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Very severe immune aplastic anemia after mRNA vaccination against COVID-19 responds well to immunosuppressive therapy: clinical characteristics and comparison to previous reports

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Abstract
OBJECTIVE: Various hematologic side effects of the Coronavirus Disease 2019 (COVID-19) vaccination has been reported, and most of them are thought to be related to autoimmune pathways. To the best of our knowledge, only few cases of post-COVID-19 vaccination aplastic anemia (AA) have been reported and there is no reported Korean case of COVID-19 vaccine-induced AA yet. We present a case of severe immune-mediated AA that developed after the administration of a messenger ribonucleic acid (mRNA) gene-based spike protein vaccine against COVID-19, which responded well to immunosuppressive therapy, and discuss the probable pathogenesis of AA and the implication of vaccination along with a comparison of previous cases reported. METHODS: A 53-year-old Korean man developed sudden pancytopenia three months after COVID-19 vaccination. To evaluate the cause of pancytopenia, a bone marrow study was performed. RESULTS: A diagnosis of AA was made through the bone marrow study and he received triple immunosuppressive therapy (IST). After triple IST for five months, his blood cell count was improved and maintained without transfusion and his follow-up bone marrow examination showed improved cellularity. CONCLUSION: COVID-19 vaccine might be associated with the development of immune-mediated AA. Prompt hematologic evaluation should be performed when there are symptoms or signs suggestive of cytopenia after COVID-19 vaccination. Although the clinical outcome of post-vaccination AA varies, a good prognosis can be possible for patients with COVID-19 vaccination-induced AA.
All Author(s)
S. Woo ; B. Kim ; S. C. Lee ; M. S. Kim ; Y. A. Yoon ; Y. J. Choi
Issued Date
2022
Type
Article
Keyword
Aplastic anemiaSARS-CoV-2COVID-19vaccineimmunosuppressive therapy
Publisher
Taylor & Francis
ISSN
1024-5332 ; 1607-8454
Citation Title
Hematology
Citation Volume
27
Citation Number
1
Citation Start Page
1191
Citation End Page
1195
Language(ISO)
eng
DOI
10.1080/16078454.2022.2140986
URI
http://schca-ir.schmc.ac.kr/handle/2022.oak/809
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