Hostname: page-component-745bb68f8f-b95js Total loading time: 0 Render date: 2025-02-06T11:10:31.583Z Has data issue: false hasContentIssue false

Long-term status of middle-ear aeration post canal wall down mastoidectomy

Published online by Cambridge University Press:  03 July 2019

T Ezulia*
Affiliation:
Otorhinolaryngology, Head and Neck Surgery, University Malaya Medical Centre, Kuala Lumpur, Malaysia
B S Goh
Affiliation:
Otorhinolaryngology, Head and Neck Surgery, University Kebangsaan Malaysia Medical Centre, Kuala Lumpur, Malaysia
L Saim
Affiliation:
Otorhinolaryngology, Head and Neck Surgery, KPJ Tawakkal Specialist Hospital, Kuala Lumpur, Malaysia
*
Author for correspondence: Dr Tengku Ezulia Binti Tengku Nun Ahmad, Department of Otorhinolaryngology, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia E-mail: tengkuezulia@gmail.com
Rights & Permissions [Opens in a new window]

Abstract

Background

Retraction pocket theory is the most acceptable theory for cholesteatoma formation. Canal wall down mastoidectomy is widely performed for cholesteatoma removal. Post-operatively, each patient with canal wall down mastoidectomy has an exteriorised mastoid cavity, exteriorised attic, neo-tympanic membrane and shallow neo-middle ear.

Objective

This study aimed to clinically assess the status of the neo-tympanic membrane and the exteriorised attic following canal wall down mastoidectomy.

Methods

All post canal wall down mastoidectomy patients were recruited and otoendoscopy was performed to assess the neo-tympanic membrane. A clinical classification of the overall status of middle-ear aeration following canal wall down mastoidectomy was formulated.

Results

Twenty-five ears were included in the study. Ninety-two per cent of cases showed some degree of neo-tympanic membrane retraction, ranging from mild to very severe.

Conclusion

After more than six months following canal wall down mastoidectomy, the degree of retracted neo-tympanic membranes and exteriorised attics was significant. Eustachian tube dysfunction leading to negative middle-ear aeration was present even after the canal wall down procedure. However, there was no development of cholesteatoma, despite persistent retraction.

Type
Main Articles
Copyright
Copyright © JLO (1984) Limited, 2019 

Introduction

Cholesteatoma is characterised by a cyst-like, expansile lesion of the temporal bone, lined with stratified squamous epithelium that contains desquamated keratin.Reference Dornelles, Costa, Meurer and Schweiger1 Eustachian tube dysfunction with negative pressure of the middle ear is the most likely mechanism for cholesteatoma development and recurrence after surgery.Reference Alves, Pereira, Ribeiro and Fregnan2Reference Schuknecht10

Studies have also suggested that there is abnormal proliferation of epithelium in cholesteatoma patients. Some reseachers,Reference Michaels11Reference Jove, Vassalli, Raslan and Applebaum23 including Bujia et al.,Reference Bujia, Sudhoff, Holly, Hildmann and Kastenbauer20 found that cholesteatoma epithelium proliferates at a higher rate than normal epidermis. Previous studies on cholesteatoma formationReference Huang, Yan and Huang24Reference Hulka and McElveen33 have indicated the possible involvement of: cytokeratins (e.g. Weiss et al.Reference Weiss, Eichner and Sun25), epidermal growth factor (e.g. Kojima et al.,Reference Kojima, Shiwa, Kamide and Moriyama26 Li et al.Reference Li, Jiang and Wang27 and Barbara et al.Reference Barbara, Raffa, Murè, Manni, Ronchetti and Monini28) and its receptor, and keratinocyte growth factor (e.g. Kojima et al.,Reference Kojima, Matsuhisa, Shiwa, Kamide, Nakamura and Ohno29 and Yamamoto-Fukuda et al.Reference Yammamoto-Fukuda, Aoki, Hishikawa, Kobayashi, Takahashi and Koji30) and its receptor.

