发布求助
文献互助 智能选刊 最新文献

Journal of Neonatal Surgery最新文献

筛选
英文 中文
A case of prenatally diagnosed prune belly syndrome variant and congenital pouch colon in the United States: A case report 美国一例产前诊断为梅干-腹部综合征变异型和先天性袋状结肠的病例报告
Journal of Neonatal Surgery Pub Date : 2021-09-25 DOI: 10.47338/jns.v10.1012
M. Yilma, Karen Trang, M. Schwab, M. Bowman, M. Sugi, J. Courtier, L. Baskin, D. Ozgediz
{"title":"A case of prenatally diagnosed prune belly syndrome variant and congenital pouch colon in the United States: A case report","authors":"M. Yilma, Karen Trang, M. Schwab, M. Bowman, M. Sugi, J. Courtier, L. Baskin, D. Ozgediz","doi":"10.47338/jns.v10.1012","DOIUrl":"https://doi.org/10.47338/jns.v10.1012","url":null,"abstract":"Background: Prune belly syndrome (PBS) and congenital pouch colon (CPC) are rare congenital syndromes with a low incidence in the United States (U.S.) with most CPC cases being from India. In this case report, we describe, to the best of our knowledge, the first PBS variant and CPC patient in the U.S.\u0000Case Presentation: A 30-year-old G2P0010 woman was referred to a tertiary center after an 18-week ultrasound showed a fetal abdominal mass. A prenatal MRI showed a dilated loop of bowel containing a mixture of urine and meconium, oligohydramnios, and a protuberant abdominal wall. Born at 37 weeks, the child’s physical exam was notable for a distended abdomen with thin abdominal musculature, non-palpable bilateral testes, no anal opening, and flat buttocks. Intra-operatively, a dilated cecum/ascending colon was noted with an abrupt change in caliber at the transverse colon, bilateral enlarged ureters, a left testis at the internal ring and no visualized right testis. A colostomy and mucous fistula were created 5 cm from the sigmoid pouch.\u0000Conclusion: While most reported cases of CPC undergo single stage repair (one operation) at 1 day of life, our patient underwent the first procedure of a staged repair at 16 hours of life given his clinical instability at the time as well as his unknown urological anatomy in the setting of urinary obstruction. This case demonstrates the importance of fetal imaging, multidisciplinary approach at a tertiary care center, and reinforces a staged repair when necessary.","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45453697","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Meconium obstruction in a premature neonate: An etiology that may simulate spontaneous intestinal perforation 早产新生儿胎便梗阻:一种可能模拟自发性肠穿孔的病因
Journal of Neonatal Surgery Pub Date : 2021-09-23 DOI: 10.47338/jns.v10.1013
James G. Glasser
{"title":"Meconium obstruction in a premature neonate: An etiology that may simulate spontaneous intestinal perforation","authors":"James G. Glasser","doi":"10.47338/jns.v10.1013","DOIUrl":"https://doi.org/10.47338/jns.v10.1013","url":null,"abstract":"A surgeon expects either necrotizing enterocolitis (NEC) or spontaneous intestinal perforation (SIP) in preemies with pneumoperitoneum. But there is another cause wherein the operative findings simulate meconium ileus [1]: The terminal ileum and colon are tiny and obstructed by inspissated meconium; The bowel proximal to the obstruction may be diffusely dilated, or there may be aneurysmal (segmental) dilatation, which may be single or multiple; Resection with ileostomy is all that is attempted in these tiny, fragile babies; Surprisingly, when the ileostomy is closed 4-6 weeks later, the bowel appears to be normal, the obstruction has cleared and the caliber disparity has disappeared, which suggests that immaturity was causative of the obstruction and the occasional aneurysmal dilatation.","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":"186 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70820170","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Intraluminal pyloric duplication cyst- a rare cause of non-bilious vomiting in a neonate: A case report 幽门腔内重复囊肿——新生儿非胆汁性呕吐的罕见原因：一例报告
Journal of Neonatal Surgery Pub Date : 2021-09-23 DOI: 10.47338/jns.v10.1006
Ravi Patcharu, Jaiprakash Yadav, K. Chand, Badal Parikh
{"title":"Intraluminal pyloric duplication cyst- a rare cause of non-bilious vomiting in a neonate: A case report","authors":"Ravi Patcharu, Jaiprakash Yadav, K. Chand, Badal Parikh","doi":"10.47338/jns.v10.1006","DOIUrl":"https://doi.org/10.47338/jns.v10.1006","url":null,"abstract":"Background: Duplications of the alimentary tract are rare congenital malformations, out of which, true pyloric duplications constitute only 2.2%. They present with non-bilious vomiting and mimic hypertrophic pyloric stenosis (HPS). Pyloric duplications that are intraluminal are not separately visible at laparotomy, making their diagnosis difficult. \u0000Case presentation: Our case is a neonate with an intraluminal pyloric duplication cyst who presented with recurrent vomiting. The radiological evaluation suggested a duplication cyst medial to the second part of the duodenum towards the stomach’s lesser curvature with features of gastric outlet obstruction. Intraoperatively, a cystic mass of 1 x 2 cm intraluminally was found on opening the pylorus which was excised and pyloroplasty was done. Postoperatively the baby was discharged in a stable condition.\u0000Conclusion: Intraluminal pyloric duplication cysts are rare and the clinical presentation mimics HPS. They should be considered as a differential diagnosis in a neonate presenting with features of gastric outlet obstruction.","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45779660","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cystic hygroma and esophageal atresia with tracheoesophageal fistula: Is there a genetic association? 囊性水肿和食管闭锁伴气管食管瘘:是否有遗传关系?
