Acquired hemophilia A and plasma cell neoplasms: a case report and review of the literature
Abstract Background Acquired hemophilia A is a rare autoimmune disease with clinically often significant bleeding diathesis resulting from circulating autoantibodies inhibiting coagulation factor VIII. Half of acquired hemophilia A cases are associated with an underlying disorder, such as autoimmune...
Main Authors: | Katarzyna A. Jalowiec, Martin Andres, Behrouz Mansouri Taleghani, Albulena Musa, Martina Dickenmann, Anne Angelillo-Scherrer, Alicia Rovó, Johanna A. Kremer Hovinga |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2020-10-01
|
Series: | Journal of Medical Case Reports |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s13256-020-02505-7 |
Similar Items
-
Disappearance of Acquired Hemophilia A after Complete Remission in a Multiple Myeloma Patient
by: Vanessa Innao, et al.
Published: (2017-05-01) -
Abnormalities of primary and secondary hemostasis in multiple myeloma: insights from studies on thrombopoiesis, the coagulation system, and the bone marrow microenvironment
by: Jahan Abdi, et al.
Published: (2025-03-01) -
Acquired von Willebrand syndrome and lymphoproliferative disorders: A case report
by: Christophe Nicol, et al.
Published: (2020-05-01) -
Acquired Hemophilia
by: Şinasi Özsoylu
Published: (2014-12-01) -
Acquired platelet dysfunction in newly diagnosed myeloma
by: Joshua Mortimer, et al.
Published: (2021-02-01)