https://jneonatalsurg.com/ojs/index.php/jns/issue/feed Journal of Neonatal Surgery 2024-04-04T00:24:34-04:00 Dr. Muhammad Bilal Mirza blmirza@gmail.com Open Journal Systems <p class="style58" style="text-align: justify; line-height: 16.5pt; background: white; margin: 12.0pt 0in 12.0pt 0in;"><span style="font-size: 11.5pt; font-family: 'Arial',sans-serif; color: black;"><strong>Journal of Neonatal Surgery (ISSN: 2226-0439)</strong> is a peer-reviewed, open-access, electronic journal promoting the dispersion of quality research in Neonatal Surgery. It is the only journal dedicated to Neonatal Surgery- a developing specialty. The journal also provides an opportunity for learning "Medical Writing" for young pediatric and neonatal surgeons. Our editorial team works hard to guide new writers in this field. The journal publishes quality research that will improve outcomes of neonatal surgery, especially in resource-constrained settings. Our main aim is to reduce morbidity and mortality of neonatal surgery by publishing the latest trends in this discipline, in a special context to developing countries. We invite pediatric and neonatal surgeons for their quality contributions to the Journal of Neonatal Surgery and for helping us achieve these goals.</span></p> https://jneonatalsurg.com/ojs/index.php/jns/article/view/1294 Extremely low birth weight (ELBW) neonates for emergency surgery- A challenge for the Anesthesiologist: A case series 2024-02-14T11:06:59-05:00 Preeti Goyal Varshney doc_1998@rediff.com Madhurima Sinharay drmadhurimasinharay@gmail.com Anshu Gupta anug71@yahoo.co.in Maitree Pandey maitreepandey@gmail.com <p>Background: Extremely Low Birth Weight (ELBW) newborns, defined as those with a birth weight of 1000 grams or less, present challenging anesthetic scenarios. Emergency surgeries in these infants elevate their vulnerability to various complications.</p> <p>Case Presentation: We present a case series involving 5 ELBW neonates who underwent emergency surgery. Three of them were at a post-conceptual age (PCA) of ≥ 33 weeks and underwent procedures for congenital birth defects, including esophageal atresia, ileal atresia, and gastroschisis. The remaining two neonates, with a PCA of 29-30 weeks, underwent surgery for necrotizing enterocolitis (NEC).</p> <p>Conclusion: The compromised physiology resulting from distinct disease processes and the underdeveloped systems of ELBW preterm neonates necessitate focused care and strategic anesthesia. This approach is crucial to mitigate morbidity and mortality risks in such vulnerable patients.</p> 2024-03-14T00:00:00-04:00 Copyright (c) 2023 Preeti Goyal Varshney, Madhurima Sinharay, Anshu Gupta, Maitree Pandey https://jneonatalsurg.com/ojs/index.php/jns/article/view/1279 Single-center experience of fetus in fetu: A case series 2023-12-08T08:51:51-05:00 G Habachi habachighada92@gmail.com I Sabolic sabolici@gmail.com M Mesic mrkmesic@yahoo.com A Ksia amineks@yahoo.fr M ben Fredj myriam.benfredj@yahoo.fr S ben Youssef sabrine.benyoussef@yahoo.com S Sfar samisfar@gmail.com N Kechiche kechichenahla@gmail.com R Lamiri lamiri.rachida@yahoo.fr M Mekki mongi_mekki@yahoo.fr M Belghith belghithmohsen.58@gmail.com M Messoud marwa.mesaoud@gmail.com S Mosbahi sana_mosbahi@yahoo.fr L Sahnoun slassaad13@gmail.com <p>Background: Fetus in fetu is a rare congenital malformation resulting from abnormal embryogenesis in a monochorionic diamniotic twinning gestation. This study aimed to document our experience with this anomaly in a developing country.</p> <p>Methods: This retrospective analysis covers cases of fetus in fetu diagnosed at our institution between 1999 and 2023. Patients presenting with an intracorporeal mass containing a vertebral column and an appropriate arrangement of organs and limbs around the axis were included in the study.</p> <p>Results: Five female patients with fetus in fetu were identified. The timing of diagnosis varied from incidental antenatal ultrasound discovery to postnatal abdominal mass presentation. The initial diagnosis involved radiological and serological investigations, confirmed by histopathology after surgical excision. The mean age at the time of surgery was 44 days. All patients underwent complete excision of the fetal mass, resulting in excellent postoperative outcomes and no recurrences.</p> <p>Conclusion: Fetus in fetu is a pediatric rarity and must be distinguished from a teratoma mass, which carries a high malignant potential. Histological and genetic studies may contribute to understanding the pathogenesis and etiology of the disease.