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Journal articles on the topic 'Duodenoduodenostomi'

Author: Grafiati

Published: 5 June 2025

Last updated: 15 July 2025

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1

Saraç, Ahmet, Abdi Abdishakur Mohamed, Mohamed Shukri Said, Adan Mesut Kayse, and Ali Abdullahi Yusuf. "A Rare Cause of Congenital Duodenal Obstruction: Preduodenal Portal Vein." Life and Medical Sciences 1, no. 1 (2020): 33–35. https://doi.org/10.54584/lms.2022.7.

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<strong>Abstract</strong> Preduodenal portal vein (PDPV) is a rare cause of duodenal obstruction. While half of PDPV cases present with obstructive findings in the neonatal period, the other half are diagnosed incidentally at advanced ages. In half of the obstructed PDPV cases, the cause of obstruction is another congenital anomaly. In our case, the aberrant ventral extension of the pancreas with PDPV caused incomplete duodenal obstruction by compressing the duodenum externally. <strong>Özet</strong> Preduodenal portal ven (PDPV), duodenal tıkanıklığın nadir bir n

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2

Saraç, Ahmet, Abdi Abdishakur Mohamed, Mohamed Shukri Said, Adan Mesut Kayse, and Ali Abdullahi Yusuf. "A Rare Cause of Congenital Duodenal Obstruction: Preduodenal Portal Vein." Life and Medical Sciences 1, no. 1 (2020): 33–35. https://doi.org/10.5281/zenodo.5656761.

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<strong>Abstract</strong> Preduodenal portal vein (PDPV) is a rare cause of duodenal obstruction. While half of PDPV cases present with obstructive findings in the neonatal period, the other half are diagnosed incidentally at advanced ages. In half of the obstructed PDPV cases, the cause of obstruction is another congenital anomaly. In our case, the aberrant ventral extension of the pancreas with PDPV caused incomplete duodenal obstruction by compressing the duodenum externally. <strong>Özet</strong> Preduodenal portal ven (PDPV), duodenal tıkanıklığın nadir bir nedenidir. Yenidoğan d&oum

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3

Gunasekaran, Ganesh, Alvin Wee, John Rabets, Charles Winans, and Venkatesh Krishnamurthi. "Duodenoduodenostomy in pancreas transplantation." Clinical Transplantation 26, no. 4 (2011): 550–57. http://dx.doi.org/10.1111/j.1399-0012.2011.01563.x.

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4

Kay, Saundra, Suzanne Yoder, and Steve Rothenberg. "Laparoscopic duodenoduodenostomy in the neonate." Journal of Pediatric Surgery 44, no. 5 (2009): 906–8. http://dx.doi.org/10.1016/j.jpedsurg.2009.01.025.

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5

Balasubramanian, Satya, Madhu Ramasundaram, and Jegadeesh Sundaram. "Congenital duodenal obstruction due to duodenal atresia along with annular pancreas, intestinal malrotation and preduodenal portal vein." BMJ Case Reports 18, no. 2 (2025): e264877. https://doi.org/10.1136/bcr-2025-264877.

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A newborn delivered by emergency lower segment caesarean section at 35 weeks of gestation suspected duodenal atresia antenatally with maternal ultrasonogram showing double bubble sign. After birth, the baby was stabilised and taken up for laparotomy and was found to have duodenal atresia along with intestinal malrotation, annular pancreas and preduodenal portal vein (PDPV). Ladd’s procedure with Kimura’s duodenoduodenostomy was performed. In a similar previously reported case study, a gastrojejunostomy was conducted;5here, we were able to do a duodenoduodenostomy which is a better physiologica

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6

Peterson, Danielle M., Eric M. Pauli, and Kathryn L. Martin. "Endoscopic visualization of annular pancreas after duodenoduodenostomy." VideoGIE 5, no. 1 (2020): 22–23. http://dx.doi.org/10.1016/j.vgie.2019.09.004.

