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- Reina Takabayashi, Osamu Nishikido, Kazuko Nagano, Akiko Doi, Ryou Nishisako, and Takeshi Tateda.
- Department of Anesthesiology, St. Mariannna University School of Medicine, Yokohama City Seibu Hospital, Yokohama 216-0811.
- Masui. 2007 Oct 1; 56 (10): 1198-9.
AbstractMay-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.
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