Results 11 to 20 of about 620,878 (264)

Right paraduodenal hernia presenting with strangulated obstruction with intestinal malrotation: a case report. [PDF]

J Surg Case Rep
A paraduodenal hernia is a rare cause of an internal hernia that may require massive bowel resection; prompt diagnosis and surgical treatment are essential.
Tanaka H, Mitsutomoe S, Nagao N, Komori S, Suetsugu T, Iwata Y, Watanabe T, Tanaka C, Kawai M.   +8 more
europepmc   +4 more sources

Congenital Intestinal Malrotation in Newborns: Laparoscopic Ladd's Procedure versus Open Laparotomy.

Journal of the College of Physicians and Surgeons--Pakistan : JCPSP, 2023
OBJECTIVE To assess the efficacy and safety of laparotomic or laparoscopic Ladd's procedure in newborns with congenital malrotation. STUDY DESIGN Descriptive study.
Shu-Qing Wu, Bin Zhong, Fang Shu, P. Zhang, Yun Xiao   +4 more
semanticscholar   +3 more sources

Delayed laparoscopic cholecystectomy in a case of acute cholecystitis and intestinal malrotation type I

Clinics and Practice, 2019
In adults, intestinal malrotation is an oligosymptomatic entity that is occasionally discovered during the course of diagnostic studies for other causes.
Ana Arias, Carlos Ordieres, Adrian Huergo, Marta Posadilla, Pedro Amor, Ana Milla   +5 more
doaj   +3 more sources

Diagnostic Challenges in Adult Intestinal Malrotation: A Case Report and Literature Review. [PDF]

Cureus
Adult intestinal malrotation is a rare anatomical anomaly that typically manifests during infancy but can also present in adulthood. Symptoms are mainly digestive, with a long history of intermittent abdominal pain and epigastralgia.
Abdillahi Mahamoud C, Egueh Nour A, Bouknani N, Benslima N, Rami A.   +4 more
europepmc   +2 more sources

Adult Intestinal Malrotation Treated with Laparoscopic Ladd Procedure

Case Reports in Surgery, 2022
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.
Noritoshi Mizuta, Takuya Kikuchi, Yoshiyuki Fukuda   +2 more
doaj   +2 more sources

Abdominoscrotal Hydrocele with Intestinal Malrotation: A Rare Association [PDF]

Case Reports in Radiology, 2012
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.
Sonal Jain, Ragini Singh, Surendra Kumar Singh, Vikram Singh, Kumar Shantanu   +4 more
doaj   +2 more sources

A Rare Cause of Acute Abdomen in Adults: Intestinal Malrotation

Haseki Tıp Bülteni, 2017
Intestinal malrotation is a congenital anomaly of the midgut. The incidence of intestinal malrotation is 1 in 500 live births. It is rarely seen in adults.
Mürşit Dinçer, Gamze Çıtlak, Muzaffer Akıncı   +2 more
doaj   +2 more sources

Adult-onset congenital intestinal malrotation: A case report and literature review. [PDF]

Medicine (Baltimore)
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.
Yin MD, Hao LL, Li G, Li YT, Xu BL, Chen XR.   +5 more
europepmc   +2 more sources

CT facilitates improved diagnosis of adult intestinal malrotation: a 7-year retrospective study based on 332 cases

Insights into Imaging, 2021
Objective To classify adult intestinal malrotation by CT. Methods This retrospective study enrolled adults diagnosed with intestinal malrotation who underwent abdominal CT at our institution between June 1, 2013, and August 30, 2020.
Ziman Xiong, Yaqi Shen, John N. Morelli, Zhen Li, Xuemei Hu, Daoyu Hu   +5 more
doaj   +2 more sources

Intestinal malrotation with multiple congenital anomalies

Journal of Pediatric Surgery Case Reports, 2022
Intestinal malrotation (IM) occurs secondary to abnormal midgut rotations. It is a common and often devastating cause of neonatal bowel obstruction. Associated anomalies in IM is high, up to 60%.
M.J. Human, N. Tshifularo, Y. Hawu
doaj   +2 more sources