Next Article in Journal
Nivolumab Hypersensitivity Reactions a Myth or Reality in Solid Tumors—A Systematic Review of the Literature
Next Article in Special Issue
Zinc Finger Proteins in Head and Neck Squamous Cell Carcinomas: ZNF540 May Serve as a Biomarker
Previous Article in Journal
Medical Assistance in Dying in Oncology Patients: A Canadian Academic Hospital’s Experience
Previous Article in Special Issue
A Study of Peripheral Blood Parameters to Predict Response to Induction Chemotherapy and Overall Survival in Advanced Laryngeal Squamous Cell Carcinoma
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Transoral Approach to Parotid Tumors: A Review of the Literature

Division of Otorhinolaryngology, Department of Surgical Sciences, University of Turin, 10126 Turin, Italy
*
Author to whom correspondence should be addressed.
Curr. Oncol. 2022, 29(12), 9416-9427; https://doi.org/10.3390/curroncol29120740
Submission received: 31 October 2022 / Revised: 21 November 2022 / Accepted: 28 November 2022 / Published: 1 December 2022
(This article belongs to the Special Issue Advances in Squamous Cell Carcinoma of the Head and Neck)

Abstract

:
Different surgical techniques have been proposed for parapharyngeal space tumors, including transcervical, transparotid, trans-mandibular, infratemporal, and transoral. The choice of the correct approach depends on the size, localization and nature of the tumor. The transoral approach can be used for benign prestyloid masses, such as tumors of the deep lobe of the parotid gland. It guarantees a short hospitalization without skin scars. The narrowed access represents the main limitation of this technique. This review will summarize and analyze the current knowledge about the transoral approach to parotid lesions. Thirty-seven studies were included in a qualitative and quantitative synthesis. The novelty of this review is the quantitative analyses of the clinical data reported in the included studies.

1. Introduction

Parapharyngeal space (PPS) is located laterally to the pharynx and has the shape of an inverted pyramid extended from the cranial base to the greater cornu of the hyoid bone [1,2]. PPS is divided into prestyloid and retrostyloid compartments by stylohyoid ligament and muscles. Prestyloid space contains the deep lobe of the parotid gland, lymph nodes, ascending pharyngeal artery, ascending palatine artery, and fat, while retrostyloid space contains internal jugular vein, internal carotid artery, cranial nerves (from IX to XII), and lymph nodes (Figure 1) [2].
PPS tumors are uncommon, representing only 0.5% of head and neck neoplasms. Most of them are benign and originate from the deep lobe of the parotid gland [3,4,5]. Magnetic resonance imaging (MRI) with gadolinium and fine needle aspiration cytology (FNAC) represent the gold standard for determining the diagnosis and thus the correct management of the patient. Other radiological examinations may include computed tomography (CT) with contrast, ultrasound scan and magnetic resonance angiography, which is recommended especially for vascularized tumors [6].
Different approaches to PPS tumors have been proposed, such as transcervical, transparotid, transmandibular, infratemporal, and transoral [7,8]. The choice of the surgical approach is based on the type and localization of the tumor and its relationships with neurovascular structures [7,9]. The transoral approach can be used for benign prestyloid masses, such as tumors of the deep lobe of the parotid gland [8].
The transoral approach is performed through an incision near the anterior tonsillar pillar mucosa, thus exposing prestyloid space under the superior pharyngeal constrictor muscle. Stylopharyngeal and styloglossus muscles are important landmarks for the transoral approach to PPS, since they divide pre- and retrostyloid spaces. Therefore, they represent the structures that should not be crossed to avoid severe vascular and nervous damages [10].
This review aims to summarize and analyze the current knowledge about the transoral approach to parotid lesions, with particular attention to tumor features and potential complications.

2. Materials and Methods

A review of the English literature was performed through several databases (PubMed, Scopus, accessed on 30 October 2022) to identify articles published before 30 October 2022. A primary search was performed using the terms “parotid AND transoral AND (tumor OR cancer OR adenoma OR warthin)”. Search strategies were adapted for each database. The references of selected publications were then examined to identify further reports that were not found by database searching, and the same selection criteria were applied.
The inclusion criteria were clinical trials, cohort studies, case-control studies, case series, and case reports, regarding the transoral approach for parotid gland tumors. Exclusion criteria were as follows: non-human studies, non-English literature, transoral approach for non-salivary tumors, and insufficient clinical data (i.e., tumor origin) reported in the paper.
The abstracts of all relevant articles were examined using the inclusion criteria for applicability. The references of the selected publications were reviewed to identify further reports that were not found by database searching. Two independent reviewers (AL, AB), working separately, extracted the data from all the eligible studies, which were subsequently cross-checked. All retrieved full-texts articles were included in the review by a consensus of all the authors.
Tumor volume (V) was calculated assuming ellipsoid shape (l = length, w = width, h = height) [11]:
V = 4 3 × π × l 2 × w 2 × h 2
If the third dimension (h) was not reported, its approximation was [11]:
h = 2 3 × l

