702 results match your criteria: "Imaging in Ileal Atresia"

Challenges in managing neonatal ileal atresia in limited-resource settings: a case report.

Pan Afr Med J

November 2024

President´s Office, Region Authorities and Local Governments, Region Health Management Team, Kigoma, Tanzania.

Article Synopsis
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Colonoscopy diagnosis of recurrent abdominal pain in a 4-year-old boy with intestinal duplication cyst involving colon, appendix, and ileum: a case report.

J Med Case Rep

September 2024

Department of General Surgery, School of Medicine, Shanghai Children's Hospital, Shanghai Jiao Tong University, No. 355, Luding Road, Shanghai, 200062, China.

Article Synopsis
  • Intestinal duplication cysts are rare congenital malformations that can affect any part of the gastrointestinal tract, often leading to symptoms that mimic other abdominal issues in children, making diagnosis difficult.
  • A 4-year-old boy experienced recurrent abdominal pain and vomiting, and despite initial negative tests, a later barium examination revealed a significant mass related to an intestinal duplication cyst involving the colon, appendix, and ileum.
  • After surgical resection of the cyst, the patient showed improvement without recurrence of symptoms for 5 years, highlighting the importance of using colonoscopy as a diagnostic tool for challenging cases.
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Accelerated T2-weighted MRI of the bowel at 3T using a single-shot technique with deep learning-based image reconstruction: impact on image quality and disease detection.

Acad Radiol

August 2024

NYU Langone Health Department of Radiology, 660 1st Avenue, New York, NY 10016 (B.D., B.B., S.B., S.K., A.R., F.F., H.C.); NYU Long Island Department of Radiology, Mineola, NY 11501 (B.D., B.B., B.B., S.B., A.R., F.F., M.K., H.C.).

Rationale And Objective: A single-shot T2-weighted deep-learning-based image reconstruction (DL-HASTE) has been recently developed allowing for shorter acquisition time than conventional half-Fourier acquisition single-shot turbo-spin echo (HASTE). The purpose of this study was to compare image quality of conventional 6 mm HASTE with DL-HASTE at 4 mm and 6 mm slice thickness.

Materials And Methods: 91 patients (51 female; mean±SD age: 44±10years) who underwent 3T MR enterography from 5/15/2023-7/15/2023 including pelvic conventional HASTE and DL-HASTE were included.

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Quantitative MRI in children with Crohn's disease - where do we stand?

Pediatr Radiol

October 2024

Department of Radiology, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Kasota Building MLC 5031, Cincinnati, OH, 45229, USA.

Crohn's disease (CD) is a chronic inflammatory condition that affects the gastrointestinal tract, particularly the ileum and colon. This disease is characterized by recurrent bouts of intestinal inflammation with subsequent bowel wall damage, including scarring (i.e.

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Ileal venous malformation in a pediatric patient.

J Clin Ultrasound

November 2024

Department of Ultrasound, West China Second University Hospital, Sichuan University, Chengdu, China.

A 16-month-old girl presented with ileal venous malformation. Ultrasound facilitated a preoperative diagnosis, leading to a successful surgical resection. The study emphasizes the critical role of identifying sonographic features like intestinal wall thickening, a serpiginous mass with sluggish blood sinuses, and rich vascular flow for accurate diagnosis and timely treatment.

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BACKGROUND Reversed intestinal malrotation is an extremely rare disease, with an incidence of 1 in 250 000. In Japan, application of robotic-assisted colorectal cancer surgery is expected to increase. There are no reports of robot-assisted surgery for cecal cancer with reversed intestinal malrotation.

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Diagnosis and resolution of olmesartan-associated sprue-like enteropathy confirmed by capsule endoscopy: a case report and literature review.

Clin J Gastroenterol

October 2024

Division of Gastroenterology and Hepatology, Graduate School of Medical and Dental Sciences, Niigata University, 1-757, Aasahimachi-dori, Chuo-ku, Niigata, Japan.

Herein, we describe a case of olmesartan-associated sprue-like enteropathy, in which improvement in villous atrophy was confirmed using small bowel capsule endoscopy. The patient was a 69-year-old woman who had persistent watery diarrhea (20 bowel movements/day) for 1 year and experienced a weight loss of 10 kg in the same period. Abdominal computed tomography revealed no abnormalities, and blood test results revealed no inflammatory reactions.

