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Table 3 Patient profiles showing presence or absence of clinical presentations and gene mutations

From: Proto-oncogene mutations in middle ear cholesteatoma contribute to its pathogenesis

Patient

age

analysis

type

stage

ossicles destruction

Granulation

dura exposure

Facial nerve exposure

Labilynthin fistura

Facial palsy

variants

2

38

exome

PF

II

< 50%

+

+

myc

3

17

exome

PF

Ib

< 50

 

4

57

exome

PF

II

> 50

+

+

+

Notch

5

73

exome

PT

II

> 50

+

Notch

6

54

exome

PF

II

< 50

 

7

28

Taget capture

PF

II

< 50

+

 

8

59

Taget capture

PF

III LF

< 50

+

+

+

+

Myc

9

49

Taget capture

PF

II

< 50

+

+

+

 

10

41

Taget capture

PF

II

< 50

+

 

11

49

Taget capture

R

 

> 50

+

+

 

12

64

Taget capture

R

 

< 50

Notch

13

73

Taget capture

secondary

II

< 50

+

+

 

14

29

Taget capture

PF

III LF

> 50

+

+

+

+

 

15

64

Taget capture

PF

III LF

> 50

+

+

+

+

Notch

16

57

Taget capture

C

III FP

< 50

+

+

+

+

 

17

60

Taget capture

secondary

II

< 50

+

 

18

74

Taget capture

PT

Ia

< 50

Notch

19

33

Taget capture

PF

Ib

< 50

+

 

21

56

Taget capture

PF

Ib

< 50

 

24

5

Taget capture

PF

II

< 50

 

25

17

Taget capture

R

  

 

26

6

Taget capture

PF

II

< 50

+

 
  1. PF, pars flaccida (attic cholesteatoma); PT, pars tensa; R, recurrent; C, congenital; LF, labyrinthine fistula; FP, facial palsy