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Journal articles on the topic 'Intestinal Malrotation'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 July 2025

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1

Pimenta, Joana, Gabriel Gomes, Ricardo Escrevente, and Emília Duro. "Intestinal neoplasia reveals intestinal malrotation." Journal of Case Reports and Images in Surgery 9, no. 1 (2023): 1–3. http://dx.doi.org/10.5348/100115z12jp2023ci.

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2

de Blaauw, Ivo, Julia van Ling, Sanne M. B. I. Botden, and Kim Heiwegen. "Malrotation in Congenital Diaphragmatic Hernia: Is It Really a Problem?" European Journal of Pediatric Surgery 30, no. 05 (2019): 434–39. http://dx.doi.org/10.1055/s-0039-1692165.

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Abstract Introduction Congenital diaphragmatic hernia (CDH) has been associated with other congenital malformations, such as intestinal rotation abnormalities. However, there is no standard evaluation and treatment of intestinal rotation during initial CDH repair. This study evaluates intestinal malrotation in CDH patients. Materials and Methods All patients with a CDH treated in a high-volume center between 2000 and 2015 were retrospectively evaluated. Demographics, gastrointestinal characteristics, surgical treatment, and abdominal outcomes (acute surgery, small bowel obstruction, and volvul

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3

Sipahi, Mesut, Kasim Caglayan, Ergin Arslan, Mustafa Fatih Erkoc, and Faruk Onder Aytekin. "Intestinal Malrotation: A Rare Cause of Small Intestinal Obstruction." Case Reports in Surgery 2014 (2014): 1–4. http://dx.doi.org/10.1155/2014/453128.

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Background. The diagnosis of intestinal malrotation is established by the age of 1 year in most cases, and the condition is seldom seen in adults. In this paper, a patient with small intestinal malrotation-type intraperitoneal hernia who underwent surgery at an older age because of intestinal obstruction is presented.Case. A 73-year-old patient who presented with acute intestinal obstruction underwent surgery as treatment. Distended jejunum and ileum loops surrounded by a peritoneal sac and located between the stomach and transverse colon were determined. The terminal ileum had entered into th

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4

Blumberg, Karen. "Intestinal Malrotation." Radiology 202, no. 2 (1997): 584. http://dx.doi.org/10.1148/radiology.202.2.584-a.

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5

Dietz, David W., Matthew R. Walsh, Sharon Grundfest-Broniatowski, Ian C. Lavery, Victor W. Fazio, and David P. Vogt. "Intestinal Malrotation." Diseases of the Colon & Rectum 45, no. 10 (2002): 1381–86. http://dx.doi.org/10.1007/s10350-004-6429-0.

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6

Trofimov, Victor V., and Olga G. Mokrushina. "Current understanding of the treatment of newborns with intestinal malrotation: a systematic review." Russian Journal of Pediatric Surgery, Anesthesia and Intensive Care 11, no. 4 (2021): 537–44. http://dx.doi.org/10.17816/psaic993.

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This review aimed to analyze and organize information on the treatment of newborns with bowel malrotation. A systematic review was conducted using the databases PubMed, Web of Science, Google Scholar, Scopus, and eLibrary and journals of Pediatric Surgery, Russian Bulletin of Pediatric Surgery, Anesthesiology and Reanimatology, and Pediatric Surgery from 2010 to 2020. The search terms were as follows: malrotation, neonatal, infant, newborn, intestinal malrotation, malrotation, neonatal period, Ledds syndrome, and midgut volvulus. All journal issues were reviewed for the selected period.

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7

Gnanadev, Praveen, Rohit Krishnappa, Hariprasad Ramachandra Naidu Taluru, et al. "A rare presentation of midgut malrotation as an acute intestinal obstruction and perforation in an adult." International Surgery Journal 7, no. 10 (2020): 3459. http://dx.doi.org/10.18203/2349-2902.isj20204156.