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7

Oh, Chaeyoun, Sanghoon Lee, Suk-Koo Lee, and Jeong-Meen Seo. "Laparoscopic duodenoduodenostomy with parallel anastomosis for duodenal atresia." Surgical Endoscopy 31, no. 6 (2016): 2406–10. http://dx.doi.org/10.1007/s00464-016-5241-y.

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8

Rusu, Simona, Ahmad Zaghal, and Muhammad Choudhry. "Surgical Decision Making in Preduodenal Portal Vein: Report of Two Cases in Neonates." European Journal of Pediatric Surgery Reports 06, no. 01 (2018): e40-e42. http://dx.doi.org/10.1055/s-0038-1661409.

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AbstractPreduodenal portal vein (PDPV) is a rare anomaly that can cause duodenal obstruction. PDPV is associated with other congenital anomalies, mainly cardiac and gastrointestinal. Treatment usually consists of bypassing the obstruction by duodenoduodenostomy. We report two cases of PDPV in association with atrial isomerism and malrotation with different surgical management.

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9

Habib, Zakaria, Muhammad Awan, and Mila Kolar. "Laparoscopic Duodenoduodenostomy in a Newborn with Situs Inversus Totalis." Journal of Laparoendoscopic & Advanced Surgical Techniques 18, no. 4 (2008): 654–56. http://dx.doi.org/10.1089/lap.2007.0201.

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10

Greenfeld, Jonathan I., and Arnold G. Coran. "Duodenoduodenostomy for congenital obstruction of the duodenum in infants." Operative Techniques in General Surgery 2, no. 4 (2000): 283–86. http://dx.doi.org/10.1053/otgn.2000.19146.

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11

Badiola, Izaskun, Eva Las Navas, Amaia Sanz, Begoña Estraviz, and Francisco Javier Ibañez. "Laparoscopic Side-to-Side Duodenoduodenostomy for Adult Annular Pancreas." Cirugía Española (English Edition) 92, no. 9 (2014): 630–31. http://dx.doi.org/10.1016/j.cireng.2013.05.010.

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12

Rothenberg, Steven S. "Laparoscopic duodenoduodenostomy for duodenal obstruction in infants and children." Journal of Pediatric Surgery 37, no. 7 (2002): 1088–89. http://dx.doi.org/10.1053/jpsu.2002.33882.

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13

Mahmood Mosa Mahmood, Alaa Mohammed Ali Al Baazi, and Athir Ahmed Kadium. "Management of Congenital Duodenal Obstruction by Diamond-Shaped Duodenoduodenostomy." Indian Journal of Forensic Medicine & Toxicology 15, no. 3 (2021): 772–77. http://dx.doi.org/10.37506/ijfmt.v15i3.15404.

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A prospective study of 20 patients with clinical diagnosis of duodenal obstruction done at pediatric surgery center in AL Khanssa maternity and children Teaching Hospital in Mosul from December 2006-January 2010, a detailed case-record of 20 consecutive newborn patients treated for duodenal obstruction. The aims of the study was to analyze our experience and to evaluate the clinical presentation, diagnosis, postoperative care, and outcome in infants with duodenal obstruction.The 20 patients were classified according to classification system modified from James A. O’Neill: duodenal web, atresia

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14

Zuccarello, Biagio, Antonella Spada, Antonio Centorrino, Nunzio Turiaco, Maria Rosaria Chirico, and Saveria Parisi. "The Modified Kimura's Technique for the Treatment of Duodenal Atresia." International Journal of Pediatrics 2009 (2009): 1–5. http://dx.doi.org/10.1155/2009/175963.