3. Review of the Literature

A total of 400 published papers were identified through database searches. After abstract screening for eligibility, 63 articles were considered eligible. Among these, we included 37 articles in qualitative and quantitative synthesis after full-text assessment. The other 26 papers were excluded for the following reasons: non-parotid tumors (n = 6), not transoral approach (n = 8), and incomplete clinical data (n = 12) (Figure 2).
Among the papers that matched the inclusion criteria, 14 publications were case reports and 23 were retrospective studies. One hundred and thirty-nine cases were included in the review (Table 1).
Based on available data, the mean age was 49.44 ± 15.73 years (range 14–78 years), with a male/female ratio of 67/72 (48.2% male, 51.8% female). The maximum tumor size ranged from 10 to 90 mm (mean 48.01 ± 15.29 mm, calculated on 116 patients). The maximum size was greater than 50 mm in 59 cases (42.4%). The mean tumor volume, calculated on 100 patients, was 36.52 ± 32.20 cm3 (range 0.35–141.99 cm3). Therefore, the transoral approach may be a feasible technique also for large tumors of the deep parotid lobe that involve PPS.
Pleomorphic adenoma was reported in most cases (116 patients, 84.1%). Other histotypes were basal cell adenoma (9 patients, 6.5%), carcinoma ex pleomorphic adenoma (6 patients, 4.3%), Warthin tumor (3 patients, 2.2%), mucoepidermoid carcinoma (2 patients, 1.4%), oncocytoma (1 patient, 0.7%), and adenocarcinoma (1 patient, 0.7%). Histology was not reported in one case (0.7%). The transoral approach was used for benign masses in most cases (129 patients, 92.8%, Figure 3). Indeed, benign capsulated masses may be removed through a blunt dissection with a lower risk of injury of vascular PPS structures than malignant lesions that infiltrate surrounding tissues. Preoperative imaging (MRI) is mandatory to evaluate the presence of a tumor capsule or pseudocapsule and correctly select patients for the transoral approach (well-circumscribed masses with a clear cleavage plane from great vessels). Extensive tumors without smooth borders and/or surrounding the facial nerve or major vascular structures may not be suitable for this approach. Moreover, the transoral approach has not been used for retrostyloid masses in the selected studies.
A pure transoral approach was performed in 125 cases (89.9%), while a combined transcervical/transparotid and transoral approach was used in 14 patients (10.1%). Robotic surgery was reported in 55 cases (39.5%) of pure transoral approach and 11 cases (7.9%) of combined approaches. An endoscopic-assisted transoral approach was described in 41 cases (29.5%). Robotic systems and endoscopes were used to improve the visualization of the mass and PPS structures. Indeed, the main limitations of the transoral approach include a poor visualization of PPS major neurovascular structures with possible uncontrollable bleeding, capsule disruption and tumor spillage, and incomplete tumor removal. According to the size and localization of the mass, 0-, 30-, and 45-degree endoscopes were used for the dissection of tumors’ lateral, superior, and deep margins. The development of endoscopy and surgical robotics reduced such disadvantages and increased the feasibility of the transoral approach. However, surgeons must be able to convert the procedure to a transcervical/transparotid approach if needed (impossibility of complete transoral removal, uncontrollable bleeding). Furthermore, trismus is a contraindication for the transoral approach.
Complications were reported in nine cases (6.5%). They were represented by pharyngeal dehiscence (two cases), deep neck space seroma/sialocele (two cases), facial nerve palsy (two cases), and hyperemia of the skin near angulus mandibulae (one case). Two cases described by Boyce et al. had a complication. However, since other patients with non-parotid tumor histology were reported without matching complications, we could not identify those related to parotid tumors (Figure 4) [31]. All the reported complications were solved. No severe bleeding was reported. However, surgeons must be aware of possible severe bleeding from great vascular structures and ready for a prompt transcervical ligation of external carotid artery. A medial displacement of the internal carotid artery should be considered a contraindication for the transoral approach. Severe postoperative pain was not reported in any cases. Wound closure was usually performed in more than one layer to reduce the risk of postoperative wound dehiscence.
The mean follow-up was 26.57 ± 36.58 months (range 1–192 months). However, follow-up was not reported in 31 cases (22.3%). One case of pleomorphic adenoma recurred after 39 months. The low recurrence rate suggests that the transoral approach for selected benign masses has a low risk of capsule disruption and/or incomplete tumor removal. One case of mucoepidermoid carcinoma with positive margins after transoral removal underwent a superficial parotidectomy with traditional open approach. An indication to a pure transoral approach for malignant tumors of the deep parotid lobe involving PPS must be accurately evaluated and reserved to highly selected cases.
The success of the transoral approach for tumors of the deep parotid lobe depends on the correct identification and exposure of the mass to allow the complete removal, prevent recurrence and ensure good functional outcomes, taking into account the risks of PPS surgery.
The main limitations of the published studies include the small number of patients, the short follow-up and the lack of a randomized control group that underwent an external approach.