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Application of small bowel capsule endoscopy in children with Meckel's diverticulum.

Eur J Gastroenterol Hepatol

July 2024

Department of Gastroenterology, Ministry of Education Key Laboratory of Child Development and Disorders, China International Science and Technology Cooperation Base of Child Development and Critical Disorders, Chongqing Key Laboratory of Pediatrics, National Clinical Research Center for Child Health and Disorders, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders.

Background: Meckel diverticulum (MD) is an important cause of gastrointestinal bleeding in children. Small bowel capsule endoscopy (SBCE) is a first-line examination method applied to patients with obscure gastrointestinal bleeding, but there are few studies on its application in children with MD. This article aims to provide evidence in favor of the auxiliary diagnosis of MD in children by analyzing its characteristics using SBCE.

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Analysis of Ileal Atresia from Prenatal Ultrasound to Postoperative Follow-up: Two Case Reports.

Curr Med Imaging

August 2024

Department of Medical Ultrasound, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Medicine and Health Key Laboratory of Abdominal Medical Imaging, Jinan, Shandong Province, China.

Background: Congenital ileal atresia is a rare neonatal disease, the most common type of intestinal malformation in newborns, and one of the most common causes of congenital intestinal obstruction. It can cause various digestive system symptoms, including abdominal distension, vomiting, abnormal bowel movements, etc. In severe cases, it can be life-threatening.

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Article Synopsis
  • Maldevelopment of the fetal bowel can lead to intestinal atresia, a rare condition causing congenital bowel obstruction; this report focuses on a case detected during a routine ultrasound at 22 weeks of gestation.
  • A 24-year-old woman with gestational diabetes underwent ultrasound and was diagnosed with bowel issues, prompting counseling about potential complications; by 33 weeks, the condition worsened and surgery was performed after birth.
  • The case underscores the significance of prenatal ultrasounds in identifying fetal abnormalities, demonstrates effective management of intestinal atresia, and highlights the challenges of coexisting conditions like gestational diabetes.
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Objective: To investigate the diagnostic utility of multimodal ultrasound for fetal bowel dilatation (FBD) in different parts of the bowel and to examine its prognostic potential in FBD.

Methods: This retrospective study analyzed 86 fetuses with a dilated bowel identified via ultrasound in a 10-month postnatal follow-up. Both two- and three dimensional (2D and 3D, respectively) ultrasound volume imaging were used to characterize dilation across different bowel sections.

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Crohn's disease.

Lancet

March 2024

Department of Gastroenterology and Hepatology, University Hospitals Leuven and KU Leuven, Leuven, Belgium. Electronic address:

Crohn's disease is a chronic inflammatory disease of the gastrointestinal tract that might lead to progressive bowel damage and disability. The exact cause of Crohn's disease is unknown, but evidence points towards multifactorial events causing dysregulation of the innate immune system in genetically susceptible people. Commonly affecting the terminal ileum and proximal colon, Crohn's disease inflammation is often discontinuous and patchy, segmental, and transmural.

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Analysis of the clinical diagnosis and treatment of fetal meconium peritonitis.

J Matern Fetal Neonatal Med

December 2024

Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fuzhou, China.

Background: The purpose of this study was to improve diagnostic and therapeutic standards by examining the clinical features, treatment, and prognosis of fetal meconium peritonitis (FMP), as well as the diagnostic efficacy of ultrasound for FMP.

Methods: The clinical data of 41 infants and pregnant women diagnosed with meconium peritonitis (MP) and treated at the Fujian Maternal and Child Health Hospital from January 2013 to January 2020 were analyzed retrospectively. Clinical data, imaging data, complications, treatment strategies, pregnancy outcomes, neonatal prognoses, and follow-up outcomes were all analyzed.

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Background: Patent omphalomesenteric duct is one of the birth defects included in the spectrum of vitelline duct abnormalities. It is a rare anomaly with estimated prevalence of 0.13-0.

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Pachydysostosis of the fibula in a case of familial adenomatous polyposis.