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Background/Purpose. Kimura's diamond-shaped-duodenoduodenostomy (DSD) is a known technique for the correction of congenital intrinsic duodenal obstruction. We present a modification of the technique and review the advantages of this new technique.Methods. From 1992 to 2006, 14 newborns were treated for duodenal atresia. We inverted the direction of the duodenal incisions: a longitudinal incision was made in the proximal duodenum while the distal was opened by transverse incision.Results. Our “inverted-diamond-shaped-duodenoduodenostomy” (i-DSD) allowed postoperative oral feeding to start on da

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15

Ruhimat, Albireza, and Ahmad Yani. "048. Roux-En-Y Duodenojejunostomy as Surgical Treatment for Congenital Duodenal Obstruction: A Case Report." JBN (Jurnal Bedah Nasional) 8, no. 2 (2024): 48. http://dx.doi.org/10.24843/jbn.2024.v08.is02.p048.

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Background: Congenital duodenal obstruction is an anatomical abnormality in newborn. Various intrinsic and extrinsic etiologies can cause duodenal obstruction. The surgical treatment that commonly performed on duodenal obstruction in neonates is duodenoduodenostomy. However, several etiologies conditions such as preduodenal portal vein (PDPV) and pancreatic annulare cause duodenoduodenostomy is nearly impossible to be performed, so an alternative treatment is necessary. Case: This case describes female neonate with congenital duodenal obstruction which had been suspected since in pregnancy due

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16

Badiola, Izaskun, Eva Las Navas, Amaia Sanz, Begoña Estraviz, and Francisco Javier Ibañez. "Duodenoduodenostomía laterolateral laparoscópica por páncreas anular del adulto." Cirugía Española 92, no. 9 (2014): 630–31. http://dx.doi.org/10.1016/j.ciresp.2013.05.012.

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17

Ozden, Onder, Seref Selcuk Kılıc, Murat Alkan, Gokhan Tumgor, and Recep Tuncer. "Biliary Atresia Splenic Malformation Syndrome: A Single Center Experience." Acta Medica 50, no. 4 (2019): 36–41. http://dx.doi.org/10.32552/2019.actamedica.355.

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Abstract: Introduction: The cause of biliary atresia (BA) is not understood exactly as well as biliary atresia splenic malformation (BASM) syndrome. BA is destructive biliary fibrosis; the etiology may be multifactorial. Association of cytomegalovirus (CMV) and BA have been shown in many reports but CMV and BASM have not been mentioned in the literature. So we aimed to report BASM experiences, an association of CMV infection and need of duodenoduodenostomy if preduodenal portal vein exists. Materials and Methods: The data were collected retrospectively from Cukurova University whic

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18

Ribeiro, Bruno Jucá, Nicoli Tamie Yoshimi, Camila Dufrayer Fânzeres Monteiro Fortes, et al. "Pancreatic transplantation with duodenoduodenostomy drainage: technique, normal radiological appearance and complications." Abdominal Radiology 45, no. 2 (2019): 479–90. http://dx.doi.org/10.1007/s00261-019-02267-x.

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19

Schenker, P., M. Flecken, O. Vonend, A. Wunsch, T. Traska, and R. Viebahn. "En Bloc Retroperitoneal Pancreas–Kidney Transplantation With Duodenoduodenostomy Using Pediatric Organs." Transplantation Proceedings 41, no. 6 (2009): 2643–45. http://dx.doi.org/10.1016/j.transproceed.2009.06.113.

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20

Sharma, Prmila, Naresh Pawar, and Arun Kumar Gupta. "Congenital intrinsic duodenal obstruction: Clinical study and predictors of neonatal surgical mortality." Journal of Neonatal Surgery 11 (February 20, 2022): 9. http://dx.doi.org/10.47338/jns.v11.1034.

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Background: This study was aimed to analyze the clinical profile and the predictors of neonatal surgical mortality of congenital intrinsic duodenal obstruction (CIDO). Methods: This is a case series of 67 patients with CIDO (duodenal atresia and stenosis) admitted at our teaching institute, from October 2018 to June 2020. The demographic data, clinical presentation, diagnostic methods, location & type of duodenal atresia, the operative procedure performed, and neonatal surgical mortality (NSM) predictors such as birth weight, age on presentation, associated anomalies, duration of surgery,

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21

De Ugarte, Daniel A., Eric P. Dutson, and Darryl T. Hiyama. "Annular Pancreas in the Adult: Management with Laparoscopic Gastrojejunostomy." American Surgeon 72, no. 1 (2006): 71–73. http://dx.doi.org/10.1177/000313480607200117.