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Midgut malrotation is a congenital anomaly seen usually in childhood. Its presentation as an acute intestinal obstruction is extremely rare in adults usually identified intra operatively. A high index of suspicion is always required when dealing with any case of acute intestinal obstruction. We report a case of young adult who presented with symptoms of acute intestinal obstruction and was diagnosed intra-operatively as cecal volvulus with impending perforation caused by midgut malrotation. Malrotation of the intestinal tract is seen due to aberrant embryology. The presentation of intestinal m

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8

Torre, Ana, Andreia Amado, Susana Graça, and Antónia Póvoa. "Caecum volvulus as a late presentation of intestinal malrotation in an adult: a challenging diagnosis." BMJ Case Reports 15, no. 2 (2022): e247645. http://dx.doi.org/10.1136/bcr-2021-247645.

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Intestinal malrotation is usually diagnosed in early childhood. It results from failure of the normal gut rotation during embryological development. We present a case of a 62-year-old woman with a delayed presentation of an intestinal malrotation. She was admitted in the emergency department with an acute intestinal obstruction. Exploratory laparotomy revealed Ladd’s band with caecum volvulus and intestinal malrotation. Ladd’s procedure and right hemicolectomy were performed with uneventful recovery. Since both caecum volvulus and intestinal malrotation are rare events, particularly in adultho

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9

Daniel, Guillaume, and Aurélien Dupré. "Partial intestinal malrotation." Clinics and Research in Hepatology and Gastroenterology 37, no. 5 (2013): 442–43. http://dx.doi.org/10.1016/j.clinre.2013.01.005.

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10

Nishio, Yosuke, Yoshihiko Kawano, and Shinya Hara. "Nutcracker syndrome complicated with intestinal malrotation." BMJ Case Reports 12, no. 10 (2019): e231230. http://dx.doi.org/10.1136/bcr-2019-231230.

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Nutcracker syndrome (NCS) is a pathological condition in which the left renal vein (LRV) is compressed between the superior mesenteric artery (SMA) and aorta. NCS can predispose patients to the onset of chronic kidney disease because of persistent increase in LRV pressure. Although NCS in children is often idiopathic, it can also be caused by underlying pathologies such as retroperitoneal tumours. To the best of our knowledge, there have been no reports regarding paediatric cases of NCS complicated with intestinal malrotation. Here, we report the case of a 12-year-old girl with intestinal malr

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11

Emeka, Chukwubuike Kevin. "Intestinal Malrotation in Children: Experience of a Tertiary Care Hospital in a Developing Country." Janaki Medical College Journal of Medical Science 8, no. 2 (2020): 37–42. http://dx.doi.org/10.3126/jmcjms.v8i2.33976.

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Background and Objectives: Intestinal malrotation is a congenital disorder resulting from abnormal rotation of the intestine during fetal development. The aim of this study was to evaluate our experience in the management of pediatric patients with intestinal malrotation. Material and Methods: This was a retrospective study of children aged 3 years and below who were treated for intestinal malrotation between January 2014 and December 2018 at the pediatric surgery unit of Enugu State University Teaching Hospital (ESUTH) Enugu, Nigeria. Results: Sixty-one patients had laparotomy for

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12

Wada, Yusuke, Takeshi Yamashita, Yoshiaki Ozawa, et al. "Laparoscopic Management of Intestinal Malrotation With Cocoon Deformity: A Case Report." International Surgery 101, no. 9-10 (2016): 426–30. http://dx.doi.org/10.9738/intsurg-d-16-00042.1.

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Intestinal malrotation is diagnosed and treated mostly in infancy and childhood, but it is rarely encountered in adults. Here, we present a case of adult intestinal malrotation with cocoon deformity that was managed by a laparoscopic procedure. A 71-year-old man presented with intermittent abdominal pain, nausea, and vomiting. Preoperative findings from abdominal computed tomography, upper gastrointestinal contrast imaging, and enema examination showed intestinal malrotation without volvulus. Diagnostic laparoscopy revealed nonrotation of the midgut, and most of the small bowels were contained

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13

Jain, Sonal, Ragini Singh, Surendra Kumar Singh, Vikram Singh, and Kumar Shantanu. "Abdominoscrotal Hydrocele with Intestinal Malrotation: A Rare Association." Case Reports in Radiology 2012 (2012): 1–3. http://dx.doi.org/10.1155/2012/354514.

