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十二指肠狭窄:体重增长不佳新生儿的诊断难题

Duodenal Stenosis: A Diagnostic Challenge in a Neonate With Poor Weight Gain.

作者信息

Win Ma Khin Khin, Mensah Carole, Kaushik Kunal, Pierre Louisdon, Adeyinka Adebayo

机构信息

Pediatrics, The Brooklyn Hospital Center, Brooklyn, USA.

出版信息

Cureus. 2020 Jun 11;12(6):e8559. doi: 10.7759/cureus.8559.

DOI:10.7759/cureus.8559
PMID:32670696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7358904/
Abstract

Cases of isolated duodenal stenosis in the neonatal period are minimally reported in pediatric literature. Causes of small bowel obstruction such as duodenal atresia or malrotation with midgut volvulus have been well documented and are often diagnosed due to their acute clinical presentation. Duodenal stenosis, however, causes an incomplete intestinal obstruction with a more indolent and varying clinical presentation thus making it a diagnostic challenge. We present a neonate with a unique case of congenital duodenal stenosis. The neonate presented with poor weight gain and frequent "spit-ups" as per the mother at the initial newborn visit. The clinical presentation was masked as the patient was being fed infrequently and with concentrated formula. We postulate that this may be due to the fact that the mother was an adolescent and relatively inexperienced with newborn care. During the hospital course, the patient had recurrent episodes of emesis with notable electrolyte abnormalities including hypochloremia and metabolic alkalosis. Further investigation with an abdominal X-ray showed dilated loops of bowel. Pyloric stenosis was ruled out via abdominal ultrasound. An upper gastrointestinal (GI) series ultimately confirmed a diagnosis of duodenal stenosis and the infant underwent surgical repair with full recovery. Congenital duodenal stenosis may have atypical presentations in neonates requiring pediatricians to have a high index of suspicion for diagnosis and to ensure timely therapy.

摘要

新生儿期孤立性十二指肠狭窄病例在儿科文献中报道极少。小肠梗阻的病因,如十二指肠闭锁或合并中肠扭转的肠旋转不良,已有充分记载,且常因其急性临床表现而得以诊断。然而,十二指肠狭窄导致不完全性肠梗阻,临床表现更为隐匿且多样,因此构成诊断挑战。我们报告一例患有先天性十二指肠狭窄的独特新生儿病例。该新生儿在初次新生儿访视时,据其母亲称存在体重增加不佳及频繁“吐奶”的情况。由于喂养不频繁且使用浓缩配方奶,临床表现被掩盖。我们推测这可能是因为母亲是青少年,且相对缺乏新生儿护理经验。在住院期间,患儿反复呕吐,伴有明显的电解质异常,包括低氯血症和代谢性碱中毒。腹部X线进一步检查显示肠袢扩张。通过腹部超声排除了幽门狭窄。上消化道造影最终确诊为十二指肠狭窄,患儿接受手术修复并完全康复。先天性十二指肠狭窄在新生儿中可能有非典型表现,需要儿科医生高度怀疑以进行诊断并确保及时治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7645/7358904/7974c29a8fe4/cureus-0012-00000008559-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7645/7358904/74b50521a2cf/cureus-0012-00000008559-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7645/7358904/603b1c972e1e/cureus-0012-00000008559-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7645/7358904/7974c29a8fe4/cureus-0012-00000008559-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7645/7358904/74b50521a2cf/cureus-0012-00000008559-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7645/7358904/603b1c972e1e/cureus-0012-00000008559-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7645/7358904/7974c29a8fe4/cureus-0012-00000008559-i03.jpg

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Congenital duodenal obstruction: causes and imaging approach.先天性十二指肠梗阻:病因及影像学检查方法
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