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先天性小肠肌层缺如(一例报告)

Congenital absence of small intestinal musculature (one case report).

作者信息

Miyagawa S, Nakaba H, Takao T, Yoshikawa K, Satani M

出版信息

Z Kinderchir. 1985 Feb;40(1):55-7. doi: 10.1055/s-2008-1059713.

Abstract

Intestinal obstruction due to congenital absence of the small intestinal musculature in a neonate is presented. This report represents the seventh known case of this abnormality. In addition, in our case ectopic oesophageal mucosa and ectopic gastric mucosa is detected. The aetiology of this condition is unknown, and the diagnosis must simply depend on pathological examination of biopsy samples taken from appropriate regions. Unfortunately the regions of this disease have no continuity. Therefore, course of treatment cannot be established as the extent of the region cannot be correctly identified. To detect change of colour tone of the bowel may be helpful in the treatment of the disease.

摘要

本文报告了一例因先天性小肠肌肉组织缺失导致肠梗阻的新生儿病例。这是已知的该异常情况的第七个病例。此外,在我们的病例中还检测到异位食管黏膜和异位胃黏膜。这种情况的病因尚不清楚,诊断必须仅依赖于从适当区域采集的活检样本的病理检查。不幸的是,这种疾病的区域没有连续性。因此,由于无法正确识别该区域的范围,所以无法确定治疗方案。检测肠道色调的变化可能有助于该病的治疗。

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