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Abdominoscrotal hydrocele is an uncommon clinical entity and so is intestinal malrotation. We report a case of 15 year old boy who presented with lump in abdomen previously diagnosed as mesenteric cyst on ultrasound. A multislice CT scan and repeat ultrasound not only diagnosed the case as abdominoscrotal hydrocele but also detected intestinal malrotation with positive whirl sign. This is the first reported case of abdominoscrotal hydrocele with intestinal malrotation.

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14

Khiali.R*, Haicheur.E.H Naitslimane.N Drai.K Messaoudi.A Lotmani.F.Z Araoui.M Bendjeddou.S Bahache.N Taieb.M. "Situs Inversus Abdominus and Intestinal Malrotation in an Adult with Ladd's Band." INTERNATIONAL JOURNAL OF MEDICAL SCIENCE IN CLINICAL RESEARCH AND REVIEW 6, no. 1 (2023): 313–15. https://doi.org/10.5281/zenodo.7654104.

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<strong>ABSTRACT</strong>: Intestinal malrotation has been recognized as a cause of obstruction in infants and children and may be complicated by intestinal ischemia; it is very rare in adults. It is a congenital anomaly of foetal intestinal rotation and it is mostly discovered in early childhood as acute intestinal obstruction. The situs inversus abdominus is a rare entity but not pathological, and it is exceptionally associated with intestinal malrotation. The Ladd’s Band extends from the underside of the liver to the cecum, dangerously bringing the proximal jejunum and terminal ileum

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15

Cabanilla-Manuntag, Ma Corazon, Jan Paolo Cruz, Sofia Isabel Manlubatan, and Marc Paul Lopez. "Malrotation in the Adult, a Forgotten Etiology of Partial Gut Obstruction: A Report of Two Cases." Philippine Journal of Surgical Specialties 78, no. 1 (2023): 20–25. http://dx.doi.org/10.61662/pcs_huwd3185.

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Ninety percent of cases of malrotation have shown signs and symptoms of intestinal obstruction by the first year of life. It is thus an often-overlooked etiology in adult patients. Evidence-based recommendations are also limited because of the paucity of cases. This paper discusses the two cases of malrotation from diagnosis to surgical management at a tertiary academic hospital. Both are previously well adult male patients with virgin abdomen who presented with vomiting and signs of intestinal obstruction. During medical decompression, CT scan with triple contrast clinched the diagnosis of ma

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16

Khan, Yousuf, Sunil Yadav, and Ashraf Elkholy. "Waugh's Syndrome: Report of Two Children with Intussusception." European Journal of Pediatric Surgery Reports 05, no. 01 (2017): e29-e31. http://dx.doi.org/10.1055/s-0037-1604264.

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AbstractWaugh's syndrome (WS) is the rare association of intussusception and intestinal malrotation. We present two such cases in a 5-month-old infant and a 9-year-old girl. Both patients presented with intussusception and were diagnosed with malrotation during workup and surgical exploration. We conclude that the possibility of intestinal malrotation must be taken into consideration while managing children with intussusception.

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17

Draus, John M., David S. Foley, and Sheldon J. Bond. "Laparoscopic Ladd Procedure: A Minimally Invasive Approach to Malrotation without Midgut Volvulus." American Surgeon 73, no. 7 (2007): 693–96. http://dx.doi.org/10.1177/000313480707300711.

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The management of intestinal malrotation without midgut volvulus is controversial. Some advocate the Ladd procedure in all patients with malrotation, whereas others propose a more selective approach. We attempted the laparoscopic Ladd procedure on nine patients who were diagnosed with intestinal malrotation without volvulus. Patient records were retrospectively reviewed. Data were collected on patient presentation, operative procedure, hospital course, and outcome. The laparoscopic Ladd procedure was successfully completed in eight patients (aged 10 weeks to 25 years). One patient required con

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18

Hoeffel, J. C. "Intestinal malrotation in infants." American Journal of Roentgenology 160, no. 6 (1993): 1362–63. http://dx.doi.org/10.2214/ajr.160.6.8292122.

