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Acquired hemophilia A following COVID-19 vaccine: a case report.
Emna, Bouselama; Kmira, Zahra; Hajer, Ben Ismail; Nadia, Sassi; Yossra, Dhaha; Amina, Bouatay; Yosra, Ben Youssef; Haifa, Regaieg; Abderrahim, Khelif.
  • Emna B; Department of Clinical Hematology, Farhat Hached University Hospital, Sousse, Tunisia.
  • Kmira Z; Department of Clinical Hematology, Farhat Hached University Hospital, Sousse, Tunisia. Kmira_zahra@yahoo.fr.
  • Hajer BI; Department of Clinical Hematology, Farhat Hached University Hospital, Sousse, Tunisia.
  • Nadia S; Department of Clinical Hematology, Farhat Hached University Hospital, Sousse, Tunisia.
  • Yossra D; Laboratory of Hematology, Sahloul University Hospital, Sousse, Tunisia.
  • Amina B; Laboratory of Hematology, Sahloul University Hospital, Sousse, Tunisia.
  • Yosra BY; Department of Clinical Hematology, Farhat Hached University Hospital, Sousse, Tunisia.
  • Haifa R; Department of Clinical Hematology, Farhat Hached University Hospital, Sousse, Tunisia.
  • Abderrahim K; Department of Clinical Hematology, Farhat Hached University Hospital, Sousse, Tunisia.
J Med Case Rep ; 17(1): 125, 2023 Mar 27.
Article in English | MEDLINE | ID: covidwho-2258231
ABSTRACT

BACKGROUND:

In the literature, reported cases of Acquired hemophilia A (AHA) induced by COVID-19 vaccination occurred after Adenoviral Vector Deoxyribonucleic Acid (DNA)- and SARS-CoV-2 Messenger Ribonucleic acid (mRNA)-Based vaccines. Here, and to the best of our knowledge, we report the first case of AHA occurring after an inactivated Sinovac-coronavac COVID-19 vaccine. CASE PRESENTATION A 69-year-old Tunisian male patient consulted for severe left leg pain limiting physical mobility due to a 5*6 cm large ecchymosis located at the left inner thigh, having spontaneously appeared 5 days prior consultation and without notion of trauma. The patient had no known personal medical history. He had received the second dose of CoronaVac-SinoVac vaccine 30 days prior to consultation. Further physical examination revealed the presence of two other ecchymoses one at the inner face of the right forearm, starting at the wrist reaching the elbow and the other at the left flank of the abdomen. Diagnosis of AHA was based on clinical presentation and confirmed with prolonged a PTT, Factor VIII deficiency and the presence of an FVIII inhibitor. The patient was successfully treated with corticosteroids and low dose Rituximab.

CONCLUSION:

Clinicians should consider AHA in front of prolonged aPTT with or without spontaneous bleedings even after inactivated virus COVID-19.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Hemophilia A Type of study: Case report / Diagnostic study / Prognostic study Topics: Long Covid / Vaccines Limits: Aged / Humans / Male Language: English Journal: J Med Case Rep Year: 2023 Document Type: Article Affiliation country: S13256-023-03850-z

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Hemophilia A Type of study: Case report / Diagnostic study / Prognostic study Topics: Long Covid / Vaccines Limits: Aged / Humans / Male Language: English Journal: J Med Case Rep Year: 2023 Document Type: Article Affiliation country: S13256-023-03850-z