Results 51 to 60 of about 2,191 (165)

Autoimmune gastritis with a gastric hamartomatous inverted polyp and two hyperplastic polyps: a case report

Journal of International Medical Research, 2023
We report an unusual case of autoimmune gastritis (AIG) complicated with a submucosal tumor (SMT) and two pedunculated polyps in a 60-year-old man. The patient was admitted for epigastric distention, heartburn, and anorexia.
Jun-zhen Hou, Ning-ning Dong, Bing Yue, Fan-dong Meng, Yong-jun Wang   +4 more
doaj   +1 more source

PRKD3 Overexpression May Improve Survival and Suppresses Proliferation in Colorectal Cancer

Cancer Reports, Volume 9, Issue 4, April 2026.
ABSTRACT Objective The study aimed to explore PRKD3 protein expression in colorectal cancer and its clinical implications. Methods PRKD3 expression was assessed in 189 paired colorectal cancer tissues and their corresponding adjacent non‐cancerous counterparts using tissue microarray‐based immunohistochemistry. The associations of PRKD3 expression with
Bin Zhang, Chen Chang, Jingli Chen, Yue Cao, Yu Chang, Lele Liu, Wensheng Li, Guorong Wang   +7 more
wiley   +1 more source

Solitary Peutz-Jeghers Polyp in a Paediatric Patient

Case Reports in Gastroenterology, 2010
Hamartomatous polyps of Peutz-Jeghers are mostly found in patients affected by Peutz-Jeghers syndrome (PJS), but they can be rarely encountered in the general population. It is unclear whether a solitary Peutz-Jeghers polyp (PJP) is an incomplete form of
Giuseppe Retrosi, Lorenzo Nanni, Fabio Maria Vecchio, Carlo Manzoni, Raffaella Canali, Gaia Busato, Claudio Pintus   +6 more
doaj   +1 more source

Toward Timely Diagnosis of Pancreatic Cancer: Revolutionizing Early Detection Through Genomics, Artificial Intelligence, and Noninvasive Biomarkers

Journal of Gastroenterology and Hepatology, Volume 41, Issue 3, Page 895-913, March 2026.
ABSTRACT Background Pancreatic ductal adenocarcinoma (PDAC) remains one of the most aggressive cancers, typically diagnosed at an advanced stage due to its subtle and often absent early symptoms. Despite representing only 3% of new cancer cases, it is projected to become the second leading cause of cancer‐related deaths by 2030.
Muhammad Masroor Hussain, Sana Qammar, Ju‐Mei Wang, Ao‐Qiang Zhai, Fu‐yu Li, Hai‐jie Hu   +5 more
wiley   +1 more source

Peutz-Jeghers syndrome: Quantitative study on enterochromaffin cells in hamartomatous intestine polyps [PDF]

Srpski Arhiv za Celokupno Lekarstvo, 2013
Introduction. Peutz-Jeghers (PJ) syndrome is a rare familial disorder with the autosomal transmission characterized by multiple intestinal polyps, mucocutaneous pigmentation and increased incidence of various malignancies. Some clinical manifestations
Krstić Miljan, Katić Vuka, Stojnev Slavica, Mihailović Dragan, Mojsilović Marijola, Radovanović Zoran, Živković Vladimir   +6 more
doaj   +1 more source

Cerebrovascular Malformations Associated With Hereditary Hemorrhagic Telangiectasia and HHT‐Like Syndromes: A Comparative Overview

European Journal of Neurology, Volume 33, Issue 2, February 2026.
Hereditary hemorrhagic telangiectasia (HHT) and several HHT‐like syndromes, including Wyburn–Mason, Cobb, Klippel–Trénaunay, Parkes Weber, neurofibromatosis type 1, PHACE(S), capillary malformation–AVM (CM‐AVM), Juvenile polyposis/HHT overlap, HHT type 5, PTEN hamartoma tumor syndrome, and blue rubber bleb nevus syndrome, share overlapping ...
Matteo Palermo, Carmelo Lucio Sturiale
wiley   +1 more source

Peutz-Jeghers polyp: A Retrospective Study on Twelve Cases Received at the Department of Pathology, Bangabandhu Sheikh Mujib Medical University

Bangabandhu Sheikh Mujib Medical University Journal, 2012
Background: Peutz Jegher syndrome is a rare inherited condition characterized mainly by gastrointestinal hamartomatous polyposis and mucocutaneous pigmentation.
Tamanna Choudhury, Suraiya Enam, Ferdousy Begum, Md. Taufiq, Mohammed Kamal   +4 more
doaj   +1 more source

Gastric hamartomatous polyps in the absence of familial polyposis coli [PDF]

Cancer, 1980
Hamartomatous polyps in the stomach have been described as gastric lesions of familial polyposis coli. Four cases of multiple gastric hamartomatous polyps not associated with polyposis coli were encountered. Histologically, all these polyps consisted of normal oxyntic glands with numerous cystic dilatations of the glandular lumens of various sizes ...
M, Tatsuta, S, Okuda, H, Tamura, H, Taniguchi   +3 more
openaire   +2 more sources

Ovarian Sex Cord Stromal Tumor With Annular Tubules: A Rare Diagnosis in Young Women

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT Ovarian sex cord‐stromal tumor with annular tubules (SCTAT) is a rare neoplasm with distinct clinicopathological features in its sporadic and syndromic forms, the latter commonly associated with Peutz‐Jeghers syndrome. Although imaging may suggest a sex cord‐stromal origin, definitive diagnosis relies on histopathological examination.
Prescillia Marques, Thiago Vieira, Raquel Brodbeck Ilgenfritz, Dusan Djokovic   +3 more
wiley   +1 more source

A Successful Live Birth After Double Fertility Preservation With Embryo Cryopreservation and MPA Therapy Combined With Hysteroscopic Resection for Metachronous Breast and Endometrial Cancer in Women With Cowden Syndrome: A Case Report

Reproductive Medicine and Biology, Volume 25, Issue 1, January/December 2026.
ABSTRACT Case Cowden syndrome is an autosomal‐dominantly inherited rare condition caused by germline pathogenic variants of the PTEN gene. Multiple tumor development at a younger age in this syndrome may warrant different modalities of fertility preservation.
Itsuki Kajimura, Michio Kitajima, Shoko Miura, Chiaki Eishi, Riko Matsuda, Kanako Matsumoto, Ayumi Harada, Yuriko Kitajima, Yuri Hasegawa, Megumi Matsumoto, Keitaro Matsumoto, Kiyonori Miura   +11 more
wiley   +1 more source