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Letter to the Editors-in-Chief| Volume 202, P182-183, June 2021

Cerebral venous thrombosis and thrombocytopenia post-COVID-19 vaccination

      We report the case of a 50-year-old white man who had always been in good health. He was a voluntary periodic blood donor (his last whole blood donation was on December 1, 2020) and all laboratory checks performed before donations, including blood cell count, were always within the normal range. His personal and family history was negative for thrombotic or hemorrhagic disorders. He had never suffered from COVID-19 and all molecular screens for SARS-CoV-2 (performed routinely every month as he worked in the public administration) were always negative. On March 4, 2021, he received the first dose of the anti-COVID-19 vaccine produced by AstraZeneca without any immediate adverse reaction. Seven day later (11 March 2021) he suffered from a worsening headache but, despite this symptom, he continued to work under analgesic medications. On March 15, 2021 the patient was referred unconscious to the emergency room of the city hospital of Mantua (Italy). Computed tomography (CT) scans of the brain showed intra-parenchymal hemorrhage in the left cerebral hemisphere while CT angiography of intracranial circle vessels showed multiple small bleeding spots in the context of the left parenchymal hemorrhage and lack of opacification of the left transverse and sigmoid sinuses, compatible with cerebral venous sinus thrombosis (CVST). The patient was immediately transferred to the Intensive Care Unit and underwent urgent neurosurgery in a desperate attempt to stop and remove the intracerebral hemorrhage, but 18 h after the intervention he died. Overall, the patient was transfused with 9 red blood cell units and 4 platelet apheresis units. Thromboelastogram (TEG6S, Haemonetics) studies performed before and during the operation showed a prolonged reaction time, decreased platelet function and the absence of fibrinogen, measured with a functional fibrinogen assay, with a consequent markedly reduced maximum amplitude of the clot (8.4 mm, normal range 52–69 mm) only partially and temporarily restored by an infusion of fibrinogen concentrate (10 g total). The most relevant abnormal laboratory results (Table 1), performed on admission to hospital, were severe thrombocytopenia and hypofibrinogenemia associated with factor XIII deficiency. In addition, heterozygous MTHFR C677T together with increased levels of homocysteine, which have been associated with an increased CVST risk [
      • Boncoraglio G.
      • Carriero M.R.
      • Chiapparini L.
      • et al.
      Hyperhomocysteinemia and other thrombophilic risk factors in 26 patients with cerebral venous thrombosis.
      ,
      • Gogu A.E.
      • Jianu D.C.
      • Dumitrascu V.
      • et al.
      MTHFR gene polymorphisms and cardiovascular risk factors, clinical-imagistic features and outcome in cerebral venous sinus thrombosis.
      ], and concomitant folate deficiency were observed. Notably, like previous observations by other investigators [
      • Brodard J.
      • Kremer Hovinga J.A.
      • Fontana P.
      • Studt J.D.
      • Gruel Y.
      • Greinacher A.
      COVID-19 patients often show high-titer non-platelet-activating anti-PF4/heparin IgG antibodies.
      ,
      • Greinacher A.
      • Thiele T.
      • Warkentin T.E.
      • Weisser K.
      • Kyrle P.
      • Eichinger S.
      A prothrombotic thrombocytopenic disorder resembling heparin-induced thrombocytopenia following coronavirus-19 vaccination.
      ], anti-PF4 antibodies were detected. Further studies are needed to assess the pathogenesis of thrombocytopenia (i.e., immune-mediated or protein spike-mediated) [
      • Zhang S.
      • Liu Y.
      • Wang X.
      • et al.
      SARS-CoV-2 binds platelet ACE2 to enhance thrombosis in COVID-19.
      ] and its relationship with the development of CVST following anti-COVID vaccination.
      Table 1The patient's basal laboratory profile (abnormal results are shown in bold).
