Okay you guys, I need opinions from anyone who's had head and neck surgery.
Would you believe I'm going to have to have surgery AGAIN in less than a year after valve surgery? I'm telling you it just keeps getting better and better.
I noticed a less than small grape size node-like thingy last spring right under my earlobe. I was in the midst of psychological panic over aortic stensosis/bicuspid valve at the time so it really wasn't the top thing on my mind but I did point it out to my surgeon and he wasn't "concerned". Everybody else told me to stop obcessing and get over myself.
Fast forward to last week. It's still there. I had mentioned it to two of my personal Docs and a couple I work with and got a 50/50 check it out/it's okay response. I decided to side with my paranoia and went to see a Head and neck Doc. He called a pathologist to jab a needle in my neck 4011 times and the next day I was told the "good news": I have a pleomorphic adenoma or "mixed tumor" on my left partid gland. It is benign right now but such "aliens" do have a tendency to turn cancerous so the thing must come out. What is it with my body that things want to blow up? First it was my aorta and now it's this ditsel on my neck. It also makes me nervous because I work in CT surgery and used to do ENT/head and neck. Makes one wonder if you really can get the diseases in which you work.
Anyway, the head and neck guy started with the regular song and dance of "you'll have to go off the coumadin" and I told him absolutely not unless I am bridged with heparin or lovenox and if he didn't agree I would take my business elsewhere. I believe this intrigued him as he admitted he had never had a patient who could not stop their anticoagulation. I did get support troups in the form of his partner the ear Doc with whom I used to work who refered me to him. He informed him he had had a couple of patients like me and it was doable. I believe the guy is deep into research about it at this time.
I would like this guy to operate on me as he has excellent credentials for the procedure I need. I am very impressed that he outright diagnosed me prior to the Path report and my friend, the other ENT guy highly recommends him.
I've been researching through this forum but basically have only found treatment with uterine ablations, colonoscopy, and dermatologic procedures. I've also searched the net as well as Al's bridging outline. There seems to be conflicting opinions between Heparin and Lovenox. I've had great success with lovenox the few times my INR has been subtherapeutic and hope I can go that route. I guess what I'd like to know is if anyone has had parotid or submandibular gland surgery after valve replacement with mechanical valve and how your anti coagulant therapy was adjusted. I can't be the only one who's faced this can I?
Would you believe I'm going to have to have surgery AGAIN in less than a year after valve surgery? I'm telling you it just keeps getting better and better.
I noticed a less than small grape size node-like thingy last spring right under my earlobe. I was in the midst of psychological panic over aortic stensosis/bicuspid valve at the time so it really wasn't the top thing on my mind but I did point it out to my surgeon and he wasn't "concerned". Everybody else told me to stop obcessing and get over myself.
Fast forward to last week. It's still there. I had mentioned it to two of my personal Docs and a couple I work with and got a 50/50 check it out/it's okay response. I decided to side with my paranoia and went to see a Head and neck Doc. He called a pathologist to jab a needle in my neck 4011 times and the next day I was told the "good news": I have a pleomorphic adenoma or "mixed tumor" on my left partid gland. It is benign right now but such "aliens" do have a tendency to turn cancerous so the thing must come out. What is it with my body that things want to blow up? First it was my aorta and now it's this ditsel on my neck. It also makes me nervous because I work in CT surgery and used to do ENT/head and neck. Makes one wonder if you really can get the diseases in which you work.
Anyway, the head and neck guy started with the regular song and dance of "you'll have to go off the coumadin" and I told him absolutely not unless I am bridged with heparin or lovenox and if he didn't agree I would take my business elsewhere. I believe this intrigued him as he admitted he had never had a patient who could not stop their anticoagulation. I did get support troups in the form of his partner the ear Doc with whom I used to work who refered me to him. He informed him he had had a couple of patients like me and it was doable. I believe the guy is deep into research about it at this time.
I would like this guy to operate on me as he has excellent credentials for the procedure I need. I am very impressed that he outright diagnosed me prior to the Path report and my friend, the other ENT guy highly recommends him.
I've been researching through this forum but basically have only found treatment with uterine ablations, colonoscopy, and dermatologic procedures. I've also searched the net as well as Al's bridging outline. There seems to be conflicting opinions between Heparin and Lovenox. I've had great success with lovenox the few times my INR has been subtherapeutic and hope I can go that route. I guess what I'd like to know is if anyone has had parotid or submandibular gland surgery after valve replacement with mechanical valve and how your anti coagulant therapy was adjusted. I can't be the only one who's faced this can I?