</p> 2024-04-13T00:00:00-04:00 Copyright (c) 2023 G Habachi, I Sabolic, M Mesic, A Ksia, M ben Fredj , S ben Youssef, S Sfar, N Kechiche, R Lamiri, mongi mekki, mohsen belghith, marwa messoud, sana mosbahi, lassad sahnoun https://jneonatalsurg.com/ojs/index.php/jns/article/view/1255 Apple-Peel intestinal atresia: A systematic review 2023-10-04T22:15:33-04:00 Francesco Laconi flaconi@chu-reims.fr Charline Bischoff cbischoff@chu-reims.fr Theo Michailos theo.michailos@gmail.com Ongoly Okiemy M'Inserret omiokiemy@chu-reims.fr Emmanuelle Kremer emmanuelle.kremer@univ-reims.fr Marie-Laurence Poli-Merol mlpolime@chu-reims.fr <p>Background: Apple-peel bowel atresia (APA) is rare and thus lacks proper management guidelines. This systematic review analyzes various interventions found in the literature for this type of atresia and highlights the outcomes of each intervention with their complications.</p> <p>Methods: The relevant literature on PubMed, Scopus, Embase, and Cochrane was reviewed from November 2020 to January 2021. Articles published in English, French, Italian, or Spanish between 1990 and 2020, focusing on APA, were included. Data on demography, clinical profile, management provided, time to achieve full feed, length of hospital stay, complications, etc., reviewed.</p> <p>Results: A total of 2495 articles were found, of which only 48 met the inclusion criteria. Among these, 125 patients were treated, with 15 deaths. The most frequently employed intervention was primary resection, with or without tapering, while ostomy creation was less commonly used. The most frequent complication across all techniques appeared to be cholestasis, followed by stenosis of the anastomosis and sepsis. Additionally, there were a total of 7 cases of short bowel syndrome (SBS).</p> <p style="font-weight: 400;">Conclusion: The management of apple-peel atresia seems variable in various centers of different countries. The review failed to assess which interventions could lead to faster full enteral feeding. The distal part of the anastomosis must be considered as an active part in the resumption of bowel function.</p> 2024-05-14T00:00:00-04:00 Copyright (c) 2023 Francesco Laconi, Charline Bischoff, Theo Michailos, Ongoly Okiemy M'Inserret, Emmanuelle Kremer, Marie-Laurence Poli-Merol https://jneonatalsurg.com/ojs/index.php/jns/article/view/1253 Inguinal hernia repair in newborns: A systematic literature review 2023-10-27T08:07:22-04:00 Rachida Lamiri lamiri.rachida@yahoo.fr Fatma Chebab fatmachebab902017@gmail.com Nahla Kechiche kechichenahla@gmail.com Salma Mani salmamanihs@hotmail.com Hayet Ben Hmida benhamidahayet@yahoo.fr Maroua El Ouaer maroua.elouaer.b@gmail.com Sawsen Chakroun sawsenchakroun1@gmail.com Amine Ksia amineks@yahoo.fr Mongi Mekki mongi_mekki@yahoo.fr Mohsen Belghith belghithmohsen.58@gmail.com Nahla Hmidi nh.nahlahamdi@gmail.com Lassaad Sahnoun slassaad13@gmail.com <p>Background: Inguinal hernia (IH) is a prevalent condition in children necessitating surgical repair. However, determining the optimal timing (early or delayed) of inguinal herniotomy in neonates and preterm infants remains debatable. While open herniotomy traditionally serves as the standard inguinal hernia repair (IHR) procedure, laparoscopic repair has gained traction in recent decades. Our study aims to scrutinize both the optimal timing and approach to inguinal hernia repair in neonates and preterm infants.</p> <p>Methods: We conducted a literature review on surgical repair of IH in neonates and preterm infants published between 1999 and 2024.</p> <p>Results: Twenty studies met the inclusion criteria for this review. All studies were retrospective, predominantly originating from Europe and the United States. Thirteen out of the 20 studies focused solely on preterm infants. Patient sample sizes ranged from 30 to 8037, totaling 14533 patients. Most studies indicate that delaying inguinal hernia repair in newborns and preterm infants does not increase the risk of incarceration or recurrence. Moreover, postponing repair until after discharge from the NICU correlates with a shorter postoperative hospital stay and notably diminishes the risk of long-term postoperative ventilator dependence, thereby mitigating potential perioperative complications. Hence, this approach seems safe for certain patients whose families can reliably access appropriate surgical care.</p> <p>Conclusion: Significant disparities exist in the timing of inguinal hernia repair for newborns and preterm infants across various pediatric surgery centers. Current evidence suggests delayed inguinal hernia repair may be a viable option for selected patients. Regarding the optimal approach in this population, laparoscopy appears safe and effective.