歯肉出血を契機に発見された後天性第Ⅹ因子欠乏症の1例
Factor X deficiency is a coagulation disorder caused by lack of factor X, which is a vitamin K-dependent clotting factor synthesized in the liver. The disease can be inherited or acquired. This case report describes a male patient who was given a diagnosis of acquired factor X deficiency after havin...
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Published in | 日本口腔外科学会雑誌 Vol. 64; no. 2; pp. 78 - 82 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | Japanese |
Published |
社団法人 日本口腔外科学会
20.02.2018
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ISSN | 0021-5163 2186-1579 |
DOI | 10.5794/jjoms.64.78 |
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Abstract | Factor X deficiency is a coagulation disorder caused by lack of factor X, which is a vitamin K-dependent clotting factor synthesized in the liver. The disease can be inherited or acquired. This case report describes a male patient who was given a diagnosis of acquired factor X deficiency after having gingival bleeding. [Case and Progress] An 80-year-old man had undergone detailed examinations for the cause of anemia in another hospital. Hemorrhagic lesions were not found, and gingival bleeding was suspected as the cause of anemia. Therefore, he visited our hospital for further evaluation of gingival bleeding. Because gingival bleeding was caused by periodontal disease, we extracted the right mandibular second molar and left maxillary second molar under local anesthesia. Because of persistent intermittent gingival bleeding, we referred the patient to a hematologist. The blood examination revealed prolonged prothrombin time and decreased factor X activity, and he was given a diagnosis of acquired factor X deficiency on the basis of his past medical history. Although we performed local hemostatic treatment and medical therapy, it took us about 40 days to arrest the hemorrhage. |
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AbstractList | Factor X deficiency is a coagulation disorder caused by lack of factor X, which is a vitamin K-dependent clotting factor synthesized in the liver. The disease can be inherited or acquired. This case report describes a male patient who was given a diagnosis of acquired factor X deficiency after having gingival bleeding. [Case and Progress] An 80-year-old man had undergone detailed examinations for the cause of anemia in another hospital. Hemorrhagic lesions were not found, and gingival bleeding was suspected as the cause of anemia. Therefore, he visited our hospital for further evaluation of gingival bleeding. Because gingival bleeding was caused by periodontal disease, we extracted the right mandibular second molar and left maxillary second molar under local anesthesia. Because of persistent intermittent gingival bleeding, we referred the patient to a hematologist. The blood examination revealed prolonged prothrombin time and decreased factor X activity, and he was given a diagnosis of acquired factor X deficiency on the basis of his past medical history. Although we performed local hemostatic treatment and medical therapy, it took us about 40 days to arrest the hemorrhage. |
Author | 高山, 智宏 橘川, 芳明 吉濱, 直哉 小川, 芙美 雨河, 茂樹 大西, 徹郎 |
