Home         Forums  

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

AA Aplastic anemia

Reply
 
Thread Tools Search this Thread
  #1  
Old Wed Jul 11, 2012, 07:26 PM
BrianFlaigmore BrianFlaigmore is offline
Member
 
Join Date: Jul 2012
Location: San Diego CA USA
Posts: 27
AA and liver failure

Hey all, my name is Brian, I'm 26, and I am new to the forum although I've been reading and gaining encouragement from it for some time. Last month I underwent a MUD BMT at the City of Hope and to this point am doing very well. But as I sit here on this side of transplant it's kind of fun (kind of) to put the pieces together from the past crazy year. It all began last July when I had a week of upper right quadrant pressure and increasing depression. Eventually when my eyes and skin began to turn yellow I decided to go to the ER. My ALT was well above 2000 and after a litany of tests it showed I was a complete mystery. Some would call is seronegative autoimmune hepatitis, but after seeing many hepatologist on this as my platelets began to fall some said there was no markers for this and that it was toxic. Either way we never got a complete answer and probably will never know. My question is does anyone else with AA have a history of liver problems? Thank you much!
__________________
26m Mystery liver failure 6/11 treated with prednisone. Falling counts, Rituxan attempted for Evans syndrome 11/11. Tx dependent and SAA dx 12/11. hATG 2/12, no response. MUD BMT 5/6/12. Living life!

Last edited by BrianFlaigmore : Thu Jul 12, 2012 at 04:57 PM. Reason: spelling
Reply With Quote
  #2  
Old Thu Jul 12, 2012, 04:56 PM
Karenish Karenish is offline
Member
 
Join Date: Feb 2011
Location: Stafford, United Kingdom
Posts: 100
Not as such however I am not totally confident that mine isnt something to do with the liver...the reason....
up until about 7 years ago my blood results were always normal. Then as I was fast approaching 50 my GP said she would give me an MOT, when the results came back she said everything was normal except my bilirubin level which was very high, but not to worry as it was probably genetic and that I had something which I cant recall the name of now, but that it wasn't anything to be concerned about just that if i got stressed or ill I would find the whites of my eyes go yellow and my skin might too.......I didn't worry and carried on with my life until a couple of years later i 2010....when I became unwell and got diagnosed with VSAA. Coincidence? I will never know.
Reply With Quote
  #3  
Old Mon Jul 16, 2012, 02:42 AM
BrianFlaigmore BrianFlaigmore is offline
Member
 
Join Date: Jul 2012
Location: San Diego CA USA
Posts: 27
Thanks for the information. I don't know if I'm the only one (probably not) who tries to think of things that I did which could have caused this. I know that I read somewhere that 2% of AA patients had viral hepatitis, so I was just wondering if there is any more of a correlation with liver problems in general. I'm +38 today and last week we found out that my ALT and AST were getting kind of high, so we hope that the appointment tomorrow shows that the numbers have evened out.
__________________
26m Mystery liver failure 6/11 treated with prednisone. Falling counts, Rituxan attempted for Evans syndrome 11/11. Tx dependent and SAA dx 12/11. hATG 2/12, no response. MUD BMT 5/6/12. Living life!
Reply With Quote
  #4  
Old Tue Jul 24, 2012, 07:24 PM
ssdavi71416 ssdavi71416 is offline
Member
 
Join Date: Mar 2012
Location: Atlanta Georgia
Posts: 105
Back in Oct 2011 I had high AST and ALT 900 and 350. Then in Nov I developed what was eventually diagnosed as reactive arthritis. I also had what was thought to be a gall bladder attack on Dec 22. I then began to loose platelet counts beginning in Jan 2012. platelets were125, 117, 50, 30. Now I have SAA and had ATG treatment in the beginning of April. So theshort answer for me is it seems possible that there is a link.
Reply With Quote
  #5  
Old Mon Jul 30, 2012, 02:02 AM
BrianFlaigmore BrianFlaigmore is offline
Member
 
Join Date: Jul 2012
Location: San Diego CA USA
Posts: 27
Thanks for the reply. It sounds like you have had a very active immune system. Did you have many allergies before, or any other autoimmune problems?
__________________
26m Mystery liver failure 6/11 treated with prednisone. Falling counts, Rituxan attempted for Evans syndrome 11/11. Tx dependent and SAA dx 12/11. hATG 2/12, no response. MUD BMT 5/6/12. Living life!
Reply With Quote
  #6  
Old Mon Jul 30, 2012, 02:27 PM
evansmom evansmom is offline
Member
 
Join Date: Nov 2007
Location: Ontario, Canada
Posts: 203
Hi Brian,

When my son was getting his BMT for AA, there was a boy in the next isolation room recovering from his BMT. His AA presented a few weeks after he suddenly, like over the course of 2 days, became jaundiced and his liver seemed to be failing. He was diagnosed with auto-immune hepatitis which did lead to his auto-immune AA. Both were cured with his BMT.

Best wishes,

Nicole
__________________
Nicole, mom to Evan (20); diagnosed SAA November 2007, hATG mid-November 2007, no response after 6 months, unrelated 9/10 BMT June 2008, no GVH, health completely restored thanks to our beloved donor Bryan from Tennessee.

www.caringbridge.org/visit/evanmacneil
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
High liver enzymes mnsnyl AA 3 Wed Jan 4, 2012 09:31 AM
New: Dad has AA Laurie AA 10 Mon Jan 1, 2007 05:56 AM


All times are GMT -4. The time now is 02:46 AM.


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