</p> 2024-05-20T00:00:00-04:00 Copyright (c) 2023 Rachida Lamiri, Fatma Chebab, Nahla Kechiche , Salma Mani, Hayet Ben Hmida, Maroua El Ouaer, Sawsen Chakroun, Amine Ksia, Mongi Mekki, Mohsen Belghith, Nahla Hmidi, Lassaad Sahnoun https://jneonatalsurg.com/ojs/index.php/jns/article/view/1242 Gastric perforation in neonates: Our experience 2023-08-30T20:37:10-04:00 Fransua Sharafeddin fransuasharafeddin@llu.edu Brandon Edelbach bedelbach@students.llu.edu Alexandra Vacaru alexandravacaru@students.llu.edu Georgi Mladenov gmladenov@llu.edu Donald Moores dmoores@llu.edu Yogen Singh ysingh@llu.edu Andrei Radulescu aradulescu@llu.edu <p>Background: Neonatal gastric perforation (NGP) is a life-threatening condition with a high mortality rate. It accounts for 7% of all gastrointestinal tract (GIT) perforations. The number of NGP cases has been increasing due to the rise in premature and low birth weight neonates. In this study, we present our experience with gastric perforation in neonates.</p> <p>Methods: This retrospective study analyzed all cases of gastric perforation in neonates that were treated at Loma Linda University Medical Center's Neonatal Intensive Care Unit (NICU) between the years 2000 and 2023. The study looked at several variables including patient demographics, birth weight, age at admission and surgery, comorbidities, use of non-steroidal anti-inflammatory drugs (NSAIDs) and steroids, and mortality rate.</p> <p>Results: We treated 15 patients with neonatal gastric perforation (NGP) during the study tenure. The median age at admission was 2 days, with 67% admitted within that timeframe. Surgery occurred at a median age of 5.5 days, and the median birth weight was 2.075 kg, with 26.67% below 1 kg. Males comprised 67%, and 60% had patent ductus arteriosus. Steroids were given to 46.66%, and 30-day mortality was 26.67%, with higher rates among males. Idiopathic cases were common, with notable etiologies including ischemia, necrosis, and congenital anomalies. Primary surgical repair was the main modality, and perforations occurred at various locations. Two cases had necrotizing enterocolitis. Six patients had favorable outcomes, while others experienced mild to moderate complications.</p> <p style="font-weight: 400;">Conclusion: Our research supports the idea that males have a worse outcome in terms of both prevalence and survival rates in neonatal gastric perforation (NGP) patients. However, our findings did not confirm the notion that NGP mortality risk is higher in neonates with low birth weight. We also discovered that the median time between admission and surgery in our study group was 1.5 days, emphasizing the importance of early detection of NGP in neonates. Early diagnosis can lead to better decision-making regarding treatment options and surgical intervention.</p> 2023-12-31T00:00:00-05:00 Copyright (c) 2023 Fransua Sharafeddin, Brandon Edelbach, Alexandra Vacaru, Georgi Mladenov, Donald Moores, Yogen Singh, Andrei Radulescu https://jneonatalsurg.com/ojs/index.php/jns/article/view/1240 Somatostatin analog (octreotide) and sirolimus immunosuppressive therapy in the treatment of chyloperitoneum and chylothorax in newborns and infants 2023-08-30T20:37:52-04:00 A Gurskaya gurskaya.as@nczd.ru M Sulavko sulavko.ma@nczd.ru E Ekimovskaya ekimovskaia.ev@nczd.ru R Bayazitov bayazitov.rr@nczd.ru O Nakovkin nakovkin.on@nczd.ru I Karnuta karnuta.iv@nczd.ru A Klepikova klepikova.aa@nczd.ru D Akhmedova akhmedova.dm@nczd.ru R Hagurov hagurov@gmail.com G Sagoyan sagoyan-garik@mail.ru <p>Background: Chyloperitoneum (CP) and chylothorax (CT) are rare conditions that have a high mortality rate and unclear treatment options. Their incidence in neonates ranges from 1 in 20000 to 1 in 187000 live births. This study aims to evaluate the effectiveness of synthetic somatostatin analog (octreotide) and sirolimus therapy in treating chylous pleural and peritoneal collections in newborns and infants.</p> <p>Methods: We conducted a retrospective analysis of 10 children with either chylothorax or chyloperitoneum, treated in our department between 2018 and 2023. The study was approved by the Local Independent Ethics Committee of The National Medical Research Center of Children's Health, under Protocol №7, dated 11 May 2023. The parents voluntarily signed an informed consent form for the off-label use of the drug. We reviewed the medical records for demographic information, clinical presentation, management, and outcome.</p> <p>Results: Our study looked at patients aged between 0 and 5.5 months, with seven cases of chyloperitoneum and three cases of chylothorax. We initially used octreotide, which was then switched to sirolimus if there was no improvement. Octreotide was effective in five children after 10-18 days of treatment, while the effect of sirolimus was observed 8-14 days after starting treatment. One patient, who had a history of a giant omphalocele with primary closure, experienced complications after 8 weeks of sirolimus therapy, including bilateral knee arthritis, leukopenia, and lymphopenia. Fortunately, there were no fatal outcomes.