4. Conclusions and Future Perspectives

Selecting the best approach for PPS tumors originating from the parotid deep lobe is based on the volume and extension of the mass to be removed and its putative nature. With these two parameters being established, the less invasive approach that provided sufficient exposure with a low and acceptable complication rate was then chosen. The transoral approach can be selected for benign lesions of the deep parotid lobe that involve prestyloid space. The literature reported a low complication rate with a good recovery in such cases. The novelty of this review was the quantitative analyses of the clinical data reported in the included studies. Further studies with larger samples are mandatory to better understand the role of the transoral approach for PPS tumors with a particular focus on robotic and endoscopic-assisted surgery.

Author Contributions

Conceptualization, G.R. and G.P.; methodology, G.R.; formal analysis, G.R.; investigation, A.L. and A.B.; resources, G.R.; data curation, G.R.; writing—original draft preparation, A.L. and A.B.; writing—review and editing, G.R., A.A., A.C. and G.P.; visualization, G.R.; supervision, G.P.; project administration, G.P. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Acknowledgments

We thank Riccardo Accattatis for the anatomical representation of the parapharyngeal space (Figure 1).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Abemayor, E.; Lufkin, R. Enhancing access to the parapharyngeal space. Laryngoscope 2002, 112, 757–759. [Google Scholar] [CrossRef] [PubMed]
  2. Dallan, I.; Seccia, V.; Muscatello, L.; Lenzi, R.; Castelnuovo, P.; Bignami, M.; Montevecchi, F.; Tschabitscher, M.; Vicini, C. Transoral endoscopic anatomy of the parapharyngeal space: A step-by-step logical approach with surgical considerations. Head Neck 2011, 33, 557–561. [Google Scholar] [CrossRef]
  3. Kuet, M.L.; Kasbekar, A.V.; Masterson, L.; Jani, P. Management of tumors arising from the parapharyngeal space: A systematic review of 1,293 cases reported over 25 years. Laryngoscope 2015, 125, 1372–1381. [Google Scholar] [CrossRef] [PubMed]
  4. Khafif, A.; Segev, Y.; Kaplan, D.M.; Gil, Z.; Fliss, D.M. Surgical management of parapharyngeal space tumors: A 10-year review. Otolaryngol.—Head Neck Surg. 2005, 132, 401–406. [Google Scholar] [CrossRef] [PubMed]
  5. Olsen, K.D. Tumors and surgery of the parapharyngeal space. Laryngoscope 1994, 104, 1–28. [Google Scholar] [CrossRef]
  6. Shirakura, S.; Tsunoda, A.; Akita, K.; Sumi, T.; Suzuki, M.; Sugimoto, T.; Kishimoto, S. Parapharyngeal space tumors: Anatomical and image analysis findings. Auris Nasus Larynx 2010, 37, 621–625. [Google Scholar] [CrossRef]
  7. Lombardi, D.; Ferrari, M.; Paderno, A.; Taboni, S.; Rampinelli, V.; Barbara, F.; Schreiber, A.; Mattavelli, D.; Tomasoni, M.; Farina, D.; et al. Selection of the surgical approach for lesions with parapharyngeal space involvement: A single-center experience on 153 cases. Oral Oncol. 2020, 109, 104872. [Google Scholar] [CrossRef]
  8. Bass, R.M. Approaches to the diagnosis and treatment of tumors of the parapharyngeal space. Head Neck Surg. 1982, 4, 281–289. [Google Scholar] [CrossRef]
  9. Allison, R.S.; van der Waal, I.; Snow, G.B. Parapharyngeal tumors: A review of 23 cases. Clin. Otolaryngol. Allied Sci. 1989, 14, 199–203. [Google Scholar] [CrossRef]
  10. Laccourreye, O.; Orosco, R.K.; Rubin, F.; Holsinger, F.C. Styloglossus muscle: A critical landmark in head and neck oncology. Eur. Ann. Otorhinolaryngol. Head Neck Dis. 2018, 135, 421–425. [Google Scholar] [CrossRef]
