首页> 外文期刊>Pediatric radiology >Neonatal intestinal obstruction simulating meconium ileus in infants with long-segment intestinal aganglionosis: radiographic findings that prompt the need for rectal biopsy.
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Neonatal intestinal obstruction simulating meconium ileus in infants with long-segment intestinal aganglionosis: radiographic findings that prompt the need for rectal biopsy.

机译:新生儿肠梗阻模拟长段肠神经节病婴儿胎粪肠梗阻:影像学检查提示需要进行直肠活检。

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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.
机译:背景:长段肠神经节病患儿涉及整个结肠,回肠,有时空肠的小肠的初步临床表现和影像学发现可模仿胎粪肠梗阻。这使得放射科医生和外科医生难以诊断。目的:记录并描述最初被认为患有胎粪性肠梗阻的长节段肠神经节病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年间在我们机构中出现的6例长段肠神经节病的新生儿,表现为胎粪肠梗阻。我们检查了临床表现以及影像学,手术和病理学发现。此外,从文献中鉴定出17个案例,并将其纳入讨论范围。结果:共检查23例。在我们系列的所有6例新生儿的腹部X光片中都注意到右下腹腔内钙化,并在文献报道的17例新生儿中的13例中得到了描述。同样,我们系列的6名新生儿中有5名和16名历史性新生儿中有14名存在小结肠(未报道)。结论:在小肠梗阻和小结肠的新生儿中,右下象限管腔内钙化的存在应该引起对长节段肠神经节病的怀疑,即使手术结果是典型的胎粪肠梗阻,也应进行活检。

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