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19

VELOSO, H. "Intestinal malrotation in adults." American Journal of Gastroenterology 97, no. 9 (2002): S201—S202. http://dx.doi.org/10.1016/s0002-9270(02)05097-9.

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20

Adams, Stephen D., and Michael P. Stanton. "Malrotation and intestinal atresias." Early Human Development 90, no. 12 (2014): 921–25. http://dx.doi.org/10.1016/j.earlhumdev.2014.09.017.

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21

Yin, Meng-Di, Li-Liang Hao, Guang Li, Yu-Tao Li, Bao-Li Xu, and Xin-Rui Chen. "Adult-onset congenital intestinal malrotation: A case report and literature review." Medicine 103, no. 8 (2024): e37249. http://dx.doi.org/10.1097/md.0000000000037249.

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Background: Intestinal malrotation is an infrequent congenital anomaly primarily observed in neonates, and adult-onset cases are exceedingly rare. Studies on adult congenital intestinal malrotation are limited. Methods: A case with congenital intestinal malrotation is reported in our study. The clinical data were collected and the treatment process and effect were evaluated. Results: A 45-year-old female who had been experiencing vomiting for over 40 years was admitted to our hospital. According to the result of CT scan, intestinal volvulus accompanied by bowel obstruction was suspected. Then

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22

Mares, Asya Zubillaga, Alejandra Nuñez-Venzor, Fátima Chávez-Hernandez, Erika Barlandas-Quintana, and Maria Fernanda Lopez-Godinez. "Laparoscopic management in an adult patient with intestinal obstruction secondary to congenital midgut malrotation: a case report and review of the literature." International Surgery Journal 9, no. 12 (2022): 2055. http://dx.doi.org/10.18203/2349-2902.isj20223172.

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Intestinal malrotation is the failure of the fetal intestine to complete a 270-degree counter clockwise rotation around the superior mesenteric artery, resulting in positional and fixation abnormalities of the small and large intestine. Adult presentation is uncommon with an estimated incidence of 0.2 to 0.5%. There is no consensus on treatment in patients with asymptomatic intestinal malrotation in adults. The aim of this document was to report and review a case of intestinal malrotation conditioning intestinal obstruction in an adult patient with successful laparoscopic management. We conclu

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23

Ovejero Gómez, VJ, MV Bermúdez García, A. Pérez Martín, and D. Morales García. "Intestinal malrotation clinical approach in adult patients." Cirugía Andaluza 34, no. 3 (2023): 382–87. http://dx.doi.org/10.37351/2023343.11.

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Resumen La malrotación intestinal es un proceso congénito que afecta a la fijación final del tracto intestinal generando malfunción intestinal. Sus manifestaciones clínicas graves son más frecuentes en la edad pediátrica. Su diagnóstico en el adulto suele ser casual o asociado a episodios no específicos de dolor abdominal que podrían evolucionar a volvulación y fenómenos isquémicos sobre segmentos intestinales dependientes de la arteria mesentérica superior, llegando a comprometer la vida del paciente. Exponemos nuestra experiencia en dos pacientes con diagnóstico confirmado de malrotación int

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24

Chandler, Courtney, and Kelsy L. Fisher. "Sonographic Findings of Midgut Malrotation With Volvulus: A Case of Upper Intestinal Obstruction in a Neonate." Journal of Diagnostic Medical Sonography 34, no. 5 (2018): 385–89. http://dx.doi.org/10.1177/8756479317754054.

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Midgut malrotation is a congenital condition resulting from incomplete normal intestinal rotation after physiologic gut herniation. While it can remain asymptomatic over an entire lifetime, midgut volvulus is most likely to occur during early life. While an upper gastrointestinal series is the imaging modality of choice for definitive diagnosis, sonography is a safe and effective modality capable of indicating midgut malrotation, especially in pediatric patients. This case study illustrates the sonographic findings associated with intestinal malrotation with volvulus and discusses the etiology

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Sekioka, Akinori, Kunihiko Tsuboi, Yoko Shono, and Yukito Adachi. "Anatomical challenge: a rare coexistence of caecal cancer and isolated duodenal malrotation." BMJ Case Reports 15, no. 10 (2022): e251627. http://dx.doi.org/10.1136/bcr-2022-251627.

