Journal List > J Korean Assoc Oral Maxillofac Surg > v.50(4) > 1516088412

Kim, Lee, Park, and Kim: Three-dimensional analysis of decompression efficacy and influencing factors in the maxillofacial cystic lesions: a retrospective study

Abstract

Objectives

To evaluate the effectiveness of decompression and various parameters that may affect volume change in cystic lesions.

Patients and Methods

This retrospective study included patients who visited the Department of Oral and Maxillofacial Surgery at Ewha Womans University Medical Center between 2012 and 2022 for decompression of cystic lesions of the jaw. To measure volume changes, pre- and post-decompression cone-beam computed tomography was performed and reconstructed in three dimensions using Mimics 25.0 software (Materialise NV). A comparative analysis was performed based on sex, age, initial cyst volume, location, degree of cortical layer expansion, and pathologic diagnosis using the Mann–Whitney U and Kruskal–Wallis tests.

Results

In all 20 cases, the duration of decompression was 7.84±3.35 months, and all patients successfully completed the decompression period without any complications. Significant differences were observed in the reduction rate and shrinkage speed based on the degree of cortical layer expansion. However, only the shrinkage speed (not the reduction rate) showed a significant difference with respect to the initial cyst volume. Significant differences were not observed based on sex, age, location, or pathologic diagnosis.

Conclusion

Although the present study involved a small number of cases, the effectiveness of decompression was confirmed. In particular, 3D analysis overcame the shortcomings of previous studies of decompression and allowed earlier resection. Further studies with more patients are required to provide a rationale for these results and identify factors that influence decompression.

I. Introduction

An odontogenic cyst is a connective tissue-lined space filled with soft or hard substances. The osmotic pressure inside a cyst is higher than in the surrounding area, allowing the entry of foreign tissue and resulting in increased fluid in the cavity and destruction of surrounding bone tissue. These cysts are common within the jaw and are usually slow-growing, asymptomatic, and sometimes remain undetected until they are very large. In such cases, invasion of important anatomical structures such as the inferior alveolar nerve and maxillary sinus, tooth displacement, root resorption, nerve damage, and jaw bone fracture may occur1,2.
Various treatments have been used for managing these cysts, ranging from decompression only to marsupialization, enucleation, and resection or a combination of decompression and enucleation3,4. In developing a treatment plan for a cyst, features such as patient age, anatomical location of the lesion, lesion size, and histological diagnosis should be considered to obtain a better prognosis. Although invasive surgery (such as enucleation and resection) is usually considered the treatment of choice for cyst removal, conservative treatment should be considered if serious complications such as facial deformities, jaw bone fractures, tooth damage, or nerve damage are anticipated following surgery4-9.
Decompression is a common conservative procedure in which the surgeon creates a window between the cyst and external environment, reducing the pressure of the cystic fluid in the cavity to stimulate growth of the osteoblasts10 and induce bone deposition toward the cystic wall10,11. If these methods result in a reduction in lesion size to not affect important anatomical structures such as the teeth or nerves, additional surgery may be performed to excise the remaining cyst2,12.
Although the efficacy of decompression has been reported in several previous studies, the factors affecting cyst volume reduction and the rate of shrinkage remain controversial. The reduction in the size of the bone defects following decompression is commonly evaluated using panoramic radiographic imaging13,14. Thus, information on the three-dimensional (3D) relationship between cystic lesions and major anatomical structures is limited15,16, limiting determination of their exact size. These limitations hinder the ability to identify factors influencing cyst size changes after decompression and plan subsequent treatment strategies.
Thus, assuming that 3D assessment of volumetric changes in cystic lesions before and after decompression surgery could provide a more accurate evaluation of the efficacy of decompression surgery and help identify factors that may influence volume changes, cone-beam computed tomography (CBCT) was used to evaluate the effectiveness of decompression and analyze parameters that may affect the volume change in cystic lesions.

II. Patients and Methods

1. Study design and sample

This retrospective study followed the ethical standards of the Declaration of Helsinki and was approved by the Institutional Review Boards of Ewha Womans University Medical Center, Ewha Womans University Mokdong Hospital (No. 2022-09-003), and Ewha Womans University Seoul Hospital (No. 2022-09-010-002). Informed consent was obtained.
Patients who visited the Department of Oral and Maxillofacial Surgery at Ewha Womans University Mokdong Hospital or Ewha Womans University Seoul Hospital between 2012 and 2022 and who underwent decompression for cystic lesions of the jaw were selected. Twenty-six patients met the inclusion criteria (20 at Ewha Womans University Mokdong Hospital and six at Ewha Womans University Seoul Hospital).
The inclusion criteria were the following: histopathological diagnosis of odontogenic cysts, decompression based on the treatment plan, CBCT performed at least once for preoperative and postoperative comparisons, and at least 6 months of follow-up. The following patients were excluded: patients who did not follow-up after decompression, had missing CT data, were illiterate, did not understand the decompression procedure or did not provide consent, were unable to perform self-cleaning, were pregnant, or had local infection or systemic diseases such as osteoporosis that could affect bone metabolism.

