Results 51 to 60 of about 4,831 (162)

Peutz–Jeghers Syndrome in a Young Ethiopian Male: A Case Report

Case Reports in Gastrointestinal Medicine
Peutz–Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by hamartomatous polyps in the gastrointestinal (GI) tract, pigmented mucocutaneous lesions, and an increased risk of cancer.
Abate Bane Shewaye, Kaleb Assefa Berhane
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

A classical case of Peutz–Jeghers syndrome with brief review of literature

Human Pathology: Case Reports, 2016
PJS is an autosomal dominant genetic disease associated with melanin pigment spots on the oral mucosa, lips, nasal alae, palm and soles, as well as hamartomatous polyps in the alimentary canal.
T. Santosh, M.K. Patro, J. Nayak, B. Behera   +3 more
doaj   +1 more source

Non-familial juvenile polyposis of the stomach with gastric cancers: a case report

Surgical Case Reports, 2018
Background Juvenile polyposis is an autosomal dominant inherited disease characterized by the development of numerous hamartomatous and nonneoplastic polyps of the gastrointestinal tract.
Tomoko Jogo, Eiji Oki, Minako Fujiwara, Junji Kurashige, Ryota Nakanishi, Masahiko Sugiyama, Yuichiro Nakashima, Hiroshi Saeki, Shinichi Tsuruta, Masataka Nishimura, Yoshinao Oda, Yoshihiko Maehara   +11 more
doaj   +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

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

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

Characteristics of Small Bowel Polyps Detected in Cowden Syndrome by Capsule Endoscopy

Case Reports in Gastrointestinal Medicine, 2015
Cowden syndrome is an uncommon, autosomal dominant disease characterized by multiple hamartomas and hyperplastic lesions in the skin, mucous membrane, brain, breast, thyroid, and gastrointestinal tract.
Keita Saito, Eiki Nomura, Yu Sasaki, Yasuhiko Abe, Nana Kanno, Naoko Mizumoto, Rika Shibuya, Kazuhiro Sakuta, Makoto Yagi, Kazuya Yoshizawa, Daisuke Iwano, Takeshi Sato, Shoichi Nishise, Yoshiyuki Ueno   +13 more
doaj   +1 more source

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

Hamartomatous Polyp of the Nasopharynx: A Rare Case Report

Indian Journal of Otolaryngology and Head & Neck Surgery, 2017
We report a case of a rare hamartomatous polyp originating from the left nasopharyngeal wall in a 4 year old female child. The characteristic microscopic appearance was neither fitting clearly into any of the known types of hamartomas i.e. epithelial, mesenchymal and mixed nor into the category of a teratoma.
Amitav, Shukla, Trishna, Kakad, Saloni, Shah, Anita S, Bhaduri   +3 more
openaire   +3 more sources