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Intestinal malrotation is a congenital anomaly, treated mostly during childhood. A small number of cases are incidentally found in adulthood, during operation for other abdominal diseases, such as colon cancer.Here, we present a case of caecal cancer with isolated duodenal malrotation, a subtype of intestinal malrotation, discovered incidentally during the operation for the cancer. Although the anatomical abnormality made the operation more complicated, laparoscopic resection was safely performed with oncologically adequate lymphadenectomy, owing to intraoperative confirmation of anatomy and c

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Roldán Aviña, JP, I. Serrano Borrero, S. Merlo Molina, L. Herrera Gutiérrez, and F. Muñoz Pozo. "Intestinal malrotation in adults: incidental diagnosis." Revista Andaluza de Patología Digestiva 44, no. 4 (2021): 142–44. http://dx.doi.org/10.37352/2021444.3.

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27

Pradiptha, Nyoman T., and Ketut Wiargitha. "Adult intestinal malrotation: a case report." International Journal of Research in Medical Sciences 7, no. 12 (2019): 4807. http://dx.doi.org/10.18203/2320-6012.ijrms20195561.

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Midgut malrotation is an incomplete rotation of the intestine which occurs during foetal development and usually presents in the neonatal period. The bowel is not fixed adequately and is thus held by a precariously narrow-based mesentery. The incidence of malrotation has been estimated at 1 in 6000 live births, it is rare for malrotation to present in adulthood. Author report a 40-year-old man presented to emergency department with generalized abdominal pain. His symptoms began 2 days before admission. The patient really weak and his mental state was somnolence. His abdomen was slightly extend

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Hernando-Almudí, Ernesto, Rafael Cerdán-Pascual, Cristina Vallejo-Bernad, Joaquín Martín-Cuartero, María Sánchez-Rubio, and Carmen Casamayor-Franco. "Adult intestinal malrotation associated with intestinal volvulus." Cirugía y Cirujanos (English Edition) 85, no. 5 (2017): 424–27. http://dx.doi.org/10.1016/j.circen.2017.11.004.

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29

Shahverdi, Ehsan, Mehdi Morshedi, Maryam Allahverdi Khani, Mohammad Baradaran Jamili, and Fatemeh Shafizadeh Barmi. "Utility of the CT Scan in Diagnosing Midgut Volvulus in Patients with Chronic Abdominal Pain." Case Reports in Surgery 2017 (2017): 1–3. http://dx.doi.org/10.1155/2017/1079192.

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Symptomatic intestinal malrotation first presenting in the adults is rare. Midgut volvulus is the most common complication of malrotation in the adults. Because of more differential diagnosis, Computed Tomography (CT) scan can play an important role in the evaluation of patients with this abnormality. The whirl pattern around the superior mesenteric artery found on CT scan in patients with midgut volvulus is pathognomonic and diagnostic. We describe a case of intestinal malrotation complicated by midgut volvulus in an adult patient. The preoperative CT findings were pathognomonic.

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VIDAL, Eduardo Arevalo, Francisco Abarca RENDON, Trino Andrade ZAMBRANO, et al. "INTESTINAL MALROTATION IN PATIENTS UNDERGOING BARIATRIC SURGERY." ABCD. Arquivos Brasileiros de Cirurgia Digestiva (São Paulo) 29, suppl 1 (2016): 24–26. http://dx.doi.org/10.1590/0102-6720201600s10007.

