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Good Morning, I was diagnosed with Splenic Marginal Zone Lymphoma B-cell Non-Hodgins around 2 years ago.  I had my spleen removed last June in order to make a true diagnosis of cancer.  I know this type of cancer is slow growing and is rare.  I was wondering if anyone that has this cancer had a relapse and if any scans or tests were done to detect a relapse.  I know this cancer can invade a major organ and I just want to be proactive so when I do relapse I will know as soon as possible (the doctor told me I would relapse in 5-10 years). I would appreciate any and all feedback.  Thank you.

Max Former Hodgkins Stage 3's picture
Max Former Hodg...
Posts: 3311
Joined: May 2012

I recall several SMZL writers here in the last two years or thereabout, Concern. A couple within two months or so. As a generality, indolent (slow-growing) cancers are more prone to relapse, not less (I know this from my non-spleenic form of HL).   Usually relapse is confirmed via CT/PET.  Spleenic may necessitate more specialized tests whith which I am unfamiliar.  Presumably, you are in some form of long-term followship, which most Best Practices centers insist upon.  By this I mean at least 5 years, but I am in lifetime annual checks, per my cancer centers insistence.  I assume you are in at least six-month oncology visits at this point, which are ordinarily extended to one annual after about 2 or 3 years in full remission.

I recommend you go to the CNS Email funtion and privately email screen names djwilzig and dan6807 .  Email both separately, to increse privacy.

Both of these individuals have written to the Boards since 2016, as you no doubt noted yourself on the other thread that you began here on.    Depending on their personal settings, the CNS system will send them an email telling them that they received mail for the Boards.  This will make them aware of discussion regarding SMZL, even if they no longer visit the Boards very often.  Good luck.  Just a suggestion, to get faster response. I get these emails frequently, and they are confidential and much quicker than hoping a reader will just spot something at random on the Boards.

I'm sure some of these or other folks with personal SMZL experiences will write soon,


cuddlefish's picture
Posts: 3
Joined: Jul 2016


I also have SMZL, though mine was diagnosed only last year. In my case, the spleen was left in place and I am receiving infusions (and now injections) of a monoclonal antibody drug called Rituxan. These "maintenance" treatments will continue another year and then I'll be cut free like you. Because our cancer does not typically show in lymphnodes, I think that we will be monitored by blood work to determine when we need further treatment. From my research, this does not typically progress into other organs. As I am choosing to think about it, it is very likely that we will simply need to be treated every several years, as our blood numbers indicate. When I received my diagnosis, the oncologist reassured me, " This probably won't be what kills you". I hope that helps you a llittle.


Posts: 1
Joined: Dec 2017

I was originally  diagnosed with monoclonal b-cell lymphocytes in 2013/14.  Since  then I have been feeling fatigued and in June of this year after a bone marrow  biopsy,  I was re-diagnoised with smzl.  My main problem  right now is anemia and related fatigue. I am not receiving any treatment at the moment. Will be going to  city of hope in December for 2nd opinion.  Does anyone else battle with anemia?

Kmsparky's picture
Posts: 3
Joined: Jan 2018

I was diagnosed in December 2017.  I presented with a spleen of 22cm, fatigue, anemia and low platelets.  Bone marrow is 75% B cells and the B cells are also in my peripheral blood. Currently am being treated with rituximab (3/4 treatments completed). I was diagnosed with an enlarged spleen (14.9 cm) in 2013 but it was not followed up.  I meet with my onc on Feb. 22.  Not sure where we will go from there but I can tell you that after the first infusion, within days i noticed my spleen was beginning to shrink.

lindary's picture
Posts: 658
Joined: Mar 2015

I was diagnosed with anemia when I was about 13. Fortunately an over the counter iron pill has worked for me and still does.When I was going through treatment I would be asked about feeling tired. My reponse "I always feel that way to some extent".  Still do but some of it is my sitting around too much.

Posts: 413
Joined: Jan 2017

I had anemia really bad about 1 year before I was diagnosed with lymphoma. Ironized yeast tablets along with b-12 was what my doc recommended and it really seemed to help. The yeast is easier on you than straight iron supplements (Gas).

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