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胎粪栓综合征的当前意义

Current significance of meconium plug syndrome.

作者信息

Keckler Scott J, St Peter Shawn D, Spilde Troy L, Tsao KuoJen, Ostlie Daniel J, Holcomb George W, Snyder Charles L

机构信息

Department of Surgery, The Children's Mercy Hospital, Kansas City, MO 64108, USA.

出版信息

J Pediatr Surg. 2008 May;43(5):896-8. doi: 10.1016/j.jpedsurg.2007.12.035.

Abstract

BACKGROUND

The significance of meconium plug syndrome is dependent on the underlying diagnosis. The incidence of pathologic finding, particularly Hirschsprung's disease, contributing to the presence of these plugs, has been debated. However, there are little recent data in the literature. Therefore, we reviewed our experience with meconium plugs as a cause of abdominal distension to evaluate the associated conditions and incidence of Hirschsprung's disease.

METHODS

We reviewed the records of newborns with meconium plugs found in the distal colon on contrast enema from 1994 to 2007. Demographics, radiologic findings, histologic findings, operative findings, and clinical courses were reviewed.

RESULTS

During the study period, 77 patients were identified. Mean gestational age was 37.4 weeks and birth weight, 2977 g. Hirschsprung's disease was found in 10 patients (13%). One had ultrashort segment disease and another had total colonic aganglionosis. Maternal diabetes was identified in 6 patients. No patients were diagnosed with cystic fibrosis, meconium ileus, malrotation, or intestinal atresia.

CONCLUSION

Meconium plugs found on contrast enema are associated with a 13% incidence of Hirschsprung's disease in our experience. Although all patients with plugs and persistent abnormal stooling patterns should prompt a rectal biopsy and genetic probe, the incidence of Hirschsprung's and cystic fibrosis may not be as high as previously reported.

摘要

背景

胎粪栓综合征的意义取决于潜在诊断。导致这些栓子出现的病理发现,尤其是先天性巨结肠的发生率,一直存在争议。然而,近期文献中相关数据较少。因此,我们回顾了以胎粪栓作为腹胀原因的经验,以评估相关情况及先天性巨结肠的发生率。

方法

我们回顾了1994年至2007年期间在结肠造影灌肠时发现远端结肠有胎粪栓的新生儿记录。对人口统计学、放射学发现、组织学发现、手术发现及临床病程进行了回顾。

结果

在研究期间,共确定了77例患者。平均胎龄为37.4周,出生体重为2977克。10例患者(13%)被诊断为先天性巨结肠。1例为超短段型疾病,另1例为全结肠无神经节症。6例患者被诊断为母亲患有糖尿病。没有患者被诊断为囊性纤维化、胎粪性肠梗阻、肠旋转不良或肠闭锁。

结论

根据我们的经验,结肠造影灌肠时发现的胎粪栓与13%的先天性巨结肠发生率相关。虽然所有有栓子且排便模式持续异常的患者都应进行直肠活检和基因检测,但先天性巨结肠和囊性纤维化 的发生率可能不像先前报道的那么高。

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