Acquired amegakaryocytic thrombocytopenic purpura progressing into aplastic anemia
In this article, we report a case of newly acquired AATP without an associated autoimmune disease, refractory to corticoids, intravenous immunoglobulin (IVIG) and second-generation TPO (thrombopoietin) agonists, which have recently been approved for the treatment of thrombocytopenia. Finally, in acc...
Gespeichert in:
| Hauptverfasser: | , , , |
|---|---|
| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2017
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| In: |
Prague medical report
Year: 2017, Jahrgang: 118, Heft: 4, Pages: 147-155 |
| ISSN: | 2336-2936 |
| DOI: | 10.14712/23362936.2017.16 |
| Online-Zugang: | Resolving-System, kostenfrei, Volltext: http://dx.doi.org/10.14712/23362936.2017.16 Verlag, kostenfrei, Volltext: https://pmr.lf1.cuni.cz/118/4/0147/ |
| Verfasserangaben: | Jan Philipp Novotný, Birgit Köhler, Regina Max, Gerlinde Egerer |
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| 520 | |a In this article, we report a case of newly acquired AATP without an associated autoimmune disease, refractory to corticoids, intravenous immunoglobulin (IVIG) and second-generation TPO (thrombopoietin) agonists, which have recently been approved for the treatment of thrombocytopenia. Finally, in accordance with other reports, disease progression into aplastic anemia has occurred. | ||
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