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Journal of Neonatal Surgery

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https://www.readbyqxmd.com/read/27896175/congenital-cecal-duplication-cyst-mimicking-as-intramural-mass
#1
Kamal Nain Rattan, Sunita Singh, Shruti Bansal, Megha Ralli, Ritika Vashisht
No abstract text is available yet for this article.
October 2016: Journal of Neonatal Surgery
https://www.readbyqxmd.com/read/27896174/congenital-pouch-colon-with-rectal-atresia-a-rare-association
#2
Bilal Mirza, Muhammad Saleem
No abstract text is available yet for this article.
October 2016: Journal of Neonatal Surgery
https://www.readbyqxmd.com/read/27896173/closed-gastroschisis-with-vanished-small-bowel-and-jejunal-atresia
#3
R S Sisodiya, S S Panda, C K Gupta, S K Sinha
No abstract text is available yet for this article.
October 2016: Journal of Neonatal Surgery
https://www.readbyqxmd.com/read/27896172/congenital-hernia-of-the-umbilical-cord-associated-with-type-iiia-ileal-atresia
#4
Rahul Gupta, Praveen Mathur, Pradeep Kumar Gupta
No abstract text is available yet for this article.
October 2016: Journal of Neonatal Surgery
https://www.readbyqxmd.com/read/27896171/isolated-jejunal-duplication-cyst-associated-with-intestinal-malrotation-in-a-newborn
#5
Prasanta Kumar Tripathy, Pradeep Kumar Jena, Hiranya Kishor Mohanty
No abstract text is available yet for this article.
October 2016: Journal of Neonatal Surgery
https://www.readbyqxmd.com/read/27896170/postoperative-gastric-perforation-in-a-newborn-with-duodenal-atresia
#6
Anko Antabak, Marko Bogović, Jurica Vuković, Ruža Grizelj, Vinka Barbarić Babić, Dino Papeš, Tomislav Luetić
Gastric perforation (GP) in neonates is a rare entity with high mortality. Although the etiology is not completely understood, it mostly occurs in premature neonates on assisted ventilation. Combination of duodenal atresia and gastric perforation is very rare. We present a case duodenal atresia who developed gastric perforation after operetion for duodenal atresia. Analysis of the patient medical record and histology report did not reveal the etiology of the perforation.
October 2016: Journal of Neonatal Surgery
https://www.readbyqxmd.com/read/27896169/rare-association-of-extended-total-colonic-aganglionosis-and-intestinal-malrotation
#7
Iulia Stratulat-Chiriac, Danielle Mc Laughlin, Brice Antao
Total colonic aganglionosis occurring together with malrotation is a rare occurrence and may pose diagnostic and management dilemmas for the paediatric surgeon. We report a case of a neonate that presented with extended total colonic aganglionosis and malrotation, along with a spectrum of central nervous system and renal abnormalities. The clinical and radiological features and potential diagnostic and management pitfalls are discussed along with a literature review of this exceptionally infrequent association...
October 2016: Journal of Neonatal Surgery
https://www.readbyqxmd.com/read/27896168/duodenal-atresia-associated-with-apple-peel-atresia-and-situs-inversus-abdominus-a-case-report
#8
H Ben Hamida, R Hadj Salem, K Ben Ameur, A Rassas, F Z Chioukh, R Sakka, N Kechiche, M Bizid, L Sahnoun, K Monastiri
Duodenal atresia is rarely associated with situs inversus abdominus. We report a case of duodenal atresia associated with small bowel atresia of apple peel type and situs inversus abdominus.
October 2016: Journal of Neonatal Surgery
https://www.readbyqxmd.com/read/27896167/imperforate-anus-with-jejunal-atresia-complicated-by-intestinal-volvulus-a-case-report
#9
Hae Soo Joung, Alexandra Leon Guerrero, Sandra Tomita, Keith A Kuenzler
Anorectal malformations (ARMs) commonly co-occur with other congenital anomalies, particularly VACTERL (vertebral, anorectal, cardiac, tracheal, esophageal, renal, limb, and duodenal) associations. However, this collection of associations is not comprehensive, and other concurrent anomalies may exist that can be missed during the standard work-up of patients with ARMs. We present a rare case of a neonate with a low ARM with concurrent jejuno-ileal atresia that was diagnosed after the correction of the ARM when the patient developed segmental volvulus...
