Jack - I read with interest your post from May '09. How did you decide to proceed? I just found out yesterday that I have a 4CM arachnoid cyst on my posterior fossa as well. This is in addition to a Type 1 Chiari Malformation...don't know which is causing my problems yet.
I'm curious to know what path you pursued and how it has worked out. Thank you.
Hi Andrew. Following my post in May 09, at the recommendation of my Neurosurgeon, I had gone to see an ENT in June to rule out any inner (vestibular) problems that might be causing my dizziness, nausea and equilibrium problems. I didn't want to rush into surgery for fear that it may not correct my problems (or maybe make them worse). My ENT ordered a battery of tests, which in the end pointed to the Cyst as a cause of my problems.
Feeling that my symptoms were too much to take and live with, I decided to opt for surgery. I had a craniotomy and cyst fenestration in July performed by Dr. Saahi Ghatan at Lennox Hill Hospital in NYC. The surgery lasted about 2 hours and I was in the hospital for a total of 3 days (one in the ICU). I spent about one month home from work recovering. I had some mild pain and headaches along with a plethora of mild to moderate symptoms for about the first two months, not to mention feeling wiped out after only a couple of hours of regular activity. I was pretty worried in the begginning, but I am now at the three month mark and am happy to report that I feel good, relatively symptom free (no nausea, dizziness, vision problems), barring some problems with short term memory and concentration. I am told by other people who've had the surgery that it takes about 6 months to a year to get back any deficits relating to the surgery.
In any event, I am happy with the results from the surgery (knock on wood). I am markedly better now than before the surgery. Again, it's been only three months, but I am optimistic that I will only improve going forward. I was lucky enough to find a fantastic Neurosurgeon who specializes in treating ACs and was patient enough to allow me to take my time to do my research to feel comfortable with going under the knife.
How have you been feeling? What are your symptoms? Since most AC's are not life threatening, I would not rush into anything. I'm sure you were shocked by the finding and just want to get the thing out of your head. I was totally freaked out in the beginning. My recommendation to you is to take your time. Don't panic. Get a bunch of opinions from Neursurgeons who have experience treating AC's and do your research. You have to weigh the cost-benefit of surgery versus living with the symptoms (and your long term prognosis).
Feel free to ask me any questions your might have.
Good Luck and Take Care.
My 20 year old daughter underwent a craniotomy one week ago to fenestrate an arachnoid cyst that was deteriorating her optic nerve. She is developmentally challenged, but very high functioning and on the austism spectrum. Behavioral changes 2 years ago led to an MRI, which led to an incidental finding of the cyst. Subsequent follow-up exams over the past 2 years had shown that there had been additional deterioration of her vision and surgery was recommended. After consultation with 2 top neuro opthalmologists and 2 neuro surgeons, we scheduled the surgery.
We were told that she would experience pain and bad headaches post-op. It was expected that she would be in the hospital for 3-4 days, take approx 2 weeks to be back on her feet and 1-2 months before she gets her full energy back.
Well, she was out of the hospital in 2 days and hasn't had to take as much as a tylenol for pain. Remarkably, she was sitting up in recovery (against orders) and trying to leave the ICU to go home, just a few hours after surgery. She didn't sleep and was so agitated about being away from home, that the team felt she would be much better off recouperating at home.
Now home, she is still suffering from severe sleeplessness and anxiety. She's only getting about 1-2 hours sleep each day and is hyper focused on the staples in her head. She told me today that she hasn't yawned in 3 days. All I want her to do is rest, but she can't seem to do that at all. She hasn't had a reasonable amount of sleep since she was under anesthesia.
The doctor believes that this can be a manifestation of the anxiety related to her autism, coupled with the trauma of surgery and being on steriods for the past week. I am hopeful, now that she's off the steriods and can look forward to the staples being removed next week that she'll be able to sleep and rest. Ultimately, I think she's just going to crash and sleep...hopefully, very soon.
So far she hasn't been enjoying the basic things she loves...TV, Video Games and talking on the phone with friends hold no interest to her right now. She's running on empty and does nothing but some photo imaging on the computer and obsess about the staples.
She's got some minor memory issues and is much more quiet than is typical. That could also be from lack of sleep. I'm her mother...I worry. But, I won't rush to judgement -- it's only been a week. I just want her to sleep for a while.