Journal of Neonatal Surgery Pub Date : 2021-09-12 DOI: 10.47338/jns.v10.997
Sravanthi Vutukuru, N. Peters, S. Dogra, R. Samujh
{"title":"Cystic hygroma and esophageal atresia with tracheoesophageal fistula: Is there a genetic association?","authors":"Sravanthi Vutukuru, N. Peters, S. Dogra, R. Samujh","doi":"10.47338/jns.v10.997","DOIUrl":"https://doi.org/10.47338/jns.v10.997","url":null,"abstract":"Background: Tracheoesophageal fistula (TEF) is associated with many other congenital anomalies like cardiac, renal, and vertebral, but the association with cystic hygroma is very rare.\u0000Case Presentation: We report a neonate, antenatally diagnosed with cystic hygroma of the neck and incidentally diagnosed to have TEF. The baby was operated on after adequate stabilization and the cystic hygroma was managed with injection sclerotherapy. The genetic analysis for the FOX genes complex has been done in this case and the results showed no association between the two.\u0000Conclusion: There is a need for future studies to find out if the association between cystic hygroma and TEF is by chance or if any embryological or genetic cause can be attributed to it.","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48916396","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Congenital segmental dilatation of intestine with different morphology: A case report 先天性不同形态节段性肠扩张1例
Journal of Neonatal Surgery Pub Date : 2021-09-12 DOI: 10.47338/jns.v10.1021
Bilal Mirza, Sumaira Noor Maham, N. Talat
{"title":"Congenital segmental dilatation of intestine with different morphology: A case report","authors":"Bilal Mirza, Sumaira Noor Maham, N. Talat","doi":"10.47338/jns.v10.1021","DOIUrl":"https://doi.org/10.47338/jns.v10.1021","url":null,"abstract":"Background: Congenital segmental dilatation of intestine is a rare entity characterized by a localized dilated segment of the intestine. It manifests as neonatal intestinal obstruction. Occurrence with another surgical anomaly may masquerade it and complicate the treatment course.\u0000Case Presentation: A 1-day-old male neonate with anorectal malformation underwent colostomy as first stage of the treatment. The stoma did not function postoperatively. At repeat surgery, congenital segmental dilatation of the ileum, with slightly different morphology, was found. Resection of the lesion and ileostomy were formed. Postoperative course remained uneventful.\u0000Conclusion: Congenital segmental dilatation of intestine may be missed at initial surgery. Complete surgical resection is curative.","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49575614","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
The Raveenthiran Syndrome—Ectopic testis within Spigelian hernia: Few additional remarks Raveenthiran综合征——Spigelian疝内异位睾丸：几点补充意见
Journal of Neonatal Surgery Pub Date : 2021-09-09 DOI: 10.47338/jns.v10.1024
Venkatachalam Raveenthiran
{"title":"The Raveenthiran Syndrome—Ectopic testis within Spigelian hernia: Few additional remarks","authors":"Venkatachalam Raveenthiran","doi":"10.47338/jns.v10.1024","DOIUrl":"https://doi.org/10.47338/jns.v10.1024","url":null,"abstract":"I read, with great interest, the article by Sinacer et al. on the association of congenital Spigelian hernia with cryptorchidism, polydactyly, and anal stenosis.[1] Although this association is known since 1895, only in 2005 it was recognized as a new syndrome.[2,3] Since then there has been an increasing awareness about this clinical entity.[4] In 2015 Moles-Morenilla et al. named it ‘Raveenthiran syndrome’ and classified it into two types: type-1 is an exclusive association of Spigelian hernia and ectopic testis while type-2 is Spigelian hernia and ectopic testis associated with other anomalies.[5] Accordingly, the newborn reported by Sinacer et al. belongs to type-2 Raveenthiran syndrome.","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41893546","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Type III wide colonic atresia: An etiological introspection III型宽结肠闭锁的病因反思
Journal of Neonatal Surgery Pub Date : 2021-08-23 DOI: 10.47338/jns.v10.1020
M. Hassan
{"title":"Type III wide colonic atresia: An etiological introspection","authors":"M. Hassan","doi":"10.47338/jns.v10.1020","DOIUrl":"https://doi.org/10.47338/jns.v10.1020","url":null,"abstract":"","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-08-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47475769","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Congenital Spigelian hernia in a neonate associated with several anomalies: A case report 新生儿先天性Spigelian疝合并几种异常:1例报告
Journal of Neonatal Surgery Pub Date : 2021-08-13 DOI: 10.47338/jns.v10.972
