microlaryngoscopy (Fig.6.11).
Fig. 6.10 Image showing blue laser application to RRP in the subglottic region in a contact mode. Note blanching of the lesion
Fig. 6.11 Laryngeal image following two sessions of blue laser therapy in the ofce showing widening of the airway
Fig. 6.9 A pre-operative view of the larynx showing extensive disease in the supraglottis with spread of the papillomatous lesion to the subglottic region. Note nar­rowing of the airway
6.2.4 Case 4: Bilateral Vocal FoldRRP
A 42-year-old male patient, non-smoker, known to be pre-diabetic, presented with history of hoarseness of few months’ duration associated with mild dyspnea and frequent episodes of chok­ing, but no dysphagia/odynophagia. On percep­tual evaluation, he had grade 3 dysphonia, grade 3 roughness, and grade 1 breathiness and strain. On laryngeal examination he had papillomatous lesion involving both vocal folds and the anterior commissure, with satellite lesions over the medial surface of the arytenoid on the right side. The patient underwent suspension microlaryngos-
6.2 Case Presentations
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copy, biopsy of the lesion, and Thulium laser therapy under general anesthesia. On follow- up 3 weeks after the surgery, he had marked improve­ment in his voice and breathing. Four months later, the patient presented with recurrence of his symptoms and worsening of his voice. Laryngeal examination showed recurrence of the disease in both vocal folds. The patient was scheduled for ofce-based blue laser therapy and cidofovir injection (Figs.6.12 and 6.13; Video 6.4). The set­ting used was 10 W, 20 ms pulse duration, and 300 ms pause time. On follow-up, the exam showed 50% regression in the size of the lesion.
Fig. 6.12 Intraoperative view showing the 400nm blue laser glass ber aiming at the papillomatous lesion. (Video
6.4 Blue laser therapy of glottic recurrent respiratory pap­illomatosis. The laser is used in contact and non-contact mode) (▶ https://doi.org/10.1007/000- ang)
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Fig. 6.14 An endoscopic image (i-scan) showing the blue laser beam targeting the base of tongue lesion. Note the punctate surface of the papilloma
6.2.5 Case 5: Base ofTongue Papilloma
A 63-year-old man presented to the Voice Clinic (ALH) for further evaluation of his throat after being diagnosed incidentally with a base-of­tongue papillomatous lesions. The patient is a non-smoker and had no history of systemic dis­eases. On presentation, he had a normal voice and denied any symptoms related to the laryngo­pharyngeal complex. Repeated laryngeal exami­nation conrmed the presence of a 2 × 2 cm papillomatous lesion at the base of tongue. The patient underwent blue laser therapy in an ofce setting under local anesthesia. The glass ber was introduced through the working channel of the exible endoscope, and the laser was used in a non-contact mode initially to induce blanching of the lesion and then in a contact mode to ablate the tissue (Fig.6.14). Examination 3 weeks later showed complete regression of the lesion.
Fig. 6.13 An image showing the 25-gauge exible nee­dle directed toward the surgical bed for cidofovir injection
6.2.6 Case 6: Posterior Pharyngeal Wall Papilloma
A 45-year-old male who presented for routine follow-up for a previously treated in-ofce) left vocal fold granuloma (grade 3) was found to have a papilloma on the posterior pharyngeal wall. The patient underwent biopsy of the lesion using
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6 Blue Laser Therapy ofRecurrent Respiratory Papillomatosis
the transnasal exible endoscope with a working channel and one soft tissue lesion measuring 0.3 × 0.3 × 0.2 cm was submitted for pathologic examination. Results showed squamous papil­loma, negative for dysplasia, and malignancy. The patient underwent ofce-based blue laser for posterior pharyngeal wall papilloma excision (Fig. 6.15). Three weeks following the surgery, the patient had complete regression of the lesion and a well-healing wound (Fig.6.16).
Fig. 6.15 An image showing the blue laser in a contact mode on the papillomatous lesion of the posterior pharyn­geal wall. The tip of the glass ber can be used to curet the lesion
6.2.7 Case 7: Posterior Laryngeal Papilloma
This 60-year-old male with recurrent laryngeal papillomatosis presented with dysphonia. The patient had multiple laryngeal surgical procedures. His laryngeal examination demon­strated posterior laryngeal papilloma (Fig.6.17).
