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Masui ; 56(10): 1198-9, 2007 Oct.
Article in Japanese | MEDLINE | ID: mdl-17966627

ABSTRACT

May-Hegglin anomaly (MHA) is a rare hereditary disorder characterized by thrombocytopenia and giant thrombocytes and continuous appearance of inclusion bodies (Dohle like corpuscles) in the cytoplasm of granulocytes. A 26-year-old woman with MHA underwent cesarean delivery under general anesthesia, although she had no history of bleeding. The platelet count was 4.9x10(4) microgl(-1) the day before surgery. There was no unusual bleeding during and after the operation and we did not give her platelet transfusion.


Subject(s)
Anesthesia, General , Anesthesia, Obstetrical , Blood Platelets/pathology , Cesarean Section , Granulocytes/ultrastructure , Inclusion Bodies/pathology , Pregnancy Complications, Hematologic , Thrombocytopenia , Female , Humans , Perioperative Care , Platelet Count , Pregnancy , Pregnancy Outcome
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