October 2016: Journal of Neonatal Surgery
https://www.readbyqxmd.com/read/27896166/congenital-middle-mesocolic-hernia-a-rare-cause-of-neonatal-intestinal-obstruction
#10
Elias Chamely, Brice Antao
Congenital mesocolic hernia is an extremely rare, but serious cause of intestinal obstruction in children. Given the rarity of this condition, delays in diagnosis and management can have catastrophic consequences. Congenital mesocolic hernias are usually caused by an abnormal rotation of primitive mid-gut and are divided into left and right congenital mesocolic hernias. We report and discuss the clinical and radiological features and management of a neonate with an extremely rare variant, congenital middle mesocolic hernia along with a literature review of this rare condition...
October 2016: Journal of Neonatal Surgery
https://www.readbyqxmd.com/read/27896165/jejunal-windsock-deformity-a-rare-cause-of-incomplete-neonatal-intestinal-obstruction
#11
Vijai Datta Upadhyaya, Basant Kumar, Amrit Gupta, Kirti Naranje, Anita Singh
Incomplete intestinal obstruction due to windsock web of the jejunum is uncommonly noticed in neonates. We present a male neonate, prenatally suspected case of proximal bowel obstruction, who was found to have features of incomplete intestinal obstruction due to windsock deformity in jejunum. The difficulty in the diagnosis and management is discussed along with relevant literature review.
October 2016: Journal of Neonatal Surgery
https://www.readbyqxmd.com/read/27896164/more-distally-located-duodenal-webs-a-case-series
#12
Rahul Gupta, Praveen Mathur, Sharanabasappa Gubbi, Pradeep Kumar Gupta, Ramendra Shukla, Anu Bhandari
Duodenal atresia is a frequent cause of intestinal obstruction in the newborn. Obstruction due to duodenal web is infrequent, but its location other than second part of duodenum is rare with only a few cases reported in the literature. We are reporting three patients where we found duodenal webs at unusual locations. In one neonate the web was located at third part of duodenum and in other two patients the web was present at duodeno-jejunal junction (DJ).
October 2016: Journal of Neonatal Surgery
https://www.readbyqxmd.com/read/27896163/varied-presentation-of-congenital-segmental-dilatation-of-the-intestine-in-neonates-report-of-three-cases
#13
Binod Kumar Rai, Bilal Mirza, Imran Hashim, Muhammad Saleem
Congenital segmental dilatation (CSD) of the intestine is a rare developmental anomaly characterized by sharply demarcated dilatation of a gastrointestinal segment and may present with intestinal obstruction. We report three cases of CSD of the intestine in neonates with varied presentation. First patient was mistaken as pneumoperitoneum on abdominal radiograph, which led to initial abdominal drain placement. The 2nd patient was a case of anorectal malformation associated with congenital pouch colon (CPC) and CSD of ileum; and the third case presented as neonatal intestinal obstruction and found to have CSD of ileum...
October 2016: Journal of Neonatal Surgery
https://www.readbyqxmd.com/read/27896162/preduodenal-portal-vein-associated-with-duodenal-obstruction-of-other-etiology-a-case-series
#14
Punit Srivastava, Mishraz Shaikh, Bilal Mirza, Richa Jaiman, Muhammad Arshad
DuodenalPreduodenal portal vein is a rare and interesting entity which often causes duodenal obstruction. It is also associated with other congenital anomalies. We report here three cases of preduodenal portal vein associated with other anomalies causing duodenal obstruction not related to direct compression by portal vein itself.
October 2016: Journal of Neonatal Surgery
https://www.readbyqxmd.com/read/27896161/distinct-presentations-of-hernia-of-umbilical-cord
#15
REVIEW
Bilal Mirza, Waqas Ali
Hernia of umbilical cord is a well-known entity which presents with herniation of small bowel into the proximal part of umbilical cord. It has very good prognosis after surgical repair. Occasionally, it can have distinct presentations and varied malformations at the umbilicus which have bearing on the course of treatment and final outcome. Herein, we describe various presentations and malformations associated with hernia of umbilical cord. Embryological extrapolation is attempted for the malformations at umbilicus...
