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肉碱棕榈酰转移酶缺乏症:一种诊断不足的疾病?

Carnitine palmitoyltransferase deficiency: an underdiagnosed condition?

作者信息

Katzir Z, Hochman B, Biro A, Rubinger D I, Feigel D, Silver J, Friedlaender M M, Popovtzer M M, Smetana S

机构信息

Nephrology and Hypertension Unit,E. Wolfson Medical Center, Holon, Israel.

出版信息

Am J Nephrol. 1996;16(2):162-6. doi: 10.1159/000168991.

Abstract

Two apparently healthy adults were admitted because of acute muscle cramps, severe weakness, and red urine excretion. Patient No. 1 developed the symptoms following intense exercise and patient No. 2 during a febrile infection. Both of them experienced such episodes in the past, but these were medically misinterpreted. Their present manifestations were accompanied by renal failure which subsided gradually and was found to be a result of rhabdomyolsis and myoglobinuria. Further investigations yielded a deficiency of carnitine palmitoyltransferase as a background to the acute muscular destruction. Examination of a sister of patient No. 2 who had a similar past history revealed the same metabolic disorder. Carnitine palmitoyltransferase deficiency, as a cause of nontraumatic rhabdomyolysis, is a distinct entity in the pathogenesis of acute renal failure. Our experience (3 patients within 2 years) makes us presume that this condition is not as rare as hitherto reported and should rather be considered in cases of 'nonhematuric' red urine and acute renal failure.

摘要

两名看似健康的成年人因急性肌肉痉挛、严重虚弱和排出红色尿液而入院。1号患者在剧烈运动后出现症状,2号患者在发热感染期间出现症状。他们两人过去都曾经历过此类发作,但当时被医学误诊。他们目前的表现伴有肾衰竭,肾衰竭逐渐消退,发现是横纹肌溶解症和肌红蛋白尿所致。进一步检查发现肉碱棕榈酰转移酶缺乏是急性肌肉破坏的背景原因。对2号患者有类似既往病史的一名姐妹进行检查,发现了相同的代谢紊乱。肉碱棕榈酰转移酶缺乏作为非创伤性横纹肌溶解症的一个病因,在急性肾衰竭的发病机制中是一个独特的实体。我们的经验(两年内3例患者)使我们推测,这种情况并不像迄今报道的那样罕见,在出现“非血尿性”红色尿液和急性肾衰竭的病例中应予以考虑。

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