2. Surgical procedures for decompression

All patients underwent a standardized protocol as described below. Patients underwent CBCT imaging between 2012 and 2022 prior to the surgery at Ewha Womans University Mokdong Hospital using the CT scanner DINNOVA 3 (HDX Corp.) at a measurement value of 90 kVp (voltage), quality standard of 10 mA (tube current), and field of view (FOV) of 20×19 cm and between 2019 and 2022 at Ewha Womans University Seoul Hospital using the CT scanner Osstem T1 (Osstem Implant Co., Ltd.) at a measurement value of 95 kVp (voltage), quality standard of 6 mA (tube current), and FOV of 15×9 cm.
An incision was made under local anesthesia (2% lidocaine with 1:100,000 epinephrine; Yuhan Corp.) to perform decompression. A handpiece with a burr was used to create an opening to access the cyst, and a portion of the cystic membrane tissue was dissected and biopsied for histological confirmation. A disposable suction catheter (PVC; MediForce) was cut to the required length and diameter (12-16 Fr) based on the size of the lesion, inserted into the cyst, sutured to the oral mucosa using 4-0 Ethilon (Ethicon) to maintain patency, and irrigated with normal saline several times. In cases where suturing to prevent catheter dislodgement was difficult, acrylic resin was used to fabricate an obturator that could be worn by the patient as shown in Fig. 1. If an impacted third molar or some other tooth was present that could be extracted without complications, the tooth was extracted. Postoperatively, 250 mg amoxicillin and 385 mg ibuprofen were prescribed for 7 days, and the patient used a 0.2% chlorhexidine mouthwash daily. The patient was instructed to return to the clinic every week for 1 month after the procedure and to self-rinse with saline 2-3 times daily. Thereafter, the patient was followed up monthly, and if the catheter became contaminated or had fallen out, it was immediately replaced with a new catheter. CBCT was performed every 2 months to determine the timing of resection based on the size of the lesion and its relationship with the surrounding structures.(Fig. 2) Enucleation was performed when the cystic boundaries were sufficiently clear to minimize damage to the surrounding structures.

3. Data collection

The duration of decompression was calculated as the date of CBCT at the first visit to the department to that of the last CBCT performed before resection. To measure the total volume of each patient’s cystic lesion, the Digital Imaging and Communications in Medicine files were entered into Mimics 25.0 software (Materialise NV). The cross-sectional boundary of the cystic lesion was used to delineate the lesion area using the difference in Hounsfield units in the CBCT images in all directions where the cyst was observed. After establishing the cross-sectional boundary of the lesion, the cyst was reconstructed three-dimensionally to measure its volume.(Fig. 3) The area marked as the cyst was reviewed and corrected along all axes of the CBCT image. The volume change following decompression was visually verified using the same method. In the mandible, the cyst was near the anatomical structures, such as the inferior alveolar nerve, and separation of the nerve and cyst lesion was confirmed during decompression and follow-up. To minimize error, a single clinician (SML) performed the procedure.

4. Parameters considered for evaluating the factors affecting decompression

To determine the factors influencing the effectiveness of decompression, a comparative analysis was performed based on patient sex and age, initial cyst volume, lesion location, degree of cortical layer expansion, and pathologic diagnosis. The criteria for these factors were based on previous studies: age was set at 30 years based on a study by Ihan Hren et al.17, and the initial volume of the cyst was set at 10,000 mm3 based on a study by Anavi et al.18. In addition, based on existing studies, the criteria were set and compared, and the reduction rate and shrinkage speed of the cysts were calculated19. Cases were categorized as severe when the degree of cortical layer expansion extended >1.5-fold buccolingually compared with the opposite normal site, and cases extending <1.5-fold were classified as mild19. To minimize bias, two reviewers independently assessed the data during the data collection and analysis process, and any ambiguous cases were resolved through discussion.

5. Statistical analysis

Data were analyzed using IBM SPSS Statistics for Windows, version 23.0 (IBM Corp.). The Mann–Whitney U and Kruskal–Wallis tests were used for statistical analyses. Statistical significance was set at P<0.05.