  11. Sápi, J.; Kovács, L.; Drexler, D.A.; Kocsis, P.; Gajári, D.; Sápi, Z. Tumor Volume Estimation and Quasi-Continuous Administration for Most Effective Bevacizumab Therapy. PLoS ONE 2015, 10, e0142190. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Goodwin, W.J.; Chandler, J.R. Transoral excision of lateral parapharyngeal space tumors presenting intraorally. Laryngoscope 1988, 98, 266–269. [Google Scholar] [CrossRef] [PubMed]
  13. Luna-Ortiz, K.; Navarrete-Alemán, J.E.; Granados-García, M.; Herrera-Gómez, A. Primary parapharyngeal space tumors in a Mexican cancer center. Otolaryngol.—Head Neck Surg. 2005, 132, 587–591. [Google Scholar] [CrossRef] [PubMed]
  14. Rahbar, R.; Grimmer, J.F.; Vargas, S.O.; Robson, C.D.; Mack, J.W.; Perez-Atayde, A.R.; Marcus, K.J.; Grier, H.E.; Healy, G.B.; McGill, T.J. Mucoepidermoid carcinoma of the parotid gland in children: A 10-year experience. Arch. Otolaryngol. Head Neck Surg. 2006, 132, 375–380. [Google Scholar] [CrossRef] [Green Version]
  15. Bozza, F.; Vigili, M.G.; Ruscito, P.; Marzetti, A.; Marzetti, F. Surgical management of parapharyngeal space tumors: Results of 10-year follow-up. Acta Otorhinolaryngol. Ital. 2009, 29, 10–15. [Google Scholar]
  16. O’Malley, B.W.; Quon, H.; Leonhardt, F.D.; Chalian, A.A.; Weinstein, G.S. Transoral robotic surgery for parapharyngeal space tumors. ORL J. Otorhinolaryngol. Relat. Spec. 2010, 72, 332–336. [Google Scholar] [CrossRef] [PubMed]
  17. Betka, J.; Chovanec, M.; Klozar, J.; Taudy, M.; Plzák, J.; Kodetová, D.; Lisý, J. Transoral and combined transoral-transcervical approach in the surgery of parapharyngeal tumors. Eur. Arch. Otorhinolaryngol. 2010, 267, 765–772. [Google Scholar] [CrossRef]
  18. Kovacić, M.; Rudić, M.; Kranjcec, Z. Transoral excision of a parapharyngeal space tumor: Case report. Coll. Antropol. 2012, 36 (Suppl. 2), 193–195. [Google Scholar]
  19. De Virgilio, A.; Park, Y.M.; Kim, W.S.; Byeon, H.K.; Lee, S.Y.; Kim, S.H. Transoral robotic surgery for the resection of parapharyngeal tumor: Our experience in ten patients. Clin. Otolaryngol. 2012, 37, 483–488. [Google Scholar] [CrossRef]
  20. Hwang, S.; Choroomi, S.; McArdle, B.; Jacobson, I. Giant de novo pleomorphic adenoma arising from the parapharyngeal space. Case Rep. Otolaryngol. 2013, 2013, 742910. [Google Scholar]
  21. Park, Y.M.; De Virgilio, A.; Kim, W.S.; Chung, H.P.; Kim, S.H. Parapharyngeal space surgery via a transoral approach using a robotic surgical system: Transoral robotic surgery. J. Laparoendosc. Adv. Surg. Tech. A 2013, 23, 231–236. [Google Scholar] [CrossRef] [PubMed]
  22. Hussain, A.; Ah-See, K.W.; Shakeel, M. Trans-oral resection of large parapharyngeal space tumors. Eur. Arch. Otorhinolaryngol. 2014, 271, 575–582. [Google Scholar] [CrossRef]
  23. Chen, W.L.; Wang, Y.Y.; Zhang, D.M.; Huang, H.Q. Endoscopy-assisted transoral resection of large benign parapharyngeal space tumors. Br. J. Oral Maxillofac. Surg. 2014, 52, 970–973. [Google Scholar] [CrossRef] [PubMed]
  24. Samoy, K.; Lerut, B.; Dick, C.; Kuhweide, R.; Vlaminck, S.; Vauterin, T. Transoral robotic surgery for parapharyngeal lesions: A case series of four benign tumors. B-ENT 2015, 11 (Suppl. 24), 55–59. [Google Scholar]
  25. Li, S.Y.; Hsu, C.H.; Chen, M.K. Minimally invasive endoscope-assisted trans-oral excision of huge parapharyngeal space tumors. Auris Nasus Larynx 2015, 42, 179–182. [Google Scholar] [CrossRef] [PubMed]
  26. Iseri, M.; Ozturk, M.; Kara, A.; Ucar, S.; Aydin, O.; Keskin, G. Endoscope-assisted transoral approach to parapharyngeal space tumors. Head Neck 2015, 37, 243–248. [Google Scholar] [CrossRef]
  27. Chan, J.Y.K.; Tsang, R.K.; Eisele, D.W.; Richmon, J.D. Transoral robotic surgery of the parapharyngeal space: A case series and systematic review. Head Neck 2015, 37, 293–298. [Google Scholar] [CrossRef]
  28. Woo, S.H. Endoscope-assisted transoral accessory parotid mass excision. Head Neck 2016, 38, E7–E12. [Google Scholar] [CrossRef]