</p> <p>Conclusion: Sirolimus therapy is effective in treating newborns with chylothorax or chyloperitoneum, with a low risk of complications even in those cases not responding to octreotide therapy. It is recommended that octreotide therapy should not exceed 10 days, after which sirolimus can be prescribed.</p> 2024-01-03T00:00:00-05:00 Copyright (c) 2023 Aleksandra Gurskaya, Mariya Sulavko, Ekaterina Ekimovskaya, Rimir Bayazitov, Oleg Nakovkin, Inna Karnuta, Anna Klepikova, Dinara Akhmedova, Ruslan Hagurov, Garik Sagoyan, Yelena Dyakonova, Andrey Fisenko https://jneonatalsurg.com/ojs/index.php/jns/article/view/1250 The outcomes of specific surgically correctable congenital gastro-intestinal malformations at a tertiary level neonatal intensive care unit in South Africa 2023-10-15T00:56:40-04:00 Ilhaam Abrahams ilhaama@sun.ac.za Lizelle Van Wyk lizelle@sun.ac.za Corne De Vos cdevos@sun.ac.za <p>Background: The outcome of neonates with congenital surgically correctable gastro-intestinal (GIT) malformations is poorly described in low middle income countries.</p> <p>Methods: A 5-year retrospective descriptive analysis of neonates admitted to a tertiary level neonatal intensive care unit (NICU), with congenital, surgically correctable GIT malformations, was performed. The primary outcome was the 30-day postoperative mortality as well as survival to 1 year. Secondary outcomes included patient demographics, clinical presentation as well as the burden of disease in our study population.</p> <p>Results: Eighty-four neonates met study criteria. The mean gestational age was 35 weeks (SD 3.19) and birthweight 2518g (SD 789.3). The most common congenital malformations were intestinal atresia (39%) followed by omphaloceles (21%). Associated systemic malformations were common (39%). The majority of neonates (88%) underwent surgery at a median age of 2 days (IQR 1.5-5). Ventilation was required in 19% of neonates preoperatively and 65% postoperatively. Full feeds were achieved at a median age of 13 days (IQR 9-18) after surgery. The 30 day-postoperative survival rate was 97% with a survival to discharge or transfer of 86%. Data for one year survival was available for 80% of neonates with a one-year survival rate of 75%.</p> <p>Conclusion: The 30-day postoperative survival was high in neonates with congenital, surgically correctable GIT malformations. Outcomes and burden on the healthcare system was dependent on the type of lesion. With early diagnosis and referral to a tertiary centre, good outcomes can be achieved. Neonates with congenital GIT malformations should have long term follow up to monitor growth and neurodevelopment as well as to address the high mortality post discharge.</p> 2023-12-31T00:00:00-05:00 Copyright (c) 2023 Dr Ilhaam Abrahams, Prof Lizelle Van Wyk, Dr Corne De Vos https://jneonatalsurg.com/ojs/index.php/jns/article/view/1275 Predictors of postoperative mortality among neonates after major-risk surgery: A one-year experience from a Tunisian hospital 2023-11-29T22:54:53-05:00 Manel Kammoun manelkammoun6@gmail.com Anouar jarraya jarraya_anouar@medecinesfax.org Hechem bradai hechembradi4@gmail.com Hind ketata ketatahind@gmail.com Hasna Bouchaira hasna_bouchaira@medecinesfax.org Olfa Cherif olfa.cherif96@gmail.com Amel Ben Hamed benhamad.amel@gmail.com Faiza Safi faiza.safi@gmail.com Riadh Mhiri riadh.mhiri@rns.tn <p>Background: Neonatal surgery in developing countries remains a high-risk modality p and its outcomes depend on various patient-related, system-related, and management-related factors. This study aims to describe our experience in managing newborns requiring surgical interventions and to investigate the primary predictors of postoperative mortality.</p> <p>Methods: In this observational study, we included all newborns aged less than 28 days who underwent surgery in the pediatric surgery department under general anesthesia with tracheal intubation for major-risk surgery. Patients were categorized into two groups based on the outcome (survival or death) during the two months following surgery. Following a comparison of the two groups, univariable and multivariable logistic regression analyses were conducted to explore predictors of perioperative mortality among neonates.