Most previous studies that assessed patients after canal wall down mastoidectomy focused on cholesteatoma recurrence rates, causes of recurrence,Reference Gantz, Wilkinson and Hansen34Reference Segalla, Nakao, Anjos and Penido38 hearing outcomes (pre- and post-operatively)Reference Vartianinen and Nuutinen39,Reference Harkness, Brown, Fowler, Grant, Ryan and Topham40 and surgery-related complications.Reference Hirsch, Kamerer and Doshi17Reference Proops, Hawak and Parkinson22,Reference Abramson and Huang35

Materials and methods

This cross-sectional study involved the clinical observation and evaluation of middle-ear aeration in patients who had undergone canal wall down mastoidectomy for cholesteatoma and other pathologies at least six months previously at a tertiary centre (KPJ Tawakkal Specialist Hospital or University Kebangsaan Malaysia Medical Centre).

We identified the post-operative canal wall down mastoidectomy patients with dry, non-discharging ears on follow up. Patients who presented with recurrence, discharge or granulation on follow up were excluded.

Otoendoscopic findings were categorised according to Sade's modified (1979) classification for pars tensa retractions of the neo-tympanic membrane,Reference Sade and Sade41 and Tos and Poulsen's modified (1980) classification for attic retractions,Reference Tos and Poulsen42 as shown in Figures 1 and 2 respectively.

Fig. 1. Representative clinical photographs showing the status of the neo-tympanic membrane following canal wall down mastoidectomy (modified Sade classificationReference Sade and Sade41): (a) normal (no retraction); (b) mild (dimple or slight retraction); (c) moderate (deeper retraction not reaching promontory); (d) severe (localised retraction reaching promontory); and (e) very severe (complete retraction to the promontory (atelectasis)).

Fig. 2. Representative clinical photographs showing the status of the exteriorised attic following canal wall down mastoidectomy (modified Tos and Poulsen classificationReference Tos and Poulsen42): (a) normal (no retraction); (b) mild (single shallow pocket); (c) moderate (multiple shallow pockets); (d) severe (single deep pocket); and (e) very severe (multiple deep pockets).

Results

Demographics

A total of 24 patients were recruited; 1 patient had undergone bilateral canal wall down mastoidectomy, hence the study included 25 ears. The age of the sample population ranged from 7 to 69 years (mean age of 39 years). Nine patients (37.5 per cent) were female and 15 (62.5 per cent) were male. The majority of the study population were Malaysian (66.6 per cent); the remainder were Chinese (16.6 per cent), Indian (13.2 per cent) or other (0.4 per cent).

Data for 14 ears (56 per cent) were collected from KPJ Tawakkal Specialist Hospital during the period from 1st May 2014 to 31st November 2014. Data for 11 ears (44 per cent) were collected from the Otorhinolaryngology Clinic at the University Kebangsaan Malaysia Medical Centre during the period from 1st December 2014 to 31st May 2015.

There was an almost equal distribution of left and right ears. The left ear was affected in 52 per cent of cases, and the right ear was implicated in 48 per cent.

Of the 25 ears, canal wall down mastoidectomy was performed for: cholesteatoma in 22 ears (88 per cent), chronic mastoiditis in 2 ears, and mastoid abscess secondary to recurrent otitis media in 1 ear. The time since canal wall down mastoidectomy amongst our study population is shown in Figure 3. Most of the patients had undergone the canal wall down procedure between two and four years previously (40 per cent).

Fig. 3. Time since canal wall down (CWD) mastoidectomy.

Neo-tympanic membrane status

The status of the neo-tympanic membrane after canal wall down mastoidectomy, for the 25 ears in this study, is shown in Table 1.

Table 1. Status of neo-tympanic membrane post canal wall down mastoidectomy in this study

The data show that 92 per cent of ears had some degree of neo-tympanic membrane retraction (ranging from mild to very severe). *Total n = 25

Exteriorised attic status

Table 2 shows the status of the exteriorised attic following canal wall down mastoidectomy for the 25 ears in this study.

Table 2. Status of exteriorised attic post canal wall down mastoidectomy in this study

*Total n = 25

Middle-ear aeration

As aeration of the middle ear following canal wall down mastoidectomy is dependent on both the neo-tympanic membrane and exteriorised attic, we combined the findings for both the neo-tympanic membrane and the exteriorised attic. Thus, we devised a new means of classifying middle-ear aeration post canal wall down mastoidectomy. Our proposed classification is shown in Table 3.

