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Old Tue Jun 24, 2014, 11:45 AM
Hopeful Hopeful is offline
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Join Date: Jan 2009
Location: California, USA
Posts: 766
Hi Steve,

Let me preface by saying that I am not a doctor just a bone marrow failure patient with 5.5 years of experience

It seems like the immunohistochemistry is just listing possible reasons why those markers would be expressed. I use to just get my markers with no explanations. So that was why I was concerned about the GI stoma notation.

Based on the rest of the report, it could be MDS or it could be something else. The traditional "smoking guns" are cytogenetic abnormalities, blasts, or significant dysplasia. He does have dysplasia in his platelet line, but he also doesn't have a lot of platelet precursors (megakaryocytes). So to me, it is not obvious.

I would seek out that third opinion from an MDS Center of Excellence. Also, keep aggressively pursing a switch in the medicines.
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55 yo female, dx 9/08, AA/hypo-MDS, subclinical PNH, ATG/CsA 12/08, partial response. small trisomy 6 clone, low-dose cyclosporine dependent
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