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. 2022 Aug;198(3):595-599.
doi: 10.1111/bjh.18235. Epub 2022 May 10.

Characteristics, management and outcome of acquired amegakaryocytic thrombocytopenia

Anais Roeser  1 , Guillaume Moulis  2   3 , Mikael Ebbo  4 , Louis Terriou  5 , Elsa Poullot  6 , Bertrand Lioger  7 , Marie Chilles  8 , Helene Labussière-Wallet  9 , Christelle Mausservey  10 , Micheline Pha  11 , Mathieu Puyade  12 , Stephane Cheze  13 , Nicolas Limal  1 , Marc Michel  1 , Bertrand Godeau  1 , Matthieu Mahévas  1
Affiliations

Characteristics, management and outcome of acquired amegakaryocytic thrombocytopenia

Anais Roeser et al. Br J Haematol. 2022 Aug.
No abstract available

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References

REFERENCES

    1. Simkins A, Maiti A, Short NJ, Jain N, Popat U, Patel KP, et al. Acquired amegakaryocytic thrombocytopenia and red cell aplasia in a patient with thymoma progressing to aplastic anemia successfully treated with allogenic stem cell transplantation. Hematol Oncol Stem Cell Ther. 2019;12(2):115-8.
    1. Ja K, My E, Lf L. Rapid progression of acquired amegakaryocytic thrombocytopenia to aplastic anemia. South Med J. 1997;90(1):91-4.
    1. Novotný JP, Köhler B, Max R, Egerer G. Acquired Amegakaryocytic thrombocytopenic purpura progressing into aplastic anemia. Prague Med Rep. 2017;118(4):147-55.
    1. Slater LM, Katz J, Walter B, Armentrout SA. Aplastic anemia occurring as amegakaryocytic thrombocytopenia with and without an inhibitor of granulopoiesis. Am J Hematol. 1985;18(3):251-4.
    1. Hoffman R, Bruno E, Elwell J, Mazur E, Gewirtz AM, Dekker P, et al. Acquired amegakaryocytic thrombocytopenic purpura: a syndrome of diverse etiologies. Blood. 1982;60(5):1173-8.

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