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先天性巨结肠症新生儿肠段扩张症的 Cajal 间质细胞紊乱。

Disorders of interstitial cells of Cajal in a neonate with segmental dilatation of the intestine.

机构信息

Department of Pediatric Surgery, Hokkaido University Graduate School of Medicine, Sapporo 060-8638, Japan.

出版信息

J Pediatr Surg. 2010 Jun;45(6):e11-4. doi: 10.1016/j.jpedsurg.2010.03.024.

Abstract

Localized myopathy of the muscular layers may be an important factor contributing to segmental dilatation of the intestine (SDI). Only one report has described SDI of the jejunum in a neonate showing no abnormality of the interstitial cells of Cajal (ICC). The present report describes the very rare case of a neonatal girl with segmental dilatation of the distal duodenum and proximal jejunum with irregular arrangements of Auerbach's plexus and ICC and the successful surgical treatment of SDI. We review the literature on this type of relationship between abnormality of ICC and SDI and discuss the clinical features of this complication. Furthermore, the possible neuropathic cause of SDI complicated with disorders of ICC was explored in this report.

摘要

局部性肌层疾病可能是导致肠节段性扩张(SDI)的一个重要因素。仅有一份报告描述了一例表现出Cajal 间质细胞(ICC)无异常的新生儿空肠 SDI。本报告描述了一例非常罕见的新生儿女性病例,其表现为远端十二指肠和近端空肠的节段性扩张,其 Auerbach 神经丛和 ICC 排列不规则,SDI 手术治疗成功。我们回顾了关于 ICC 异常与 SDI 之间这种关系的文献,并讨论了这种并发症的临床特征。此外,本报告还探讨了伴有 ICC 紊乱的 SDI 的可能神经病变原因。

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