  29. Dallan, I.; Fiacchini, G.; Turri-Zanoni, M.; Seccia, V.; Battaglia, P.; Casani, A.P.; Cristofani-Mencacci, L.; Sellari-Franceschini, S. Endoscopic-assisted transoral-transpharyngeal approach to parapharyngeal space and infratemporal fossa: Focus on feasibility and lessons learned. Eur. Arch. Otorhinolaryngol. 2016, 273, 3965–3972. [Google Scholar] [CrossRef]
  30. Casale, M.; Capuano, F.; Sabatino, L.; Pace, A.; Oliveto, G.; Vella, P.; Moffa, A.; Salvinelli, F. A safe transoral surgical approach to parapharyngeal tumor arising from deep lobe of parotid gland. SAGE Open Med. Case Rep. 2016, 4, 2050313X1668213. [Google Scholar] [CrossRef]
  31. Boyce, B.J.; Curry, J.M.; Luginbuhl, A.; Cognetti, D.M. Transoral robotic approach to parapharyngeal space tumors: Case series and technical limitations. Laryngoscope 2016, 126, 1776–1782. [Google Scholar] [CrossRef] [PubMed]
  32. Wu, T.T.; Bao, Y.Y.; Zhou, S.H.; Wang, Q.Y.; Shen, L.F. Basal cell adenoma in the parapharyngeal space resected via trans-oral approach aided by endoscopy: Case series and a review of the literature. Medicine 2018, 97, e11837. [Google Scholar] [CrossRef] [PubMed]
  33. Meng, L.Z.; Zhong, Q.; Fang, J.G.; Ma, H.Z.; Wang, J.H.; Wei, Y.X. Early experience in endoscopic transoral resection for parapharyngeal space tumors. Ear Nose Throat J. 2018, 97, E5–E9. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. Maglione, M.G.; Guida, A.; Pavone, E.; Longo, F.; Aversa, C.; Villano, S.; Ionna, F. Transoral robotic surgery of parapharyngeal space tumors: A series of four cases. Int. J. Oral Maxillofac. Surg. 2018, 47, 971–975. [Google Scholar] [CrossRef]
  35. Duek, I.; Sviri, G.E.; Billan, S.; Gil, Z. Minimally Invasive Surgery for Resection of Parapharyngeal Space Tumors. J. Neurol. Surg. B Skull Base 2018, 79, 250–256. [Google Scholar] [CrossRef] [PubMed]
  36. Mani, S.; Mathew, J.; Thomas, R.; MIchael, R.C. Feasibility of Transoral Approach to Accessory Parotid Tumors. Cureus 2019, 11, e4003. [Google Scholar] [CrossRef] [Green Version]
  37. Chen, Z.; Chen, Y.L.; Yu, Q.; Zhou, S.H.; Bao, Y.Y.; Shang, D.S.; Ruan, L.X. Excision of tumors in the parapharyngeal space using an endoscopically assisted transoral approach: A case series and literature review. J. Int. Med. Res. 2019, 47, 1103–1113. [Google Scholar] [CrossRef]
  38. Shen, L.F.; Chen, Y.L.; Zhou, S.H. Three unusual parapharyngeal space masses resected via the endoscopy-assisted transoral approach: Case series and literature review. J. Int. Med. Res. 2020, 48, 0300060520936068. [Google Scholar] [CrossRef]
  39. Moffa, A.; Fiore, V.; Rinaldi, V.; Moffa, A.P.; Magaldi, L.E.; Casale, M.; Cassano, M. Management of Parapharyngeal Space Tumor Using Transoral Robotic Surgery: The Tonsillar Fossa Battlefield. J. Craniofac. Surg. 2020, 31, 1819–1821. [Google Scholar] [CrossRef]
  40. Li, L.; London, N.R.; Li, S.; Chen, X.; Carrau, R.L. Endoscopic Transoral Approach for Resection of Basal Cell Adenoma Arising in Parapharyngeal Space. J. Neurol. Surg. B Skull Base 2020, 82, 675–681. [Google Scholar] [CrossRef]
  41. Yavuz, H.; Vural, O. Transoral Approach to the Giant Deep Lobe Parotid Gland Pleomorphic Adenoma. J. Craniofac. Surg. 2021, 32, E491–E493. [Google Scholar] [CrossRef] [PubMed]
  42. Voora, R.S.; Stramiello, J.; Funk, E.; Califano, J. Transoral Excision of a Large Accessory Parotid Gland Tumor. Ear Nose Throat J. 2021, 01455613211036237. [Google Scholar] [CrossRef] [PubMed]
  43. Tsunoda, A.; Kishimoto, S.; Tou, M.; Anzai, T.; Matsumoto, F.; Oba, S.; Ikeda, K. Endoscopy-Aided Combined Intraoral and Cervical Approach for a Huge Parapharyngeal Benign Tumor. Ear Nose Throat J. 2021, 100, 1041S–1044S. [Google Scholar] [CrossRef] [PubMed]