III. Results

Among the 26 patients who underwent decompression, six were not included in the study due to failure to attend follow-up appointments at the scheduled times, catheter dislodgement preventing tracking, or missing CBCT images. In all 20 cases (17 at Ewha Womans University Mokdong Hospital and three at Ewha Womans University Seoul Hospital), the duration of decompression was 7.84±3.35 months, and all patients successfully completed the decompression period without any complications such as infection or edema. Furthermore, enucleation was safely performed, and no patients complained of signs of nerve damage. Demographic information regarding the participants is presented in Table 1, and pathological information about the odontogenic cyst is shown in Supplementary Table 1.
Table 2 shows the volume reduction rate and shrinkage speed of 20 odontogenic cysts based on the clinical and radiologic parameters. Significant differences were observed in the cyst volume reduction rate and shrinkage speed based on the degree of cortical layer expansion. Analysis of the degree of cortical layer expansion revealed a reduction rate of 62.0% in 12 mild cases and of 74.0% in eight severe cases, with a P-value of 0.045. In addition, the shrinkage speed was 557.1 mm3/month in mild cases and 1045.8 mm3/month in severe cases, with a P-value of 0.025. However, only shrinkage speed showed a significant difference with respect to the initial cyst volume. For this volume, 16 of 20 patients had a reduction rate of 69.6% when the volume was <10,000 mm3 and of 67.6% when ≥10,000 mm3 (P=0.925). The shrinkage speed was 637.1 mm3/month when the volume was <10,000 mm3 and 1,703.2 mm3/month when ≥10,000 mm3 (P=0.038). Significant differences were not observed based on sex, age, location, or pathologic diagnosis.

