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J Rhinol > Volume 32(1); 2025 |
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Availability of Data and Material
The datasets generated or analyzed during the study are available from the corresponding author on reasonable request.
Conflicts of Interest
Yeon Hee Im who is on the editorial board of the Journal of Rhinology was not involved in the editorial evaluation or decision to publish this article. All remaining authors have declared no conflicts of interest.
Author Contributions
Conceptualization: Yeon Hee Im. Data curation: Soo Whan Kim, Chan-Soon Park, Dong-Hyun Kim. Formal analysis: Soo Whan Kim. Investigation: Dong-Hyun Kim. Methodology: Chan-Soon Park. Resources: Dong-Hyun Kim. Supervision: Yeon Hee Im. Validation: Chan-Soon Park. Writing—original draft: Yeon Hee Im. Writing—review & editing: Yeon Hee Im.
Acknowledgments
Fig. 1 was created with the assistance of Research Factory (https://www.rfactory.kr/). We thank for their contribution to the design of Fig. 1.
Study | Study type | Number of patients (M/F) | Mean or median age (yr) | Follow-up periods (mon; mean or median) | Pathology (n) | Complications, n (%) | Recurrence, n (%) | Other outcomes |
---|---|---|---|---|---|---|---|---|
Zhou et al. [1] (2013) | Retrospective cohort study | 17 (NA) | NA | 7–60 | Recurrent MS IP (10) | Epiphora: 0 (0.0%) | 1 in MS IP (5.9%) | |
Nasal polyp in the MS (2) | Dry nose: 0 (0.0%) | |||||||
MS cyst (4) | Numbness: 0 (0.0%) | |||||||
Postoperative bleeding (1) | ||||||||
Comoglu et al. [38] (2016) | Retrospective cohort study | 12 (7/5) | 22.0±5.7 | 8–21 (14.2) | Antrochoanal polyp (12) | NLD injury: 2 (16.7%) | 0 (0.0%) | |
Epiphora: 0 (0.0%) | ||||||||
Synechia requiring removal: 1 (8.3%) | ||||||||
Suzuki et al. [18] (2017) | Retrospective cohort study | 51 (30/21) | 58.7±12.6 | 2–138 | MS IP (51) | Epiphora: 0 (0.0%) | 1 (2.0%) | |
Dry nose: 0 (0.0%) | ||||||||
Numbness: 7 (13.7%) | ||||||||
Prolonged numbness: 0 (0.0%) | ||||||||
External nasal deformities: 0 (0.0%) | ||||||||
Persistent crusting: 0 (0.0%) | ||||||||
Zhou et al. [19] (2018) | Retrospective cohort study | 71 (42/29) | 52.2±12.1 | 13–134 (37.3) | MS IP (71) | NLD injury: 0 (0.0%) | 5 (7.0%) | |
Numbness: 11 (15.5%) | ||||||||
Prolonged numbness: 5 (7.0%) | ||||||||
Nasal alar retraction: 4 (5.6%) | ||||||||
Lin et al. [24] (2018) | Retrospective cohort study | 15 (12/3) | 49.5±15.3 | 6–28 (16.5) | Tumor in the MS (12) | NLD injury: 0 (0.0%) | 1in sinonasal inflammation (6.7%) | |
Sinonasal inflammation (3) | ||||||||
Hildenbrand et al. [41] (2019) | Retrospective cohort study | 17 (13/4) | 54.3 | 24–69 (45.9) | MS IP (17) | Numbness: 4 (23.5%) | 0 (0.0%) | |
Epiphora: 0 (0.0%) | ||||||||
Prolonged numbness: 3 (17.6%) | ||||||||
Nasal alar retraction: 0 (0.0%) | ||||||||
Persistent crusting: 0 (0.0%) | ||||||||
Lin and Chen [40] (2020) | Retrospective cohort study | 21 (16/5) | 51.7±14.5 | 1.4–41.5 (12.7) | Sinonasal papilloma in the MS (9) | Epistaxis: 1 (4.8%) | 0 (0.0%) | SNOT-22 and VAS scores significantly improved among non-papilloma cases but not in papilloma cases. |
Other tumors involving MS (7) | Numbness: 11 (52.4%) | |||||||
Mucocele in the MS (1) | Prolonged numbness: 0 (0.0%) | |||||||
Orbital wall fracture (1) | ||||||||
Sinonasal inflammation (3) | ||||||||
Tomoum et al. [5] (2020) | Prospective cohort study | 25 (10/15) | 37.0±12.0 | 6–14 (10.9) | Antrochoanal polyp (13) | NLD injury: 0 (0.0%) | 1 in antrochoanal polyp (4.8%) | All patients showed significant improvement in SNOT-22 scores. |