Table 3. Ezulia et al. classification of middle-ear aeration post canal wall down mastoidectomy

The classification of middle-ear aeration post canal wall down mastoidectomy for the 25 ears in this study is shown in Table 4.

Table 4. Classification of middle-ear aeration post canal wall down mastoidectomy in this study

*Total n = 25

Discussion

Several classifications of tympanic membrane retraction exist, more of which concern the pars tensa than the pars flaccida. However, there has been no previous attempt to grade the status of the neo-tympanic membrane after canal wall down mastoidectomy. The traditional Sade classification demonstrates the progression of retraction in the non-operated ear,Reference Sade and Sade41 and can be used as a basis for a new classification.

In our attempt to arrive at a reasonable grading for the status of the neo-tympanic membrane after canal wall down mastoidectomy, based on our review of 25 ears, we used Sade's classification,Reference Sade and Sade41 which has been accepted universally and is often used to grade otitis media effusion. Sade's classification was used as a basis for our grading because the (neo)tympanic membrane and middle-ear cleft may still be present post canal wall down mastoidectomy. Presumably, there was still aeration of the middle ear following canal wall down mastoidectomy. However, in the neo-tympanic membrane, the pars tensa was stiffer, possibly because of scarring. The volume of the middle ear was also smaller. The ossicles might be eroded or abnormal.

We used retraction pockets as the basis for our grading because the majority of the epithelial cover of the exteriorised attic developed retraction. Initially, we suspected that this factor might be related to pre-operative findings, regardless of whether the ossicles were present, absent or malformed intra-operatively. We assumed that the post-operative exteriorised attic might not appear as retraction pockets in patients with an absent or eroded head of malleus and body of incus. We suspected that patients who still had remnants of either the malleus or body of incus would show retraction pockets. However, there was no correlation between the intra-operative reports and post-operative findings. In our study, some patients who had remnants of the head of malleus and short process of the incus intra-operatively still developed a non-retracted exteriorised attic post-operatively, and vice versa. Thus, the presence or absence of ossicles might not be a strong determining factor for the degree of exteriorised attic retraction.

Theoretically, the desquamated keratin debris forms cholesteatoma at the retraction site. Nevertheless, in our study, some of the patients developed the debris faster than others. It was assumed that retractions of the neo-tympanic membrane and exteriorised attic were severe if middle-ear aeration was poorer, requiring more frequent ear toileting to clear the debris at the retraction site. However, no association was found between the grade of middle-ear aeration and the frequency of ear toileting in our sample.

Eustachian tube dysfunction and poor middle-ear aeration were persistent after canal wall down mastoidectomy, as evidenced by all of our 25 ears. In this study, there was no new cholesteatoma development. This may support the theory that retraction pockets and negative pressure in the middle ear are not the only determinants of cholesteatoma development. Cytokeratins and keratinocyte growth factors have a possible role in cholesteatoma development.Reference de Zinis, Tonni and Barezzani18Reference Bujia, Sudhoff, Holly, Hildmann and Kastenbauer20

  • Neo-tympanic membrane and exteriorised attic retraction was significant in patients with a longer duration since canal wall down mastoidectomy

  • Eustachian tube dysfunction leading to negative middle-ear aeration persisted after a canal wall down procedure

  • However, these patients never fully developed cholesteatoma despite persistent retraction

  • The findings suggest that retraction pockets are not the only factor determining cholesteatoma formation

Our classification of middle-ear aeration was based on clinical assessment. A combination of clinical assessment and objective measurement of middle-ear pressure would allow more accurate determination and classification of middle-ear aeration. Ikeda et al. used computed tomography (CT) scanning to measure the middle-ear aeration in a reconstructed middle-ear cavity post canal wall down mastoidectomy.Reference Ikeda, Yoshida, Ikui and Shigihara43 The CT scan evaluation was conducted approximately one year post-operatively. The state of re-aeration of the reconstructed middle-ear cavity was classified as: ‘re-aerated’, in cases where the CT scan showed obvious aeration, or ‘non-aerated’, in cases where no aerated space could be identified. In 73 of the 103 ears, re-aeration in the reconstructed mastoid cavity, epitympanum and middle ear could be evaluated post-operatively. In their study, the rate of re-aeration in the middle ear (82.4 per cent) was better than that in the epitympanum and mastoid cavity (63.5 per cent and 36.5 per cent respectively). Our study was comparably more cost effective.