IV. Discussion

In this retrospective study, the volume changes in maxillofacial cysts following decompression were analyzed using CBCT, and the effectiveness of decompression for the treatment of cysts was evaluated by assessing the influence of patients’ sex and age, initial cyst volume, lesion location, degree of cortical layer expansion, and pathological diagnosis. Because volume reduction after decompression occurs in three dimensions, measuring the volume or reduction rate of a lesion using two-dimensional panoramic images is not accurate. Thus, 3D analysis using CT is useful for more accurate assessment of cyst volume or involvement of adjacent structures because the boundaries of the lesion are accurately shown20,21. However, conventional CT is expensive and involves high radiation exposure, hindering additional scans during follow-up. In contrast, CBCT is useful due to its low cost and low exposure and has recently become a key diagnostic tool in dentistry, providing 3D images of the maxillofacial area22. Although differences may exist between multidetector CT (MDCT) and CBCT23, recent studies have suggested that these differences are not significant. Furthermore, studies have been performed in which CBCT was used for decompression in the maxillofacial area24.
Those previous results were the basis for the present study, although two different CBCT systems were used. After Mimics software was used to adjust for the three cases impacted by the different systems, the results were not significantly different; therefore, those three cases were included in the analysis.
In the present study, sex and age were not correlated with volume loss. Lizio et al.3, Gao et al.25, and Kubota et al.26 found no correlation between age and volume reduction, while Park et al.2, Anavi et al.18, and Song et al.27 did report such a correlation.
Song et al.27 reported that the volume reduction rate was associated with the original size of the cystic lesion before decompression, and other studies reported that volume reduction increased with cyst size19,28. However, Anavi et al.18 reported a significantly higher rate of reduction for smaller cysts than for larger cysts. In the present study, significant correlation was not observed in the rate of reduction; however, the shrinkage speed was significantly higher for larger cystic lesions (P<0.05).
Regarding the location of the cyst in the jaw, the mean volume reduction rates were 70.3% and 68.5%, with mean shrinkage speeds of 1,207.6 mm3/month and 657.9 mm3/month in the maxilla and mandible, respectively. Although the maxilla showed a higher reduction rate and faster shrinkage speed, the difference was not statistically significant. The higher rate of volume reduction and shrinkage speed in the maxilla may occur because most cysts in that area are associated with the maxillary sinus, which contains air. However, the mandible is a large, hard, U-shaped bone that can hinder volume reduction compared with the maxilla.
In the present study, several factors that may influence cyst volume changes were evaluated, and a significant difference was found in the degree of cortical layer expansion (P<0.05). However, in previous studies, significant differences were not observed in the rate of cyst volume reduction with the degree of cortical layer expansion19,27.
In several studies, volumetric changes following pathologic diagnosis and decompression have been evaluated27,29. Gao et al.25 reported that decompression was more effective for radicular cysts (RCs) than for odontogenic keratocysts (OKCs) or unicystic ameloblastomas. Similar results were obtained by Kubota et al.26, who reported faster shrinkage speed after decompression in RCs than in OKCs or dentigerous cysts (DCs). In contrast, Kim et al.30 reported greater shrinkage in DCs than in OKCs or RCs after decompression. However, Anavi et al.18 reported a few significant intergroup differences in shrinkage speed among RCs, DCs, and OKCs. In the present study, intergroup differences in the rate of reduction and shrinkage speed were not observed (P>0.05).
The factors influencing decompression remain controversial due to variations in conditions and analytical methods across studies. Notably, the results of the present study differed from previous studies due to the relatively small sample size; however, the effectiveness of decompression was confirmed. For large odontogenic cysts in the oral and maxillofacial regions, decompression can minimize damage to the adjacent structures and reduce the amount of bone grafting required, decreasing the treatment cost and risk of graft failure14,31,32. The ability of decompression to reduce the extent or difficulty in performing the surgery, especially in children and older adult patients, leads to more favorable treatment outcomes compared with conventional resection33. Complications have been reported more frequently when immediate excision is performed without decompression or marsupialization of extensive jaw cysts. In the literature, the prevalence of permanent sensory disturbances ranges from 2.0%-18.0%, temporary sensory disturbance from 8.0%-35.0%, and incomplete ossification from 12.0%-40.0%18,34-36. Although the need for additional surgery following sufficient reduction of the cyst volume after decompression is a disadvantage, the resulting histological changes are conducive for resection, as shown in Fig. 4 for the present study. The epithelial lining was confirmed to be thicker and easier to enucleate after decompression7. Marker et al.6 reported that histologic changes facilitated enucleation in 23 OKC cases. However, response to decompression can vary by case, and regular follow-up is essential.
The disadvantages of decompression include a long treatment duration, discomfort, and varying results that greatly depend on patient cooperation37,38. Regarding the decompression period, Enislidis et al.39 reported an average shrinkage of 81% in 446 days, Lizio et al.3 reported an average reduction of 49.86% in 5.7 months, and Song et al.27 reported a 48.28% reduction in volume in six months. Marker et al.6 recommended 12 months of decompression for odontogenic cysts, and Anavi et al.18 recommended 33 months for the maxilla and 22 months for the mandible. Park et al.40 calculated the half-life of an odontogenic cyst to be 270 days. In the present study, the duration of decompression was determined by observing the changes in the lesion. Furthermore, the enucleation was completed without any unusual complications. Compared with the duration of decompression in several previous studies, a short period of decompression was performed in the present study, and the rate of decompression was fast until 3-6 months after the procedure and then gradually slowed.(Supplementary Fig. 1) This finding is consistent with that of Tomomatsu et al.41, who showed a significant difference in the first 3-4.5 months and recommended enucleation be performed at 4.5 months. Although the duration of decompression varies widely by case, the ideal duration of decompression should be considered until the time when resection can be performed without damaging important anatomical structures2,29. The performance of 3D analysis is expected to allow enucleation at an earlier time than in previous cases, somewhat compensating for the shortcomings of decompression. However, the present study had several limitations. The number of cases was relatively small, and there were only a few cases for each pathological diagnosis. In addition, even with appropriate software, standardizing the Hounsfield units obtained from CBCT is difficult compared with those of MDCT, and the results may vary by CBCT machine. This may introduce bias in the statistical analysis of volume changes and the efficacy of decompression. Furthermore, the study was limited to Korean patients, which may introduce regional and racial biases.

V. Conclusion

In the present study, 20 cases were analyzed to measure volume change during decompression of odontogenic cysts. Although the present study involved a small number of cases, the effectiveness of decompression was confirmed. In particular, 3D analysis overcame the shortcomings of previous studies of decompression and allowed earlier resection. Further studies with more patients are required to provide a rationale for these results and identify factors that influence decompression.

Supplementary Materials

Supplementary data is available at http://www.jkaoms.org.

Notes

Authors’ Contributions

H.Y.K. and S.M.L. obtained the data and wrote the manuscript. J.H.P. and S.J.K. reviewed and revised the manuscript. All authors read and approved the final manuscript.

Ethics Approval and Consent to Participate

This retrospective study followed the ethical standards of the Declaration of Helsinki and was approved by the Institutional Review Boards of Ewha Womans University Medical Center, Ewha Womans University Mokdong Hospital (No. 2022-09-003), and Ewha Womans University Seoul Hospital (No. 2022-09-010-002). Informed consent was obtained.

