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Granulocyte tranfusion

F J Barriga, M E Legues, P Bertin
PURPOSE: We present a patient with severe aplastic anemia who had partial engraftment with full chimerism after allogeneic bone marrow transplantation from an HLA identical sibling. PATIENTS AND METHODS: A 3-year-old girl with severe aplastic anemia (SAA) received a bone marrow transplantation (BMT) from an HLA identical brother 9 months after her diagnosis. Before BMT she was red blood cell tranfusion dependent, had an absolute neutrophil count (ANC) of 1,000-1,500 x 10(9)/1 and a platelet count of 15-19,000 x 10(9)/1...
May 1996: Journal of Pediatric Hematology/oncology
J Blaschke, N E Goeken, J S Thompson, F R Dick, R D Gingrich
Multiple infections and severe neutropenia were found in a previously healthy 29 year old man with no history of similar syndromes in the family, drug ingestion or exposure to environmental toxins. There was no evidence at the time of presentation of diseases previously associated with agranulocytosis (e.g., neoplasia, thyrotoxicosis, chronic infection, collagen-vascular disease or leukoagglutinating antibody). His serum contained a nonagglutinating, complement-dependent, cytotoxic antibody, however, reactive with peripheral blood granulocytes from 35 per cent of normal donors...
May 1979: American Journal of Medicine
I E Fortuny, D C Hadlock, B J Kennedy, J J McCullough
No abstract text is available yet for this article.
March 8, 1975: Lancet
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