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Annular pancreas is an uncommon congenital anomaly associated with duodenal atresia in neonates. Rarely, the condition may manifest later in life. These symptoms include abdominal pain, nausea, and vomiting and usually arise due to obstruction to gastric emptying. Abdominal CT scan with high resolution and angiography protocol and magnetic resonance imaging are useful in confirming the presence of annular pancreas. Operative management involves bypassing the obstructed duodenum. Duodenoduodenostomy is routinely performed in neonates with annular pancreas. In adults, the duodenum is less mobile

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22

Lindahl, J. P., R. Horneland, E. Nordheim, et al. "Outcomes in Pancreas Transplantation With Exocrine Drainage Through a Duodenoduodenostomy Versus Duodenojejunostomy." American Journal of Transplantation 18, no. 1 (2017): 154–62. http://dx.doi.org/10.1111/ajt.14420.

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23

Son, Tran Ngoc, Nguyen Thanh Liem, and Hoang Huu Kien. "Laparoscopic Simple Oblique Duodenoduodenostomy in Management of Congenital Duodenal Obstruction in Children." Journal of Laparoendoscopic & Advanced Surgical Techniques 25, no. 2 (2015): 163–66. http://dx.doi.org/10.1089/lap.2014.0263.

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24

Hackett, Eileen S., Hayley M. Lang, Andre Desrochers, Sylvain Nichols, and Susan Lawson Fubini. "Duodenoduodenostomy for obstruction of the sigmoid flexure of the duodenum in cattle." Veterinary Surgery 47, no. 5 (2018): 623–28. http://dx.doi.org/10.1111/vsu.12901.

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25

Suismaya, Ni Luh Gede Wahyuni, I. Made Kardana, and Kadek Deddy Ariyanta. "Annular pancreas in two cases after diamond-shaped anastomosis duodenoduodenostomy: case reports." Intisari Sains Medis 11, no. 2 (2020): 445–51. http://dx.doi.org/10.15562/ism.v11i2.581.

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Background: Annular pancreas is an infrequent congenital disorder characterized as a partial or complete pancreatic tissue around the descending part of the duodenum. Prenatal control is essential in the early detection of the annular pancreas. Initial management might increase better prognosis. We report two cases of the annular pancreas in Sanglah General Hospital, Denpasar, Bali in 2016-2019 to describe the clinical characteristics and outcome of different ages in annular pancreas managed by diamond-shaped duodenoduodenostomy.Case Description: The first case was a six days old baby boy with

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26

Chandrasekharam, VVS. "Laparoscopic duodenoduodenostomy in neonates: Report of two cases and review of the literature." Journal of Indian Association of Pediatric Surgeons 20, no. 3 (2015): 150. http://dx.doi.org/10.4103/0971-9261.154666.

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27

Chen, Lily Ye, Victor F. Cabrera-Bou, and Adela T. Casas-Melley. "Dual duodenojejunostomies in the repair of megaduodenum, duodenal stenosis and prior missed diagnosis of annular pancreas." BMJ Case Reports 15, no. 2 (2022): e248219. http://dx.doi.org/10.1136/bcr-2021-248219.

