Hello,
I also was diagnosed with a mucinous borderine tumor and had a complete hysterectomy. My Gyn. Onc. at MD Anderson suggested that as a follow up I have a ct scan every 3 months for the 1st year, every 4 months the 2nd year and every 6 months for 3-5 th years. Also having ca-125 and a cea test done on same interval. It was during one of my ct scans that new tumors were discovered...thankfully very early and my prognosis is great. My cancer is acting unusual so don't assume you will have a recurrence but I strongly believe there should be some type of follow up. Also if you don't have a copy get a copy of your pathology report. I strongly suggest a second opinion. I went MD Anderson for my second opinion...I see from your proile you don't live in the US but I would go see another Gyn. Oncologist at a cancer hospital if you can. They may say the same thing your local doc said but peace of mind is worth it. Good Luck. Julie
I had a low malignant potential ovarian mass (otherwise known as borderline). It was not mucinous (sorry, can't remember the term for it), but I had a radical hysterectomy done. My gynecologic oncologist, who is one of the best in the country, emphasized that this is NOT cancer since the cells are atypical and not malignant. However, it is also not "benign." It's somewhere in between. The treatment is follow up exams. He said that if it reoccurs in "20 or 30 years" it will again be a borderline mass.
You definitely need a second opinion and with a doctor that can speak coherently about your situation. Although a lot of oncologists remove the appendix during a radical hysterectomy, I can't believe they are focusing on this or using it as a justification for the diagnosis.
That is just messed up. It is definitely NOT correct that mucinous borderline tumors are benign. I didn't look at your profile but by the use of the term "theatre" I am assuming you are not in the U.S. Is there any reason you can't get a second opinion? You need one Dr who can tell you what is really going on. I can't believe that they can't even tell you where the tumor came from and it is outrageous that there would be no mention of it
in the report. I have full blown cancer and not once was my appendix ever an issue. You need help that you are not getting and you need to fight like crazy to get the help you need. Below is a website that has a lot of info on this topic that I think will help to explain things to you better than your Drs did. Good luck to you.
Jan
ovariancancer.jhmi.edu/lmp.cfm
Your doctors definitely have left you with some unanswered questions. If you are unable to see anyone for a second opinion you could try posting your question in the expert forum to Dr. Goodman. I have found her to be very helpful. Good luck to you. Marie