Fungal ball in the MS (10) | ||||||||
Displaced tooth in MS (2) | ||||||||
Seresirikachorn et al. [20] (2023) | Retrospective cohort study | 40 (15/25) | 52.8±17.0 | (50.1± 25.2) | Pyriform aperture stenosis (2) | Epiphora: 0 (0.0%) | NA | |
Antrochoanal polyp (2) | Numbness: 4 (10.0%) | |||||||
Mucocele in the MS (1) | Synechia requiring removal: 2 (5.0%) | |||||||
Fungal ball in the MS (4) | External nasal deformities: 0 (0.0%) | |||||||
Rhinosinusitis (8) | ||||||||
Neoplasms (20) | ||||||||
Vinciguerra et al. [8] (2023) | Retrospective cohort study | 50 (27/23) | 48.8±16.5 | (22.8±13.9) | MS IP (26) | Epiphora: 1 (2.0%) | 0 (0.0%) | |
Odontogenic cyst (17) | Numbness: 9 (18.0%) | |||||||
Antrochoanal polyp (6) | Epistaxis: 1 (2.0%) | |||||||
V2 Schwannoma (1) | ||||||||
Liang et al. [54] (2024) | Retrospective cohort study | 122 (68/54) | 50.8±12.8 | 13–192 (86.6) | MS IP (122) | Numbness: 29 (23.8%) | 4 (3.3%) | VAS scores showed significant postoperative improvement. |
Prolonged numbness: 5 (4.1%) |
Study | Study type | Number of patients (M/F) | Mean or median age (yr) | Follow-up periods (mon; mean or median) | Pathology (n) | Complications, n (%) | Recurrence, n (%) | Other outcomes |
---|---|---|---|---|---|---|---|---|
Yu et al. [22] (2018) | Retrospective cohort study | 71 (44/27) | 52 | 37–73 | MS IP (71) | Epiphora: PLRA – 0 (0.0%), MMA+CLA – 0 (0.0%), EMM – 1 (3.3%), MMA – 0 (0.0%) | PLRA – 1 (5.0%) | |
• PLRA–20 | Dry nose: PLRA – 0 (0.0%), MMA+CLA – 0 (0.0%), EMM – 1 (3.3%), MMA – 0 (0.0%) | MMA+CLA – 1 (14.3%) | ||||||
• MMA+CLA – 7 | Numbness: PLRA – 0 (0.0%), MMA+CLA – 1 (14.3%), EMM – 0 (0.0%), MMA – 0 (0.0%) | EMM – 2 (6.7%) | ||||||
• EMM – 30 | Epistaxis: PLRA – 0 (0.0%), MMA+CLA – 0 (0.0%), EMM – 1 (3.3%), MMA – 1 (7.1%) | MMA – 2 (14.3%) | ||||||
• MMA – 14 | ||||||||
Lee et al. [34] (2019) | Retrospective cohort study | 40 (32/8) | • PLRA – 53.6±10.7 | (12.4±11.7) | MS IP (38) | Epiphora: PLRA – 0 (0.0%), CLA – 0 (0.0%) | PLRA – 0 (0.0%) | The duration of numbness was significantly shorter in the PLRA group. |
• PLRA – 10 | • CLA – 53.7±14.2 | Ameloblastoma in the MS (8) | Numbness: PLRA – 3 (30.0%), CLA – 11 (36.7%) | CLA – 0 (0.0%) | ||||
• CLA – 30 | Ossifying fibroma in the MS (1) | Facial pain: PLRA – 0 (0.0%), CLA – 2 (6.7%) | ||||||
Epistaxis: PLRA – 0 (0.0%), CLA – 0 (0.0%) | ||||||||
Nakayama et al. [17] (2020) | Retrospective cohort study | 45 (34/11) | • PLR – 54.1±12.9 | 16–104 (45.3±22.9) | MS IP (45) | NLD injury: PLRA – 0 (0.0%), ESS±CLA – 0 (0.0%) | PLRA – 0 (0.0%) | A Kaplan-Meier plot revealed a significantly lower risk of recurrence for PLRA than for ESS±CLA. |
• PLRA – 27 | • ESS±CLA – 55.1±15.6 | Epiphora: PLRA – 0 (0.0%), ESS±CLA – 0 (0.0%) | ESS±CLA – 3 (16.6%) | |||||
• ESS±CLA* – 18 | Numbness: PLRA – 1 (3.7%), ESS±CLA – 1 (5.6%) | |||||||
Mohankumar et al. [39] (2022) | Prospective cohort study | 60 (NA) | NA | 12 (12) | Maxillary sinusitis (24) | Epiphora: PLRA – 3 (10.0%), MMA – 0 (0.0%) | PLRA – 1 in antrochoanal polyp (3.3%) | No significant difference in improvement in SNOT-22 scores between the groups |
• PLRA – 30 | Allergic fungal sinusitis (8) | Numbness: PLRA – 1 (3.3%), MMA – 0 (0.0%) | MMA – 6 in antrochoanal polyp (20.0%) | |||||
• MMA – 30 | Antrochoanal polyp (24) | Facial swelling: PLRA – 3 (10.0%), MMA – 1 (10.0%) | ||||||
Dentigerous cyst (4) | Facial pain: PLRA – 5 (16.7%), MMA – 3 (10.0%) | |||||||
Vinciguerra et al. [56] (2023) | Retrospective cohort study | 52 (29/23) | • PLRA – 57.5±11.1 | (29.5±14.4) | MS IP (52) | Epiphora: PLRA – 1 (3.8%), EMM – 10 (38.5%) | PLRA – 0 (0.0%) | |
