Home         Forums  

Go Back   Marrowforums > Bone Marrow Failure Diseases > Bone Marrow Failure
Register FAQ Search Today's Posts Mark Forums Read

Bone Marrow Failure Causes, treatment approaches, terminology, related diseases

Reply
 
Thread Tools Search this Thread
  #1  
Old Tue Jul 5, 2011, 11:47 AM
Kashnav Kashnav is offline
Member
 
Join Date: Jul 2011
Posts: 1
Myelofibrosis on a background of essential thrombocytosis

Hi,

I am 65 year old male. I was diagnosed by "Essential thrombocytosis" 4 years back and was prescribed hydroxyurea (also known as hydroxycarbamide) for reduction of the platelet count to the normal range. I'm also diabetic from past 20 years.

Frequency of hydroxyurea usage - one tablet on one day and two tablet on next consecutive day.

Been experiencing low platelet, Heamoglobin and high Leukocytes of late.

Latest CBC report shows below numbers -

Hemoglobin : 6.8 g/dl
RBC : 1.85 million/cummm
Total Leucocytes Count : 10110 cells/cumm
Platelet Count : 56220 cells/cumm

As per suggestion from oncologists done a Bone Marrow aspiration and trephine biopsy below is impression "Myelofibrosis on a background of essential thrombocytosis"

Detailed report is below

Report - Peripheral blood smear shows normocytic normochromic red cells with round macrocytes. There is a prominent leucoerythroblastic reaction. Thrombocytopenia + Bone marrow aspiration yielded a 'dry tap' hence cannot be commented upon. Biopsy shows adequate number of bony trabeculae. Intervening marrow shows large areas of fibrosis. Section is negative for granulomas.

Questions -

Does above imply i have developed Myelofibrosis ?

Are there any tests that need to be done to diagnose the condition or extent of involvement?

What are treatment options available?

Can it be treated with tablets or require chemotherapy / radiation?

Please suggest, your advice is appreciated.

Thanks,
Kashnav
Reply With Quote
  #2  
Old Tue Jul 5, 2011, 03:47 PM
DanL DanL is offline
Member
 
Join Date: Dec 2010
Location: Denver, CO
Posts: 590
Kashnav,

One seemingly logical step would be to get tested for v617f jak2 protein. presence of this protein, which can be checked from a blood draw, would increase the likelihood of response to one of the new clinical trial drugs know as JAK inhibitors. There are several good reports on about 3 different JAK1/2 inhibitors.

another question though, has your doctor commented on an increased spleen size? splenamegaly along with marrow fibrosis is usually necessary for a diagnoses of Primary Myelofibrosis.
__________________
MDS RCMD w/grade 2-3 fibrosis. Allo-MUD Feb 26, 2014. Relapsed August 2014. Free and clear of MDS since November 2014 after treatment with Vidaza and Rituxan. Experiencing autoimmune attack on CNS thought to be GVHD, some gut, skin and ocular cGVHD. Neuropathy over 80% of body.
Reply With Quote
Reply


Thread Tools Search this Thread
Search this Thread:

Advanced Search

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

vB code is On
Smilies are On
[IMG] code is On
HTML code is Off
Forum Jump

Similar Threads
Thread Thread Starter Forum Replies Last Post
Mom is 75 years old and has myelofibrosis misterno Tell Your Story 4 Sat Aug 8, 2015 12:25 PM
MDS vs Myelofibrosis? lacanada1 MDS 3 Tue Apr 17, 2012 05:53 PM
Ruxolitinib : a treatment for Myelofibrosis vpolasa Drugs and Drug Treatments 2 Sat Dec 3, 2011 04:39 PM
Newbie with question about myelofibrosis membengal Bone Marrow Failure 7 Mon Oct 19, 2009 02:25 PM
Is Myelofibrosis part of the MDS family? tamtam MDS 2 Tue Apr 7, 2009 09:15 PM


All times are GMT -4. The time now is 07:33 PM.


Powered by vBulletin® Version 3.6.7
Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.
Forum sites may contain non-authoritative and unverified information.
Medical decisions should be made in consultation with qualified medical professionals.
Site contents exclusive of member posts Copyright © 2006-2020 Marrowforums.org