In the operating room, the posterior laryn­geal mass was hard and extended inferiorly for more than 1/2 cm, arytenoid cartilage motion was restricted on palpation. Cidofovir was injected beneath the lesion. The initial inci­sions have made around the lesion using sharp instruments. The lesion was dense and hemor­rhagic, and the nal cut was made using blue laser at 10 W, 60 ms pulse time, and 150 ms pulse pause which eliminated hemorrhage and produced no char (Figs.6.18 and 6.19). Total 82 joules were used during the procedure. Both arytenoids were freely mobile at the end of the surgery (Fig. 6.20, Video 6.5). No papilloma recurrence 3 months after the surgery (Fig.6.21).
Fig. 6.16 An endoscopic view of the posterior pharyn­geal wall 3 months following surgery showing complete regression of the papillomatous lesion
Fig. 6.17 Intraoperative surgical view showing posterior laryngeal mass. (Video 6.5 Surgical video showing poste­rior laryngeal papilloma resection using blue laser) (▶ https://doi.org/10.1007/000- anh)
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Fig. 6.18 Intraoperative views showing blue laser using to resect the laryngeal papilloma
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Fig. 6.20 Intraoperative view showing complete papil­loma resection
Fig. 6.19 Intraoperative views showing blue laser using to resect the laryngeal papilloma
Fig. 6.21 Laryngeal examination showing no papilloma recurrence 3 months after the surgery
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6 Blue Laser Therapy ofRecurrent Respiratory Papillomatosis
6.3 Surgical Steps inOce­Based Blue Laser Therapy ofRRP
Step 1: The patient is seated in the upright posi­tion in a standard examination chair. A pad behind his or her head may be placed to stabilize the head during the procedure.
Step 2: Topical anesthesia to the larynx and pharynx is applied using a transnasal, transoral, or percutaneous cervical approach.
Step 3: A exible laryngoscope with a work­ing channel and a side-port suction is introduced through the nasal cavity to perform indirect laryngoscopy.
Step 4: The laser glass ber is introduced through the working channel until the tip of the ber is seen at the end of the endoscope. Note that the introduction of the glass ber is done while the scope is not exed to avoid injury to the working channel. The glass ber can be introduced when the exible endoscope is either in the nasal cavity or before inserting the endoscope in the nose.
Step 5: The exible endoscope with the glass ber is introduced through the nasopharynx, oro­pharynx, and hypopharynx until the targeted lesion is observed.
Step 6: The glass ber is pushed more distally and directed toward the site of the lesion.
Step 7: The laser is used in the non-contact mode and contact mode.
Step 8: Toward the end of the laser therapy, a cup forceps may be introduced through the work­ing channel of the endoscope to remove necrotic tissue in the surgical bed.
Step 9: Cidofovir solution at a concentration that varies between 2.5 and 15 mg/ml may be injected in the bed of the lesion using a 25-guage exible needle that is inserted through the work­ing channel of the endoscope. Alternatively, a transoral needle may be used under exible laryngoscopic guidance.
References
1. Wiatrak BJ, Wiatrak DW, Broker TR, Lewis L.Recurrent respiratory papillomatosis: a longitudi­nal study comparing severity associated with human
papilloma viral types 6 and 11 and other risk fac­tors in a large pediatric population. Laryngoscope. 2004;114(S104):1–23.
2. Buchinsky FJ, Valentino WL, Ruszkay N, Powell E, Derkay CS, Seedat RY, etal. Age at diagnosis, but not HPV type, is strongly associated with clinical course in recurrent respiratory papillomatosis. PLoS One. 2019;14(6):e0216697.
3. McKaig RG, Baric RS, Olshan AF. Human pap­illomavirus and head and neck cancer: epide­miology and molecular biology. Head Neck. 1998;20(3):250–65.
4. Syrjanen S, Puranen M. Human papillomavi­rus infections in children: the potential role of maternal transmission. Crit Rev Oral Biol Med. 2000;11(2):259–74.
5. Formánek M, Jančatová D, Komínek P, Matoušek P, Zeleník K. Laryngopharyngeal reux and her­pes simplex virus type 2 are possible risk factors for adult-onset recurrent respiratory papillomatosis (prospective case–control study). Clin Otolaryngol. 2017;42(3):597–601.
6. Gallagher TQ, Derkay CS. Recurrent respiratory papillomatosis: update 2008. Curr Opin Otolaryngol Head Neck Surg. 2008;16(6):536–42.
7. Ruiz R, Achlatis S, Verma A, Born H, Kapadia F, Fang Y, et al. Risk factors for adult-onset recur­rent respiratory papillomatosis. Laryngoscope. 2014;124(10):2338–44.
