Results 31 to 40 of about 510 (145)

Molecular and clinicopathological analysis of three cases of gastric juvenile polyposis

JGH Open, Volume 6, Issue 8, Page 531-538, August 2022., 2022
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, Yuka Yanai, Tsutomu Takeda, Takuo Hayashi, Yoichi Akazawa, Noboru Yatagai, Hiroya Ueyama, Hidetaka Eguchi, Akihito Nagahara, Takashi Yao, Tsuyoshi Saito   +10 more
wiley   +1 more source

Immunoglobulin G4‐related disease accompanying a small intestinal ulcer: A case

DEN Open, Volume 2, Issue 1, April 2022., 2022
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, Akinori Mizoguchi, Kazuyuki Narimatsu, Shun Takahashi, Dai Hirata, Shinji Ono, Yusuke Onoyama, Seiya Suzuki, Tomoaki Horiuchi, Nanoka Chiya, Keisuke Ikeyama, Hiroyuki Tahara, Akira Tomioka, Suguru Ito, Rina Tanemoto, Shin Nishii, Kenichi Inaba, Nao Sugihara, Yoshinori Hanawa, Kazuki Horiuchi, Akinori Wada, Yoshihiro Akita, Masaaki Higashiyama, Shunsuke Komoto, Kengo Tomita, Shinya Yoshimatsu, Susumu Matsukuma, Ryota Hokari   +27 more
wiley   +1 more source

PTEN Hamartoma Syndrome in a Child Presenting With Malrotation, Panintestinal Polyps, Severe Anemia, and Protein‐Losing Enteropathy

JPGN Reports, Volume 2, Issue 3, August 2021., 2021
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, Atif A. Ahmed, Caitlin E. Lawson, Thomas Attard   +3 more
wiley   +1 more source

The pathology of gastric and duodenal polyps: current concepts

Histopathology, Volume 78, Issue 1, Page 106-124, January 2021., 2021
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, Baek H Kim, Gregory Y Lauwers   +2 more
wiley   +1 more source

Polyposis of gastrointestinal tract after COVID-19 mRNA vaccination: a report of two cases [PDF]

Clinical Endoscopy
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

Chemical Gastroenterocolitis after Dental Root Canal Therapy with Camphorated and Mentholated Chlorophenol

Case Reports in Gastrointestinal Medicine, Volume 2021, Issue 1, 2021., 2021
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, Ernst-Wolfgang Kolbe, Günther Winde, Michael Kaspari, Chia-Tung Shun   +4 more
wiley   +1 more source

The Diagnosis of Cronkhite-Canada Syndrome with CT Enterography: A Clinical Case Analysis

CT Lilun yu yingyong yanjiu, 2023
Cronkhite-Canada syndrome (CCS) is a rare cause of chronic diarrhea and malabsorption where patients develop multiple polyps throughout the gastrointestinal (GI) tract, accompanied by ectodermal changes.
Xuesong ZHAO, Fei MIAO, Jing SUN, Yihan DONG, Huan ZHANG, Fuhua YAN, Bei DING   +6 more
doaj   +1 more source

Cronkhite-Canada Syndrome (CCS)—A Rare Case Report [PDF]

Journal of Clinical and Diagnostic Research, 2015
Cronkhite-Canada syndrome (CCS) is an extremely rare non-inherited condition characterized by gastrointestinal hamartomatous polyposis, alopecia, onychodystrophy, hyperpigmentation, weight loss and diarrhoea.
SUBRATA CHAKRABARTI
doaj   +1 more source

A case of Cronkhite-Canada syndrome.

Nishi Nihon Hifuka, 1986
51才女子。初診の1ヵ月前より, 消化器症状, 頭部, 眉毛部の脱毛および顔面, 四肢末端の瀰漫性褐色色素沈着を生じた。手掌の皮膚病理組織像では, 基底層のメラニンの増加を認めた。Cronkhite-Canada症候群が疑われたため, 内科にて精査したところ, 消化管ポリポーシスの合併が証明されたため, 本症と確定診断した。内科入院後, onychotrophiaも出現した。治療は, 経静脈強化栄養とプレドニソロン内服投与が行われ, 消化器症状は改善し, 皮膚症状も爪と, 手背の色素沈着を除いて軽快した。
HATANO, Taketsugu, TSUDA, Shingo, SASAI, Yoichiro, IWAO, Tadashi, YAMAUCHI, Kazuaki   +4 more
openaire   +1 more source

Cronkhite-Canada Syndrome Associated with Metastatic Colon Cancer

Case Reports in Gastroenterology, 2018
Cronkhite-Canada syndrome is characterized by gastrointestinal and ectodermal manifestations. In this paper, we describe a 64-year-old Iranian male, presenting with Cronkhite-Canada syndrome with metastatic colon cancer.
Shirin Haghighi, Sima Noorali, Amir Houshang Mohammad Alizadeh   +2 more
doaj   +1 more source