Member Comments are provided by individuals and reflect their personal opinions only. Under NO circumstances should you act on any advice or opinion posted in this forum.  ALWAYS check with your personal physician before taking any action regarding your health! MedHelp International and our partners, sponsors and affiliates have no obligation to monitor any comments posted on this site, or the content and/or accuracy of such exchanges. MedHelp International does not endorse the views of any user.

Waldenstrom's Macroglobulinemia Community

This patient support community is for discussions relating to Waldenstrom's Macroglobulinemia, non-Hodgkin lymphoma, monoclonal gammopathy of unknown significance (MGUS), multiple myeloma, and plasmapheresis.
 | 

Intermittent M-Spike

by ScarlettRae, Apr 17, 2008 10:54PM
I realize this is a WM forum - but I am unsure where to turn.   I am a 41 yr old with a 10 yr history of IgM monoclonal paraprotienemia (w/elevated B2 Microglobulins).  Additionally, I have been treated for hypercalcemia and had all other possible causes (ie: parathyroid disorder, myeloma) ruled out.  I have a chronic irom defiency anemia which has been treated with IV Imferon - however, my iron stores disappear after 2 years.  I had a hysterectomy 5 years ago to  see if that would resolve the anemia - to no avail.  I have my SPE & labs done every 3-6 months and have yet to find out what could cause an intermittent M-spike.  My doc (who I trust implicitly) has no clue.  But we just keep treating the symptoms as they appear.  Is this a normal profile for early WM?  Additionally, my latest labs show that the Fe deficiency is back however my hemoglobin is elevated.  Any suggestions or infor would be very much appreciated.

Scarlett
Member Comments

by Dennis MD, Apr 27, 2008 10:00AM
To: ScarlettRae
Hi Scarlett.
How are you doing?
Just have some clarifications.  What are your other signs and symptoms?  What other laboratory examinations were already done?  Have you had a bone marrow biopsy?
Excess lymphoplasmacytic cells, absence of lytic bone disease, and presence of hepatosplenomegaly or lymphadenopathy, or both characterize Waldenstrom’s Macroglobulinemia (WM).  Common symptoms include severe fatigue, bleeding, and bone pain.  Laboratory evaluation usually shows anemia, elevated erythrocyte sedimentation rate (ESR), elevated beta 2 microglobulin, and monoclonal IgM protein in serum.  Hypercalcemia is common in patients with multiple myeloma as a result of bone destruction.  
I suggest further examinations in order to have a definite diagnosis.  There are diagnostic criteria for WM.  Perhaps a referral to a hematologist will help.
Please do post your clarifications.
Good luck.

by wezee, Aug 31, 2008 12:12AM
i jhave just been dia with waldstrom aneima lympoohoma  Pretty scarry. can aynone give me any words of wisdom and help thank you
Post Comment
To
Comment
Post Comment
Recent Activity
Comment on Seems Like
Sep 03 by laypeople
Made it to Texas
Aug 24 by alagirl
Comment on Haven't left yet
Aug 24 by alagirl
Comment on Haven't left yet
Aug 23 by scratchinghead
Haven't left yet
Aug 22 by alagirl
Comment on Topamax and Another...
Aug 21 by alagirl
Comment on Topamax and Another...
Aug 21 by alagirl
Comment on Topamax and Another...
Aug 21 by alagirl
Expert Activity
Early Diagnosis of Peripheral Arter... 
Aug 31 by Lee Kirksey, MD
5 Steps to Medical Debt
Aug 30 by Adam R. Tanase, D.C.
Coronary Artery Disease - Risk fact... updated
Aug 26 by Cleveland Clinic