臨床血液
Online ISSN : 1882-0824
Print ISSN : 0485-1439
ISSN-L : 0485-1439
臨床研究
難治性ITPについて
山内 勝世篠原 建次松本 昇三輪 史朗
著者情報
ジャーナル 認証あり

1978 年 19 巻 3 号 p. 199-206

詳細
抄録
Refractory idiopathic thrombocytopenic purpura (refractory ITP) is defined as ITP of greater than 7 months' duration and which failed to respond to both corticosteroids and splenectomy. Among 19 cases, 2 were refractory ITP. One case was 32-year-old male with ecchymoses and gum bleeding. Platelet count was 8,000/mm3. He had been treated with prednisolone and azathioprine, then splenectomized. These treatments revealed no effect and now he is followed in our out-patient clinic. Another case was 63-year-old male with tarry stool, ecchymoses, petechiae and anemia. Prednisolone was administered and splenectomy was performed. After that, azathioprine, then vincristine was administered. Although tarry stool stopped, the effect was not satisfactory.
In refractory ITP, it can be suggested that liver as well as spleen contributes significantly as a site of production of anti-platelet antibody and the sequestration of affected platelets. We discussed the immunosuppressants for the treatment of refractory ITP, reviewing previously reported cases.
著者関連情報
© 1978 一般社団法人 日本血液学会
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