By all accounts, the surgery was a success. She is getting her strength back, is healing nicely and it seems as though some of her vision has been restored.
Emotionally...I believe that she has a long recovery ahead of her.
I wonder how are you feeling now after a year of getting surgery done on your brain, I am a 32 year old male, 3 months ago a Neurologist found a cyst (Arachnoid cyst) of the size of a "Golf ball" behind my cerebellum through MRI scan. The only symptoms I got are that my right leg feels kinda numb and I feels tingling sensations, I am not sure but today my right arm also feels weird like numbed, I already went to see a Neurosurgeon and he said that I don't need no Surgery, because my symptoms are not related to the cyst, but I think I am getting worst,
my question is, should I get a second opinion? and if should I get surgery?.
I am a 31 year old male with an arachnoid cyst on my spine from t-5 through t-9. If anyone has had this problem before please tell me what I can do for this.
I too have been diagnosed with an AC in my right posterior fossa. I have done alot of research on this subject since and have been symptomatic for a long time and recently getting worse. I saw a neurologist this past Monday and he was such a jerk. He said of course (as I was told most do) that this is a birth malformation and that it would'nt cause all of these symptoms. I KNOW that this is what it is. What else is going to cause a perfectly healthy 35 yr old to be dizzy all the time, have memory and concentration issues, erratic hb, migraines, seeing spots, etc? I've gone to doctors for years and they've treated the symptoms only and not seen the big picture. This doctor made me so upset. He reminded me of why I had given up. He asked me if I'd like to see the surgeon and I said "yes please", so theyre referring me to one. i really hope that I do get as lucky as you did with your first neuro surgeon and they say "lets do this". i never in my wildest dreams would have conceived the notion of wanting brain surgery but i will tell you, if this is the surgery that is going to make all of this or most of it go away so that i don't have to live feeling like a hollow shell anymore, bring it on! I can stand a few months of pain to exchange for this and I'll rather take my chances than live like this forever.
i was diagnosed with a large posteria fossa, and mines the size of an advocado lol, scared the hell out of me, what strikes me as very funny is every time i come on these sites every one with cysts have the same symptoms as me, coincidence?? i realy dont think so, and same as you happygirl i to see spots, blue ones, i bugged my neurosegeon for 6 months n now has agreed to put in a shunt, and im very relieved, in fact i cant wait to go under the knife, ive been ill now for 18 months, ,,, fingers crossed, martin
I was diagnosed with 5 AC in the frontal lobe back in 2003 and had surgery dec 2004 aged 23. I opted for the less invasive operation to drain 4 out of the 5 so I had Key hole surgery things didnt go to plan as the equipment was faulty as they couldnt see what where they were going, I suffered a bleed on the brain and had a stroke. It took nearly a year of therapy and living in a rehabilitaion centre and today Im back to being normal(ish) back at work and enjoying my career.
Today I went for a routine check on my last AC and with my usual symptoms and a few new ones (Dizziness, sickness and double/blurred vision - Had my glasses prescription changed 3 times within 18 months) my surgeon has told me that I have 3 options:
1) Do nothing and live with the symptoms - Avoiding contact sports or banging my head as it can knock the AC and cause another mass bleed, possible severe disability.
2) He operates and cuts the last cyst so the fluid can be dispersed but it will fill up as there is a void the size of an apple so it will fill probably within 6 hours of surgery OR
3) he fits a shunt - Which I think this will be the way forward!!!
Im 30 now and I thought all this was sorted out. I lost 6 months of my life due to memory loss. Didnt know my family and how to spell their names, forgot there was a Sunday in the days of the week ( to this day still get the mick taken out of me and laugh about it!!) and learning how to walk talk and care for myself again, Ive come too far, do I want to take another risk! I suppose I could look at it, Life is a risk and we will never know what if until we have taken at least ONE big risk. But 2, I dont know!? At least ive got time to do research and think and discuss with family and close friends.
If anyone is diagnosed with AC the one bit of advice I can give you is talk with family but the final discision is down to one person, you!! They are going on the same journey as you and with all the help and support they give you it will make you stronger!!
