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  1. 学術雑誌論文
  2. 琉球医学会
  3. 琉球大学保健学医学雑誌
  4. 4巻1号
  1. 部局別インデックス
  2. その他

[原著]放射線療法が奏効したKasabach-Merritt症候群の2例

http://hdl.handle.net/20.500.12000/0002016281
http://hdl.handle.net/20.500.12000/0002016281
a63b9fef-069f-48e2-80af-9c3f9801725d
名前 / ファイル ライセンス アクション
v4p95.pdf v4p95.pdf
Item type デフォルトアイテムタイプ(フル)(1)
公開日 2014-07-18
タイトル
タイトル [原著]放射線療法が奏効したKasabach-Merritt症候群の2例
言語 ja
作成者 大城, 隆

× 大城, 隆

ja 大城, 隆

平山, 清武

× 平山, 清武

ja 平山, 清武

喜友名, 琢也

× 喜友名, 琢也

ja 喜友名, 琢也

名嘉真, 武男

× 名嘉真, 武男

ja 名嘉真, 武男

外間, 之雄

× 外間, 之雄

ja 外間, 之雄

Ohshiro, Takashi

× Ohshiro, Takashi

en Ohshiro, Takashi

Hirayama, Kiyotake

× Hirayama, Kiyotake

en Hirayama, Kiyotake

Kiyuna, Takuya

× Kiyuna, Takuya

en Kiyuna, Takuya

Nakama, Takeo

× Nakama, Takeo

en Nakama, Takeo

Hokama, Yukio

× Hokama, Yukio

en Hokama, Yukio

アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
権利情報
言語 ja
権利情報 琉球医学会
内容記述
内容記述タイプ Other
内容記述 We have recently encountered two cases of Giant hemangioma with thrombocytopenia, so-called Kasabach-Merritt Syndrome, responded well to radiotherapy. The first case, a 3-month-old girl was hospitalized in October 1980 because of thrombocytopenia and hemangioma around the right ear after birth. On admission, the size of hemangioma showed a 7.5cm×6.5cm. Coagulation studies included a platelet count of 57,000/mm^3, prolonged bleeding time and slightly increased FDP titer. The prothrombin time and partial thromboplastin time were normal, but fibrinogen was decreased. Fragmented erythrocyte was seen in peripheral blood. The second case, a 4-month-old boy was admitted in November 1980 with rapidly enlarging hemangioma in the right upper arm. Hematological findings were as follows: hemoglobin was 9.8g/dl.; platelets, 29,000/mm^3; bleeding time, 8 minutes; prothrombin time, 11.2 seconds compared to a control of 13 seconds; partial thromboplastin time, 24.2 seconds with a control of 30 seconds; fibrinogen level, 208mg/dl; and FDP titer, 40-80$ \mu $g/ml. The patients were treated with radiotherapy under diagnosis of hemangioma complicated with coagulopathy. The total doses we administered were of 600 rads at the first case, and 800 rads at the second case. Thereafter, the size of the hemangioma decreased gradually, and the coagulation abnormalities were corrected to normal within one to three months. For Kasabach-Merritt syndrome, various treatment, for example, surgical excision, corticosteroid therapy or radiotherapy were attempted up to date. We suggests that radiotherapy is more effective and safe treatment rather than the others.
内容記述タイプ Other
内容記述 論文
出版者
言語 ja
出版者 琉球大学医学部
言語
言語 jpn
資源タイプ
資源タイプ journal article
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 0285-9270
収録物識別子タイプ NCID
収録物識別子 AN00250763
収録物名
言語 ja
収録物名 琉球大学保健学医学雑誌=Ryukyu University Journal of Health Sciences and Medicine
書誌情報
巻 4, 号 1, p. 95-102
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