Results 31 to 40 of about 1,754 (178)

Intussusception secondary to Meckel's diverticulum in a 3-month-old girl. Case report

Revista Médica del Hospital General de México, 2018
A 3-month-old female patient is presented, with ileo-ileal intussusception secondary to Meckel's diverticulum. The patient underwent emergency surgery due to a diagnosis of intestinal obstruction secondary to intussusception.
I. Camacho-Guerrero, L. Ramírez-Patiño
doaj   +1 more source

Two Contrasting Scintigraphy‐Negative Pediatric Meckel's Diverticula Identified and Localized by Intestinal Ultrasound and Double‐Balloon Enteroscopy: A Report of Two Cases

DEN Open, Volume 7, Issue 1, April 2027.
ABSTRACT Scintigraphy‐negative Meckel's diverticulum (MD) is diagnostically challenging in children, particularly when the underlying pathology differs between cases. Technetium‐99m pertechnetate scintigraphy is widely used for diagnosis; however, false‐negative results may occur when ectopic gastric mucosa is absent or when the diverticulum is ...
Saki Kasai, Masumi Nagata, Keisuke Jimbo, Nobuyasu Arai, Yuichiro Miyake, Mitsuyoshi Suzuki, Takahiro Kudo, Go Miyano, Hiromichi Shoji   +8 more
wiley   +1 more source

COMPLICAȚIILE DIVERTICULULUI MECKEL. REVISTA LITERATURII

Arta Medica, 2022
Obiective. Scopul articolului a fost de a analiza datele din sursele existente de literatură, referitor la complicațiile diverticulului Meckel. Material  și  metode.  Au  fost  studiate  un  număr  de  publicații  științifice  ce  prezintă  informații 
Iurii Bazeliuc, Alin Bour
doaj  

“Learning from my experience”: Acute abdomen - Perforated Meckel's diverticulitis

European Journal of Radiology Open, 2019
This is a case report documenting the risk in imaging misinterpretation of a pediatric patient that presented with an acute abdomen. Computed Tomography (CT) demonstrated an inflamed blind ending loop of bowel in the pelvis without an obvious cecal ...
William Janika Brackett, Shikha Khullar-Gupta   +1 more
doaj   +1 more source

Intussusception caused by an inverted Meckel diverticulum: a rare cause of small bowel obstruction in adults

The Pan African Medical Journal, 2011
Adult intussusception due to Meckel s diverticulum is an uncommon cause of intestinal obstruction. However, the surgeon should still be suspicious of this condition since the non specific symptoms and the rarity of it make a preoperative diagnosis ...
Mahdi Bouassida, Bilel Feidi, Mechaal Ben Ali, Mohamed Fadhel Chtourou, Marouene Krifa, Selim Sassi, Fathi Chebbi, Mohamed Mongi Mighri, Hassen Touinsi, Sadok Sassi   +9 more
doaj   +1 more source

Perforated Meckel's Diverticulum in a 22‐Year‐Old Male: A Case Report

Clinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT Meckel's diverticulum (MD), the most common congenital anomaly of the gastrointestinal tract, results from incomplete regression of the vitelline duct. Although often asymptomatic, complications occur in 4%–7% of cases, with perforation being a rare but life‐threatening presentation that may mimic other acute abdominal emergencies.
Munira Abdul Aziz, Hamza Shakil, Haris Mahmood, Rawdah Shakil, Muhammad Ali, Kamil Ahmad Kamil   +5 more
wiley   +1 more source

Heterotopic pancreas in Meckel′s diverticulum in a 7-year-old child with intussusception and recurrent gastrointestinal bleeding: Case report and literature review focusing on diagnostic controversies

African Journal of Paediatric Surgery, 2014
Meckel′s diverticulum, the most common congenital abnormality of the small intestine, may be associated to heterotopic pancreas, often diagnosed incidentally on histopathological examination.
Guanà Riccardo, Bucci Valeria, Carbonaro Giulia, Cerrina Alessia, Ferrero Luisa, Teruzzi Elisabetta, Mussa Alessandro, Morra Isabella, Schleef Jürgen   +8 more
doaj   +1 more source

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12 ‐Related Developmental Disorders

American Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1619-1650, July 2026.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source

Essential embryology for the Canadian pathologists’ assistant

Anatomical Sciences Education, Volume 19, Issue 7, Page 1134-1156, July 2026.
Abstract Pathologists' assistants (PAs) are pivotal in healthcare, conducting autopsies and examining tissues under a pathologist's guidance. Embryology knowledge is crucial for PAs to accurately assess anomalies and identify pathologies. Yet, it is often overlooked in academic PA training programs.
Samantha H. Nacci, William Tsui, Fang‐I Lu, Avrum I. Gotlieb, Danielle C. Bentley   +4 more
wiley   +1 more source

MECKEL'S DIVERTICULUM – REVISITED [PDF]

Medical Journal Armed Forces India, 1997
Twenty five cases of Meckel's diverticulum were studied between 1985-1995. Eight of these were symptomatic and in the remaining 17 it was an incidental finding. The symptomatic patients presented with intestinal obstruction (5 cases), perforated peritonitis (2 cases) and intussusception (1 case). All cases of acute appendicitis were also subjected to a
H S, Bindra, S V, Soman, A K, Srivastava
openaire   +2 more sources