Eur J Med Genet

April 2024

Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal; University Clinic of Genetics, Faculty of Medicine, Universidade de Coimbra, Coimbra, Portugal; Clinical Academic Center of Coimbra, Coimbra, Portugal. Electronic address:

Background: Familial Adenomatous Polyposis (FAP) is a colorectal cancer (CRC) predisposition syndrome caused by germline APC mutations and characterised by an increased risk of CRC and colonic polyps and, in certain forms, of specific prominent extraintestinal manifestations, namely osteomas, soft tissue tumours and dental anomalies. Pachydysostosis of the fibula is a rare clinical entity defined by unilateral bowing of the distal portion of the fibula and elongation of the entire bone, without affectation of the tibia.

Clinical Report: We report a 17-year-old male, who presented with a non-progressive bowing of the right leg detected at 18 months of age caused by a fibula malformation (later characterized as pachydysostosis) and a large exophytic osteoma of the left radius, noticed at the age of 15 years, without gastrointestinal symptoms.

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Article Synopsis
  • The study looked at two types of surgery methods, Three-column osteotomies (TCOs) and anterior column realignment (ACR), to see how they affect the spine.
  • They found that out of 69 patients, about 20% developed a problem called PJK after surgery, and ACR was linked to a higher chance of getting this problem compared to TCO.
  • TCO also led to better improvements in spine shape and alignment compared to ACR.
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Background: Unexpected hypermetabolic activity is often encountered in the gastrointestinal tract when PET/CT is performed for various indications, prompting endoscopic evaluation. Our aim was to characterize the types of lesions seen in segments of the gastrointestinal tract with unexpected PET/CT abnormalities as well as clinically significant lesions seen on endoscopy which did not produce a PET/CT abnormality to guide the endoscopist tasked with evaluating these imaging findings.

Methods: We retrospectively reviewed a database of endoscopies performed at City of Hope Comprehensive Cancer Center between January 1, 2016 and September 30, 2021 for an indication of "abnormal PET.

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Background: Multidisciplinary management of patients with an ileoanal pouch requires dedicated imaging to identify structural problems of the pouch associated with dysfunction. The purpose of this study is to provide a framework for interpretation of magnetic resonance imaging (MRI) scan of the ileoanal pouch to enable surgeons and radiologists to work cohesively, optimise diagnosis and ultimately improve patient care.

Methods: We propose a protocol for structured MRI assessment of the ileal pouch, aiming to provide surgeons a systematic report of the anatomy, its variations and pouch complications.

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Intussusception occurs when a part of the intestine enters another segment of the intestine causing bowel obstruction. It is common in children but not in adults with only <5% of prevalence of all intussusceptions. Most of the cases have an underlying neoplastic pathology.

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Alimentary tract duplications are heterogenous congenital anomalies of the digestive tract. Their form of presentation is varied, and they may lead to different complications, depending on their natural course. Infection is a rare complication, but it cannot be ignored because of its severity.

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Background: Fetal small bowel obstruction (SBO) is a serious condition with high morbidity and mortality rates. Prenatal ultrasound is an important tool for detecting SBO, but the optimal cutoff value for intestinal diameter remains undefined.

Objective: This study aimed to investigate the ultrasonic characteristics of fetal SBO and determine the optimal cutoff value for intestinal diameter to enhance prenatal ultrasound diagnosis.

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Endoscopic removal of a huge cecum fecalith hidden behind the ileocecal stricture in a patient with Crohn's disease.

Gastrointest Endosc

April 2024

Department of Gastrointestinal Endoscopy, Guangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Diseases, Biomedical Innovation Center, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

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Residual abnormalities on CTE predict adverse outcomes in Crohn's disease with endoscopic healing.

Dig Liver Dis

February 2024

Department of Radiology, The Sixth Affiliated Hospital, Sun Yat-sen University. 26th Yuancun the second Road, Guangzhou, Guangdong Province, 510655, China; Biomedical Innovation Center, The Sixth Affiliated Hospital, Sun Yat-sen University, China. Electronic address:

Background: Residual abnormalities on computed tomography enterography (CTE) in Crohn's disease (CD) with endoscopic healing (EH) may have prognostic implications and affect therapeutic strategy.

Methods: CD patients with EH who underwent CTE between March 2015 and June 2022 were enrolled. CTE findings of the terminal ileum and the most severe segment of colon at the time of EH were assessed respectively for each patient.

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