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Duodenal stenosis and atresia are some of the most common forms of congenital bowel obstruction. The gold standard approach to treatment is duodenoduodenostomy, while rare, gastrojejunostomy and duodenojejunostomies may still be used. We report a case of a 7-year-old male presenting with annular pancreas with duodenal stenosis that was diagnosed at birth as primary duodenal atresia and repaired by gastrojejunostomy with a Braun enteroenterostomy. Through successful reoperation with dual duodenojejunostomy and subsequent management, we treated the sequelae of the initial repair, including megad

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28

Gogan, M. V. LS Boris, Koto Toualouth Lafia, Codjo Serge Metchihoungbe, CA Médard Amoussou, MGI Sergine Dossou, and Michel Armand Fiogbe. "Duodenal atresia, annular pancreas, and situs inversus totalis- rare association in a newborn: A case report." Journal of Neonatal Surgery 12 (September 5, 2023): 26. http://dx.doi.org/10.47338/jns.v12.1218.

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Background: Simultaneous occurrence of duodenal atresia, annular pancreas, and situs inversus totalis is an exceedingly rare clinical condition. This may pose management-related challenges to the treating surgeon. Case Presentation: We report a case with a preoperative diagnosis of duodenal atresia and situs inversus. Intraoperatively, an annular pancreas encircling the duodenum was found. Instead of duodenoduodenostomy, a duodenojejunal anastomosis was performed. The postoperative course remained uneventful. The patient is doing fine on a 6-month follow-up. Conclusion: The simultaneous presen

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29

Li, Bing, Bing W. Chen, and Lin S. Xia. "Laparoscopic side‐to‐side duodenoduodenostomy versus diamond‐shaped anastomosis for annular pancreas in the neonate." ANZ Journal of Surgery 91, no. 7-8 (2021): 1504–8. http://dx.doi.org/10.1111/ans.16959.

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30

Dewberry, Lindel C., Raphael N. Vuille-dit-Bille, Ann M. Kulungowski, and Stig Somme. "A Single Surgeon Laparoscopic Duodenoduodenostomy Case Series for Congenital Duodenal Obstruction in an Academic Setting." Journal of Laparoendoscopic & Advanced Surgical Techniques 28, no. 12 (2018): 1517–19. http://dx.doi.org/10.1089/lap.2018.0215.

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31

Bethell, George S., Dina Fouad, Enitan Ogundipe, and Mohammed Choudhry. "Delayed finding of congenital duodenal obstruction following congenital diaphragmatic hernia repair." BMJ Case Reports 16, no. 1 (2023): e253394. http://dx.doi.org/10.1136/bcr-2022-253394.

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Congenital diaphragmatic hernia (CDH) is encountered in just under 1 in 6000 live births, while congenital duodenal obstruction is seen once every 8000 live births. These congenital anomalies have only been reported together as part of the VACTERL syndrome and therefore in isolation represent an incredibly rare occurrence. This is a case report of a girl born at 34 weeks gestation who had an antenatal diagnosis of left CDH. Five days following operative repair of this, there was extensive pneumoperitoneum and pneumothorax. Upper gastrointestinal contrast study showed a perforation of the duode

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32

Walter, Martin, Martin Jazra, Stylianos Kykalos, et al. "125 Cases of duodenoduodenostomy in pancreas transplantation: a single‐centre experience of an alternative enteric drainage." Transplant International 27, no. 8 (2014): 805–15. http://dx.doi.org/10.1111/tri.12337.

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33

Kovács, Tamás, Péter Vörös, Tibor Verebély, and Zsuzsanna Antal. "Gastric Transposition after Duodenoduodenostomy in Infants with Combined Esophageal and Duodenal Atresia—Report of Three Cases." European Journal of Pediatric Surgery 22, no. 06 (2012): 470–72. http://dx.doi.org/10.1055/s-0032-1313344.

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34

Silva, Vanessa Lima do Nascimento, Maria Clara Lustosa Veras, Valeska Nayra Diógenes Oliveira Batista, et al. "Atresia Duodenal: Desafios no Diagnóstico Precoce e Manejo Terapêutico em Recém-Nascidos." Brazilian Journal of One Health 2, no. 2 (2025): 617–26. https://doi.org/10.70164/bjoh.v2i2.139.

