Endoscopic ultrasonography‐guided tumor ablation
S. Lakhtakia, D. Seo
semanticscholar +1 more source
Porto‐sinusoidal vascular disorder in a pediatric patient with prolidase deficiency: A case report
Abstract Prolidase deficiency (PD) is a rare autosomal recessive disorder affecting collagen turnover, leading to diverse clinical manifestations including dermatologic lesions, hepatosplenomegaly, and vascular anomalies. Liver involvement in PD is poorly understood, with few reported cases.
Melissa Castro+5 more
wiley +1 more source
Comparison of sedation with pentazocine or pethidine hydrochloride for endoscopic ultrasonography in outpatients: A single-center retrospective study. [PDF]
Urabe M+12 more
europepmc +1 more source
Evaluation of Colorectal Villous Adenomas and Carcinomas Using Endoscopic Ultrasonography
Taikan Yamamoto+9 more
openalex +2 more sources
Abstract Hereditary angioedema (HAE) is a rare genetic condition caused by deficient or dysfunctional C1 inhibitor protein (C1INH) resulting in episodic angioedema of the skin, upper airway, and gastrointestinal tract. HAE most often presents within the first two decades of life and may cause severe abdominal pain, nausea, diarrhea, and emesis, making ...
Stephanie L. Rager+2 more
wiley +1 more source
Early Chronic Pancreatitis Findings by Endoscopic Ultrasonography (EUS) in Asymptomatic Patients with Pancreas Divisum. [PDF]
Nagahama M+6 more
europepmc +1 more source
A case of lactobezoar: Outpatient management in a neonate
Abstract A lactobezoar is a conglomerate of undigested and partially digested milk components and is the most common form of bezoar in infants. Described treatments include hospitalization for intravenous fluids and cessation of feeds, endoscopy with administration of N‐acetyl cysteine, and surgical or endoscopic removal.
Shivani Kamal+3 more
wiley +1 more source
Peroral pancreatoscopy-guided lithotripsy via an endoscopic ultrasonography-guided pancreatogastrostomy. [PDF]
Murakami M+6 more
europepmc +1 more source
ABSTRACT Sickle cell anemia (SCA) is a genetic disorder that presents with a variety of systemic complications, including gastrointestinal (GI) manifestations. These GI symptoms can overlap with those of digestive autoimmune diseases (DAD) such as inflammatory bowel disease (IBD) and autoimmune hepatitis (AIH), complicating the diagnosis and management.
Saray Mesonero Cavia+3 more
wiley +1 more source
Reactive autoimmune‐like enteropathy in the setting of a chlamydia infection: A case report
Abstract A 16‐year‐old female presenting with acute left‐sided abdominal pain, diarrhea, nausea, and vomiting associated with a 20‐lb weight loss. She was found to have positive chlamydia polymerase chain reaction upon admission. She underwent endoscopy and colonoscopy, with pathology revealing marked inflammation, complete villous blunting with ...
Sarah Masten+3 more
wiley +1 more source