Samira Sinacer, Bilal Zakaria Semari, Soumia Khemari, Ahlem Kharchi, Assia Haif, Zineddine Soualili
{"title":"Congenital Spigelian hernia in a neonate associated with several anomalies: A case report","authors":"Samira Sinacer, Bilal Zakaria Semari, Soumia Khemari, Ahlem Kharchi, Assia Haif, Zineddine Soualili","doi":"10.47338/jns.v10.972","DOIUrl":"https://doi.org/10.47338/jns.v10.972","url":null,"abstract":"Background: Spigelian hernia (SH) is a rare entity characterized by a defect of the anterior abdominal wall located along the Spigelian line, it may be congenital or acquired.Association with other anomalies is worth reporting.\u0000Case Presentation: A 22-day-old male newborn was admitted with strangulated right inguinal hernia and operated on emergently. Clinical examination also revealed a Spigelian hernia in the left lower abdominal quadrant with bilateral cryptorchidism, associated with polydactyly of the small right finger and anal stenosis. At surgery, the SH contained a part of the small intestine and the ipsilateral undescended testis.\u0000Conclusion: Pediatric SH is rare, but its association with undescended ipsilateral testis is frequent. Other abnormalities can be concomitant to this association.","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":"398 ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-08-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41315499","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Outcomes following the establishment of Qatar’s quaternary neonatal general surgical service in a hospital with a “Tabula Rasa” for service development 在一家拥有“Tabula Rasa”的医院建立卡塔尔四级新生儿普通外科服务后的结果
Journal of Neonatal Surgery Pub Date : 2021-08-09 DOI: 10.47338/jns.v10.975
B. Khalil, Abdalla E. Zarroug, Abubakr Elawad, S. Moussa, C. Donnelly, Saleem Mammoo, G. Brisseau, Alison R Bedford Russell, H. Hummler
{"title":"Outcomes following the establishment of Qatar’s quaternary neonatal general surgical service in a hospital with a “Tabula Rasa” for service development","authors":"B. Khalil, Abdalla E. Zarroug, Abubakr Elawad, S. Moussa, C. Donnelly, Saleem Mammoo, G. Brisseau, Alison R Bedford Russell, H. Hummler","doi":"10.47338/jns.v10.975","DOIUrl":"https://doi.org/10.47338/jns.v10.975","url":null,"abstract":"Background: Sidra Medicine is the first dedicated Children and Maternity hospital in the State of Qatar. This paper describes the preparations for and results of activating quaternary neonatal surgical services in a brand new, \"greenfield\" hospital. We believe that these are the first published national results of neonatal general surgical services from the Gulf region.\u0000Methods: A review of surgical babies below four weeks corrected age from 1st of April 2018 – 31st of March 2020 was undertaken. Patient demographics, primary diagnosis, surgical procedures, 30-day postoperative mortality, overall mortality, and cause of death were recorded.\u0000Results: One hundred and sixty-nine babies (169) were identified (44.4% term and 55.6% preterm). Major surgery included laparotomy (76), congenital diaphragmatic hernia repair (20), surgery for anorectal malformations (25), and esophageal atresia (13). One set of conjoined twins were also separated successfully.  Fourteen babies died, resulting in overall mortality of 8.3 %. Excluding babies who died of life-limiting conditions, two babies died within 30 days of surgery, resulting in 30 days postoperative mortality rate of 1.2 %.\u0000Conclusions: The neonatal surgical mortality rate is comparable with those from top international centers. This low rate could be attributed to the high level of expertise preceded by months of preparations.","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-08-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44079020","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Jejunal atresia with ileojejunal knotting: An unusual presentation 空肠闭锁伴回空肠结:一种不寻常的表现
Journal of Neonatal Surgery Pub Date : 2021-07-23 DOI: 10.47338/JNS.V10.951
N. Pawar, Pramila Sharma, P. Mittal, V. Chaturvedi
{"title":"Jejunal atresia with ileojejunal knotting: An unusual presentation","authors":"N. Pawar, Pramila Sharma, P. Mittal, V. Chaturvedi","doi":"10.47338/JNS.V10.951","DOIUrl":"https://doi.org/10.47338/JNS.V10.951","url":null,"abstract":"      ","PeriodicalId":34201,"journal":{"name":"Journal of Neonatal Surgery","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45106041","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
首页 上一页
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整，为了账户安全，请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
请完成安全验证×
相关产品
×
本文献相关产品
联系我们：info@booksci.cn Book学术提供免费学术资源搜索服务，方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号：481959085
Book学术官方微信