Results 41 to 50 of about 3,754 (176)

Essential embryology for the Canadian pathologists’ assistant

open access: yesAnatomical Sciences Education, EarlyView.
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   +4 more
wiley   +1 more source

Spontaneous perforation of Meckel's diverticulum: a case report and review of literature

open access: yesThe Pan African Medical Journal, 2015
Meckel's diverticulum is the commonest congenital abnormality of the gastrointestinal tract. Hemorrhage, obstruction and inflammation are the three main categories of complications resulting from Meckel's diverticulum. Spontaneously perforation of Meckel'
Robleh Hassan Farah   +8 more
doaj   +1 more source

Paediatric development of radiopharmaceutical imaging agents and radioligand therapeutics

open access: yesBritish Journal of Clinical Pharmacology, EarlyView.
Abstract This review focuses on the development of radiopharmaceutical imaging agents and radioligand therapeutics for paediatric use. Nuclear medicine plays an important role in the diagnosis and treatment of various childhood conditions, including cancers, infections and brain disorders.
Justin L. Hay   +5 more
wiley   +1 more source

Littré’s hernia: a rare complication of Meckel’s diverticulum

open access: yes, 2017
Littré’s hernia is caused by the protrusion of Meckel’s diverticulum through an orifice in the abdominal wall. Meckel’s diverticulum is the most common congenital anomaly of the gastrointestinal tract that is generally asymptomatic and only manifests in ...
Suman Saurav Rout, Prakash Kumar Sahoo
core   +1 more source

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

open access: yesAmerican 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   +4 more
wiley   +1 more source

Small bowel segment with Meckel’s diverticulum volvulus related to short mesodiverticular band: a case report

open access: yesJournal of Medical Case Reports, 2023
Background Meckel’s diverticulum is a remnant of the omphalomesenteric duct and occurs in only about 2% of people. Mesodiverticular band is the congenital remnant of the vitelline artery and is an even less often occurring phenomenon.
Michał Zieliński   +3 more
doaj   +1 more source

A case report of inverted Meckel's diverticulum

open access: yesRadiology Case Reports, 2021
Inverted Meckel's diverticulum is an entity often discovered incidentally or through a clinical evaluation for gastrointestinal bleeding. While rare, inverted Meckel's diverticulum should be considered in the evaluation of a patient presenting with ...
Elizabeth Rhodes, BS   +3 more
doaj   +1 more source

Obstructing Meckel's diverticulum associated with Infantile Hypertrophic Pyloric Stenosis

open access: yesJournal of Pediatric Surgery Case Reports, 2019
Infantile Hypertrophic Pyloric Stenosis (IHPS) with Meckel's diverticulum presenting as an intraluminal cyst is a very rare presentation. We are reporting a case presenting with persistent non-bilious vomiting after each feed.
Amit kumar sinha   +4 more
doaj   +1 more source

Jejunal Diverticulosis as a Rare Cause of Severe Obscure Gastrointestinal Bleeding in an Elderly Patient: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Jejunal diverticulosis is a rare cause of obscure gastrointestinal bleeding (OGIB) that can present with life‐threatening hemorrhage. We report a 69‐year‐old male with recurrent melena, severe anemia, and hemodynamic instability requiring multiple transfusions. Upper and lower endoscopy were nondiagnostic, and CT angiography failed to localize
Mahmoud Draidi   +5 more
wiley   +1 more source

Bilateral Gonadoblastoma in a 12‐Year‐Old Girl 4 Years After Wilms' Tumor: A Rare Pediatric Case

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT This case of a 12‐year‐old patient who developed bilateral gonadoblastoma 4 years after treatment for Wilms tumor highlights the importance of rigorous, risk‐adapted long‐term surveillance and careful evaluation of incidental gonadal findings, even in asymptomatic patients.
Ahmed Quraish   +4 more
wiley   +1 more source

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