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特发性横纹肌溶解症

Idiopathic rhabdomyolysis.

作者信息

Savage D C, Forbes M, Pearce G W

出版信息

Arch Dis Child. 1971 Oct;46(249):594-607. doi: 10.1136/adc.46.249.594.

Abstract

The clinical, biochemical, and pathological findings in 2 children with idiopathic rhabdomyolysis are reported. Hypocalcaemic tetany, a previously unrecognized complication of severe muscle damage, was seen in one child and was associated with hyperphosphataemia and hyperphosphaturia consequent on the rhabdomyolysis. Respiratory distress and an acute tubular necrosis contributed to her eventual death. The second child recovered; an intracellulr granular material of unknown nature was seen in his muscle biopsy on electron microscopy. The literature of idiopathic recurrent rhabdomyolysis occurring in childhood is reviewed.

摘要

报告了2例特发性横纹肌溶解症患儿的临床、生化和病理检查结果。其中1例患儿出现了低钙性手足搐搦,这是此前未被认识到的严重肌肉损伤并发症,与横纹肌溶解继发的高磷血症和高磷尿症有关。呼吸窘迫和急性肾小管坏死导致了她最终死亡。第2例患儿康复;在其肌肉活检的电子显微镜检查中发现了一种性质不明的细胞内颗粒物质。本文对儿童期发生的特发性复发性横纹肌溶解症的文献进行了综述。

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