  44. Jbali, S.; Khaldi, A.; Touati, S.; Gritli, S. Surgical Approaches to Parapharyngeal Space Tumors: An Example and Review of the Literature. Case Rep. Surg. 2021, 2021, 3536145. [Google Scholar] [CrossRef] [PubMed]
  45. Shin, B.J.; Lee, D.H.; Lee, J.K.; Lim, S.C. Surgical Treatment of Parapharyngeal Space Salivary Gland Tumor. J. Craniofac. Surg. 2022, 33, e676–e679. [Google Scholar] [CrossRef] [PubMed]
  46. Salzano, G.; Togo, G.; Maglitto, F.; Borriello, G.; Perri, F.; Audino, G.; Vaira, L.A.; Maglione, M.G.; Petrocelli, M.; Califano, L.; et al. Trans-Oral Robotic Surgery: 14 Cases of Pleomorphic Adenoma of the Parapharyngeal Space. J. Craniofac. Surg. 2022, 33, 1587–1590. [Google Scholar] [CrossRef]
  47. Lenzi, R.; Matteucci, J.; Muscatello, L. Endoscopic transoral approach to accessory parotid gland. Auris Nasus Larynx 2022, 49, 511–514. [Google Scholar] [CrossRef]
  48. Cadena-Piñeros, E.; Moreno-Torres, A.; Correa-Marin, J.; Melo-Uribe, M.A. Transoral robotic surgery for parapharyngeal carcinoma ex-pleomorphic adenoma: A case report. Cancer Rep. 2022, 5, e1692. [Google Scholar] [CrossRef]
Figure 1. Anatomical representation of the parapharyngeal space. Abbreviations: CN, cranial nerve; ICA, internal carotid artery; IJV, internal jugular vein; m./mm., muscle(s).
Figure 1. Anatomical representation of the parapharyngeal space. Abbreviations: CN, cranial nerve; ICA, internal carotid artery; IJV, internal jugular vein; m./mm., muscle(s).
Curroncol 29 00740 g001
Figure 2. Review of the English literature through PubMed and Scopus, accessed on 30 October 2022. Primary search was performed using the terms “parotid AND transoral AND (tumor OR cancer OR adenoma OR Warthin)”.
Figure 2. Review of the English literature through PubMed and Scopus, accessed on 30 October 2022. Primary search was performed using the terms “parotid AND transoral AND (tumor OR cancer OR adenoma OR Warthin)”.
Curroncol 29 00740 g002
Figure 3. Tumor histology in transoral approach (n, %). Abbreviations: AC, adenocarcinoma; BCA, basal cell adenoma; CXPA, carcinoma ex pleomorphic adenoma; MEC, mucoepidermoid carcinoma; NR, not reported; O, oncocytoma; PA, pleomorphic adenoma; WT, Warthin tumor.
Figure 3. Tumor histology in transoral approach (n, %). Abbreviations: AC, adenocarcinoma; BCA, basal cell adenoma; CXPA, carcinoma ex pleomorphic adenoma; MEC, mucoepidermoid carcinoma; NR, not reported; O, oncocytoma; PA, pleomorphic adenoma; WT, Warthin tumor.
Curroncol 29 00740 g003
Figure 4. Complications in transoral approach.
Figure 4. Complications in transoral approach.
Curroncol 29 00740 g004
Table 1. Transoral approach to parotid tumors: review of the literature.
Table 1. Transoral approach to parotid tumors: review of the literature.
ReferenceYear of PublicationAge (y)SexLength (mm)Width (mm)Height (mm)Volume (cm3)HistologyApproachComplications/RecurrencesFollow-Up (Months)
Goodwin et al. [12]198866FNRNRNRNAPATONone120
Goodwin et al. [12]198873FNRNRNRNAPATONone180
Goodwin et al. [12]198868MNRNRNRNAPATORecurred after 39 months39
Goodwin et al. [12]198864MNRNRNRNAPATONone74
Goodwin et al. [12]198869FNRNRNRNABCATONone21
Goodwin et al. [12]198858FNRNRNRNAPATONone22
Luna–Ortiz et al. [13]200537M90NRNRNAPATC + TONone19
Rahbar et al. [14]200614MNRNRNRNAMECTOPositive margins, addressed by superficial parotidectomy13
Bozza et al. [15]200923M30NRNRNAPATONone192
Bozza et al. [15]200953F30NRNRNAPATONone168
O’Malley et al. [16]201052F25NRNRNAPATORSNone37
O’Malley et al. [16]201075F60NRNRNAPATORSPharyngeal dehiscence35
O’Malley et al. [16]201058F43NRNRNAPATORSNone33
O’Malley et al. [16]201069F58NRNRNAPATORSNone32
O’Malley et al. [16]201035F31NRNRNAPATORSPharyngeal dehiscence32
O’Malley et al. [16]201064F32NRNRNAPATORSNone31