Conflict of Interest

No potential conflict of interest relevant to this article was reported.

References

1. Manor E, Kachko L, Puterman MB, Szabo G, Bodner L. 2012; Cystic lesions of the jaws - a clinicopathological study of 322 cases and review of the literature. Int J Med Sci. 9:20–6. https://doi.org/10.7150/ijms.9.20. DOI: 10.7150/ijms.9.20. PMID: 22211085. PMCID: PMC3222086.
crossref
2. Park HS, Song IS, Seo BM, Lee JH, Kim MJ. 2014; The effectiveness of decompression for patients with dentigerous cysts, keratocystic odontogenic tumors, and unicystic ameloblastoma. J Korean Assoc Oral Maxillofac Surg. 40:260–5. https://doi.org/10.5125/jkaoms.2014.40.6.260. DOI: 10.5125/jkaoms.2014.40.6.260. PMID: 25551089. PMCID: PMC4279975.
crossref
3. Lizio G, Sterrantino AF, Ragazzini S, Marchetti C. 2013; Volume reduction of cystic lesions after surgical decompression: a computerised three-dimensional computed tomographic evaluation. Clin Oral Investig. 17:1701–8. https://doi.org/10.1007/s00784-012-0869-z. DOI: 10.1007/s00784-012-0869-z. PMID: 23099727.
crossref
4. Wakolbinger R, Beck-Mannagetta J. 2016; Long-term results after treatment of extensive odontogenic cysts of the jaws: a review. Clin Oral Investig. 20:15–22. https://doi.org/10.1007/s00784-015-1552-y. DOI: 10.1007/s00784-015-1552-y. PMID: 26250795.
crossref
5. Nakamura N, Mitsuyasu T, Mitsuyasu Y, Taketomi T, Higuchi Y, Ohishi M. 2002; Marsupialization for odontogenic keratocysts: long-term follow-up analysis of the effects and changes in growth characteristics. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 94:543–53. https://doi.org/10.1067/moe.2002.128022. DOI: 10.1067/moe.2002.128022. PMID: 12424446.
crossref
6. Marker P, Brøndum N, Clausen PP, Bastian HL. 1996; Treatment of large odontogenic keratocysts by decompression and later cystectomy: a long-term follow-up and a histologic study of 23 cases. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 82:122–31. https://doi.org/10.1016/s1079-2104(96)80214-9. DOI: 10.1016/S1079-2104(96)80214-9. PMID: 8863300.
7. Pogrel MA, Jordan RC. 2004; Marsupialization as a definitive treatment for the odontogenic keratocyst. J Oral Maxillofac Surg. 62:651–5. discussion 655–6. https://doi.org/10.1016/j.joms.2003.08.029. DOI: 10.1016/j.joms.2003.08.029. PMID: 15170272.
crossref
8. Cranin AN, Madan S, Fayans E. 1994; Novel method of treating large cysts of jaws in children. N Y State Dent J. 60:41–4.
9. Chiapasco M, Rossi A, Motta JJ, Crescentini M. 2000; Spontaneous bone regeneration after enucleation of large mandibular cysts: a radiographic computed analysis of 27 consecutive cases. J Oral Maxillofac Surg. 58:942–8. discussion 949. https://doi.org/10.1053/joms.2000.8732. DOI: 10.1053/joms.2000.8732. PMID: 10981973.
crossref
10. Castro-Núñez J. 2016; Decompression of odontogenic cystic lesions: past, present, and future. J Oral Maxillofac Surg. 74:104.e1–9. https://doi.org/10.1016/j.joms.2015.09.004. DOI: 10.1016/j.joms.2015.09.004. PMID: 26428611.
crossref
11. Bonavolontà P, Dell'Aversana Orabona G, Friscia M, Sani L, Abbate V, Iaconetta G, et al. 2019; Surgical management of large odontogenic cysts of the mandible. J Craniofac Surg. 30:e658–61. https://doi.org/10.1097/scs.0000000000005725. DOI: 10.1097/SCS.0000000000005725. PMID: 31261346.
crossref
12. de Molon RS, Verzola MH, Pires LC, Mascarenhas VI, da Silva RB, Cirelli JA, et al. 2015; Five years follow-up of a keratocyst odontogenic tumor treated by marsupialization and enucleation: a case report and literature review. Contemp Clin Dent. 6(Suppl 1):S106–10. https://doi.org/10.4103/0976-237x.152963. DOI: 10.4103/0976-237X.152963. PMID: 25821360. PMCID: PMC4374304.
crossref
13. Dolanmaz D, Etoz OA, Pampu A, Kalayci A, Gunhan O. 2011; Marsupialization of unicystic ameloblastoma: a conservative approach for aggressive odontogenic tumors. Indian J Dent Res. 22:709–12. https://doi.org/10.4103/0970-9290.93461. DOI: 10.4103/0970-9290.93461. PMID: 22406718.
14. Litvin M, Caprice D, Infranco L. 2008; Dentigerous cyst of the maxilla with impacted tooth displaced into orbital rim and floor. Ear Nose Throat J. 87:160–2. DOI: 10.1177/014556130808700313. PMID: 18404914.
15. Zhao Y, Liu B, Han QB, Wang SP, Wang YN. 2011; Changes in bone density and cyst volume after marsupialization of mandibular odontogenic keratocysts (keratocystic odontogenic tumors). J Oral Maxillofac Surg. 69:1361–6. https://doi.org/10.1016/j.joms.2010.05.067. DOI: 10.1016/j.joms.2010.05.067. PMID: 21195525.
crossref
16. Krennmair G, Lenglinger F. 1995; Imaging of mandibular cysts with a dental computed tomography software program. Int J Oral Maxillofac Surg. 24(1 Pt 1):48–52. https://doi.org/10.1016/s0901-5027(05)80856-2. DOI: 10.1016/S0901-5027(05)80856-2. PMID: 7782641.
crossref
17. Ihan Hren N, Miljavec M. 2008; Spontaneous bone healing of the large bone defects in the mandible. Int J Oral Maxillofac Surg. 37:1111–6. https://doi.org/10.1016/j.ijom.2008.07.008. DOI: 10.1016/j.ijom.2008.07.008. PMID: 18760900.
18. Anavi Y, Gal G, Miron H, Calderon S, Allon DM. 2011; Decompression of odontogenic cystic lesions: clinical long-term study of 73 cases. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 112:164–9. https://doi.org/10.1016/j.tripleo.2010.09.069. DOI: 10.1016/j.tripleo.2010.09.069. PMID: 21194990.
crossref
19. Jeong HG, Hwang JJ, Lee SH, Nam W. 2017; Effect of decompression for patients with various jaw cysts based on a three-dimensional computed tomography analysis. Oral Surg Oral Med Oral Pathol Oral Radiol. 123:445–52. https://doi.org/10.1016/j.oooo.2016.11.012. DOI: 10.1016/j.oooo.2016.11.012. PMID: 28094215.
crossref
20. Pogrel MA. 2005; Treatment of keratocysts: the case for decompression and marsupialization. J Oral Maxillofac Surg. 63:1667–73. https://doi.org/10.1016/j.joms.2005.08.008. DOI: 10.1016/j.joms.2005.08.008. PMID: 16243185.
crossref
