1. www.orl-marseille.com
Congenital middle ear
cholesteatomas in children
A Abbas, R Nicollas, I Sudre, H Belaïche, S Roman, JM Triglia
Dr Ali ABBAS
Pediatric ENT department
Timone Children Hospital
Marseille France
20/06/2006
2. Why?
Problem: early diagnosis
Comparative study with acquired cholesteatoma in
children
Objective: to determine criterias allowing earlier diagnosis
3. Material and methods
Monocentric and comparative prospective study from 1994 to 2005,
n = 322 cases of cholesteatoma in children
Mean follow-up = 48 months
Canal wall up procedure
Congenital cholesteatoma Acquired cholesteatoma
n=61 n=261
4 bilateral cases 14 bilateral cases
Mean age: 6 years [1,1 to 13,9] Mean age: 10 years [3,4 to 18]
Gender: 59% boys gender: 62% boys
4. Results
Clinical n=61
otalgia
non symptomatic
serous otitis media 13%
9% 31%
24%
23%
deafness otorrhea
9. Contralateral ear
Congenital (n=61) Acquired (n=261)
Normal 84% 56%
SOM 12% 13%
Chronic otitis 4% 31%
p<0,05
10. Postoperative hearing assessments
Congenital (n=61) Acquired (n=261)
Preoperative ABG (dB): 28 [26 à 59] 27 [7 à 56]
Postoperative ABG (dB): 15 [0 à 47] 17 [0 à 60]
Preoperative mean AC (dB): 38 35
p<0,05
11. Discussion
Levenson’s criterias:
– CC children with AOM
– under-estimated incidence: perforation post CC
• Location
Series Year Number of Antero-mallear Postero-
cases (%) mallear(%)
Parisier 1989 40 67,5 15
McGill 1991 41 41 0
Postic 2002 172 82 49
Nelson 2002 119 85,1 77
Our study 2006 61 83 31
12. Conclusion
location relates to postoperative hearing results
and the likelihood of residual disease
earlier diagnosis = better surgical result
Large increase in reports of CC