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首页> 外文期刊>International Journal of Surgery Case Reports >Congenital intestinal atresia associated with a mesenteric cystic lymphangioma in a low birth weight neonate: A case report
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Congenital intestinal atresia associated with a mesenteric cystic lymphangioma in a low birth weight neonate: A case report

机译:先天性肠腹腹腹部与肠系膜囊性淋巴管瘤的低出生体重新生儿:案例报告

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Introduction Congenital intestinal atresia requires emergency surgery soon after birth. Lymphangioma, a benign tumor, is caused by an anomalous lymphatic system. We report a case of congenital intestinal atresia associated with a mesenteric cystic lymphangioma in a low birth weight neonate. Presentation of case At 21 weeks of pregnancy, ultrasonography revealed a cystic lesion in the fetal abdominal cavity. At 31 weeks, magnetic resonance imaging showed dilatation of the small intestine. This low birth weight (1752?g) male infant was born by vaginal delivery at 32 weeks 3 days’ gestation. Laparotomy on day 2 of life revealed jejunal atresia and a mesenteric cyst. The cyst was removed and intestinal anastomosis was performed. Histologically, the cyst proved to be a mesenteric lymphangioma. Discussion The most popular theories regarding the mechanism of congenital intestinal atresia include reperfusion injury and intestinal tract blood flow disturbance. In this fetus, intestinal torsion had occurred around the mesenteric cystic lymphangioma, which apparently disturbed the mesenteric blood flow and caused intestinal atresia. Conclusion There have been few reports of the combination of a mesenteric cystic lymphangioma and congenital intestinal atresia. This case supports the theory that small bowel atresia and stenosis are caused by accidental blood flow disturbance.
机译:引言先天性肠道休息于出生后不久需要急诊手术。淋巴管瘤是一种良性肿瘤,是由异常淋巴系统引起的。我们举报了与肠系膜囊性淋巴管瘤的先天性肠梗出的案例,以低出生体重新生儿。妊娠21周介绍,超声检查显示胎儿腹腔中的囊性病变。在31周,磁共振成像显示出小肠的扩张。这种低出生体重(1752×g)雄性婴儿在32周的妊娠32周的阴道递送时出生。剖腹术在生命中的第2天揭示了Jejunal atresia和肠系膜囊肿。除去囊肿并进行肠吻合术。组织学上,囊肿被证明是肠系膜淋巴管瘤。讨论先天性肠梗塞机制的最受欢迎的理论包括再灌注损伤和肠道血流干扰。在这种胎儿中,肠道扭转周围发生肠系膜囊性淋巴管瘤,这显然扰乱了肠系膜血流并导致肠道腹部。结论肠系膜囊性淋巴管瘤和先天性肠闭锁的结合几乎没有报道。这种情况支持小肠闭锁和狭窄是由意外血流扰动引起的理论。

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