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A atresia duodenal é uma malformação congênita caracterizada pela obstrução parcial ou total do duodeno, resultante de uma falha na recanalização durante o desenvolvimento embrionário, entre a 9ª e a 11ª semanas de gestação. É uma das principais causas de obstrução intestinal em recém-nascidos, com incidência estimada entre 1 em 7.500 a 10.000 nascidos vivos. O diagnóstico precoce é fundamental, pois a condição pode levar a complicações graves como desidratação, desnutrição e choque hipovolêmico. A atresia duodenal é frequentemente associada a anomalias como a síndrome de Down e cardiopatias c

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35

Salluzzo, Jennifer, Stephanie G. Wood, Matthew O. Hubbard, et al. "493 Laparoscopic Duodenoduodenostomy: A Minimally Invasive Technique for the Managment of Duodenal Obstruction Due to Annular Pancreas." Gastroenterology 150, no. 4 (2016): S1185. http://dx.doi.org/10.1016/s0016-5085(16)34000-8.

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36

Chandrasekaran, Sankkarabarathi, and Anirudhan Asokaraju. "Clinical profile and predictors of outcome in congenital duodenal obstruction." International Surgery Journal 4, no. 8 (2017): 2605. http://dx.doi.org/10.18203/2349-2902.isj20173396.

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Background: Congenital duodenal obstruction is a broad term that refers to a variety of disorders like duodenal atresia, duodenal stenosis, annular pancreas, duodenal membrane and preduodenal portal vein. The aim of this study was to analyse in detail the entire clinical profile of duodenal obstruction and to study the short-term outcome.Methods: A prospective descriptive study was conducted in the Department of Paediatric Surgery, Institute of child Health and Hospital for Children, Egmore, Chennai, among all babies with suspected duodenal obstruction based on clinical symptoms and subsequent

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37

Edan, Obay. "Situs ambiguous with duodenal atresia in a neonate: A case report with literature review." Journal of Neonatal Surgery 13 (July 20, 2024): 26. http://dx.doi.org/10.47338/jns.v13.1318.

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Background: Situs ambiguous is a rare congenital anomaly characterized by an unusual and irregular distribution of the major visceral organs and vessels within the chest and abdomen. In this condition, the organs are arranged in a way that cannot be classified as either situs inversus or situs solitus. We report this case due to the rarity of this anomaly and its uncommon association with duodenal atresia in a neonate. Case Presentation: A full-term newborn female presented with repeated bilious vomiting and failure to pass meconium for five days. An erect abdominal X-ray revealed a double-bub

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38

Edan, Obay. "Situs ambiguous with duodenal atresia in a neonate: A case report with literature review." Journal of Neonatal Surgery 13 (July 20, 2024): 26. https://doi.org/10.52783/jns.v13.1318.

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Background: Situs ambiguous is a rare congenital anomaly characterized by an unusual and irregular distribution of the major visceral organs and vessels within the chest and abdomen. In this condition, the organs are arranged in a way that cannot be classified as either situs inversus or situs solitus. We report this case due to the rarity of this anomaly and its uncommon association with duodenal atresia in a neonate. Case Presentation: A full-term newborn female presented with repeated bilious vomiting and failure to pass meconium for five days. An erect abdominal X-ray revealed a double-bub

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39

Ferrer-Fàbrega, J., C. Castillo-Delgado, R. García-Pérez, et al. "Duodenoduodenostomy versus Duodenojejunostomy for Exocrine Drainage in Pancreas Transplantation. A 22-Year Single-Center Experience of Pancreas Transplantation." HPB 24 (2022): S597. http://dx.doi.org/10.1016/j.hpb.2022.05.1302.

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40

Ananthasivan, Rupa, Sudarshan Rawat, Pramesh Reddy, Pooja G. Patil, and Chittur Narendra Radhakrishnan. "Duodenal Stenosis with Diaphragmatic Hernia—A Rare Combination—Delayed Diagnoses with Barium Study." Journal of Gastrointestinal and Abdominal Radiology 02, no. 01 (2019): 069–73. http://dx.doi.org/10.1055/s-0039-1683770.