</p> <p>Results: Sixty-seven newborns were included in this study, with an early mortality incidence of 28.3%. Anesthesia management did not impact neonatal mortality. The main predictors of neonatal mortality were revision surgery [aOR=35.5; 95% CI: 1.33- 94.1], surgery duration ≥ 120 minutes [aOR=36.5; 95% CI: 1.48- 312], preoperative mechanical ventilation [aOR=3.88; 95% CI: 1.12- 30.8], and the occurrence of perioperative adverse events [aOR=5.7; 95% CI: 1–29.5] or postoperative surgical complications [aOR=32.5; 95% CI: 1.05–101].</p> <p>Conclusion: The early mortality rate after major neonatal surgery remains high in our department. It appears that preoperative poor conditions can elevate the risk. Additionally, major-risk surgeries requiring prolonged procedures and revision surgery, along with the incidence of postoperative infections, significantly increase the risk of neonatal mortality.</p> 2023-12-31T00:00:00-05:00 Copyright (c) 2023 Manel Kammoun, Anouar jarraya, Hechem bradai, Hind ketata, Hasna Bouchaira, Olfa Cherif, Amel Ben Hamed, Faiza Safi, Riadh Mhiri https://jneonatalsurg.com/ojs/index.php/jns/article/view/1306 Attrition rate among patients of Anorectal Malformations on colostomy: A matter of concern 2024-03-17T03:18:39-04:00 Parveen Kumar parveenkumar_maan@yahoo.co.in Sauradeep Dey deysauradeep@gmail.com Ashvin Damdoo ashvindam23@gmail.com Shishir Kumar shishirjha1610@gmail.com Vivek Manchanda vivek_7477@hotmail.com <p>Background: Anorectal malformations (ARM) are correctable congenital malformations with good prognosis. Traditionally it is managed by staged procedure, with diversion colostomy, followed by definitive procedure and stoma reversal in the third stage. It is recommended to complete all stages of repair by 6 months of age for better long-term continence. We had fewer patients coming for definitive surgery and stoma reversal than the patients undergoing colostomy for ARM, so we planned this study to find out the attrition rate among patients undergoing stoma for ARM and explore the reasons for the same.</p> <p>Methods: An observational study was conducted in the Pediatric Surgery department of Chacha Nehru Bal Chikitsalaya, New Delhi. All the case records of patients with ARM who underwent diversion stoma at our center from January 2018 to December 2019 were retrieved. Further follow-up case records were retrieved with the same Unique Health Identification Number (UHID). When the definitive surgery/ stoma closure was not found in the hospital records till December 2022, the parents were contacted telephonically to find out if the children had undergone definitive surgery at some other center, were awaiting surgery, or had died. The attrition was calculated as the difference between the number of patients for whom a stoma was done and the number of patients who underwent definitive surgery and stoma closure till the data acquisition.</p> <p>Results: A total of 105 patients were included in the study with male preponderance. Colostomy was done for 73.33% of patients in the neonatal period (77/105). The cloacal malformation was found in 7 (6.67%), rectal atresia in 6 (5.71%), and 9 had congenital pouch colon (8.57%). The age at stoma creation for ARM ranged from 1 day to 9.3 years (mean 0.67 ±1.96 years). Cardiac and renal anomalies were among the major associations. 28 of the neonates (26.67%) had stomal complications. Stomal issues were reported in 32.4%. Mortality was reported in 37 patients (35.24%) including 35 neonates. The attrition rate in our study was found to be 38.24% (26 out of 68). Factors contributing to attrition range from anemia and protracted waiting lists to the anesthesiologist’s pursuit of optimal patient stabilization, alongside familial or personal matters faced by caregivers.</p> <p>Conclusion: There was a high attrition rate in operated patients of ARM in whom stoma was constructed. The main reasons for the same were anemia and a long surgical waiting list.</p> 2024-05-06T00:00:00-04:00 Copyright (c) 2023 Parveen Kumar, Sauradeep Dey, Ashvin Damdoo, Shishir Kumar, Vivek Manchanda https://jneonatalsurg.com/ojs/index.php/jns/article/view/1258 Second-look surgery in a patient of malrotation with midgut volvulus 2023-11-09T13:35:13-05:00 Survesh Kumar Gupta surveshkg@gmail.com Anand Pandey dranand27@rediffmail.com Rahul Kumar Rai drrahul2004@gmail.com Nirpex Tyagi drnirpekshtyagi@yahoo.in 2024-01-03T00:00:00-05:00 Copyright (c) 2023 Survesh Kumar Gupta, Anand Pandey, Rahul Kumar Rai, Nirpex Tyagi https://jneonatalsurg.com/ojs/index.php/jns/article/view/1270 A case of anorectal malformation with human tail 2023-10-23T17:39:28-04:00 Omar Ajaj abd.o85@yahoo.com 2023-12-31T00:00:00-05:00 Copyright (c) 2023 Omar Ajaj https://jneonatalsurg.com/ojs/index.php/jns/article/view/1247 Neutrophil to Lymphocyte ratio: A promising tool in neonatal appendicitis diagnosis 2023-09-04T13:02:24-04:00 Emine Burcu Cigsar Kuzu ebcigsar@gmail.com 