      ParameterPatient's valuesNormal values
      Hemoglobin (g/dL)14.613.5–17.5
      RBC (1012/L)5.184.50–5.90
      Schistocytes on peripheral blood smear (%)<1<1
      White cells (109/L)10.874.40–11.0
      Platelets (109/L)15150–400
      Prothrombin time (INR)1.190.88–1.12
      Activated partial thromboplastin time (ratio)0.880.82–1.18
      Thrombin time (seconds)23.516–20
      Fibrinogen (mg/dL)98150–450
      D-dimer (ng/mL)>10,000<500
      Antitrombin (%)10175–125
      Protein C (%)7370–140
      Protein S (%)6072–123
      Alanine aminotransferase (IU/L)165–45
      Total bilirubin0.570.20–1.00
      C reactive protein (mg/L)17.6<5
      SARS-CoV-2 screening
       PCRNegativeNegative
       Anti-SARS-CoV-2 Ab (ECLIA, Roche)NegativeNegative
       Anti-SARS-CoV-2 IgGAb (CLIA, Diasorin) (UA/mL)6.4<12
      Lactate dehydrogenase (IU/L)337150–450
      Coagulation factor II (%)7150–150
      Coagulation factor IX (%)>15050–150
      Coagulation factor V (%)7150–150
      Coagulation factor VII (%)6850–150
      Coagulation factor VIII (%)11450–150
      Coagulation factor X (%)6950–150
      Coagulation factor XI (%)10370–120
      Coagulation factor XII (%)9970–120
      Coagulation factor XIII (%)3570–150
      VWF:Ag (%)>12050–120
      VWF:RCo (%)>15050–150
      VWF:CB (%)>15050–150
      ADAMTS13 activity (FRET assay) (%)4845–138
      Lupus anticoagulantNegativeNegative
      Anti-beta2 glycoprotein Ab
       IgG (U/mL)<0.6<7
       IgM (U/mL)<0.9<7
      Anti-cardiolipin Ab
       IgG (U/mL)2.6<10
       IgM (U/mL)0.8<10
      Thrombophilia mutations
       Factor V Leiden (G169A)AbsentAbsent
       Prothrombin (G20210A)AbsentAbsent
       MTHFR (C677T)HeterozygousAbsent
       JAK2AbsentAbsent
      Homocysteine (μmol/L)16.7<12
      Folic acid (ng/mL)0.93.9–26.8
      Vitamin B12 (pg/mL)246197–771
      Complement (g/L)
      C30.760.81–1.57
       C40.140.13–1.39
      Anti-PF4 antibodies (nm) (PF4 Enhanced ELISA, Immucor)2.6<0.4
      Anti-platelet antibodies
      PakAuto test detects specific autoantibodies against platelet glycoproteins IIb/IIIa and Ia/IIa present in plasma or serum or eluted from platelet surface. PakPlus test detects in serum anti-HLA class I antibodies and platelet-specific antibodies against glycoproteins IIb/IIIa, Ia/IIa, Ib/IX and IV.
       Autoantibodies (PakAuto ELISA, Immucor)AbsentAbsent
       Alloantibodies (PakPlus ELISA, Immucor)AbsentAbsent
      Legend: SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; PCR, polymerase chain reaction; Ab, antibodies; CLIA, chemiluminescence immunoassay; ECLIA, electrochemiluminescence assay; VWF, von Willebrand factor; Ag, antigen; RCo, ristocetin cofactor; CB, collagen binding; ADAMTS13, A Disintegrin And Metalloproteinase with a ThromboSpondin type 1 motif, member 13; FRET, fluorescent resonance energy transfer; RBC, red blood cells; ELISA, enzyme-linked immunosorbent assay.
      a PakAuto test detects specific autoantibodies against platelet glycoproteins IIb/IIIa and Ia/IIa present in plasma or serum or eluted from platelet surface. PakPlus test detects in serum anti-HLA class I antibodies and platelet-specific antibodies against glycoproteins IIb/IIIa, Ia/IIa, Ib/IX and IV.

      CRediT authorship contribution statement

      M.F.: study design and concept, writing a draft of the manuscript; S.T.: coagulation assays, writing a draft of the manuscript; M.P.: study design and concept, interpretation of the data; C.G.: coagulation assays; B.C.: coagulation assays; I.T.: coagulation assays; C.P.: interpretation of the data from clinical point of view; S.A.B.: revising the manuscript; G.C.: interpretation of the data from clinical point of view, revising the manuscript.

      Declaration of competing interest

      The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

      Acknowledgments

      The authors thank Dr. Rachel Stenner for her revision of the language of this manuscript.

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