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横结肠缺如、降结肠系膜持续存在、小肠和大肠移位:一种罕见的先天性异常,有形成肠扭转的高风险。

Absence of transverse colon, persistent descending mesocolon, displaced small and large bowels: a rare congenital anomaly with a high risk of volvulus formation.

作者信息

Shetty Prakashchandra, Nayak Satheesha B

机构信息

Department of Anatomy, Melaka Manipal Medical College (Manipal Campus), Manipal University, Manipal, India.

出版信息

Anat Cell Biol. 2014 Dec;47(4):279-81. doi: 10.5115/acb.2014.47.4.279. Epub 2014 Dec 23.

Abstract

Congenital anomalies such as positional anomalies of the right half of the colon are more common when compared to its left half. We report a rare case of congenital anomaly where the transverse colon was totally absent. Ascending colon continued as descending colon at the right colic flexure. Ascending and descending colons formed an inverted U shaped loop which was situated in the right half of the abdomen. The sigmoid colon began from the descending colon, on the right side of the midline and coursed to the left iliac fossa. The terminal part of ascending colon and entire descending colon had a persistent mesocolon. The jejunum and ileum were situated in the upper left part of the abdominal cavity. This anomaly can cause volvulus of the colon at any stage of life. Furthermore, the knowledge of this anomaly is very useful for radiologists, gastroenterologists and surgeons.

摘要

与结肠左半部分相比,诸如结肠右半部分位置异常等先天性异常更为常见。我们报告一例罕见的先天性异常病例,其中横结肠完全缺失。升结肠在右结肠弯曲处延续为降结肠。升结肠和降结肠形成一个倒U形环,位于腹部右半部分。乙状结肠从中线右侧的降结肠开始,向左侧髂窝走行。升结肠末端和整个降结肠有持续的结肠系膜。空肠和回肠位于腹腔左上部。这种异常可在生命的任何阶段引起结肠扭转。此外,了解这种异常对放射科医生、胃肠病学家和外科医生非常有用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8348/4276904/8dc0e00ab362/acb-47-279-g001.jpg

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