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

机译:缺乏横结肠持续下降的中结肠大肠和小肠移位:一种罕见的先天性异常有肠形成的高风险

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摘要

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.
机译:与结肠左半部相比,先天性异常例如结肠右半部的位置异常更为常见。我们报告了罕见的先天性异常病例,其中完全没有横结肠。右结肠弯曲时升结肠继续为降结肠。升结肠和降结肠形成倒U形的loop,位于腹部的右半部分。乙状结肠从降结肠开始,在中线的右侧,并行至左窝。升结肠的末端部分和整个降结肠具有持续的中结肠。空肠和回肠位于腹腔的左上方。这种异常会在生命的任何阶段引起结肠肠扭转。此外,这种异常的知识对于放射科医生,肠胃科医生和外科医生非常有用。

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