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Urban, C; Lackner, H; Müller, E; Benesch, M; Strenger, V; Sovinz, P; Schwinger, W.
Stem cell transplantation in 6 children with parvovirus B19- induced severe aplastic anaemia or myelodysplastic syndrome.
Klin Padiatr. 2011; 223(6):332-334 Doi: 10.1055/s-0031-1287839
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Führende Autor*innen der Med Uni Graz
Urban Ernst-Christian
Co-Autor*innen der Med Uni Graz
Benesch Martin
Lackner Herwig
Müller Ewa Christine
Ritter-Sovinz Petra
Schwinger Wolfgang
Strenger Volker
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Abstract:
Parvovirus B19 (PVB19) induced severe aplastic anaemia (SAA) or myelodysplastic syndrome (MDS) is rare, and haematopoietic stem cell transplantation (HSCT) in this condition has not been reported so far. 6 children with SAA (n=4) or MDS (n=2) caused by acute PVB19 infection underwent HSCT under the protection of intravenous immunoglobulines. The 4 children with SAA received matched HLA bone marrow from a sibling (n=3) or peripheral unrelated blood stem cells (n=1). 1 patient had delayed erythrocyte engraftment, whereas 3 patients had an uneventful transplantation course. HSCT in one of the 2 children with MDS was complicated by poor graft function, the other patient engrafted without complications. In conclusion, HSCT in children with PVB19 induced SAA or MDS is feasible, even though some patients may develop delayed engraftment or prolonged poor graft function.
Find related publications in this database (using NLM MeSH Indexing)
Adolescent -
Anemia, Aplastic - therapy
Bone Marrow Transplantation -
Child -
Delayed Graft Function - diagnosis
Erythema Infectiosum - therapy
Feasibility Studies -
Female -
Hematopoietic Stem Cell Transplantation - methods
Humans -
Immunization, Passive -
Male -
Myelodysplastic Syndromes - therapy
Parvovirus B19, Human -
Retrospective Studies -

Find related publications in this database (Keywords)
pediatrics
haematology
stem cell transplantation
parvovirus B19
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