21. Marin S, Kirnbauer B, Rugani P, Mellacher A, Payer M, Jakse N. 2019; The effectiveness of decompression as initial treatment for jaw cysts: a 10-year retrospective study. Med Oral Patol Oral Cir Bucal. 24:e47–52. https://doi.org/10.4317/medoral.22526. DOI: 10.4317/medoral.22526. PMID: 30573706. PMCID: PMC6344015.
crossref
22. Khavid A, Sametzadeh M, Godiny M, Moarrefpour MM. 2021; Comparison of the hounsfield unit values obtained from cone-beam computed tomography (CBCT) and multidetector computed tomography (MDCT) images for different bone densities. J Contemp Med Sci. 7:92–5. DOI: 10.22317/jcms.v7i2.943.
crossref
23. Liang X, Lambrichts I, Sun Y, Denis K, Hassan B, Li L, et al. 2010; A comparative evaluation of cone beam computed tomography (CBCT) and multi-slice CT (MSCT). Part II: on 3D model accuracy. Eur J Radiol. 75:270–4. https://doi.org/10.1016/j.ejrad.2009.04.016. DOI: 10.1016/j.ejrad.2009.04.016. PMID: 19423257.
crossref
24. Kwon YJ, Ko KS, So BK, Kim DH, Jang HS, Kim SH, et al. 2020; Effect of decompression on jaw cystic lesions based on three-dimensional volumetric analysis. Medicina (Kaunas). 56:602. https://doi.org/10.3390/medicina56110602. DOI: 10.3390/medicina56110602. PMID: 33182601. PMCID: PMC7696604.
25. Gao L, Wang XL, Li SM, Liu CY, Chen C, Li JW, et al. 2014; Decompression as a treatment for odontogenic cystic lesions of the jaw. J Oral Maxillofac Surg. 72:327–33. https://doi.org/10.1016/j.joms.2013.07.035. DOI: 10.1016/j.joms.2013.07.035. PMID: 24071375.
crossref
26. Kubota Y, Imajo I, Itonaga R, Takenoshita Y. 2013; Effects of the patient's age and the size of the primary lesion on the speed of shrinkage after marsupialisation of keratocystic odontogenic tumours, dentigerous cysts, and radicular cysts. Br J Oral Maxillofac Surg. 51:358–62. https://doi.org/10.1016/j.bjoms.2012.07.017. DOI: 10.1016/j.bjoms.2012.07.017. PMID: 22981336.
crossref
27. Song IS, Park HS, Seo BM, Lee JH, Kim MJ. 2015; Effect of decompression on cystic lesions of the mandible: 3-dimensional volumetric analysis. Br J Oral Maxillofac Surg. 53:841–8. https://doi.org/10.1016/j.bjoms.2015.06.024. DOI: 10.1016/j.bjoms.2015.06.024. PMID: 26212420.
crossref
28. Cho JY, Kim JW, Kim SB, Ryu J. 2020; Decompression of large cyst invading the mandibular canal leading to reduced cyst volume and increased mandibular canal length. J Oral Maxillofac Surg. 78:1770–9. https://doi.org/10.1016/j.joms.2020.05.025. DOI: 10.1016/j.joms.2020.05.025. PMID: 32579886.
crossref
29. Asutay F, Atalay Y, Turamanlar O, Horata E, Burdurlu MÇ. 2016; Three-dimensional volumetric assessment of the effect of decompression on large mandibular odontogenic cystic lesions. J Oral Maxillofac Surg. 74:1159–66. https://doi.org/10.1016/j.joms.2015.12.010. DOI: 10.1016/j.joms.2015.12.010. PMID: 26828617.
crossref
30. Kim SM, Chung SW, Cha IH, Nam W. 2009; Normal eruption guidance of unerupted permanent teeth associated with dentigerous cyst by decompression: 5 cases report. J Korean Assoc Oral Maxillofac Surg. 35:271–5.
31. Maurette PE, Jorge J, de Moraes M. 2006; Conservative treatment protocol of odontogenic keratocyst: a preliminary study. J Oral Maxillofac Surg. 64:379–83. https://doi.org/10.1016/j.joms.2005.11.007. DOI: 10.1016/j.joms.2005.11.007. PMID: 16487797.
32. Lim HK, Kim JW, Lee UL, Kim JW, Lee H. 2017; Risk factor analysis of graft failure with concomitant cyst enucleation of the jaw bone: a retrospective multicenter study. J Oral Maxillofac Surg. 75:1668–78. https://doi.org/10.1016/j.joms.2017.02.003. DOI: 10.1016/j.joms.2017.02.003. PMID: 28282517.
crossref
33. Pei J, Zhao S, Chen H, Wang J. 2022; Management of radicular cyst associated with primary teeth using decompression: a retrospective study. BMC Oral Health. 22:560. https://doi.org/10.1186/s12903-022-02572-w. DOI: 10.1186/s12903-022-02572-w. PMID: 36457003. PMCID: PMC9713984.
crossref
34. van Doorn ME. 1972; Enucleation and primary closure of jaw cysts. Int J Oral Surg. 1:17–25. https://doi.org/10.1016/s0300-9785(72)80032-2. DOI: 10.1016/S0300-9785(72)80032-2. PMID: 4634124.
crossref
35. Richter M, Laurent F, Chausse JM. 1986; Homologous cancellous bone grafts for large jaw defects caused by bone cysts. J Oral Maxillofac Surg. 44:447–53. https://doi.org/10.1016/s0278-2391(86)80009-x. DOI: 10.1016/S0278-2391(86)80009-X. PMID: 3517262.
crossref
36. Stoelinga PJ. 2001; Long-term follow-up on keratocysts treated according to a defined protocol. Int J Oral Maxillofac Surg. 30:14–25. https://doi.org/10.1054/ijom.2000.0027. DOI: 10.1054/ijom.2000.0027. PMID: 11289615.
crossref
37. Habibi A, Saghravanian N, Habibi M, Mellati E, Habibi M. 2007; Keratocystic odontogenic tumor: a 10-year retrospective study of 83 cases in an Iranian population. J Oral Sci. 49:229–35. https://doi.org/10.2334/josnusd.49.229. DOI: 10.2334/josnusd.49.229. PMID: 17928730.
crossref
38. Berdén J, Koch G, Ullbro C. 2010; Case series: Treatment of large dentigerous cysts in children. Eur Arch Paediatr Dent. 11:140–5. https://doi.org/10.1007/bf03262730. DOI: 10.1007/BF03262730. PMID: 20507812.
crossref
39. Enislidis G, Fock N, Sulzbacher I, Ewers R. 2004; Conservative treatment of large cystic lesions of the mandible: a prospective study of the effect of decompression. Br J Oral Maxillofac Surg. 42:546–50. https://doi.org/10.1016/j.bjoms.2004.06.020. DOI: 10.1016/j.bjoms.2004.06.020. PMID: 15544886.
crossref
40. Park JH, Kwak EJ, You KS, Jung YS, Jung HD. 2019; Volume change pattern of decompression of mandibular odontogenic keratocyst. Maxillofac Plast Reconstr Surg. 41:2. https://doi.org/10.1186/s40902-018-0184-y. DOI: 10.1186/s40902-018-0184-y. PMID: 30671423. PMCID: PMC6321831.
crossref
41. Tomomatsu N, Takahara N, Kurasawa Y, Terauchi M, Iwasaki T, Yoda T. 2022; Three-dimensional changes in cystic lesions of the mandible after marsupialization. J Oral Maxillofac Surg Med Pathol. 34:126–30. https://doi.org/10.1016/j.ajoms.2021.09.001. DOI: 10.1016/j.ajoms.2021.09.001.
crossref