2023-12-31T00:00:00-05:00 Copyright (c) 2023 Emine Burcu Cigsar Kuzu https://jneonatalsurg.com/ojs/index.php/jns/article/view/1261 Staged repair of esophageal atresia, tracheoesophageal fistula, and duodenal atresia in a newborn 2023-11-03T02:06:58-04:00 Christos Tsakalidis tsakalidisx@gmail.com Maria Lithoxopoulou mlithoxopoulou@yahoo.com Nikolaos Gkiourtzis gkiourtzisnikolaos@gmail.com Eftychia Drogouti edrogouti@yahoo.com Vassilios Mouravas vmouravas@auth.gr Ioannis Spyridakis ispyrida@auth.gr Elisavet Diamanti diamanti.veta@gmail.com 2024-01-14T00:00:00-05:00 Copyright (c) 2023 Christos Tsakalidis, Maria Lithoxopoulou, Nikolaos Gkiourtzis, Eftychia Drogouti, Vassilios Mouravas, Ioannis Spyridakis, Elisavet Diamanti https://jneonatalsurg.com/ojs/index.php/jns/article/view/1292 Caudal regression syndrome in a newborn in distress: A therapeutic challenge 2024-01-17T11:43:53-05:00 Rachida Lamiri lamiri.rachida@yahoo.fr Ghada Habachi habachighada92@gmail.com Nahla Kechiche kechichenahla@gmail.com Meriem Oumaima Beji meriemoumaimabeji@gmail.com Hayet Ben Hmida benhamidahayet@yahoo.fr Amine Ksia amineks@yahoo.fr Mongi Mekki mongi_mekki@yahoo.fr Lassaad Sahnoun slassaad13@gmail.com 2024-02-26T00:00:00-05:00 Copyright (c) 2023 Rachida Lamiri, Ghada Habachi, Nahla Kechiche , Meriem Oumaima Beji, Hayet Ben Hmida, Amine Ksia, Mongi Mekki, Lassaad Sahnoun https://jneonatalsurg.com/ojs/index.php/jns/article/view/1320 Palatal teratoma in a 1-day-old full-term female neonate 2024-04-04T00:24:34-04:00 Nousheen Ilyas drnousheenilyas@gmail.com Bilal Arshad dr_bilal.arshad@yahoo.com Faryal Ilyas Jhammat faryal.iqbal@hotmail.com Ali Ayyaz Kirmani drnousheenilyas@gmail.com Ahmed Imran drnousheenilyas@gmail.com Abeera Asad Rasool drnousheenilyas@gmail.com 2024-05-28T00:00:00-04:00 Copyright (c) 2023 Nousheen Ilyas, Bilal Arshad, Faryal Ilyas Jhammat, Ali Ayyaz Kirmani, Ahmed Imran, Abeera Asad Rasool https://jneonatalsurg.com/ojs/index.php/jns/article/view/1252 Amyand hernia with perforated appendix simulating as testicular torsion in a neonate: A case report 2023-09-04T13:00:03-04:00 Obay Edan obayabdedaan@uomosul.edu.iq <p>Background: Amyand hernia is defined as the presence of the vermiform appendix within the hernial sac. A perforated appendix is an uncommon complication of Amyand hernia. Rarely it may simulate a testicular torsion.</p> <p>Case Presentation: A twenty-five-day-old male infant presented with right-sided scrotal swelling, exhibiting symptoms of crying, irritability, and poor feeding over a two-day duration. The swelling was non-reducible, confined to the scrotum, and the spermatic cord showed thickening with erythematous scrotal skin. Following preparation, an inguinal incision was made, and an appendectomy and herniotomy were performed.</p> <p>Conclusion: Amyand hernia, a rare type of inguinal hernia, poses challenges in preoperative diagnosis. The occurrence of a perforated appendix is especially rare in neonates with Amyand hernia. Surgical management entails appendectomy through an inguinal incision coupled with meticulous hernia repair.</p> 2023-12-31T00:00:00-05:00 Copyright (c) 2023 Obay Edan https://jneonatalsurg.com/ojs/index.php/jns/article/view/1282 Jarcho Levin Syndrome with open neural tube defect: A case report 2024-01-25T11:39:39-05:00 Md Mokarram Ali mohdmokarramali1990@gmail.com Yogender Singh Kadian yogarin@gmail.com Saima Ejaz saimaejaz2011@gmail.com Arnav Kadian arnavkadian@gmail.com <p>Background: Jarcho Levin syndrome is a rare genetic disorder characterized by spine abnormalities and the absence of ribs. It is associated with various congenital malformations and carries significant morbidity and mortality. The simultaneous presentation of this syndrome with neural tube defects is seldom encountered.</p> <p>Case Presentation: We report a case of a 2-day-old male who presented with a lesion on his back since birth. Clinical and radiological examinations revealed thoracolumbar meningomyelocele with the absence of upper ribs on the right side and a patent foramen ovale. Subsequently, the patient underwent surgery for meningomyelocele, while the rib anomalies were managed conservatively.</p> <p>Conclusion: Jarcho Levin syndrome is a rare disorder, and its association with meningomyelocele is extremely uncommon. It should be considered in the evaluation of a patient with a neural tube defect and respiratory distress.