Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Aug;198(3):595-599.
doi: 10.1111/bjh.18235. Epub 2022 May 10.

Characteristics, management and outcome of acquired amegakaryocytic thrombocytopenia

Affiliations

Characteristics, management and outcome of acquired amegakaryocytic thrombocytopenia

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

PubMed Disclaimer

Similar articles

Cited by

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.

Supplementary concepts

LinkOut - more resources