Results 281 to 290 of about 80,240 (320)

Hereditary angioedema as a cause of recurrent abdominal pain in a pediatric patient with Crohn's disease

JPGN Reports, EarlyView.
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, Paula J. Busse, Joesph A. Picoraro   +2 more
wiley   +1 more source

Linking epidemiological and genomic data in cases of enteric fever in England to inform clinical management and public health action. [PDF]

J Antimicrob Chemother
Buczkowska M, Chattaway MA, Jenkins C, Hungerford D, Katwa P, Kirkbride H, Hawker J.   +6 more
europepmc   +1 more source

An incidental finding of mesenteric hematoma in a patient with a new diagnosis of inflammatory bowel disease

JPGN Reports, EarlyView.
Abstract Mesenteric hematomas (MHs) are relatively rare and are characterized by localized bleeding in the mesenteric vascular tree presenting with abdominal pain, vomiting, abdominal distension, masses, and hypotension. We report a case of a MH which was incidentally found in a 10‐year‐old patient with a new diagnosis of ulcerative colitis (UC).
Breanna Brown, Anna Hunter, Kimberly Trieschmann   +2 more
wiley   +1 more source

Enteric Fever Presenting With Complete Heart Block (CHB): A Rare Case of Reversible Arrhythmia. [PDF]

Cureus
Dhondge RH, Acharya S, Kumar S, Agrawal S, Nimkar SV.   +4 more
europepmc   +1 more source

A case of amebic colitis: A potentially fatal mimicker of inflammatory bowel disease

JPGN Reports, EarlyView.
ABSTRACT Amebiasis, caused by Entamoeba histolytica, can present diagnostic challenges due to its diverse clinical manifestations and potential for misdiagnosis, particularly in regions with low incidence rates. We report a case of a 9‐year‐old girl initially diagnosed with inflammatory bowel disease but later confirmed to have amebic colitis.
Fadhel Al Ateeqi, Ala K. Shaikhkhalil, Nowfala Nowshad   +2 more
wiley   +1 more source

Digestive autoimmune diseases mimicking gastrointestinal manifestations in children with sickle cell anemia: A report of three cases

JPGN Reports, EarlyView.
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, Marta García Bernal, Maria Jose López Liñan, Roger García Puig   +3 more
wiley   +1 more source

Evaluation of a point-of-care immunochromatographic assay for enteric fever in Dhaka, Bangladesh: a prospective diagnostic accuracy study.

Lancet Microbe
Munira SJ, Islam N, Prithe NT, Sarkar A, Esfandiari J, Gunasekera D, Islam S, Akter T, Garrett DO, Saha SK, Andrews JR, Saha S, Charles RC.   +12 more
europepmc   +1 more source

A pragmatic and ethical guide for addressing life‐sustaining treatments in patients with suicidal thoughts or behaviors

Journal of Hospital Medicine, EarlyView.
Nurlan Aliyev, Chad Vokoun, Lou A. Lukas
wiley   +1 more source

Decline in gut motility of cerebral palsy patients after a triggering event: A discussion on invasive versus conservative management

JPGN Reports, EarlyView.
Abstract Objectives Patients with cerebral palsy (CP) often have gastrointestinal dysmotility. An inciting event, such as infection, may lead to progressive decline in bowel motility and episodes of acute pediatric intestinal pseudo‐obstruction (PIPO).
Zoe Saenz, Elizabeth Reynolds, Jamie E. Anderson, Payam Saadai, Maheen Hassan   +4 more
wiley   +1 more source