Hi, my son (20) is diagnosed with Arachnoid Cyst near midline cerebellum after 2 MRI and numerous blood tests. Symptoms 24/7 vertigo, concentration problem, inbalance. Symptoms has persisted for the past 3 months and the Neurosurgeon we saw feels that it is not the AC that is causing the symptoms but rather extreme change in lifestyle (from a couch potato to army - stressful physical activity) that caused the headaches. He also said the AC should not cause symptoms because it has been there since birth. But you are 38years old when symptoms surfaced? My son has been out of army and resting at home for the past 3 months and symptoms remained same. I am at a lost what to do and would appreciate your experience.
I am a 17 year old and i have had a growing arachnoid cyst my whole life. I have daily unbearable headaches, the blurry vision and dizzyness you are having, and I occasionally bleed from my nose, ends of my eyes, and ears when I sleep. I also see red spots in my vision daily. I am scared of the surgery because I may die or there could be severe complications. The cyst may be worse, which is why i'm currently seeing doctors about treatment and surgery. So I feel for you and just knowing that there are more people out there like this makes me feel a little better.
I also have a Arachnoid Cyst, I had surgery last May and still struggle with headaches. My cyst started out 8.8cm x 6.7 cm. it is smaller since the last MRI but trying to get info out of a Neurosurgeon is like pulling teeth. Before surgery I dragged my leg, I would fall backwards, forwards and complained about my vision. It took an ER trip because I thought I was having a stroke to find this large cyst. I also have trouble with sleeping and still forget things and its been a year. I am tired of the run around.
I am a 48 yo engineering professional and I had an arachnoid cyst (14 cm x 5 cm x 2.5 cm) that was diagnosed in Jan that was addressed 3/28 with a Ventricular Peritoneal Shunt. The shunt drained the cyst completely and collapsed the top of my brain into the area where the cyst used to reside. The collapse of the top of the brain into the cyst area caused bleeding that had to be drained during an operation 6/1. The doctor also closed the valve in the shunt to allow for the CSF to build back up in my brain. The shunt will turned back on 7/1 when crainial pressure was at the desired pressure. desired level. The doctor also added a low pressure drain on the outside of my brain. The collapsed part of the brain continues to be collapsed. The doctor is going to leave it alone unless something else occurs. This is hte first time in six months that I am going back for a check not more surgery. I may still need more surgery but we are crossing our fingers. I still have heads daily. There we averaging 7-9 every day all days. After this third surgery they do occassional get as high as 8-9, but they are generally 5-6.
I have always had a bad short term memory that has been getting apparently worse over the past 4-5 years. In addition, my wife states (and my children agree) that my mood switches very quickly and I lose my temper very easily. I had always been a laid back and relaxed person. I realize that this is no longer the case and I am realizing that this change is very real. But, I think that the recovery from this surgery and symptoms will dissipate these symptoms. I apologize for the long winded answer, but hope fully it helps reduce someone's anxiety.
Dr.Hyrahr Shahinian, Skull Base Institute. Treats these cyst every day, he's been on The Doctors and Ellen. Has special tools he developed with NASA to perform what other surgeons can only do via open craniotomy, via minimally invasive keyhole surgery. If anyone has info or experience with this doctor please share. His claim is that he can completely remove the cyst via his methods many times going in through a small key hole made through the eyebrow.
hi please could someone help me is a 4cm arachnoid cyst classed as a large one please
Found this article as I was researching AC's as my 13yr old is suffering from a 6.5cm x 3.5cm cyst. In the past 3days she has been transferred to 2 different hospitals from the ER as the other day getting ready for school she fainted in the shower after yelling she was losing/lost her vision. She has cronic headaches, see's what she discribes as "green glittering stars", has had numerous ear issues and constantly complains of dizziness.
Check out the article and decide from there...
"Devan Perez - arachnoid cyst brain surgery for teenager
Best of luck to you...
Guys, this chat is really great. I thought I had a concussion from surfing in Southeast Asia and when I got back I had tons of blood work, was put on Prednisone (*****!) for who knows what and amoxicillin for a minor ear infection. We treated the symptoms but I still have had memory loss, dull headaches and fatigue... I am a teacher and I would lose the words I wanted to say when addressing the class. I am usually pretty sharp and I hate having my thoughts shut down! Haha. Anyways I had an MRI and a cerebellar Arachnoid Cyst was found. It is quite large and now we are watching it and gathering second opinions... Anyways, i wanted to get an update on overall feeling after surgery...Neurologist is calm and cool and claiming I have POst Concussion symptoms but I cant stop thinking about getting this thing out of myhead Starship Troopers style!