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AbstractDuodenal stenosis is part of a spectrum of disorders due to non-cannulization of the fetal gut lumen occurring in 11 to 13 weeks of fetal life. The diagnosis is often made in the neonatal period owing to bilious vomiting. The authors present a case of a 9-year-old boy who was diagnosed by an upper gastrointestinal study that showed a hugely dilated stomach filled with food residue and a dilated first part of the duodenum with an abrupt narrowing in the second part of the duodenum in keeping with duodenal stenosis. There was no associated malrotation (a known association), but the delay

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41

Medjedovic, Edin, Zlatan Zvizdic, Anis Cerovac, Sabaheta Jonuzovic-Prosic, and Emir Milisic. "Successful Pregnancy Outcome after Amnioreduction Treated Acute Polyhydramnios Caused by Duodenal Atresia." Acta Medica (Hradec Kralove, Czech Republic) 65, no. 4 (2022): 149–52. http://dx.doi.org/10.14712/18059694.2023.6.

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The aim of our manuscript is to report of a successful perinatal outcome after treatment of acute polyhydramnios caused by duodenal atresia. A 34-year-old G3P1 was referred due to polyhydramnios in the 30th week of pregnancy. Ultrasound revealed polyhydramnios, amniotic fluid index (AFI) 28, and a double bubble sign that indicated duodenal atresia and dilatated oesophagus. In the 32nd week of gestation, the volume of amniotic fluid increases, AFI 35, along with symptoms of dyspnea and abdominal pain. Due to the clinical picture and the early gestational age, it was decided to perform an amnior

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42

Patel, R. V., D. Govani, R. Patel, and D. B. Dekiwadia. "Neonatal duodenoduodenostomy and missed duodenal stenosis with windsock deformity: a rare intraoperative error of technique and judgement by an unwary surgeon." Case Reports 2014, jan15 2 (2014): bcr2013202782. http://dx.doi.org/10.1136/bcr-2013-202782.

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43

Bethell, George Stephen, Anna-May Long, Marian Knight, and Nigel J. Hall. "Congenital duodenal obstruction in the UK: a population-based study." Archives of Disease in Childhood - Fetal and Neonatal Edition 105, no. 2 (2019): 178–83. http://dx.doi.org/10.1136/archdischild-2019-317085.

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ObjectiveCongenital duodenal obstruction (CDO) comprising duodenal atresia or stenosis is a rare congenital anomaly requiring surgical correction in early life. Identification of variation in surgical and postoperative practice in previous studies has been limited by small sample sizes. This study aimed to prospectively estimate the incidence of CDO in the UK, and report current management strategies and short-term outcomes.DesignProspective population-based, observational study for 12 months from March 2016.SettingSpecialist neonatal surgical units in the UK.Main outcome measuresIncidence of

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44

Liang, Zijian, Menglong Lan, Xiaogang Xu, Fei Liu, Boyuan Tao, and Jixiao Zeng. "Diamond-shaped versus side-to-side anastomotic duodenoduodenostomy in laparoscopic management of annular pancreas in children: a single-center retrospective comparative study." Translational Pediatrics 12, no. 10 (2023): 1791–99. http://dx.doi.org/10.21037/tp-23-156.

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45

Moga, Andreea, Radu Bălănescu, Laura Bălănescu, et al. "Factors Associated with Postoperative Complications After Congenital Duodenal Obstruction Surgery: A Retrospective Study." Medicina 60, no. 10 (2024): 1722. http://dx.doi.org/10.3390/medicina60101722.