Conclusion

There was no statistically significant association between the severity of middle-ear aeration and the frequency of ear toileting in our study. There was also no association between the time since the canal wall down mastoidectomy and the severity of middle-ear aeration. In patients who underwent canal wall down mastoidectomy a long time previously, most still had a retracted neo-tympanic membrane and exteriorised attic. Eustachian tube dysfunction leading to negative middle-ear aeration persisted after the canal wall down procedure. In this study, even those patients with a high degree of middle-ear aeration and longer follow up did not develop cholesteatoma post-operatively. This suggests that retraction pockets may not be the only factor that determines cholesteatoma formation. Our findings may support recent studies that propose a significant role for cytokeratin and keratinocyte growth factor in the proliferation of primary cholesteatoma. However, once the canal wall down procedure has been performed, the local environment changes. The open cavity may suppress cytokeratins and keratinocyte growth factor; thus, cholesteatoma never fully develops in these patients.

Acknowledgement

The authors would like to express their utmost gratitude to Prof AB Zulkiflee, a senior researcher from the University of Malaya, Kuala Lumpur, who kindly edited and suggested ideas to improve the manuscript.

Competing interests

None declared

Footnotes

Dr T Ezulia takes responsibility for the integrity of the content of the paper

References

1Dornelles, C, Costa, SS, Meurer, L, Schweiger, C. Some considerations about acquired adult and pediatric cholesteatomas. Braz J Otorhinolaryngol 2005;71:536–45Google Scholar
2Alves, DL, Pereira, SB, Ribeiro, FAQ, Fregnan, JHT. Analysis of histopathological aspects in acquired middle ear cholesteatoma. Braz J Otorhinolaryngol 2008;74:835–41Google Scholar
3Park, KH, Park, SN, Chang, KH, Jung, MK, Yeo, SW. Congenital middle ear cholesteatoma in children: retrospective review of 35 cases. J Korean Med Sci 2009;24:126–31Google Scholar
4Janardhan, N, Nara, J, Peram, I, Palukuri, S, Chinta, A, Satna, K. Congenital cholesteatoma of temporal bone with Bezold's abscess: case report. Indian J Otolaryngol Head Neck Surg 2012;64:97–9Google Scholar
5Kemppainen, HO, Puhakka, HJ, Laippala, PJ, Sipilä, MM, Manninen, MP, Karma, PH. Epidemiology and aetiology of middle ear cholesteatoma. Acta Otolaryngol 1999;119:568–72Google Scholar
6Drahy, A, De Barros, A, Lerosey, Y, Choussy, O, Dehesdin, D, Marie, JP. Acquired cholesteatoma in children: strategies and medium-term results. Eur Ann Otorhinolaryngol Head Neck Dis 2012;129:225–9Google Scholar
7Tabook, SM, Abdel Tawab, HM, Gopal, NK. Congenital cholesteatoma localized to the mastoid cavity and presenting as a mastoid abscess. Case Rep Otolaryngol 2015;2015:305494Google Scholar
8Morimitsu, T. Pathogenesis of cholesteatoma. In: Cholesteatoma and Anterior Tympanotomy. Tokyo: Springer, 1997;95110Google Scholar
9Michaels, L. Origin of congenital cholesteatoma from a normally occurring epidermoid rest in the developing middle ear. Int J Pediatr Otorhinolaryngol 1988;15:5165Google Scholar
10Schuknecht, HF. The Pathology of the Ear. Cambridge, MA: Harvard University Press, 1974Google Scholar
11Michaels, L. Biology of cholesteatoma. Otolaryngol Clin North Am 1989;22:869–81Google Scholar
12Spilsbury, K, Miller, I, Semmens, JB, Lannigan, FJ. Factors associated with developing cholesteatoma: a study of 45,980 children with middle ear disease. Laryngoscope 2010;120:625–30Google Scholar
