Results 21 to 30 of about 460 (115)
Cronkhite–Canada syndrome: report of a rare case and review of the literature
Cronkhite–Canada syndrome is rarely encountered in clinical practice. Notably, most patients with Cronkhite–Canada syndrome exhibit hypoalbuminemia.
Yuping Liu +3 more
doaj +1 more source
Abstract Introduction The risk of cancer in patients with solitary colorectal juvenile polyps (JPs) is poorly investigated and several studies have reported polyps with dysplastic and adenomatous alterations. We aimed to investigate the long‐term risk of cancer and mortality in these patients by merging data from national registers and comparing them ...
Anne Marie Jelsig +5 more
wiley +1 more source
While short and long attachment caps are available for colonoscopy, it is unclear which type is more appropriate for acute hematochezia. This study has shown that long cap‐assisted colonoscopy is superior to short cap colonoscopy for the diagnosis of acute hematochezia, particularly colonic diverticular bleeding, and the detection of active bleeding ...
Mariko Kobayashi +45 more
wiley +1 more source
Cronkhite-Canada Syndrome: Report of Three Cases and Literature Review [PDF]
Cronkhite-Canada syndrome (CCS) is currently considered to be a non-genetic disorder and a relatively rare clinical condition that is characterized endoscopically by multiple polyps in the gastrointestinal tract and clinically manifested by ...
LI Shuying, LIN Yingmin, WANG Min
doaj +1 more source
Molecular and clinicopathological analysis of three cases of gastric juvenile polyposis
Strong nuclear expression of SMAD4, even under the presence of genetic alterations, seems to be closely associated with dysplastic polyps in juvenile polyposis (JP). Complete inactivation of SMAD4 was not shown to be essential for the development of dysplastic polyps in gastric JP, and other pathways seemed to be involved in the acquisition of the ...
Yuya Yamashiro +10 more
wiley +1 more source
Immunoglobulin G4‐related disease accompanying a small intestinal ulcer: A case
Abstract Immunoglobulin (Ig)G4‐related disease (IgG4‐RD) is a systemic condition associated with fibroinflammatory lesions and is characterized by elevated serum IgG4 levels and IgG4‐positive cell infiltration into the affected tissues. It has been reported that IgG4‐RD affects a variety of organs but uncommonly affects the gastrointestinal tract.
Yuta Yoshidome +27 more
wiley +1 more source
PTEN hamartoma syndrome (PTEN‐HS) is a rare syndrome including neurologic, neurodevelopmental, integumentary, endocrine, and gastrointestinal manifestations. Eosinophilic disorders of the gastrointestinal system are diverse group of disorders reported to be more common in PTEN‐HS.
Nicole Stoecklein +3 more
wiley +1 more source
The pathology of gastric and duodenal polyps: current concepts
The liberal use of upper endoscopy has led to an increased detection of gastric and duodenal polyps, which are identified in as many as 6 and 4.6% of patient examinations, respectively. Gastroduodenal polyps are a heterogeneous group of lesions that can be neoplastic or non‐neoplastic (e.g. hyperplastic or heterotopical).
Bence Kővári +2 more
wiley +1 more source
Polyposis of gastrointestinal tract after COVID-19 mRNA vaccination: a report of two cases [PDF]
Cronkhite-Canada syndrome is a rare gastrointestinal polyposis syndrome with distinctive clinical features and endoscopic findings. Diagnosis can be challenging without suspicion, and the disease carries high mortality due to complications such as ...
Jun Ho Kim, Eun Hye Oh, Dong Soo Han
doaj +1 more source
A 78‐year‐old man with a history of pancolitis, after the treatment of dental abscess with oral antibiotics and local application of camphorated and mentholated chlorophenol (CMCP), presented with abdominal pain of 4‐day duration, as well as hair loss in the area of moustache and finger nail lifting.
Mikheil Kalandarishvili +4 more
wiley +1 more source