</p> 2024-02-26T00:00:00-05:00 Copyright (c) 2023 Md Mokarram Ali, Yogender Singh Kadian, Saima Ejaz, Arnav Kadian https://jneonatalsurg.com/ojs/index.php/jns/article/view/1244 Double-blind ureteral duplication- a rare cause of a neonatal abdominal cyst: A case report 2023-11-09T13:38:38-05:00 Maria Vittoria Stern mariavittoria.stern@gmail.com Filomena Valentina Paradiso filomenavalentina.paradiso@policlinicogemelli.it Riccardo Rizzo riccardo.rizzo@policlinicogemelli.it Sara Silvaroli sara.silvaroli@policlinicogemelli.it Francesco Pierconti mariavittoria.stern@gmail.com Lorenzo Nanni lorenzo.nanni@policlinicogemelli.it <p>Background: Double-blind ureteral duplication (DBUD) is a rare condition in which one of the ureters in a duplicated system has no communication with the bladder or the renal pelvis.</p> <p>Case Presentation: We present a neonatal case of DBUD in a newborn girl, associated with a non-functional kidney, initially identified as an abdominal cystic anechoic mass during antenatal ultrasound. A stepwise diagnostic and management approach was undertaken, including prenatal and postnatal imaging, multidisciplinary consultation, and surgical intervention.</p> <p>Conclusion: Establishing a diagnosis of DBUD requires a systematic approach, incorporating comprehensive prenatal and postnatal assessments. This case is the first reported instance of DBUD diagnosed and treated in the neonatal period, highlighting the importance of early detection and intervention.</p> 2024-05-30T00:00:00-04:00 Copyright (c) 2023 Maria Vittoria Stern, Filomena Valentina Paradiso, Riccardo Rizzo, Sara Silvaroli, Francesco Pierconti, Lorenzo Nanni https://jneonatalsurg.com/ojs/index.php/jns/article/view/1305 Unveiling neonatal intestinal obstruction due to total colonic atresia: A case report 2024-03-10T10:19:40-04:00 Fawad Mueen Arbi fawad.arbi@gmail.com Muhammad Zulfiqar Anjum zulfiqar_anjum@yahoo.com Zeeshan Iqbal zhenzmars@gmail.com Seerat Fatima seeratf042@gmail.com <p>Background: Total colonic atresia is an uncommon congenital anomaly associated with neonatal intestinal obstruction, often necessitating prompt diagnosis and surgical intervention to prevent life-threatening complications. Understanding the etiology and optimal management strategies is crucial for ensuring favorable outcomes.</p> <p>Case Presentation: We present a case of a full-term male neonate with total colonic atresia, who presented with failure to pass meconium, abdominal distension, and vomiting. Diagnostic imaging confirmed intestinal obstruction, leading to surgical exploration revealing an atretic colon extending from the Ileocolic Junction to the Rectosigmoid Junction. An ileostomy was performed, followed by meticulous postoperative care, resulting in a successful resolution of symptoms and discharge from the hospital.</p> <p>Conclusion: Timely recognition and staged surgical management are paramount in addressing total colonic atresia, emphasizing the importance of early intervention for optimal patient outcomes. Long-term follow-up and comprehensive care are essential to ensure the overall well-being of affected newborns.</p> 2024-04-26T00:00:00-04:00 Copyright (c) 2023 Fawad Mueen Arbi, Muhammad Zulfiqar Anjum, Zeeshan Iqbal, Seerat Fatima https://jneonatalsurg.com/ojs/index.php/jns/article/view/1243 A remarkable case of intrauterine intussusception, ileal atresia, and complicated meconium ileus: A case report 2023-10-22T10:50:20-04:00 Jonathan Hencke j.hencke@klinikum-stuttgart.de Oliver Diez o.diez@klinikum-stuttgart.de Steffan Loff s.loff@klinikum-stuttgart.de <p>Background: Intrauterine intussusception, although very rare (&lt;2%), is a potential cause of intestinal atresia. It usually manifests as bowel obstruction during the first hours or days of life.</p> <p>Case Presentation: We report a case with fetal ascites prompting early Cesarean section, with subsequent percutaneous abdominal drainage and laparotomy. Intraoperative findings showed meconium peritonitis and type IIIa ileal atresia with intussusception of the distal part, with the necrosed intussusceptum likely causing perforation and ileal atresia; in addition, the distal ileum demonstrated signs of meconium ileus. After ileostomy creation, the postoperative course was uneventful. Cystic fibrosis was excluded via a sweat test.</p> <p>Conclusion: Prompt diagnosis and management of neonatal intestinal obstruction secondary to the unusual combination of fetal ascites, intussusception, complicated meconium ileus, and ileal atresia results in a favorable outcome.</p> 2024-05-07T00:00:00-04:00 Copyright (c) 2023 Jonathan Hencke, Oliver Diez, Steffan Loff https://jneonatalsurg.com/ojs/index.php/jns/article/view/1225 Perioperative fluid and electrolyte management in surgical neonates 2023-08-30T20:41:57-04:00 Nitin James Peters nitinjamespeters@yahoo.com Shivani Dogra shivanidogra2003@yahoo.com Sandhya Yaddanapudi sandhya.yaddanapudi@gmail.com Jai Kumar Mahajan jkmahajan@gmail.com <p>Neonates with surgical conditions may experience significant electrolyte abnormalities and dehydration of varying degrees. Increased awareness of perioperative hyponatremia and its associated morbidity has led to a shift in Pediatric fluid guidelines favoring the use of isotonic fluids. However, there is a lack of evidence-based guidelines for neonatal perioperative fluid administration, resulting in the extrapolation of fluid management principles from adults and children. This article reviews perioperative neonatal fluid management.