Fig. 1
A case involving catheter placement for decompression. A. Intraoral view after catheter placement for decompression. B. Obturator produced with acrylic resin and a catheter.
jkaoms-50-4-197-f1.tif
Fig. 2
Coronal and sagittal cone-beam computed tomography performed at follow-up after decompression; cystic lesion size decreased over the course of approximately 11 months. A. At initial diagnosis. B. Five months after decompression. C. Eleven months after decompression.
jkaoms-50-4-197-f2.tif
Fig. 3
Cystic lesion analysis in cone-beam computed tomography images. Three-dimensional reconstruction for volume measurement.
jkaoms-50-4-197-f3.tif
Fig. 4
Histopathologic changes due to decompression. A. Before decompression of an odontogenic keratocyst (H&E staining, ×200). B. After decompression with resection (H&E staining, ×100). C. Before decompression (H&E staining, ×40) of a dentigerous cyst. D. After decompression with resection (H&E staining, ×40).
jkaoms-50-4-197-f4.tif
Table 1
Patient information
Variable Total (n=20)
Sex
Male 8
Female 12
Age (yr)
≤30 11
>30 9
Initial cyst volume (mm3)
<10,000 16
≥10,000 4
Location
Maxilla 7
Mandible 13
Degree of cortical layer expansion
Mild 8
Severe 12
Pathologic diagnosis
Dentigerous cyst 11
Radicular cyst 7
OKC 2

