Results 191 to 200 of about 587,390 (283)

Delayed diagnosis of hereditary fructose intolerance presenting as chronic lean steatosis in an adolescent

open access: yesJPGN Reports, EarlyView.
Abstract Hereditary fructose intolerance (HFI) typically presents in infancy with acute metabolic crisis upon the introduction of fructose. We report a case of a 13‐year‐old female with chronic abdominal pain, short stature, and persistent mild transaminitis.
Alexandra Hurlock   +4 more
wiley   +1 more source

Case report of a gastric bezoar causing anterograde gastroduodenal intussusception requiring surgical intervention in a 15‐year‐old female

open access: yesJPGN Reports, EarlyView.
Abstract Gastroduodenal bezoars are masses of indigestible material that accumulate within the stomach and may lead to obstruction. We present a young female who presented with abdominal pain, nausea, and vomiting, and was found to have a large gastric bezoar extending into the duodenum, resulting in gastroduodenal intussusception.
Olga Ostrovetsky   +8 more
wiley   +1 more source

AI told my cat he's terminally ill

open access: yes
Journal of Hospital Medicine, EarlyView.
Jamila Mammadova
wiley   +1 more source

A joint transdisciplinary approach for paediatric inflammatory bowel disease: Integrating nursing, dietetic and psychological support

open access: yesJPGN Reports, EarlyView.
Abstract Paediatric inflammatory bowel disease (pIBD) is a long‐term, immune‐mediated condition characterised by fluctuating gastrointestinal symptoms, nutritional risk and psychosocial difficulties. Although multidisciplinary team (MDT) support is considered the gold standard, there is considerable variation in how it is delivered, and it remains ...
King‐Chi Yau, Laura Tesser, Kay Crook
wiley   +1 more source

Type II achalasia unmasked by EndoFLIP and high‐resolution manometry in a child with eosinophilic esophagitis

open access: yesJPGN Reports, EarlyView.
ABSTRACT Eosinophilic esophagitis (EoE) is a chronic immune‐mediated disease characterized by esophageal dysfunction and eosinophilic inflammation. Persistent dysphagia despite histologic remission should prompt evaluation for alternative etiologies. A 10‐year‐old male with asthma and eczema presented with progressive solid food dysphagia, daily non ...
Rasha Abi Radi Abou Jaoudeh   +2 more
wiley   +1 more source

Plummer–Vinson syndrome in a 10‐year‐old boy from Côte d'Ivoire: An exceptional paediatric case with African context

open access: yesJPGN Reports, EarlyView.
Abstract Plummer–Vinson syndrome (PVS) is characterised by the triad of dysphagia, iron‐deficiency anaemia, and proximal oesophageal webs. While well described in adults, paediatric cases remain exceptionally rare, particularly in sub‐Saharan Africa.
Paul Mike Tayou Mbobda   +2 more
wiley   +1 more source

Recurrent acute pancreatitis caused by a duodenal diverticulum: The diagnostic value of secretin‐enhanced magnetic resonance cholangiopancreatography

open access: yes
Journal of Pediatric Gastroenterology and Nutrition, EarlyView.
Dagmar H. Zeef   +5 more
wiley   +1 more source

Acinar Cell Carcinoma of the Pancreas: A Three Case Series and Literature Review. [PDF]

open access: yesNiger Med J
Nasiru R   +6 more
europepmc   +1 more source

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