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References | 8) 塚原邦弘, 宿輪昌宏, 他:後腹膜出血で発症した,第Ⅹ因子欠乏とアミロイドーシスを伴う多発性骨髄腫の1例.日内会誌 80 : 757-758, 1991. 2) 京本博行, 瀧田正亮, 他:先天性第Ⅹ因子欠乏症患者における抜歯経験.日口外誌 52 : 625-628, 2006. 1) 三輪史郎, 青木延雄, 他:血液病学.第2版, 文光堂, 東京, 1995, 1281-1282 頁 6) 森下英理子:血友病 (および von Willebrand 病) 以外の先天性凝固異常症の病態と治療.臨血 51 : 219-228, 2010. 14) Mori K, Sakai H, et al : Congential factor X deficiency Japan. Tohoku J Exp Med 133: 1-19, 1981. 15) 竹尾明子, 岡本喜之, 他:歯肉出血をきたした先天性凝固第Ⅹ因子欠乏症患者の1例.日口診誌 25 : 148-152, 2012. 10) Adewumi A and Sakhalkar V : Dental management of a patient with factor X deficiency. J Can Dent Assoc 75 : 461-464, 2009. 7) Kumar A, Mishra KL, et al : Hereditary coagulation factor X deficiency. Indian Pediatr 42 : 1240-1242, 2005. 12) Col T, Col J, et al : Inherited Factor X (Stuart-Prower Factor) deficiency and its management. MJAFI 71 : 184-186, 2015. 5) 長江千愛, 瀧 正志:その他の先天性凝固因子欠損症の診断と治療.日血栓止血会誌 21 : 297-300, 2010. 9) 榎本 愛, 長谷川温, 他:歯肉出血を契機に発見された先天性第Ⅹ因子欠乏症の1例.日口外誌 59 : 362-366, 2013. 16) 沖津庸子, 鈴木宗三, 他:後天性第Ⅹ因子低下症の一例.東北止血血栓研会誌 ⅩⅩⅢ : 12-16, 2010. 4) 高松純樹:先天性第Ⅹ因子欠乏症/ 異常症;別冊日本臨牀領域別症候群21.日本臨牀社, 大阪, 1998, 442-444 頁 13) 野間弘康, 金子 譲:抜歯の臨床.第1版, 医歯薬出版株式会社, 東京, 2000, 53-56 頁 3) 山本晃士:第Ⅹ因子;日本臨牀広範囲血液・尿化学検査/ 免疫学的検査.第7版, 日本臨牀社, 大阪,2010, 715-718 頁 11) Joost J, Kingsley K, et al : Blood product support for delivery in severe Factor X deficiency : the use of thrombin to guide therapy. Blood Transfus 5 : 204-209, 2007. |
References_xml | – reference: 3) 山本晃士:第Ⅹ因子;日本臨牀広範囲血液・尿化学検査/ 免疫学的検査.第7版, 日本臨牀社, 大阪,2010, 715-718 頁. – reference: 8) 塚原邦弘, 宿輪昌宏, 他:後腹膜出血で発症した,第Ⅹ因子欠乏とアミロイドーシスを伴う多発性骨髄腫の1例.日内会誌 80 : 757-758, 1991. – reference: 11) Joost J, Kingsley K, et al : Blood product support for delivery in severe Factor X deficiency : the use of thrombin to guide therapy. Blood Transfus 5 : 204-209, 2007. – reference: 6) 森下英理子:血友病 (および von Willebrand 病) 以外の先天性凝固異常症の病態と治療.臨血 51 : 219-228, 2010. – reference: 5) 長江千愛, 瀧 正志:その他の先天性凝固因子欠損症の診断と治療.日血栓止血会誌 21 : 297-300, 2010. – reference: 15) 竹尾明子, 岡本喜之, 他:歯肉出血をきたした先天性凝固第Ⅹ因子欠乏症患者の1例.日口診誌 25 : 148-152, 2012. – reference: 13) 野間弘康, 金子 譲:抜歯の臨床.第1版, 医歯薬出版株式会社, 東京, 2000, 53-56 頁. – reference: 12) Col T, Col J, et al : Inherited Factor X (Stuart-Prower Factor) deficiency and its management. MJAFI 71 : 184-186, 2015. – reference: 14) Mori K, Sakai H, et al : Congential factor X deficiency Japan. Tohoku J Exp Med 133: 1-19, 1981. – reference: 7) Kumar A, Mishra KL, et al : Hereditary coagulation factor X deficiency. Indian Pediatr 42 : 1240-1242, 2005. – reference: 4) 高松純樹:先天性第Ⅹ因子欠乏症/ 異常症;別冊日本臨牀領域別症候群21.日本臨牀社, 大阪, 1998, 442-444 頁. – reference: 1) 三輪史郎, 青木延雄, 他:血液病学.第2版, 文光堂, 東京, 1995, 1281-1282 頁. – reference: 2) 京本博行, 瀧田正亮, 他:先天性第Ⅹ因子欠乏症患者における抜歯経験.日口外誌 52 : 625-628, 2006. – reference: 9) 榎本 愛, 長谷川温, 他:歯肉出血を契機に発見された先天性第Ⅹ因子欠乏症の1例.日口外誌 59 : 362-366, 2013. – reference: 16) 沖津庸子, 鈴木宗三, 他:後天性第Ⅹ因子低下症の一例.東北止血血栓研会誌 ⅩⅩⅢ : 12-16, 2010. – reference: 10) Adewumi A and Sakhalkar V : Dental management of a patient with factor X deficiency. J Can Dent Assoc 75 : 461-464, 2009. |
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SubjectTerms | 後天性第Ⅹ因子欠乏症 抜歯 歯肉出血 |
Title | 歯肉出血を契機に発見された後天性第Ⅹ因子欠乏症の1例 |
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