13Chang, CC, Chen, MK. Canal-wall-down tympanoplasty with mastoidectomy for advanced cholesteatoma. J Otolaryngol 2000;29:270–3Google Scholar
14Kos, MI, Castrillon, R, Montandon, P, Guyot, JP. Anatomic and functional long-term results of canal wall-down mastoidectomy. Ann Otol Rhinol Laryngol 2004;113:872–6Google Scholar
15Cody, DTR, McDonald, TJ. Mastoidectomy for acquired cholesteatoma: follow-up to 20 years. Laryngoscope 1984;94:1027–30Google Scholar
16Quaranta, A, Cassano, P, Carbonara, G. Cholesteatoma surgery: open vs closed tympanoplasty. Am J Otol 1988;9:229–31Google Scholar
17Hirsch, BE, Kamerer, DB, Doshi, S. Single-stage management of cholesteatoma. Otolaryngol Head Neck Surg 1992;106:351–4Google Scholar
18de Zinis, LO, Tonni, D, Barezzani, MG. Single-stage canal wall-down tympanoplasty: long-term results and prognostic factors. Ann Otol Rhinol Laryngol 2010;119:304–12Google Scholar
19Belcadhi, M, Chahed, H, Mani, R, Bouzouita, K. Predictive factors of recurrence in pediatric cholesteatoma surgery. Mediterr J Otol 2008;4:118–24Google Scholar
20Bujia, J, Sudhoff, H, Holly, A, Hildmann, H, Kastenbauer, E. Immunohistochemical detection of proliferating cell nuclear antigen in middle ear cholesteatoma. Eur Arch Otorhinolaryngol 1996;253:21–4Google Scholar
21Huang, CC, Yi, ZX, Chao, WY. Effect of granulation tissue conditioned medium on the in vitro differentiation of keratinocytes. Arch Otorhinolaryngol 1988;245:325–9Google Scholar
22Proops, DW, Hawak, WM, Parkinson, EK. Tissue culture of migratory skin of the external ear and cholesteatoma: a new research tool. J Otolaryngol 1984;13:63–9Google Scholar
23Jove, MA, Vassalli, L, Raslan, W, Applebaum, EL. The effect of isotretinoin on propylene glycol-induced cholesteatoma in chinchilla middle ears. Am J Otolaryngol 1990;11:59Google Scholar
24Huang, T, Yan, SD, Huang, CC. Colony-stimulating factor in middle ear cholesteatoma. Am J Otolaryngol 1989;10:393–8Google Scholar
25Weiss, RA, Eichner, R, Sun, TT. Monoclonal antibody analysis of keratin expression in epidermal diseases: a 48- and 56-kdalton keratin as molecular markers for hyperproliferative keratinocytes. J Cell Biol 1984;98:1397–406Google Scholar
26Kojima, H, Shiwa, M, Kamide, Y, Moriyama, H. Expressive and localization of mRNA for epidermal growth factor and epidermal growth factor receptor in human cholesteatoma. Acta Otolaryngol 1994;114:423–9Google Scholar
27Li, H, Jiang, P, Wang, L. Immunohistochemical study of the epithelial hyperproliferation in middle ear cholesteatoma [in Chinese]. Zhonghua Er Bi Yan Hou Ke Za Zhi 2002;37:118–20Google Scholar
28Barbara, M, Raffa, S, Murè, C, Manni, V, Ronchetti, F, Monini, S et al. Keratinocyte growth factor receptor (KGF-R) in cholesteatoma tissue. Acta Otolaryngol 2008;128:360–4Google Scholar
29Kojima, H, Matsuhisa, A, Shiwa, M, Kamide, Y, Nakamura, M, Ohno, T et al. Expression of messenger RNA for keratinocyte growth factor in human cholesteatoma. Arch Otolaryngol Head Neck Surg 1996;122:157–60Google Scholar
30Yammamoto-Fukuda, T, Aoki, D, Hishikawa, Y, Kobayashi, T, Takahashi, H, Koji, T. Possible involvement of keratinocyte growth factor and its receptor in enhanced epithelial-cell proliferation and acquired recurrence of middle-ear cholesteatoma. Lab Invest 2003;83:123–36Google Scholar
31Vartiainen, E. Ten-year results of canal wall down mastoidectomy for acquired cholesteatoma. Auris Nasus Larynx 2000;27:227–9Google Scholar
