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Trimethoprim-Sulfamethoxazole-Induced Hepatitis in Mixed Connective Tissue Disease
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作者 takeshi sugimoto Yumiko Nobuhara +1 位作者 Seiji Kawano Akio Morinobu 《International Journal of Clinical Medicine》 2011年第5期629-632,共4页
Trimethoprim-Sulfamethoxazole (TMP-SMZ) is associated with severe hepatic toxicity or liver failure. We present a case of severe hepatic toxicity for whom TMP-SMZ was prescribed as part of treatment for mixed connecti... Trimethoprim-Sulfamethoxazole (TMP-SMZ) is associated with severe hepatic toxicity or liver failure. We present a case of severe hepatic toxicity for whom TMP-SMZ was prescribed as part of treatment for mixed connective tissue disease (MCTD). TMP-SMZ was used to prevent complications from steroid therapy, but fever and hepatic toxicity developed with repeated TMP-SMZ medication. While the drug lymphocyte stimulation test (DLST) for TMP-SMZ showed negative, the genotype for N-acetyltransferase 2 (NAT2) showed type *6/*7, which is the slow acetylating type for NAT2 activity. This finding for NAT2 genotype and the patient’s clinical history lead us to speculate that her fever and hepatic toxicity were caused by TMP-SMZ. 展开更多
关键词 HEPATIC TOXICITY Mixed CONNECTIVE Tissue Disease N-ACETYLTRANSFERASE 2 TRIMETHOPRIM-SULFAMETHOXAZOLE
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An Evans Syndrome Case Expressing Anti-Jk<sup>a</sup>Autoantibody under Condition of Primary IgA Immunodeficiency
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作者 takeshi sugimoto Ayumi Tani +9 位作者 Ikuyo Hayakawa Makoto Hashimoto Tomoko Yanai Ikuko Kubokawa takeshi Mori takeshi Kato Satoshi Hirase Nobuyuki Yamamoto Hironobu Minami Akira Hayakawa 《International Journal of Clinical Medicine》 2015年第7期496-499,共4页
Autoimmune haemolytic anaemia is a haemolytic disease resulting from an autoimmune reaction to the surface of red blood cells. A part of autoantibody is known to react with the blood type antigen. This is the case of ... Autoimmune haemolytic anaemia is a haemolytic disease resulting from an autoimmune reaction to the surface of red blood cells. A part of autoantibody is known to react with the blood type antigen. This is the case of a 14 years old female with Evans syndrome in which autoimmune haemolysis may cause from anti-Jka autoantibody reaction. As this case is complicated with primary IgA immunodeficiency syndrome, anti-Jka autoantibody may occur under the condition of primary immunodeficiency status, in which autoantibody production is accelerated. Considering the co-occurrence of autoimmune haemolytic anaemia and primary IgA immunodeficiency syndrome, analysis focusing on specificity for red blood cells antigens will be required in IgA immunodefi-ciency syndrome patients. 展开更多
关键词 Anti-Jka AUTOANTIBODY EVANS Syndrome IGA IMMUNODEFICIENCY
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