Malignant cerebral infarction after ChAdOx1 nCov-19 vaccination: a catastrophic variant of vaccine-induced immune thrombotic thrombocytopenia

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作者
M. De Michele
M. Iacobucci
A. Chistolini
E. Nicolini
F. Pulcinelli
B. Cerbelli
E. Merenda
O. G. Schiavo
E. Sbardella
I. Berto
L. Petraglia
N. Caracciolo
M. Chiara
S. Truglia
D. Toni
机构
[1] Sapienza University of Rome,Emergency Department, Stroke Unit
[2] Sapienza University of Rome,Neuroradiology Unit, Department of Human Neurosciences
[3] Sapienza University of Rome,Hematology, Department of Translational and Precision Medicine
[4] Sapienza University of Rome,Department of Experimental Medicine
[5] Sapienza University of Rome,Department of Medico
[6] Sapienza University of Rome,Surgical Sciences and Biotechnologies
[7] Sapienza University of Rome,Department of Radiological, Oncological and Pathological Sciences
[8] Sapienza University of Rome,Department of Human Neurosciences
[9] Sapienza University of Rome,Neurosurgery, Department of Human Neurosciences
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摘要
Vaccine-induced thrombotic thrombocytopenia with cerebral venous thrombosis is a syndrome recently described in young adults within two weeks from the first dose of the ChAdOx1 nCoV-19 vaccine. Here we report two cases of malignant middle cerebral artery (MCA) infarct and thrombocytopenia 9-10 days following ChAdOx1 nCoV-19 vaccination. The two cases arrived in our facility around the same time but from different geographical areas, potentially excluding epidemiological links; meanwhile, no abnormality was found in the respective vaccine batches. Patient 1 was a 57-year-old woman who underwent decompressive craniectomy despite two prior, successful mechanical thrombectomies. Patient 2 was a 55-year-old woman who developed a fatal bilateral malignant MCA infarct. Both patients manifested pulmonary and portal vein thrombosis and high level of antibodies to platelet factor 4-polyanion complexes. None of the patients had ever received heparin in the past before stroke onset. Our observations of rare arterial thrombosis may contribute to assessment of possible adverse effects associated with COVID-19 vaccination.
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