32Meuser, W. The exenterated mastoid: a problem of ear surgery. Am J Otol 1985;6:323–5Google Scholar
33Hulka, GF, McElveen, JT Jr. A randomized, blinded study of canal wall up versus canal wall down mastoidectomy determining the differences in viewing middle ear anatomy and pathology. Am J Otol 1998;19:574–8Google Scholar
34Gantz, BJ, Wilkinson, EP, Hansen, MR. Canal wall reconstruction tympanomastoidectomy with mastoid obliteration. Laryngoscope 2005;115:1734–40Google Scholar
35Abramson, M, Huang, CC. Localization of collagenase in human middle ear cholesteatoma. Laryngoscope 1977;87(5 Pt 1):771–91Google Scholar
36Haginomori, S, Takamaki, A, Nonaka, R, Mineharu, A, Kanazawa, A, Takenaka, H. Postoperative aeration in the middle ear and hearing outcome after canal wall down tympanoplasty with soft-wall reconstruction for cholesteatoma. Otol Neurol 2009;30:478–83Google Scholar
37Azevedo, AF, Soares, ABC, Garchet, HQC, Sousa, NJ. Tympanomastoidectomy: comparison between canal wall-down and canal wall-up techniques in surgery for chronic otitis media. Int Arch Otorhinolaryngol 2013;17:242–5Google Scholar
38Segalla, DK, Nakao, LH, Anjos, MF, Penido, NO. Surgical and audiological results after mastoidectomy in a medical residency service [in Spanish]. Acta Otorrinolaringol 2008;26:178–81Google Scholar
39Vartianinen, E, Nuutinen, J. Long-term hearing results of one-stage tympanoplasty for chronic otitis media. Eur Arch Otorhinolaryngol 1992;249:329–31Google Scholar
40Harkness, P, Brown, P, Fowler, S, Grant, H, Ryan, R, Topham, J. Mastoidectomy audit: results of the Royal College of Surgeons of England comparative audit of ENT surgery. Clin Otolaryngol Allied Sci 1995;20:8994Google Scholar
41Sade, J. The atelectatic ear. In: Sade, J, ed. Monograms in Clinical Otolaryngology, Secretort Otitis Media and its Sequelae. New York: Churchill-Livingstone, 1979;6488Google Scholar
42Tos, M, Poulsen, G. Attic retractions following secretory otitis. Acta Otolaryngol 1980;89:479–86Google Scholar
43Ikeda, M, Yoshida, S, Ikui, A, Shigihara, S. Canal wall down tympanoplasty with canal reconstruction for middle-ear cholesteatoma: post-operative hearing, cholesteatoma recurrence, and status of re-aeration of reconstructed middle-ear cavity. J Laryngol Otol 2003;117:249–55Google Scholar
Figure 0

Fig. 1. Representative clinical photographs showing the status of the neo-tympanic membrane following canal wall down mastoidectomy (modified Sade classification41): (a) normal (no retraction); (b) mild (dimple or slight retraction); (c) moderate (deeper retraction not reaching promontory); (d) severe (localised retraction reaching promontory); and (e) very severe (complete retraction to the promontory (atelectasis)).

Figure 1

Fig. 2. Representative clinical photographs showing the status of the exteriorised attic following canal wall down mastoidectomy (modified Tos and Poulsen classification42): (a) normal (no retraction); (b) mild (single shallow pocket); (c) moderate (multiple shallow pockets); (d) severe (single deep pocket); and (e) very severe (multiple deep pockets).

Figure 2

Fig. 3. Time since canal wall down (CWD) mastoidectomy.

Figure 3

Table 1. Status of neo-tympanic membrane post canal wall down mastoidectomy in this study

Figure 4

Table 2. Status of exteriorised attic post canal wall down mastoidectomy in this study

Figure 5

Table 3. Ezulia et al. classification of middle-ear aeration post canal wall down mastoidectomy

Figure 6

Table 4. Classification of middle-ear aeration post canal wall down mastoidectomy in this study