Suppr超能文献

长段肠神经节缺如婴儿中模拟胎粪性肠梗阻的新生儿肠梗阻:提示需要进行直肠活检的影像学表现

Neonatal intestinal obstruction simulating meconium ileus in infants with long-segment intestinal aganglionosis: radiographic findings that prompt the need for rectal biopsy.

作者信息

Cowles Robert A, Berdon Walter E, Holt Peter D, Buonomo Carlo, Stolar Charles J

机构信息

Division of Pediatric Surgery, Morgan Stanley Children's Hospital of New York-Presbyterian, Columbia University College of Physicians and Surgeons, 3959 Broadway, Rm. CHN216B, New York, NY 10032, USA.

出版信息

Pediatr Radiol. 2006 Feb;36(2):133-7. doi: 10.1007/s00247-005-0043-8. Epub 2005 Dec 3.

Abstract

BACKGROUND

The initial clinical presentation and radiographic finding of microcolon in children with long-segment intestinal aganglionosis involving the entire colon, ileum and sometimes the jejunum can mimic meconium ileus. This makes the diagnosis difficult for the radiologist and surgeon.

OBJECTIVE

To document and describe the clinical and radiographic findings in children with long-segment intestinal aganglionosis who are initially thought to have meconium ileus.

MATERIALS AND METHODS

We reviewed the cases of six neonates with long-segment intestinal aganglionosis presenting as meconium ileus at our institutions between 1978 and 2002. We examined the clinical presentation and the radiographic, surgical, and pathologic findings. In addition, 17 cases from the literature were identified and are included in the discussion.

RESULTS

A total of 23 cases were reviewed. Right lower quadrant intraluminal calcifications were noted on abdominal radiographs in all six neonates of our series and were described in 13 of the 17 neonates reported in the literature. Similarly, a microcolon was present in five of the six neonates of our series and in 14 of 16 historical neonates (one not reported).

CONCLUSION

In a neonate with small-bowel obstruction and a microcolon, the presence of right lower quadrant intraluminal calcifications should raise the suspicion of long-segment intestinal aganglionosis even if the operative findings are typical of meconium ileus and a biopsy should be performed.

摘要

背景

患有累及整个结肠、回肠甚至有时包括空肠的长段肠道神经节细胞缺乏症的儿童,其微结肠的初始临床表现和影像学表现可能类似胎粪性肠梗阻。这给放射科医生和外科医生的诊断带来困难。

目的

记录并描述最初被认为患有胎粪性肠梗阻的长段肠道神经节细胞缺乏症患儿的临床和影像学表现。

材料与方法

我们回顾了1978年至2002年间在我们机构就诊的6例表现为胎粪性肠梗阻的长段肠道神经节细胞缺乏症新生儿病例。我们检查了临床表现以及影像学、手术和病理检查结果。此外,还从文献中找出17例病例并纳入讨论。

结果

共回顾了23例病例。我们系列中的6例新生儿腹部X线片均显示右下腹腔内钙化,文献报道的17例新生儿中有13例也有此表现。同样,我们系列中的6例新生儿中有5例存在微结肠,16例既往病例中有14例(1例未报道)存在微结肠。

结论

对于患有小肠梗阻和微结肠的新生儿,即使手术所见典型为胎粪性肠梗阻,右下腹腔内钙化的存在也应引起对长段肠道神经节细胞缺乏症的怀疑,应进行活检。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验