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ABSTRACT Background: Intestinal malrotation is a rare congenital anomaly. In adults is very difficult to recognize due to the lack of symptoms. Diagnosis is usually incidental during surgical procedures or at autopsy. Aim: To review the occurrence and recognition of uneventful intestinal malrotation discovered during regular cases of bariatric surgeries. Methods: Were retrospectively reviewed the medical registry of 20,000 cases undergoing bariatric surgery, from January 2002 to January 2016, looking for the occurrence of intestinal malrotation and consequences in the intraoperative technique

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Ray, Dipankar, Gautam Chattopadhyay, and Surajit Das. "Malrotation of Intestine with Carcinoma Colon in Adult." Journal of Nepal Medical Association 52, no. 193 (2014): 726–28. http://dx.doi.org/10.31729/jnma.486.

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Malrotation of gut is a congenital anomaly and patients usually present in childhood. Occasionally it may present in adulthood. Patients are usually asymptomatic when malrotation of gut is detected during investigations or operation. Also it can cause longstanding abdominal symptoms, volvulus of gut. Rarely malrotation of gut may present with gastrointestinal neoplasm. We present a 60year old female presented with carcinoma caecum along with intestinal malrotation.

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Melkonian, Vatche, Pablo Quadri, Chintalapati R. Varma, Mustafa Nazzal, Henry B. Randall, and Minh-Tri J. P. Nguyen. "Asymptomatic Intestinal Malrotation Progressing to Midgut Volvulus in a Decompensated Alcoholic Cirrhotic Adult: A Rare Scenario Requiring Special Considerations." Case Reports in Surgery 2020 (June 17, 2020): 1–4. http://dx.doi.org/10.1155/2020/4196012.

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Intestinal malrotation usually presents in the pediatric population with midgut volvulus requiring emergency Ladd’s procedure. Rarely, it remains asymptomatic and is discovered incidentally only during adulthood when it seldom causes intestinal complications. The scenario of a cirrhotic adult being diagnosed with asymptomatic intestinal malrotation with subsequent intestinal complications is thus extremely rare and to our knowledge has not been previously reported. We describe a 56-year-old man with decompensated alcoholic cirrhosis (Child-Pugh class C, MELD score 22) who was initially observe

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Donaire, Michael, James Mariadason, Daniel Stephens, Sitaram Pillarisetty, and Marc K. Wallack. "Carcinoma of the Colon in an Adult with Intestinal Malrotation." Case Reports in Surgery 2013 (2013): 1–4. http://dx.doi.org/10.1155/2013/525081.

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Colon cancer is the third most common cancer in the USA. Intestinal malrotation diagnosed in adulthood was, until recently, a very rare phenomenon. While patients may present with intestinal obstruction or abdominal pain, the diagnosis is now often made as an incidental finding by computed tomography (CT). Surprisingly we found only seven case reports of carcinoma of the colon in patients with malrotation; CT failed to make the preoperative diagnosis in a majority. Laparoscopic colon surgery is rapidly becoming standard of care for colon cancer. We present a case of carcinoma of the colon in a

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Zavras, Nick, Konstantinos Tsilikas, and George Vaos. "Chronic Intussusception Associated with Malrotation in a Child: A Variation of Waugh’s Syndrome?" Case Reports in Surgery 2016 (2016): 1–5. http://dx.doi.org/10.1155/2016/5638451.

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Chronic intussusception is a relatively uncommon disease most commonly observed in older children. Waugh’s syndrome represents a rare entity characterized by intestinal malrotation and acute intussusception. We report a very unusual case of intestinal malrotation associated with chronic intussusception. Clinical presentation, radiological findings, and managing of this association are discussed in the light of the available literature.

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Tumminelli, Cristina, Anna Maria Chiara Galimberti, Grazia Di Leo, Daniela Codrich, Flora Maria Murru, and Giulia Gortani. "La malrotazione intestinale: cosa deve sapere il pediatra." Medico e Bambino pagine elettroniche 24, no. 3 (2021): 78–83. http://dx.doi.org/10.53126/mebxxiv078.

