首页> 外文期刊>Journal of Pediatric Surgery Case Reports >Early presenting hypertrophic pyloric stenosis with transient antroduodenal dysmotility in a preterm neonate: A case report
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Early presenting hypertrophic pyloric stenosis with transient antroduodenal dysmotility in a preterm neonate: A case report

机译:早产儿早期表现为肥厚性幽门狭窄伴短暂性十二指肠运动障碍:一例报告

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Hypertrophic pyloric stenosis (HPS) is one of the most common gastrointestinal disorders that require surgical intervention in early infancy. Clinical presentation, diagnosis, and treatment have been well established in typical cases. We herein describe an unusual case of early presenting HPS with transient postoperative feeding intolerance after complete myotomy in a preterm newborn. An ex-31-week preterm newborn (birth weight, 1760?g) with persistent feeding intolerance since the first feeding was referred for surgery on the 7th day of life. Abdominal ultrasonography (USG) revealed an elongated pyloric channel (11?mm) with thickened pyloric muscle (2.1?mm). Laparotomy was performed and confirmed suspected HPS. Pylomyotomy was successful, but feeding intolerance persisted until postoperative day 12. USG on postoperative day 12 noted antroduodenal dysmotility, and transpyloric tube feeding was started. Full feeds were reached 8 days after tube feeding, which was then converted to full oral feeding. HPS should be considered in patients who show feeding intolerance shortly after birth. USG criteria for HPS in preterm infants has not yet been established. Transient antroduodenal dysmotility could be a reason for persistent feeding intolerance after complete myotomy in preterm infants, and transpyloric tube feeding could be a treatment in such cases. Highlights ? We report a case of early presenting HPS with transient antroduodenal dysmotility. ? The patient presented with feeding intolerance 2 days after birth. ? Ultrasound findings were suggestive of HPS. ? Postoperatively, antroduodenal dysmotility was noted transiently. ? Transpyloric tube feeding during the dysmotility was successful.
机译:肥厚性幽门狭窄(HPS)是最常见的胃肠道疾病之一,在婴儿早期需要手术干预。在典型病例中,临床表现,诊断和治疗已得到很好的确立。我们在此描述了一种不寻常的病例,在早产儿完全肌切开术后,早期出现HPS伴有短暂的术后喂养不耐受。自出生后第7天起,自首次喂养以来持续喂养不耐受的31周前早产新生儿(出生体重1760 µg)被转诊。腹部超声检查(USG)显示幽门通道延长(11?mm),幽门肌肉增厚(2.1?mm)。进行了剖腹手术,并确认疑似HPS。脊髓切开术是成功的,但喂养不耐受一直持续到术后第12天。术后第12天的USG注意到十二指肠前运动障碍,并开始经幽门管喂养。管饲后8天达到全喂,然后转变为全口饲。出生后不久出现喂养不耐受的患者应考虑HPS。尚未建立早产儿HPS的USG标准。短暂性十二指肠动力不全可能是早产儿完全肌切开术后持续进食不耐受的原因,在这种情况下经幽门管喂养可能是一种治疗方法。强调 ?我们报告一例早期出现HPS伴短暂性十二指肠运动障碍。 ?该患者在出生后2天出现喂养不耐受。 ?超声检查结果提示HPS。 ?术后短暂出现十二指肠前运动障碍。 ?动力不全期间经幽门管喂养成功。

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