2022
DOI: 10.14740/jmc3921
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Acquired Hemophilia A After SARS-CoV-2 Infection: A Case Report

Abstract: Acquired hemophilia A is a rare autoimmune coagulation disorder associated to the development of neutralizing antibodies directed towards coagulation factor VIII, known as factor VIII inhibitors, in subjects with previous normal clotting system homeostasis and personal and family history negative for bleeding episodes. This condition, although variable in severity and clinical presentation, may lead to severe and life-threatening hemorrhages which can be either spontaneous or associated with traumatic events a… Show more

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Cited by 7 publications
(6 citation statements)
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References 19 publications
(12 reference statements)
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“…Namely, both onset and relapse of immune thrombocytopenic purpura [10] and immune-mediated thrombotic thrombocytopenic purpura [11] were described in the literature, along with a new condition characterized by thrombocytopenia accompanied by thrombosis and antibodies against platelet factor 4 (PF4) in the serum (defined vaccine-induced thrombotic thrombocytopenic -VITT-) [12] . Finally, like in our patient, cases of AHA onset following vaccination have been described, thus improving our knowledge of the possible underlying pathophysiological mechanisms, although establishing a specific causal relationship between the vaccine and these autoimmune disorders can be challenging due to several variables related to a single case [13] , [14] , [15] , [16] . Despite difficulties in establishing a specific correlation, several working groups, including Leone and colleagues, have reported an increase in the incidence of AHA in the months following the worldwide SARS-CoV-2 immunization period (between 14 and 52 days from vaccination day and AHA-related treatment start) [17] .…”
Section: Discussionmentioning
confidence: 90%
“…Namely, both onset and relapse of immune thrombocytopenic purpura [10] and immune-mediated thrombotic thrombocytopenic purpura [11] were described in the literature, along with a new condition characterized by thrombocytopenia accompanied by thrombosis and antibodies against platelet factor 4 (PF4) in the serum (defined vaccine-induced thrombotic thrombocytopenic -VITT-) [12] . Finally, like in our patient, cases of AHA onset following vaccination have been described, thus improving our knowledge of the possible underlying pathophysiological mechanisms, although establishing a specific causal relationship between the vaccine and these autoimmune disorders can be challenging due to several variables related to a single case [13] , [14] , [15] , [16] . Despite difficulties in establishing a specific correlation, several working groups, including Leone and colleagues, have reported an increase in the incidence of AHA in the months following the worldwide SARS-CoV-2 immunization period (between 14 and 52 days from vaccination day and AHA-related treatment start) [17] .…”
Section: Discussionmentioning
confidence: 90%
“…In the last few years, cases of AHA in COVID patients have been described, both after infection and vaccination [15][16][17][18][19][20][21][22][23][24][25]. A few cases of AHA following the viral infection have been reported in literature [15,[26][27][28][29][30]. Our first hypothesis is that SARS-CoV-2 infection acted as the immunological trigger for the development of autoantibodies.…”
Section: Discussionmentioning
confidence: 99%
“…Malignant disease has been ruled out, but the exclusion of autoimmune disease was not reported although she had fibromyalgia in medical history. Nardella et al showed a 53-year-old woman treated under the diagnosis of AHA ( 11 ). They concluded that AHA may have been associated with SARS-CoV-2 infection based on SARS-CoV-2 anti-spike antibodies, although she also had signs and symptoms of autoimmune thyroiditis.…”
Section: Discussionmentioning
confidence: 99%