</p> 2023-12-31T00:00:00-05:00 Copyright (c) 2023 Nitin James Peters, Shivani Dogra, Sandhya Yaddanapudi, Jai Kumar Mahajan https://jneonatalsurg.com/ojs/index.php/jns/article/view/1290 On the curious association of diaphragmatic hernia and Urban-Rifkin-Davis Syndrome (Autosomal Recessive Cutis Laxa-1C): A collective review of 16 cases 2024-01-16T14:32:07-05:00 V Raveenthiran vrthiran@yahoo.co.in Nagarajan Darun darunsai@gmail.com Dhayalan Pavithra pavithra.dh@lifecell.in Prakash Gambhir drprakash.s@lifecell.in <p style="font-weight: 400;"><span style="font-weight: 400;">Background: Autosomal recessive cutis laxa type-1C is also known as Urban-Rifkin-Davis syndrome (URDS). It is known to affect cardiopulmonary, integumentary, gastrointestinal, musculoskeletal and genitourinary systems. However, its frequent association with congenital diaphragmatic hernia has not previously been highlighted.</span></p> <p style="font-weight: 400;"><span style="font-weight: 400;">Case Presentation: A newborn male with cutis laxa presented with respiratory distress at birth. The cause of dyspnoea was perinatal strangulation of the stomach in hiatus hernia. After surgical repair of the hernia, his respiratory distress temporarily improved but kept recurring periodically by various mechanisms in sequence namely pulmonary hypertension, tracheomalacia, pulmonary emphysema and finally he succumbed to pneumothorax. Genetic analysis revealed his skin condition as autosomal recessive cutis laxa type-1C which is also known as URDS. Exome sequencing revealed a novel frameshift mutation c.426delC (p.Cys143Alafs*41) of the LTBP4 gene in the exon 5 of Chromosome 19. </span></p> <p style="font-weight: 400;"><span style="font-weight: 400;">Conclusion: Out of the 28 cases of URDS reported in the world literature 57% had congenital diaphragmatic hernia (CDH) and 53% of them died during infancy. Such a high incidence of CDH is not observed in other subtypes of elastic disorders. Thus, congenital diaphragmatic defects appear to be a characteristic diagnostic feature of URDS in patients with cutis laxa.</span></p> 2024-03-22T00:00:00-04:00 Copyright (c) 2023 V Raveenthiran, Nagarajan Darun, Dhayalan Pavithra, Prakash Gambhir https://jneonatalsurg.com/ojs/index.php/jns/article/view/1291 Scrotoschisis: Review in clinical and embryological perspective of a rare anomaly 2024-01-18T12:18:15-05:00 Erjan Fikri erjan.fikri@usu.ac.id Ahmad Razi Maulana Alnaz ahmadrazima@gmail.com Aqyl Hanif Abdillah aqyl.abdillah@gmail.com Salsabila Az-Zahra salsabila499@gmail.com <p>Scrotoschisis is a rare congenital anomaly affecting the scrotum and testes, characterized clinically by a defect in the scrotal wall and extrusion of testicular tissue. This literature review is based on reports gathered from PubMed, Science Direct, and Google Scholar using relevant keywords to explore the underlying basic science of this rare condition. The etiology and mechanism of scrotoschisis development remain largely unknown, with only theoretical explanations and a lack of empirical evidence regarding its pathogenesis, which is thought to be linked to embryological abnormalities during scrotal formation. Diagnosing scrotoschisis typically involves a straightforward visual examination of the extruded testes immediately after birth, although clinical presentations may vary, being either unilateral or bilateral. Surgical intervention, primarily through orchidopexy, is generally beneficial for repositioning the testes, closing defects, and preventing potential complications. The prognosis for individuals with this anomaly is generally favorable, although long-term testicular function has been inadequately documented. Further research, including additional clinical reports and investigations involving animal models or embryological studies, is warranted to enhance our understanding of this condition.</p> 2024-03-25T00:00:00-04:00 Copyright (c) 2023 Erjan Fikri, Ahmad Razi Maulana Alnaz, Aqyl Hanif Abdillah, Salsabila Az-Zahra https://jneonatalsurg.com/ojs/index.php/jns/article/view/1280 Artificial intelligence and writing: What ChatGPT says? 2023-12-04T10:54:12-05:00 Muhammad Bilal Mirza blmirza@gmail.com 2023-12-31T00:00:00-05:00 Copyright (c) 2023 Muhammad Bilal Mirza