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Intestinal malrotation includes anomalies of intestinal rotation and fixation occurred during embryogenesis. It may present with acute or chronic-intermittent symptoms or remain asymptomatic. There are several methods to identify a defect of intestinal rotation, however an upper gastrointestinal series remains the method of choice in non-acute cases. Surgical correction is performed by open laparotomy, while the laparoscopic approach is reserved only to selected cases. This article suggests an evaluation of children with suspected intestinal malrotation and gives information about its manageme

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Alhassan, Fatima, Isam Ahmed Abd Aljaleel, and Ibrahim Salih Elkheir. "Management and Outcome of Intestinal Malrotation in Paediatric Age Group in Paediatric Surgery Centers in Sudan from March 2019 to March 2020." SVOA Paediatrics 4, no. 3 (2025): 55–60. https://doi.org/10.58624/svoapd.2025.04.009.

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Background: Intestinal malrotation is a congenital abnormality of intestinal rotation and fixation that is of great interest to paediatric surgeons because it can produce volvulus of the midgut, which can have disastrous effects if diagnosed too late. This study assessed the outcomes of intestinal malrotation in paediatric surgery centers in Sudan. Methods: Medical records of all paediatric patients with symptomatic malrotation who underwent open Ladd's surgery between March 2019 and March 2020 were evaluated in this retrospective cross-sectional study. The following patient variables were ass

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Jain, Arihant, Shailesh Solanki, J. K. Mahajan, Arun Sharma, and Shivani Dogra. "Intestinal malrotation with levocardia and Spondylo-costal dysostosis: A case report." Journal of Neonatal Surgery 13 (September 17, 2024): 33. http://dx.doi.org/10.47338/jns.v13.1298.

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Background: Intestinal malrotation with midgut volvulus is usually present in the neonatal period but can present at any age, and can be associated with various congenital anomalies. These congenital defects increase the morbidity of the disease per se and require a multidisciplinary approach. Case Presentation: The index case was an eight-month-old child with intestinal malrotation, situs inversus, levo-cardia, single ventricle, and Spondylo-costal dysostosis. Here, we discuss its presentation, treatment, challenges during management, and review of pertinent literature. Conclusion: The associ

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Jain, Arihant, Shailesh Solanki, J. K. Mahajan, Arun Sharma, and Shivani Dogra. "Intestinal malrotation with levocardia and Spondylo-costal dysostosis: A case report." Journal of Neonatal Surgery 13 (September 17, 2024): 33. https://doi.org/10.52783/jns.v13.1298.

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Background: Intestinal malrotation with midgut volvulus is usually present in the neonatal period but can present at any age, and can be associated with various congenital anomalies. These congenital defects increase the morbidity of the disease per se and require a multidisciplinary approach. Case Presentation: The index case was an eight-month-old child with intestinal malrotation, situs inversus, levo-cardia, single ventricle, and Spondylo-costal dysostosis. Here, we discuss its presentation, treatment, challenges during management, and review of pertinent literature. Conclusion: The associ

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Arunachalam, Rathnaswami. "Ladd procedure in intestinal malrotation." Gastroenterology, Hepatology and Endoscopy Practice 2, no. 2 (2022): 83. http://dx.doi.org/10.4103/ghep.ghep_8_22.

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40

GLOWNIAK, JERRY V. "Intestinal Malrotation Diagnosed by Cholescintigraphy." Clinical Nuclear Medicine 13, no. 11 (1988): 835–36. http://dx.doi.org/10.1097/00003072-198811000-00017.

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41

Mitchell, John, Kurt R. Stahlfeld, and Ronald G. Cercone. "Retrocaval ureter with intestinal malrotation." Urology 62, no. 1 (2003): 142–43. http://dx.doi.org/10.1016/s0090-4295(03)00107-9.

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42

Spicer, Richard D. "Intestinal Obstruction Due to Malrotation." Journal of the Royal Society of Medicine 97, no. 10 (2004): 504. http://dx.doi.org/10.1177/0141076809701020.

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Hamidi, Hidayatullah, Yalda Obaidy, and Sahar Maroof. "Intestinal malrotation and midgut volvulus." Radiology Case Reports 11, no. 3 (2016): 271–74. http://dx.doi.org/10.1016/j.radcr.2016.05.012.

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Guvendi, Bulent, and Hayri Ogul. "Wandering Spleen and Intestinal Malrotation." Cirugía Española (English Edition) 97, no. 4 (2019): 232. http://dx.doi.org/10.1016/j.cireng.2018.10.003.

