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Grade 2/3 fibrosis
Does anyone know if this has any relevance to anything? They seem to discuss it a lot in my husband's reports, but I can't find anything to say if this is bad or good.
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Husband (61) dx RAEB1 Apr 2015 after long term bad CBCs (first discovered Apr 2008 after an unknown infection had him hospitalized), currently on watch & wait with monthly bloodwork. Myeloid Gene Panel testing done Aug 2017, showed nothing worrisome. CEBPA mutation 
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