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先天性巨结肠症中的血清及红细胞乙酰胆碱酯酶

Serum and erythrocyte acetylcholine esterase in Hirschsprung's disease.

作者信息

Okasora T, Okamoto E, Kuwata K, Toyosaka A, Ohashi S, Ueki S

出版信息

Z Kinderchir. 1983 Oct;38(5):298-300. doi: 10.1055/s-2008-1059992.

Abstract

Determination of acetylcholine esterase in serum (S-AChE) and erythrocytes (E-AChE) was carried out in nine patients with Hirschsprung's disease and 16 normal controls. S-AChE was significantly elevated in patients with Hirschsprung's disease, while no significant difference was observed in E-AChE in these two groups. In 17 patients with Hirschsprung's disease, S-AChE and E-AChE were determined after definitive operation. Twelve of these patients underwent a Duhamel type procedure in which a small part of the aganglionic bowel segment remained unresected. Five patients were treated by Swenson's procedure performing complete resection of the aganglionic bowel segment. S-AChE in patients treated by the Duhamel type procedure remained elevated, while it was as low as that in normal controls in patients who underwent Swenson's procedure. There was no significance in E-AChE in both groups. This study suggests a close relation of the level of S-AChE to the extent of the aganglionic bowel segment in Hirschsprung's disease.

摘要

对9例先天性巨结肠病患者和16名正常对照者进行了血清乙酰胆碱酯酶(S-AChE)和红细胞乙酰胆碱酯酶(E-AChE)的测定。先天性巨结肠病患者的S-AChE显著升高,而两组的E-AChE未观察到显著差异。对17例先天性巨结肠病患者在确定性手术后测定了S-AChE和E-AChE。其中12例患者接受了杜哈梅尔(Duhamel)式手术,术中一小部分无神经节肠段未被切除。5例患者接受了斯文森(Swenson)手术,即完全切除无神经节肠段。接受杜哈梅尔式手术治疗的患者S-AChE仍升高,而接受斯文森手术治疗的患者S-AChE则低至正常对照者水平。两组的E-AChE均无显著差异。本研究提示先天性巨结肠病中S-AChE水平与无神经节肠段范围密切相关。

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Observation on erythrocyte acetylcholinesterase (AChE) in infants and children with Hirschsprung's disease.
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