It has now been three months since my 3rd surgery in a four month period. The post surgery headaches was significantly more intense than the headaches prior to the surgeries. The first two surgeries had difficulties (my brain collapsed into the areas where the (14 cm x 5 cm x 2.5 cm) cyst was prior. This caused bleeding that reulted in my second surgery. After I recovered from the second surgery, I needed one more surgery to install a drain on the outside of my brain to drain the CSF without collapsing my brain again. Again, the headaches have been veritually around the clock at a level of 5-7 pain level since January.
Now that I am 3 months post the third surgery, the headaches and other sypmoms are decreasing in the frequency and intensity. The doctor says that the headaches should go back to "normal" in about 6 months. The stuttering and inability to say the word that I want should dissipate in about a year. The memory issues should clear up in about 2 years.
I do not want to scare you. Your symptoms and side effects most likely are different. However, as bad as this experience has been, I am getting past this very difficult period in my life. I hope you get past your difficulties as soon as soon as possible.
Thanks for the feedback. I have doing a lot research on my own and I have been finding some mixed results that have me going back and forth about what to pursue. I am lucky to meet with a Nuerosurgeon for a second look this week. I am pushing through the "fog" every day but myself , friends and family are trying to make light of it all..joking around yet everyne is learning about it at the same time. Exercise is hurting now, and that is killing me the most. Mine is in the back of my head, pushes on my cerebellum, yet i have little to no balance issues. My main problems are the pressure. I feel pressure in my ears, loud noises really irritate me. I get chills shooting down my body when hearing really loud noises at the school sports matches or a concert..so lately I avoid them. I require a lot of sleep. The brain fog and pressure are confusing and memory loss is present but again, I can "push" through.
What I dont want to do is "treat the symptom". Give me the reality of living with the thing or get it out. I consider myself lucky to live in a country that has the medical technology to find the cyst and if I am very lucky, treat it. I have much respect for all others on here, sharing stories, ideas, and fears. We all just have to remember to count our blessings, navigate our way through the fog (backed by those we keep close), and suffer through the pain with hope, love and patience. I will keep you all posted with my progress!
I can only speak from my experience with my doctor. I live near Boston, MA, USA. We have some of the best doctors and hospitals in the world. But I have reasearched and spoken to other doctors in other regions of the country to get some feedback regarding the treatment my Nuerosurgeon proposed prior to having the surgeries. (NOTE: I was helped by the fact that one of my brother's was a Nursing Director at a hospitl in another state. That helped me contact more Neurologists and Nuerosurgeons for remote second and thrid opinions.)
Those doctors (4 doctors) all stated that they agreed with my doctor and would only recommend surgery if symptoms were present. The mere presence of a cycst is generally not a good reason for surgery. There are significant risks anytime a doctor cuts into any part of your body, especially the brain. Most people that find that they have cycsts in thier brain find it when they are not looing for it. They typically go into the hospital for some unrelated issue (concussion, car accident, fall, etc..). They have an MRI or a CT scan and find out they have a cycst. These patients, if there are no symptoms get monitored on a regular baiss (yearly) by getting an MRI to make sure that there are no problems. Most of these people never have symptoms and never have or require surgery. People with symptoms that are severe enough have surgery.
I had double vision, speach issues, and memory loss. I am not certain if my surgeon and the doctors I consulted are outside of the norm (which I do not think that they are) do not necessarily consider headaches as a symptom. If a patient only has headaches, the doctor's may not be inlcined to operate. If the Nuerosurgeon can tie your symptoms to the abnomaly in your head, he\she may most likely undertake surgery.
All of these comments are based on my experience and my perception of the events and doctor's opinions. Your experience may differ and your doctor may have a different opinion than my doctor. However, I hope that this (very long winded answer) may somehow in some small way help you in feeling comfortable with your decision. ALWAYS REMEMBER IT IS YOUR DECISION, NOT THE DOCTOR'S. Good Luck - Tom
Hi Everyone, I have been feeling ill since January 2010 the major symptoms being chronic headache, visual dysfunction, cognitive dysfunction, fatigue and muscle pain. These symptoms have severely affected every aspect of my life. An arachnoid cyst was discovered last year by MRI in the right hand posterior fossa deforming the cerebellum in that region, it is approximately the volume of a small chicken egg with an odd shape. The radiologist’s comments were that it was not clinically significant. I saw a neurologist around 5 months ago who also said the cyst was not responsible for my symptoms.
