Miyake S, Taketa K, Izumi M, Nagashima H, Nishina Y, Kawanishi K, Ofuji T, Shimono K
Clin Chim Acta. 1980 Dec 8;108(2):323-8. doi: 10.1016/0009-8981(80)90020-0.
A rare isozyme of serum creatine kinase (CK) migrating cathodic to CK-MM on electrophoresis was found in a 30-year-old male with stomach cancer complicated by disseminated intravascular coagulation leading to massive upper gastrointestinal bleeding and marked anemia. Serum CK activity rose to a maximum of 374 U/l without detectable CK-MB isoenzyme. The patient was also characterized by a marked increase in serum lactate dehydrogenase (all isozymes elevated) and by preferential leakage of mitochondrial aspartate aminotransferase and glutamate dehydrogenase, indicating the presence of extensive tissue damage involving mitochondria. Skeletal muscle mitochondria were considered the most likely source of the additional CK isozyme.
在一名30岁男性胃癌患者中发现了一种罕见的血清肌酸激酶(CK)同工酶,该同工酶在电泳时向阴极迁移至CK-MM。该患者合并弥散性血管内凝血,导致大量上消化道出血和明显贫血。血清CK活性最高升至374 U/l,未检测到CK-MB同工酶。该患者还表现为血清乳酸脱氢酶显著升高(所有同工酶均升高),线粒体天冬氨酸氨基转移酶和谷氨酸脱氢酶优先漏出,提示存在涉及线粒体的广泛组织损伤。骨骼肌线粒体被认为是额外CK同工酶最可能的来源。