8. Kashima HK, Shah F, Lyles A, Glackin R, Muhammad N, Turner L, et al. A comparison of risk factors in juvenile-onset and adult-onset recur­rent respiratory papillomatosis. Laryngoscope. 1992;102(1):9–13.
9. Sataloff RT. Structural abnormalities of the larynx. In: Sataloff RT, editor. Professional voice: the sci­ence and art of clinical care, 3-volume set. San Diego: Plural Publishing; 2017. p.1533–86.
10. Tjon Pian Gi RE, Halmos GB, van Hemel BM, den Heuvel ER, van der Laan BF, Plaat BE, etal. Narrow band imaging is a new technique in visualization of recurrent respiratory papillomatosis. Laryngoscope. 2012;122(8):1826–30.
11. Sataloff RT, Farhad C, Shruti J.Atlas of endoscopic laryngeal surgery. New Delhi: JP Medical Ltd; 2011.
12. Dedo HH, Yu KC. CO2 laser treatment in 244 patients with respiratory papillomas. Laryngoscope. 2001;111(9):1639–44.
13. Crockett DM, McCabe BF, Shive CJ.Complications of laser surgery for recurrent respiratory papilloma­tosis. Ann Otol Rhinol Laryngol. 1987;96(6):639–44.
14. Valdez TA, McMillan K, Shapshay SM.A new laser treatment for vocal cord papilloma—585-nm pulsed dye. Otolaryngology. 2001;124(4):421–5.
15. Burns JA, Zeitels SM, Akst LM, etal. 532nm pulsed potassium-titanyl-phosphate laser treatment of laryngeal papillomatosis under general anesthesia. Laryngoscope. 2007;117(8):1500–4.
16. Burns JA, Zeitels SM, Akst LM, Broadhurst MS, Hillman RE, Anderson R.Effects of 532nm pulsed­KTP laser parameters on vessel ablation in the avian
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chorioallantoic membrane: implications for vocal fold mucosa. Laryngoscope. 2007;117(2):220–5.
17. Kuet ML, Pitman MJ. Photoangiolytic laser treat­ment of recurrent respiratory papillomatosis: a scaled assessment. J Voice. 2013;27(1):124–8.
18. Balouch B, Ranjbar PA, Alnouri G, Al Omari AI, Martha V, Brennan M, etal. Surgical outcome of low­power- density blue laser for vascular lesions of the vocal fold. J Voice. 2022;2022:S0892.
19. Zeitels SM, Burns JA, Franco RA Jr, Hillman RE, Dailey SH, Anderson RR.Ofce-based treatment of glottal dysplasia and papillomatosis with the 585­nm pulsed dye laser and local anesthesia. Ann Otol Rhinol Laryngol. 2004;113(4):265–76.
20. Mouadeb DA, Belafsky PC. In-ofce laryngeal surgery with the 585nm pulsed dye laser (PDL). Otolaryngology. 2007;137(3):477–81.
21. Koufman JA, Rees CJ, Frazier WD, Kilpatrick LA, Wright SC, Halum SL, etal. Ofce-based laryngeal laser surgery: a review of 443 cases using three wave­lengths. Otolaryngology. 2007;137(1):146–51.
22. Zeitels SM, Akst LM, Burns JA, Hillman RE, Broadhurst MS, Anderson RR. Ofce-based 532­nm pulsed KTP laser treatment of glottal papillo­matosis and dysplasia. Ann Otol Rhinol Laryngol. 2006;115(9):679–85.
23. Centric A, Hu A, Heman-Ackah YD, Sataloff RT. Ofce-based pulsed-dye laser surgery for laryngeal lesions: a retrospective review. J Voice. 2014;28(2):262.
24. Hamdan AL, Ghanem A. Un-sedated ofce-based application of blue laser in vocal fold lesions. J Voice. 2021;2021:S0892.
25. Miller BJ, Abdelhamid A, Karagama Y.Applications of ofce-based 445nm blue laser transnasal exible laser surgery: a case series and review of practice. Ear Nose Throat J. 2021;100(1):105–12.
26. Derkay CS.Task force on recurrent respiratory papil­lomas: a preliminary report. Arch Otolaryngol Head Neck Surg. 1995;121(12):1386–91.
27. Schraff S, Derkay CS, Burke B, Lawson L.American Society of Pediatric Otolaryngology members' experi­ence with recurrent respiratory papillomatosis and the use of adjuvant therapy. Arch Otolaryngol Head Neck Surg. 2004;130(9):1039–42.
