Results 61 to 70 of about 4,831 (162)

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

open access: yesReproductive 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   +11 more
wiley   +1 more source

Conservative Management on Antenatally Found Congenital Cystic Adenomatoid Malformation: A 1‐Year Follow‐Up Case Report

open access: yesCase Reports in Obstetrics and Gynecology, Volume 2026, Issue 1, 2026.
Objective We report a rare case of congenital cystic adenomatoid malformation (CCAM) diagnosed antenatally based on USG and postnatally based on babygram, CT scan, and chest x‐ray. We follow up the baby up to 1 year of age. Method This study is a retrospective case report describing the clinical presentation, diagnosis, and management of a single ...
Bambang Abimanyu   +7 more
wiley   +1 more source

Tonsillar Lymphangiomatous Polyp Mimicking a Vallecular Cyst in an Adult: A Case Report

open access: yesCase Reports in Otolaryngology, Volume 2026, Issue 1, 2026.
Introduction Tonsillar lymphangiomatous polyps are rare benign lesions characterized histologically by dilated lymphatic channels within a fibrous, adipose, or lymphoid stromal background. Although these lesions are more commonly reported in children and young adults, they are uncommon in older adults and may mimic other oropharyngeal or laryngeal ...
Mohammed A. Awadh   +7 more
wiley   +1 more source

Narrow‐band imaging with magnification for the diagnosis of colorectal adenoma in a patient with Cronkhite‐Canada syndrome

open access: yesDEN Open
Cronkhite‐Canada syndrome (CCS) is a rare disease characterized by gastrointestinal polyposis, skin pigmentation, alopecia, and abnormal nailfolds. Although colorectal cancer has been reported in patients with CCS, reports are limited regarding the ...
Hitoshi Fukase   +8 more
doaj   +1 more source

Bannayan-Rilay-Ruvalcaba syndrome presenting with recurrent lower gastrointestinal bleed: A Case Report and a review of the literature

open access: yesJournal of Digestive Endoscopy, 2013
Bannayan-Rilay-Ruvalcaba syndrome (BRRS) is a rare congenital disorder, characterized by macrocephaly, hamartomas, lipomas, and genital lentiginosis with or without PTEN gene mutations.
Jaswinder Singh Sodhi   +5 more
doaj   +1 more source

Impact of Magnification Endoscopy on Diagnostic Accuracy and Confidence in Real‐Time Histological Prediction of Colorectal Lesions: A Prospective Multicenter Study

open access: yesJournal of Gastroenterology and Hepatology, Volume 40, Issue 12, Page 2879-2889, December 2025.
Magnification endoscopy has a minimal impact on overall diagnostic accuracy for colorectal lesions; it significantly improves diagnostic confidence, leading to meaningful accuracy gains. ABSTRACT Background Accurate endoscopic diagnosis of colorectal lesions is essential for clinical management. This prospective multicenter study assessed the impact of
Kotaro Shibagaki   +14 more
wiley   +1 more source

A Clinical Analysis of the Association Between Nifedipine and Insulin Usage and the Increased Incidence of Colonic Polyps

open access: yesJGH Open, Volume 9, Issue 11, November 2025.
ABSTRACT Objective To investigate the association between the incidence of colon polyps and colon cancer and the use of clinical medications, including nifedipine and insulin, thereby providing a scientific basis for the development of chemoprevention strategies for colorectal cancer and for guiding rational clinical drug use.
Xiao‐Lin Wang   +4 more
wiley   +1 more source

Hamartomatous polyps - a clinical and molecular genetic study. [PDF]

open access: yesDanish medical journal, 2016
Hamartomatous polyps (HPs) in the gastrointestinal (GI) tract are rare compared to other types of GI polyps, yet they are the most common type of polyp in children. The symptoms are usually rectal bleeding, abdominal pain, obstipation, anaemia, and/or small bowel obstruction.
openaire   +3 more sources

Peutz-Jeghers Type Polyp of the Appendix with Review of Literature

open access: yesCase Reports in Pathology, 2019
Hamartomatous polyps of Peutz-Jeghers type are strongly associated with Peutz-Jeghers polyposis syndrome and are predominantly encountered in the small intestine. Sporadic cases are uncommonly reported. We report a case of a polyp identified incidentally
Jolanta Jedrzkiewicz   +5 more
doaj   +1 more source

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