(OKC: odontogenic keratocyst)

Table 2
Rate of reduction in cyst volume and shrinkage speed based on parameters
Parameter Reduction rate Shrinkage speed


Mean±SD Mann–Whitney U test/χ2 P-value Mean±SD Mann–Whitney U test/χ2 P-value
Sex
Male 66.2±11.1 35 0.316 697.8±619.7 38 0.440
Female 71.2±13.5 952.0±812.0
Age (yr)
≤30 69.9±14.6 48 0.909 739.9±460.1 47 0.939
>30 68.2±10.4 1,015.9±1038.7
Initial cyst volume (mm3)
<10,000 69.6±12.8 31 0.925 637.1±448.9 10 0.038*
≥10,000 67.6±13.1 1,703.2±1,094.5
Location
Maxilla 70.3±14.4 38 0.552 1,207.6±1,028.2 32 0.285
Mandible 68.5±12.1 657.9±459.7
Degree of cortical layer expansion
Mild 62.0±11.4 22 0.045* 557.1±559.5 19 0.025*
Severe 74.0±11.3 1,045.8±788.4
Pathologic diagnosis
DC 70.3±13.0 0.6091 0.738 867.0±658.4 0.3541 0.838
RC 67.4±15.1 593.3±339.4
OKC 66.0±0.66 519.4±99.9

(DC: dentigerous cyst, RC: radicular cyst, OKC: odontogenic keratocyst, SD: standard deviation)

1Kruskal–Wallis test.

*P<0.05.

TOOLS
Similar articles