28. Soma MA, Albert DM. Cidofovir: to use or not to use? Curr Opin Otolaryngol Head Neck Surg. 2008;16(1):86–90.
29. Fusconi M, Grasso M, Greco A, Gallo A, Campo F, Remacle M, et al. Recurrent respiratory papillo­matosis by HPV: review of the literature and update on the use of cidofovir. Acta Otorhinolaryngol Ital. 2014;34(6):375.
30. Wemer RD, Lee JH, Hoffman HT, Robinson RA, Smith RJ. Case of progressive dysplasia concomi­tant with intralesional cidofovir administration for recurrent respiratory papillomatosis. Ann Otol Rhinol Laryngol. 2005;114(11):836–9.
31. Broekema FI, Dikkers FG.Side-effects of cidofovir in the treatment of recurrent respiratory papillomatosis. Eur Arch Otorhinolaryngol. 2008;265(8):871–9.
32. Moore JE, Garcia A, Sanyal S, Saunders S, Portnoy JE, Hu A, etal. Degrees of dysplasia based on viral typing in patients with cidofovir use and recurrent respira­tory papillomatosis. J Voice. 2013;27(6):765–8.
33. Joura EA, Kjaer SK, Wheeler CM, Sigurdsson K, Iversen OE, Hernandez-Avila M, etal. HPV antibody levels and clinical efcacy following administration of a prophylactic quadrivalent HPV vaccine. Vaccine. 2008;26(52):6844–51.
34. Young DL, Moore MM, Halstead LA.The use of the quadrivalent human papillomavirus vaccine (gardasil) as adjuvant therapy in the treatment of recurrent respi­ratory papilloma. J Voice. 2015;29(2):223–9.
Blue Laser Therapy ofVocal Fold
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Leukoplakia
7
7.1 Introduction
Vocal fold leukoplakia is dened as a whitish dis­coloration/plaque of the vocal fold. The esti­mated annual prevalence is 4.2 per 100,000 with a male predilection [1, 2]. When present, leuko­plakia denotes a pathologic transformation of the underlying mucosa of the vocal fold which nor­mally is non-keratinizing stratied epithelium. The histologic changes may vary from cellular hyperplasia to dysplasia to carcinoma. In a review by the French Society of Phoniatrics and Laryngology, vocal fold leukoplakia and dyspla­sia are lumped together to designate “epithelial hyperplastic laryngeal lesions” (EHLL) [3]. In 2017, the WHO classication dichotomized these lesions as low-grade vs. high-grade reecting the lesion’s potential for malignant transformation [4]. Low-grade dysplasia is considered as an abnormal reactive lesion with no cellular atypia, whereas high-grade dysplasia harbors atypical cellular changes such as hyperchromatic nuclei and atypic mitosis. According to numerous stud­ies, it is estimated that around 50% of vocal fold leukoplakia contains dysplastic and/or malignant cells [5–7]. In a review of 2188 cases, Isenberg
Supplementary Information The online version con­tains supplementary material available at https://doi.
org/10.1007/978- 3- 031- 35283- 6_7. The videos can be
accessed individually by clicking the DOI link in the accompanying gure caption or by scanning this link with the SN More Media App.
etal. reported severe dysplasia/carcinoma in situ (CIS) in 15.2% of the cases, and mild/moderate dysplasia in almost one-third of the cases [5]. It is important to note that the likelihood of malignant transformation increases with the degree of dys­plasia, but that lesions with no dysplasia at the time of diagnosis still carry the risk of malignant transformation [7].
Several predisposing factors for malignant transformation of vocal fold leukoplakia have been described in the literature, the most important of which are poor vocal hygiene and smoking. It is estimated that two-thirds of patients with laryn­geal leukoplakia are smokers, and the risk of malignant transformation increases with the dura­tion of smoking [1]. In a case study of 96 patients with laryngeal cancer, Vaezi et al. found that smoking and alcohol were signicant risk factors for malignant transformation with an odd ratio of
5.46 and 1.97, respectively [8]. Similarly, laryngo­pharyngeal reux disease (LPR) has been incrimi­nated in laryngeal cancer and in the progression of leukoplakia to cancer [9, 10]. In a review on the prevalence of laryngopharyngeal reux (LPR) in 113 patients with dysphonia, Koufman et al. reported abnormal 24-hour pH monitoring in almost half the cases. Four of the six patients with vocal fold carcinoma in their study group had LPR [9]. Chen etal. investigated the pathogenic role of reux in 63 patients with laryngeal and pharyngeal cancer and reported abnormal 24-hour pH moni­toring results in 54% of their cohort [10]. Several
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2023 A.-L. Hamdan et al., Blue Laser Surgery in Laryngology,
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