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Braz. J. Anesth. (Impr.) ; 72(6): 823-825, Nov.-Dec. 2022.
Article in English | LILACS | ID: biblio-1420620

ABSTRACT

Abstract Glanzmannʼs Trombasthenia (GT) is a genetic disorder, that develops with a tendency toward bleeding and is characterized by the absence or decrease in platelet aggregation. Surgical bleeding may be difficult to control. Platelet transfusion is the main treatment, albeit refractoriness can occur. We describe the case of a patient with GT and platelet refractoriness, who was submitted to radical prostatectomy and dental extraction. The perioperative treatment with apheresis platelet concentrate and activated recombinant factor seven allowed the procedures to be performed uneventfully. We discuss the complexity of the case and the treatment option.


Subject(s)
Humans , Male , Thrombasthenia , Thrombasthenia/surgery , Factor VIIa/therapeutic use , Platelet Transfusion , Hemorrhage
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