2012
DOI: 10.1007/s13224-012-0189-x
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TA-GVHD, a Fatal Complication Following Blood Transfusion from a First-Degree Relative

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Cited by 5 publications
(3 citation statements)
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“…It is understood that having a donor from family member is actually less preferable compared to unrelated donors -as homozygosity of HLA types is more common to occur between first-degree family members, which may trigger transfusion-associated graft-versus-host-disease (TA-GVHD). 14,15 Regardless, this was the safest blood option we were able to provide concerning its kidd-incompatibility circumstances.…”
Section: Discussionmentioning
confidence: 99%
“…It is understood that having a donor from family member is actually less preferable compared to unrelated donors -as homozygosity of HLA types is more common to occur between first-degree family members, which may trigger transfusion-associated graft-versus-host-disease (TA-GVHD). 14,15 Regardless, this was the safest blood option we were able to provide concerning its kidd-incompatibility circumstances.…”
Section: Discussionmentioning
confidence: 99%
“…This finding might result from the lymphocyte insufficiency in peripheral blood, probably because that donor lymphocytes were easier to be rejected as foreign bodies (18) . Immunosuppressive regimens involving corticosteroids, antithymocyte globulin (ATG), and immune inhibitors (CsA, CTX) have yielded poor results with few documented survivors (19,20) . Some scholars even believe that "there is currently no treatment" (2) .…”
Section: Discussionmentioning
confidence: 99%
“…The bone marrow biopsy reported hypocellularity, scattered histiocytes and erythrophagocytosis in TA-GVHD. 4,6 A definitive diagnosis of TAGVHD is possible by documentation of donor-specific cells, or DNA, in the blood or tissues of the recipient by various molecular methods. 7 Hemophagocytosis and marked stromal changes seen in the trephine biopsy resulting in pancytopenia were seen in a fatal outcome TAGVHD case.…”
mentioning
confidence: 99%