I initially took their word for this but have recently done a little research into arachnoid cysts and have found there is a wealth of information to suggest that this arachnoid cyst may be responsible for my ill health. So I am struggling to understand the radiologist and neurologists opinion on this. I also had a CT scan about a year previous to the MRI scan and there was no mention of a cyst in the report from that scan.
I had a meeting with another consultant last week and told him my concerns. He is going to raise the issue with the chief neurosurgeon at Dundee, and hopefully soon I will be able to discuss the possibility of an operation to remove/decompress this cyst.
I found these following three papers particularly convincing regarding the symptoms associated with arachnoid cysts and there subsequent improvement after operation on the cyst. There is also mention of different techniques of cyst surgery and there pro’s and con’s.
Erdincler, P. et al, 1999. Posterior fossa arachnoid cysts, British Journal of Neurosurgery, 13(1), pp.10-17
Samii, P. et al, 1999. Arachnoid cysts of the posterior fossa, Surgical Neurology, 51, pp. 376-82
Helland, C.A., et al, A population based study of intracranial arachnoid cysts: clinical and neuroimaging outcomes following surgical cyst decompression in adults, J Neurol Neurosurg Psychiatry, 78, pp. 1129-1135
I t was reassuring to read on this forum that I had a lot symptoms in common with other cyst sufferers, I wish everyone good luck in their pursuit of good health.
Hello to Mrs. Jeanean419,
I read your post, you said you dragged your right leg before your surgrey, does that mean you no longer do that after you had your surgrey? I do the same but I drag my left. I was told I have foot drop caused by my cyst on my brain. I was told I have 3 and I never new I had them. One is so large they say it cover's a third of my brain. I just developed foot drop afew months after I had my baby in 5/11/12. By Jan. of this year 2012, I noticed my foot was dragging and dropping when I walk. I had no other indications I just turned 30 and I never knew I had this. I walked completly normal until about Jan. of this year 2012. I don't know what to do, I'm praying and researching. I was told it was to risky to do surgery, if they touch the wrong thing, I might not walk, talk, or wake up. I was also told not to hit my head as it may leak. I was told to just monitor it and come back in May 2013 for a followup MRI, if I have any new symptoms contact them. I don't know if it will cause other issues by waiting. What kind of surgrey did you have done, and did it stop you from dragging your leg?
I had symptoms of lightheadedness and dizzy. Had ears checked as I have had tinnitius for 15 years and doc did MRI and found Cyst at bottom of brain pushing up. She felt it had been there since birth and probably not causing my lightheadedness. Well I had the surgery and 3 months later still am not able to work due to dizzy off an on. I currently feel pressure in ears as if fluid and I think this is causing dizziness. Fri I am going back to doc to check for 2 problems that could be causing this. And I decided to start taking sinus meds as I think allergeries are causing this pressure in eardrums and that is causing the dizziness. I will keep u posted. Glad to hear u are fine. For all out there that are getting or thinking of getting this operation I watched it on Youtube first. The operation was no problem only the cathiter removal afterwards hurts worse.
Sorry for the delay in a reply, I ended up with a new neurosurgeon and had to have a second surgery because my cyst detached from the ventricles and closed up and started to fill up with protien and was growing again. I too have a short fuse and my short term memory is getting better, the problem since my surgery is the dropped foot that I woke up with after surgery and like the last time I am going through physical therapy again, I am happy that my headaches are gone for the moment. The neurosurgeon is waiting for the three month mark to do another MRI to see if the surgery worked if not a shunt will be placed, I am crossing my fingers that things are better, because I am suffering the effects from injuries from all the falling that went on before the diagnosis of the cyst-neck and lower back herniated disc and partial thickness tear in my shoulder that has become arthritic, I think I rather deal with my brain problems than be in all the pain from injuries, keeping my fingers crossed for a good follow-up
I am very keen in contacting the nuersosurgeon that you dealt with in regards to your cyst.
Could you please take the time to send the name and contact number and location of the nuerosurgeon used. That would be very much appreicated.