October 2016: Journal of Neonatal Surgery
https://www.readbyqxmd.com/read/27896160/neonatal-intestinal-obstruction-when-to-suspect-duplication-cyst-of-bowel-as-the-cause
#16
Rizwan Ahmad Khan, Shagufta Wahab, Imran Ghani
BACKGROUND: Duplication cyst is a rare cause of neonatal intestinal obstruction. Their most common location is the small intestine. The clinical presentation is extremely variable depending upon its size, location and type and the age of the patient and are mainly encountered during infancy or early childhood. The diagnosis is very difficult in neonates. This study was undertaken to study their presentation, diagnostic modality of choice and further management in neonatal age group. MATERIALS AND METHODS: This was a retrospective study performed at the Department of Paediatric Surgery, J ...
October 2016: Journal of Neonatal Surgery
https://www.readbyqxmd.com/read/27896159/intestinal-atresia-experience-at-a-busy-center-of-north-west-india
#17
Shilpi Gupta, Rahul Gupta, Soumyodhriti Ghosh, Arun Kumar Gupta, Arvind Shukla, Vinita Chaturvedi, Praveen Mathur
Objective: To evaluate the presentation, management, complications and outcome of intestinal atresia (IA) managed at our center over a period of 1 year. Materials and methods: Records of patients of IA admitted in our center from January 2015 to December 2015 were retrospectively analyzed. Demographic data, antenatal history, presenting complaints, location (duodenal, jejunoileal, colonic) of atresia, surgery performed and peri-operative complications were noted. Results: Total 78 cases of IA were included in the analyses...
October 2016: Journal of Neonatal Surgery
https://www.readbyqxmd.com/read/27896158/congenital-duodenal-obstruction-in-neonates-over-13-years-experience-from-a-single-centre
#18
Parveen Kumar, Chiranjiv Kumar, Prince Raj Pandey, Yogesh Kumar Sarin
AIM: To study the prevalence of associated anomalies with neonatal duodenal obstruction and factors impacting short-term survival. MATERIAL AND METHODS: Records of 31 neonates with neonatal duodenal obstruction could be retrieved and analyzed for a 13.5-year-period (October 2003-May 2016). M:F ratio was 1.58:1. The mean birth weight was 2.15 kg; 12 patients were preterm. Etiologies included duodenal atresia (n=23), duodenal web (n=8) and malrotation of gut (n= 6)...
October 2016: Journal of Neonatal Surgery
https://www.readbyqxmd.com/read/27896157/congenital-neonatal-intestinal-obstruction-retrospective-analysis-at-tertiary-care-hospital
#19
Vijay Singh, Manish Pathak
BACKGROUND: The purpose of this study is to analyze the etiology, clinical presentation and outcome of neonatal intestinal obstruction at our institute. MATERIALS AND METHODS: The medical record of all the patients, presented with intestinal obstruction in neonatal period during 2014 and 2015 was reviewed retrospectively for etiology, clinical features, investigations, management, and outcome. RESULTS: Out of total 53 cases of neonatal intestinal obstruction, 27 were of intestinal atresia (9 cases (17%) were of duodenal atresia, 7 (13%) were of jejunal atresia and 8 (13%) were ileal atresias and 3 cases were found with colonic atresia); 7 were malrotation, 17 were Hirschsprung's disease (HD)...
October 2016: Journal of Neonatal Surgery
https://www.readbyqxmd.com/read/27896156/modified-gut-anastomotic-technique-in-type-iii-and-type-iv-jejunoileal-atresias
#20
Kamal Nain Rattan, Deepak Kumar Garg
BACKGROUND: Type III and IV jejunoileal atresias are associated with loss of significant length of the gut and can lead to short gut syndrome if further resection of proximal dilated gut is done. We modified the anastomotic technique so that proximal dilated segment of the gut is not resected as to prevent short gut syndrome. MATERIAL AND METHODS: Medical Record of patients of Type III and IV jejuno-ileal atresias managed with modified anastomotic technique in our center during 5-years was reviewed...
October 2016: Journal of Neonatal Surgery
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