• PLRA – 26 | • EMM – 57.7±14.4 | Dry nose: PLRA – 1 (3.8%), EMM – 13 (50.0%) | EMM – 1 (38.5%) | |||||
• EMM – 26 | Numbness: PLRA – 6 (23.1%), EMM – 8 (30.8%) | |||||||
Nasal crusting: PLRA – 3 (11.5%), EMM – 14 (53.8%) | ||||||||
Epistaxis/infection requiring intervention: PLRA – 1 (3.8%), EMM – 6 (23.1%) | ||||||||
Kondo et al. [57] (2024) | Retrospective cohort study | 140 (68/72) | • PLRA – 52.9±17.9 | 3–132 (32.6±29.3) | Tumor in the MS (140) | Epiphora: PLRA – 0 (0.0%), EMMM – 0 (0.0%) | NA | |
• PLRA – 44 | • EMMM – 52.4±18.5 | Numbness: PLRA – 4 (9.1%), EMMM – 14 (14.6%) | ||||||
• EMMM – 96 | Prolonged numbness: PLRA – 1 (2.3%), EMMM – 5 (5.2%) | |||||||
Synechia requiring removal: PLRA – 2 (4.5%), EMMM – 4 (4.2%) | ||||||||
Nasal cavity stenosis: PLRA – 0 (0.0%), EMMM – 0 (0.0%) | ||||||||
Abdulla et al. [59] (2024) | NA | 30 (18/12) | 39.5±11.5 | 11–23 (14.3) | Antrochoanal polyp (4) | Epiphora: MMA+PLRA – 1 (6.7%), MMA – 0 (0.0%) | MMA+PLRA – 0 (0.0%) | Postoperative improvement in VAS score and Lund-Kennedy Endoscopic scores were significantly higher in the MMA+PLRA group. |
• MMA+PLRA – 15 | Mucocele in the MS (12) | MMA – 4 (26.7%) | ||||||
• MMA – 15 | Allergic fungal sinusitis (14) | Anterior nasal synechia: MMA+PLRA – 1 (6.7%), MMA – 0 (0.0%) |
M, male; F, female; NA, not available; PLRA, prelacrimal recess approach; MMA, middle meatal antrostomy; CLA, Caldwell-Luc approach; ESS, endoscopic sinus surgery; EMM, endoscopic medial maxillectomy; EMMM, endoscopic modified medial maxillectomy; MS, maxillary sinus; IP, inverted papilloma; NLD, nasolacrimal duct; SNOT-22, Sino-Nasal Outcome Test-22; VAS, visual analog scale
Caldwell-Luc approach | Endoscopic medial maxillectomy | Prelacrimal recess approach | |
---|---|---|---|
Benefits | • All areas of the maxillary sinus can be accessed [17] | • All areas of the maxillary sinus can be accessed [1] | • All areas of the maxillary sinus can be accessed with preserving inferior turbinate and nasolacrimal duct, maintaining nasal physiologic function [1,23,33] |
• Useful when the two-port technique is necessary, such as for tumors in infratemporal fossa [34] | • Suitable for tumorous lesions involving medial maxillary sinus wall or nasolacrimal duct [20,33] | • Lesions placed in the lateral or anterior wall of the maxillary sinus, or the alveolar recess can be manipulated [43] | |
Limitations | • Persistent facial numbness, discomfort, or edema, mucocele, and neo-osteogenesis can develop [1,5,23,34] | • Inferior turbinate and nasolacrimal duct are sacrificed, potentially causing empty nose syndrome, dry nose, epiphora, lacrimal pathway obstruction, and dacryocystitis [1,17] | • Nasolacrimal duct is directly exposed and susceptible to potential injury [38,41] |
• Infraorbital nerve or artery can be injured [34] | • Facial paresthesia due to injury of anterior superior alveolar nerve, and nasal mucosa dryness can develop [13,38,41,42] | ||
• Canine fossa puncture site may serve as a potential pathway for tumor spreading [34] | • Superomedial wall of the maxillary sinus is difficult to manage [34] | ||
• Lesions of anterior wall of the maxillary sinus, prelacrimal recess, and alveolar recess are difficult to manage [17,34,41] | • Access might be challenging if the prelacrimal recess is narrow or absent [23, 43] | ||
• Tumorous lesions involving the medial maxillary sinus wall or nasolacrimal duct might not be appropriate [20,33] |
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