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Background and Objectives: Duodenal atresia and stenosis are common causes of intestinal obstruction. Associated anomalies significantly influence early postoperative mortality, while postoperative complications impact long-term survival. Materials and Methods: Over a 13-year period from January 2010 to August 2023, a total of 74 infants and children with congenital duodenal obstruction were treated at “Grigore Alexandrescu” Children’s Emergency Hospital and met the inclusion criteria. All patients diagnosed with duodenal obstruction (both instrinsic and extrinsic causes) were included. Analys

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Chiarenza, Salvatore Fabio, Valeria Bucci, Maria Luisa Conighi, et al. "Duodenal Atresia: Open versus MIS Repair—Analysis of Our Experience over the Last 12 Years." BioMed Research International 2017 (2017): 1–7. http://dx.doi.org/10.1155/2017/4585360.

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Objective. Duodenal atresia (DA) routinely has been corrected by laparotomy and duodenoduodenostomy with excellent long-term results. We revisited the patients with DA treated in the last 12 years (2004–2016) comparing the open and the minimally invasive surgical (MIS) approach.Methods. We divided our cohort of patients into two groups. Group 1 included 10 patients with CDO (2004–09) treated with open procedure: 5, DA; 3, duodenal web; 2, extrinsic obstruction. Three presented with Down’s syndrome while 3 presented with concomitant malformations. Group 2 included 8 patients (2009–16): 1, web;

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Ohno, Koichi, Tetsuro Nakamura, Takashi Azuma, et al. "Evaluation of the portal vein after duodenoduodenostomy for congenital duodenal stenosis associated with the preduodenal superior mesenteric vein, situs inversus, polysplenia, and malrotation." Journal of Pediatric Surgery 42, no. 2 (2007): 436–39. http://dx.doi.org/10.1016/j.jpedsurg.2006.10.019.

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Mizuta, Noritoshi, Takuya Kikuchi, and Yoshiyuki Fukuda. "Adult Intestinal Malrotation Treated with Laparoscopic Ladd Procedure." Case Reports in Surgery 2022 (October 18, 2022): 1–6. http://dx.doi.org/10.1155/2022/6874885.

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Intestinal malrotation is a rare congenital disease caused by abnormal intestinal rotation and fixation of the intestinal tract in the early embryonic state. Adult cases are rare. A laparoscopic Ladd procedure for adult intestinal malrotation is increasingly reported, but owing to the rarity, some important aspects of the disease and its treatment may be overlooked. Three adult cases of intestinal malrotation that underwent surgery at our hospital between January 2019 and October 2020 were retrospectively examined about patient backgrounds, short-term results, and complications. All patients w

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Gupta, Abhaya, Apoorva Kulkarni, Paras Kothari, Shalika Jayaswal, Vishesh Dikshit, and Geeta Kekre. "Retrocolic isoperistaltic gastrojejunostomy as an alternative to Kimura's duodenoduodenostomy in low- and very low-birth-weight babies of duodenal atresia: A 5 year retrospective study." Journal of Clinical Neonatology 8, no. 2 (2019): 75. http://dx.doi.org/10.4103/jcn.jcn_95_18.

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Caicedo, Luis Armando, Juan Carlos Gómez-Vega, Óscar Javier Serrano, et al. "Derivación exocrina al duodeno en trasplante simultáneo de riñón y páncreas, experiencia en la Fundación Valle de Lili, Cali, Colombia." Revista Colombiana de Cirugía 31, no. 3 (2016): 178–84. http://dx.doi.org/10.30944/20117582.283.

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Introducción. El trasplante simultáneo de riñón y páncreas es reconocido como un tratamiento eficaz para el manejo de pacientes con diabetes mellitus, principalmente de tipo I, e insuficiencia renal crónica. Sin embargo, hoy en día aún existe dificultad para el seguimiento del injerto pancreático, ya que no existe un marcador serológico definitivo que lo permita y persiste la dificultad para la toma de biopsias. Se ha descrito una modificación en la técnica quirúrgica que permitiría el acceso endoscópico mediante una duodenoduodenostomía. Materiales y métodos. Se seleccionaron los pacien

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