Mastoid cavity obliteration
Posted , 7 users are following.
I am on the waiting list for one of these operations. I had a radical mastoid op when I was 11 am now 45 and having serious pain so after many oils ointments and sprays this seems like the last ditched attempt. Having had the op explained to me I was wondering if anyone else had had it done.
0 likes, 8 replies
guest1 Becky157
Posted
I had a mastoid obliteration during October last year. I assume you have lost hearing in your affected ear?
I lost hearing in my left ear when I was first diagnosed with cholesteatoma 11 years ago (aged 30). After 3 mastoidectomies (the first rebuilding my ear drum) to clear me of the conditoin, it was decided that as my hearing had gone in the affected ear, a mastoid obliteration would be the best choice as the cholesteatoma could never come back.
My mastoid bone, ossicles and ear canal were removed, my eustachian tube plugged with cartilage and fat from my belly transferred to the void. Now almost a year later I have had no problems with the ear and live a normal life. The only physical difference is if that instead of having an ear canal I now have a belly button where it used to be. From a visual look everything looks exactly the same as a normal ear, I just can't put cotton buds down the ear canal anymore! I'm due an MRI in November to check no skin tissue has grown back, then I will be discharged permanantly. The reason they put my tummy fat in the void is to help show up any skin tissue in the void better during any future MRI's - a bit like looking at a solid floating in a bottle of lemonade or water.
Any questions, please ask, otherwise my thoughts are with you and wish you the best with your op'. SteveM.
Becky157 guest1
Posted
I feel a bit happier now I know someone else has had it done. Can you hear in that ear now?
Beckt
guest1 Becky157
Posted
Becky157 guest1
Posted
Becky
smallen Becky157
Posted
I was watching a surgery video today and learned of this procedure. I've had bi-lateral mastoidectomy procedures when I was young.... 9, 10, 11... Don't remeber exactly how old I was. I'm 61 now. I've had numerous numerous procedures to restore hearing. Most worked "for a while" finally settled on a bunch of different types of hearing aids. Eventually - these hearing aids weren't suitable for me. I've got some pretty short ear canals and due to all the surgeries - the molds are just to hard to fit. My audiologist - in Boston, MA - suggested I try a BAHA " a bone anchored hearing aid"... I am quite happy with it .... There are currently two manufacturers of this type of aid. Works for me.
dezm Becky157
Posted
It has been nice to read the experience of others here.
karenskip Becky157
Posted
Hi becky
I had this done in 2013 and they used my skull bone and cartlidge to repair. I can hear so that's a blessing but I still get a very full feeling that drives me mad. I just want to rip my ear open sometimes when it gets too bad. Sleeping is still a problem too as lying on one particular place sends a shock. They say it's a neuroma from the surgery. My op was lengthy but I recovered eventually...long story. My ear canal was remade (attempted) they say and I just wish it was wider because sometimes I need to open it up because it feels so full. I can also feel bone just inside and it did bleed for quite some time when touched. I
have not had any recurrence although they did say it could. At the moment I am debating going to the doctors because I have got a dull ache behind again. I was also discharged from ent this year although I thought we were checked lifelong?
luis50454 Becky157
Posted
Hi there.
2 months ago I had the same operation done.
I'd like to know how you guys doing? I hope that there are no more cholesteatoma .
Does anyone developed tinnitus due to this procedure?