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Ballesteros Gómiz, E., A. Torremadé Ayats, C. Durán Feliubadaló, C. Martín Martínez, and A. Caro Tarragó. "Intestinal malrotation – volvulus: Imaging findings." Radiología (English Edition) 57, no. 1 (2015): 9–21. http://dx.doi.org/10.1016/j.rxeng.2014.07.002.

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El-Matary, Wael, Mathew Jones, Neville Wright, and Mark Dalzell. "Intestinal malrotation: an unusual presentation." European Journal of Pediatrics 162, no. 11 (2003): 812–13. http://dx.doi.org/10.1007/s00431-003-1308-6.

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Manohar, Aishwarya Emerald, M. S. Kalyan Kumar, V. Vijayalakshmi, and R. Kannan. "Concurrent intestinal malrotation and Meckel's diverticulum presenting as acute intestinal obstruction in an adult." International Surgery Journal 8, no. 6 (2021): 1904. http://dx.doi.org/10.18203/2349-2902.isj20212288.

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Intestinal malrotation is the partial or complete failure of rotation of midgut around the superior mesenteric artery, while Meckel’s diverticulum is the remnant of vitellointestinal duct and concurrence of these congenital abnormalities in an adult is considered a rarity. Till date only 3 cases of concurrent intestinal malrotation and Meckel's diverticulum have been reported. We report a 18 years male who presented with a 3 day history of abdominal pain, bilious vomiting, obstipation and chronic abdominal pain on and off since 3 years of age. During the last episode which occurred 1 year back

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Sneineh, Midhat Abu. "Technical Considerations In Performing One Anastomosis Gastric Bypass In Case of Intestinal Malrotation." Gastroenterology Pancreatology and Hepatobilary Disorders 5, no. 1 (2021): 01–02. http://dx.doi.org/10.31579/2641-5194/022.

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Intestinal malrotation is a rare congenital anomaly that originates from the failure of the normal rotation and fixation of the midgut during embryologic development. There are different types of Midgut Malrotation which includes non-rotation, incomplete rotation, reverse rotation, or anomalous fixation of the mesentery. Methods: We present a case of a 58-year-old woman with a BMI of 45.3 kg/m2. The patient underwent laparoscopic appendectomy 15 years ago and was diagnosed with a partial situs inversus. She has no other past medical conditions. Results: At the operation, four meters of small b

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Kaur, Simar, Paris Cai, Ajesh Sankar, and Rupak Sarkar. "A rare case of intestinal malrotation in pregnancy resulting in hemicolectomy postnatally." Česká gynekologie 88, no. 2 (2023): 114–18. http://dx.doi.org/10.48095/cccg2023114.

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Introduction: Small and large bowel obstruction secondary to volvulus on the background of intestinal malrotation is a very rare occurrence, especially in pregnancy. This can be associated with significant feto-maternal morbidity and mortality. Case report: We report a case of a pregnant lady who developed symptoms of subacute intestinal obstruction during the 2nd trimester of pregnancy and was subsequently diagnosed with intestinal malrotation on imaging. Though she had symptoms of abdominal pain and constipation persisting for 9 long weeks during pregnancy, there was no evidence of definite

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S., Srinivas, Reddy K. R., Balraj T. A., and Gangadhar A. "Neonatal small bowel obstruction due to malrotation: a clinical study." International Surgery Journal 4, no. 8 (2017): 2727. http://dx.doi.org/10.18203/2349-2902.isj20173107.

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Background:This study was done at Niloufer hospital and institute of child health, Hyderabad with an aim of evaluating the clinical presentation, diagnostic evaluation, management and outcome of malrotation of intestines in the neonates.Methods: Cases of neonatal small intestinal obstruction due to malrotation presenting to the Department of Pediatric Surgery, Niloufer hospital over a period of two years were evaluated.Results: A total of 38 newborns presented to our department with intestinal obstruction due to malrotation. 3/38 patients presented with extensive gangrene of midgut. 4/38 patie

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