Results 271 to 280 of about 103,530 (323)
Familial polyposis syndrome and achalasia in a young adult
JPGN Reports, EarlyView.Abstract We report the case of a 19‐year‐old White male diagnosed with familial adenomatous polyposis (FAP), Gardner's syndrome (GS) phenotype, status post total colectomy, who developed progressive dysphagia and weight loss. He was diagnosed with achalasia based on imaging and esophageal manometry.
Gabriella A. Lorusso Vivas +2 more
wiley +1 more source
JPGN Reports, EarlyView.Abstract Bloody stools are a particularly concerning symptom in neonates and infants. The differential diagnosis reaches from life‐threatening to benign conditions. We would like to present two infants, who presented to the paediatric emergency department with bloody stools and showed pneumatosis on ultrasonography, which initially led to the suspicion
Jessica Ruesen +5 more
wiley +1 more source
A clear approach: Hemostatic gel as a novel adjunct for pediatric upper gastrointestinal bleeding
JPGN Reports, EarlyView.Abstract Pediatric upper gastrointestinal bleeding (UGIB) is a significant clinical concern, with a mortality rate of approximately 2%. Endoscopic management of UGIB in children includes various techniques such as injections, mechanical devices, thermal therapies, and topical agents.
Natalia Plott +5 more
wiley +1 more source
JPGN Reports, EarlyView.Abstract Pediatric upper gastrointestinal (GI) bleeding secondary to duodenal ulceration is a potentially serious and life‐threatening condition with a broad differential diagnosis. We present a pediatric case of a pancreatic head solid pseudopapillary neoplasm (SPN) presenting with duodenal ulceration and recurrent upper GI bleeding.
Kanak V. Kennedy +10 more
wiley +1 more source
Carbohydrate malabsorption mimicking immune dysregulation: A histological challenge
JPGN Reports, EarlyView.Abstract We report a case of neonatal‐onset intractable diarrhea, where the patient's histologic findings suggested immune dysregulation. However, genetic testing revealed compound heterozygous variants in the SLC5A1 gene. This case report adds to the existing literature by demonstrating that severe carbohydrate malabsorption can cause inflammatory ...
Seyma Eroglu +4 more
wiley +1 more source
Genital Crohn's disease in pediatrics and genetic associations
JPGN Reports, EarlyView.Abstract Genital edema is a rare presentation of Crohn's disease (CD), also known as metastatic CD (MCD). This may precede, co‐occur with, or follow gastrointestinal symptoms and present a diagnostic challenge. We aimed to characterize the features, clinical courses, pathogenesis, and outcomes of patients with MCD to increase understanding and promote ...
Erica Chang +5 more
wiley +1 more source