日本口腔外科学会雑誌
Online ISSN : 2186-1579
Print ISSN : 0021-5163
ISSN-L : 0021-5163
特発性血小板減少性紫斑病 (ITP) を合併した頬粘膜癌の手術経験
三好 智三宅 実岩崎 昭憲大林 由美子谷崎 明弘長畠 駿一郎
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2001 年 47 巻 5 号 p. 293-296

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Squamous cell carcinoma of the buccal mucosa was diagnosed on biopsy. The preoperative laboratory data revealed a platelet count of 3.8 × 104/mm3. These investigations suggested the presence of idiopathic thrombocytopenic purpura (ITP). For surgical therapy, it is important to maintain normal platelet counts and to control hemostasis. A preoperative high-dose of γ-globulin therapy (400mg/kg/day for 5 days) allowed operation to be performed successfully. After the surgery and without tranfusion, abnormal bleeding did not occur. The postoperative course was uneventful, and no tumor recurrence was observed.
High-dose γ-globulin therapy appears to be reasonably safe and useful in the preoperative management of surgical patients with ITP.

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