O’Malley et al. [16]201040M70NRNRNAPATONone16
Betka et al. [17]201068F50302015.7rPATONoneNR
Betka et al. [17]201037M70504073.3rPATONoneNR
Betka et al. [17]201054F50453035.3PATONoneNR
Betka et al. [17]201072F60504062.8rPATONoneNR
Betka et al. [17]201036F50404041.9PATONoneNR
Betka et al. [17]201052F55503550.4CXPATONoneNR
Betka et al. [17]201053F55303025.9PATONoneNR
Kovačić et al. [18]201245F5050NR43.6PATONone24
De Virgilio et al. [19]201249F4032NR17.9PATORSNoneNR
De Virgilio et al. [19]201243M5540NR42.2PATORSNoneNR
De Virgilio et al. [19]201225M8555NR138.7PATP + TORSNoneNR
De Virgilio et al. [19]201231M8655NR142.0PATP + TORSNoneNR
De Virgilio et al. [19]201236M6030NR37.7PATP + TORSNoneNR
De Virgilio et al. [19]201239M3030NR9.4PATORSNoneNR
De Virgilio et al. [19]201257F4030NR16.8PATORSNoneNR
De Virgilio et al. [19]201224M5040NR34.9PATP + TORSNoneNR
Hwang et al. [20]201334M846539111.5PATC + TODeep neck space seroma that was surgically drained and treated with intravenous antibiotics3
Park et al. [21]201342MNRNRNRNAPATORSNoneNR
Park et al. [21]201331MNRNRNRNAPATORSNoneNR
Park et al. [21]201339MNRNRNRNAPATORSNoneNR
Park et al. [21]201347FNRNRNRNAPATORSNoneNR
Park et al. [21]201357FNRNRNRNAPATORSNoneNR
Park et al. [21]201329MNRNRNRNAPATORSNoneNR
Park et al. [21]201321FNRNRNRNAPATORSNoneNR
Park et al. [21]201354FNRNRNRNAPATORSNoneNR
Park et al. [21]201330MNRNRNRNAPATORSNoneNR
Hussain et al. [22]201449F60503555.0PATONone72
Hussain et al. [22]201460F50402829.3PATONone42
Chen et al. [23]201422F7070NR119.7PAEATONone21
Chen et al. [23]201433F7060NR102.6PAEATONone16
Chen et al. [23]201442M6060NR75.4PAEATONone16
Chen et al. [23]201453M4040NR22.3WTEATONone9
Chen et al. [23]201461M6050NR62.8PAEATONone8
Samoy et al. [24]201566M50NRNRNRPATORSNone9
Li et al. [25]201559F65524986.7PAEATONoneNR
Li et al. [25]201548F40353122.7PAEATONoneNR
Li et al. [25]201542F52494357.4PAEATONoneNR
Iseri et al. [26]201557F42322618.3PAEATONone6
Iseri et al. [26]201553F27313716.2NREATONone6
Iseri et al. [26]201550M59443750.3PAEATOHyperemia of the skin of angulus mandibulae6
Chan et al. [27]201534F47NRNRNAPATORSNone1
Chan et al. [27]201551F60NRNRNABCATORSNone13
Chan et al. [27]201543F54NRNRNAPATORSNone15
Woo et al. [28]201655M4040NR22.3PAEATONone6
Dallan et al. [29]201634F44NRNRNAPAEATONone14
Dallan et al. [29]201657F45NRNRNAPAEATONone14
Dallan et al. [29]201639M43NRNRNAPAEATONone14
Casale et al. [30]201667M56432227.7WTTOSmall collection of saliva, treated with drainage and intravenous antibiotics, solved after 5 daysNR
Boyce et al. [31]201674M3525177.8rPATORSYes18
Boyce et al. [31]201632F251982.0PATORSNone13
Boyce et al. [31]201670M3923157.0MECTORSNone50
Boyce et al. [31]201654M4012102.5PATORSNone5
Boyce et al. [31]201658M3020103.1PATORSNone20
Boyce et al. [31]201673F403575.1BCATORSNone2
Boyce et al. [31]201648M70703077.0PATC + TORSNone11
Boyce et al. [31]201660F42373326.9PATORSNone3
Boyce et al. [31]201670M50404041.9PATORSNone1
Boyce et al. [31]201678F221561.0OTORSNone3
Boyce et al. [31]201665M2812101.8PATORSNone10
Boyce et al. [31]201621M3417103.0PATC + TORSYes1
Boyce et al. [31]201654F231971.6PATORSNone10
Boyce et al. [31]201672F50423033.0PATORSNone1
Wu et al. [32]201852F33NRNRNRBCAEATONone11
Wu et al. [32]201848F60403037.7BCAEATONone20
Wu et al. [32]201841F4030NR16.8BCAEATONone37
Meng et al. [33]201865F50423033.0PATONone20
Meng et al. [33]201867M50403031.4CXPATONone14
Meng et al. [33]201851M60505078.5PATONone14
Meng et al. [33]201845F43403531.5PATONone14
Meng et al. [33]201866M2520174.5PATONone10
Meng et al. [33]201851F50453035.3PATONone8
Meng et al. [33]201844M42323021.1PATONone4
Meng et al. [33]201828M58423240.8PATONone3
Maglione et al. [34]201823M72623888.8PATORSNone36
Maglione et al. [34]201823F60501828.3PATORSNone39
Maglione et al. [34]201844M60302523.6PATONone42
