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[法洛四联症病例术后的舞蹈样手足徐动症]

[Postoperative choreoathetosis in a case of tetralogy of Fallot].

作者信息

Yoshii S, Mohri N, Suzuki S, Kobashiri H, Hashimoto R, Tada Y

机构信息

Department of Surgery, Yamanashi Medical University, Japan.

出版信息

Nihon Kyobu Geka Gakkai Zasshi. 1995 Jan;43(1):109-12.

PMID:7884249
Abstract

We presented a case of severe postoperative choreoathetosis which occurred in a 3-year-old boy with tetralogy of Fallot early postoperatively but almost completely recovered within two years after the operation. Because of the large coronary arterial branch on the right ventricular outflow, a small outflow incision and deep hypothermia (lowest rectal temperature was 13 degrees C) and short duration of circulatory arrest (8 minutes) were adopted. Postoperative course was uneventful till the onset of choreoathetosis on the fifth postoperative day. His symptoms and signs of choreoathetosis, oral-facial dyskinesias, hypotonia, affective changes and also pseudobulbar signs were becoming serious during the first week from the onset, but afterwards his condition started getting better gradually every week, and every month. Now, 20 months after the operation, he is almost completely recovered except for small and slow involuntary movements. Though investiations including CT, MRI and EEG were all almost normal, regional nonspecific low area of the frontal lobe and cerebellum was detected by SPECT (single photon emission computed tomography) on the 32nd and 94th postoperative days, respectively.

摘要

我们报告了一例严重的术后舞蹈手足徐动症病例,该病例发生在一名3岁法洛四联症男孩术后早期,但术后两年内几乎完全康复。由于右心室流出道有较大的冠状动脉分支,采用了小的流出道切口、深度低温(最低直肠温度为13摄氏度)和短时间的循环停止(8分钟)。术后过程平稳,直到术后第5天出现舞蹈手足徐动症。从发病开始的第一周内,他的舞蹈手足徐动症、口面部运动障碍、肌张力减退、情感变化以及假性球麻痹体征的症状和体征变得严重,但之后他的病情每周、每月都逐渐好转。现在,术后20个月,除了轻微且缓慢的不自主运动外,他几乎完全康复。尽管包括CT、MRI和EEG在内的检查几乎都正常,但分别在术后第32天和第94天通过单光子发射计算机断层扫描(SPECT)检测到额叶和小脑区域有非特异性低区。

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