Acute Myeloblastic Leukemia in a Patient with Hereditary Protein C Deficiency
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概要
- 論文の詳細を見る
The patient had been diagnosed with hereditary protein C deficiency. She recently developed acute myeloblastic leukemia (AML). Chemotherapy for AML by cytosine arabinoside, aclarubicin followed by granulocyte colony-stimulating factor (CAG) was started. Disseminated intravascular coagulation (DIC) was observed, however thromboembolic complication was not observed during the hospital course. Hematological remission was not obtained, and the patient died of pseudomembranous pancolitis. Whether the development of these rare disorders of hereditary protein C and AML are coincidental, or involve a causal relationship remains unknown.
- 社団法人 日本内科学会の論文
著者
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Matsui Kumiko
Division Of Hematology Department Of Medicine Yamaguchi Prefectural Medical Center
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Matsuda Kazuhiro
Division Of Gastroenterological And General Surgery Department Of Surgery Showa University School Of
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Tanaka Yoshinori
Division Of Molecular Genetics Institute For Enzyme Research The University Of Tokushima
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Shinohara Kenji
Division of Environment and Radiation Science, Nuclear Science and Energy Directions, Japan Atomic Energy Agency
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Yamashita Koji
Division of Hematology, Department of Medicine, Yamaguchi Prefectural Medical Center
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