Duek et al. [35]201866FNRNRNR111.0PATORSNone4
Duek et al. [35]201878FNRNRNR28.0PATC + TORSNone4
Duek et al. [35]201842MNRNRNR36.0CXPATC + TORSNone4
Duek et al. [35]201869FNRNRNR32.0CXPATC + TORSNone4
Duek et al. [35]201830MNRNRNR80.2ACTC + TORSMarginal mandibular branch weakness, completely solved within 3 months4
Duek et al. [35]201833MNRNRNR60.0PATC + TORSNone4
Duek et al. [35]201864FNRNRNR67.5PATORSNone4
Mani et al. [36]201943F1010NR0.3PATONone8
Chen et al. [37]201932M5030NR26.2PAEATONone50
Chen et al. [37]201934M5040NR34.9PAEATONone69
Chen et al. [37]201926M55452532.4PAEATONone44
Chen et al. [37]201928M70503564.1PAEATONone50
Chen et al. [37]201961M60453042.4PAEATONone31
Chen et al. [37]201956M50402020.9PAEATONone50
Chen et al. [37]201938F8060NR134.0PAEATONone25
Chen et al. [37]201945M6238NR51.0PAEATONone12
Chen et al. [37]201943M6045NR56.5PAEATONone9
Chen et al. [37]201938F58373033.7PAEATONone8
Shen et al. [38]202072M35302011.0WTTONone23
Shen et al. [38]202061M60453042.4CXPATONone51
Moffa et al. [39]202023F30NRNRNAPATORSNone12
Li et al. [40]202061F32292311.2BCAEATONone52
Li et al. [40]202066M2825207.3BCAEATONone32
Yavuz et al. [41]202170F53483445.3PATONoneNR
Voora et al. [42]202137M4030NR16.8PATONoneNR
Tsunoda et al. [43]202162M70NRNRNAPAEATONone>120
Tsunoda et al. [43]202137M70NRNRNAPAEATONone>120
Tsunoda et al. [43]202165M60NRNRNABCAEATONone>120
Jbali et al. [44]202150M5238NR35.9PATP + TOHouse–Brackmann grade III facial palsy that solves using corticosteroidNR
Shin et al. [45]202260F36NRNRNAPATONone62
Salzano et al. [46]202271M35323017.6PATORSNone6
Salzano et al. [46]202263F4020208.4PATORSNone6
Salzano et al. [46]202264F45402523.6PATORSNone6
Salzano et al. [46]202223M40302012.6PATORSNone6
Salzano et al. [46]202243M30282511.0PATORSNone6
Salzano et al. [46]202233F35302011.0PATORSNone6
Salzano et al. [46]202259F45403028.3PATORSNone6
Salzano et al. [46]202225F35282010.3PATORSNone6
Salzano et al. [46]202255F3520207.3PATORSNone6
Salzano et al. [46]202227M35303016.5PATORSNone6
Salzano et al. [46]202274F43402018.0PATORSNone6
Salzano et al. [46]202258F40352014.7PATORSNone6
Salzano et al. [46]202235F40402016.8PATORSNone6
Salzano et al. [46]202242M38252512.4PATORSNone6
Lenzi et al. [47]202276F3023217.6PAEATONone6
Cadena–Piñeros et al. [48]202259M281741.0CXPATORSNone6
Abbreviations: AC, adenocarcinoma; BCA, basal cell adenoma; CXPA, carcinoma ex pleomorphic adenoma; EATO, endoscopic assisted transoral; F, female; M, male; MEC, mucoepidermoid carcinoma; NA, not applicable; NR, not reported; O, oncocytoma; PA, pleomorphic adenoma; rPA, recurrent pleomorphic adenoma; TC, transcervical; TO, transoral; TORS, transoral robotic surgery; TP, transparotid; WT, Warthin tumor.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Riva, G.; Lorenzi, A.; Borello, A.; Albera, A.; Canale, A.; Pecorari, G. Transoral Approach to Parotid Tumors: A Review of the Literature. Curr. Oncol. 2022, 29, 9416-9427. https://doi.org/10.3390/curroncol29120740

AMA Style

Riva G, Lorenzi A, Borello A, Albera A, Canale A, Pecorari G. Transoral Approach to Parotid Tumors: A Review of the Literature. Current Oncology. 2022; 29(12):9416-9427. https://doi.org/10.3390/curroncol29120740

Chicago/Turabian Style

Riva, Giuseppe, Andrea Lorenzi, Andrea Borello, Andrea Albera, Andrea Canale, and Giancarlo Pecorari. 2022. "Transoral Approach to Parotid Tumors: A Review of the Literature" Current Oncology 29, no. 12: 9416-9427. https://doi.org/10.3390/curroncol29120740

APA Style

Riva, G., Lorenzi, A., Borello, A., Albera, A., Canale, A., & Pecorari, G. (2022). Transoral Approach to Parotid Tumors: A Review of the Literature. Current Oncology, 29(12), 9416-9427. https://doi.org/10.3390/curroncol29120740

Article Metrics

Back to TopTop