Results 71 to 80 of about 18,113 (219)
Reexamining Multisystem Desmoid Tumors Linked to Gardner’s Syndrome: A Clinical Case
Case Reports in Gastrointestinal MedicineA variation of familial adenomatous polyposis (FAP), known as Gardner’s syndrome (GS), can manifest as extraintestinal tumors, such as desmoid tumors (DTs). A key part in the diagnosing process is played by the clinician.
Haijia Zhang +3 more
doaj +1 more source
Peutz-Jeghers Syndrome: In Siblings with Palmer-Plantar Pigmentation
Journal of Indian Academy of Oral Medicine and Radiology, 2011 Peutz-Jeghers syndrome (PJS) is a rare autosomal dominant disorder characterized by typical pigmented perioral maculesn pigmented spots in the oral mucosa and digits along with hamartomatous polyps in the gastrointestinal tract.
K V Suresh +2 more
doaj +1 more source
Annals of Gastroenterological Surgery, Volume 10, Issue 4, Page 984-994, July 2026.ABSTRACT Background The Department of Gastroenterological Surgery at Kumamoto University has maintained a commitment to integrating cutting‐edge clinical practice with fundamental research, particularly concerning malignant diseases of the digestive tract.
Hideo Baba +4 more
wiley +1 more source
, 2004 Min mice have a germ-line nonsense mutation at codon 850 of the adenomatous polyposis coli (Apc) gene. These mice spontaneously develop multiple polyps in the small and large intestine at the age of 10–12 weeks.
Goonesekera, S. +7 more
core
Metastatic Unfunctional Pancreatic Neuroendocrine Tumor in Lynch Syndrome
Clinical Case Reports, Volume 14, Issue 7, July 2026.ABSTRACT Lynch syndrome (LS), a well‐known cancer risk syndrome, is caused by deleterious germline mutations in the mismatch repair genes. LS predispose patients to various types of cancers including colon adenocarcinoma. We discuss the case of a woman with LS who also developed a non‐functioning pancreatic neuroendocrine tumor (P‐NET) following ...
Fateme Salemi +5 more
wiley +1 more source
Computed tomography findings of diffuse gastrointestinal mantle cell lymphoma
Radiology Case Reports, 2017 Multiple lymphomatous polyposis is an uncommon type of primary non-Hodgkin's lymphoma, characterized by multiple lymphomatous polyps along the gastrointestinal tract.
Fernando Ide Yamauchi, MD +4 more
doaj +1 more source
An Unusual Cause of Melena: Adjacent Sigmoid Tubular Adenomas With Moderate Dysplasia—A Case Report
Clinical Case Reports, Volume 14, Issue 7, July 2026.ABSTRACT Melena usually indicates upper gastrointestinal bleeding but may rarely result from slow bleeding in the distal colon. When upper endoscopy is negative, colonoscopy is essential. Although uncommon, bleeding colonic adenomas should be considered, as endoscopic polypectomy can provide both diagnosis and definitive treatment.
Ahmad Abbas +9 more
wiley +1 more source
Search for viral particles in human papillomas [PDF]
, 1979 By electron microscopy, viral particles were searched for in specimens taken from 3 cases of verruca vulgaris, 2 cases of verruca plana, 2 cases of epidermodysplasia verruciformis, 8 cases of oral papilloma, 2 cases of nasal papilloma, 4 cases of ...
Yasui, Masazumi, Masazumi YASUI
core +1 more source
CNS Neuroscience &Therapeutics, Volume 32, Issue 7, July 2026.Repeated exposure to sevoflurane in neonatal mice leads to impaired myelin development and neurobehavioral dysfunction, a process closely associated with reduced butyrate levels in vivo. Sodium butyrate supplementation effectively ameliorates these sevoflurane‐induced abnormalities by downregulating HDAC3 and HDAC8 expression, enhancing H3K9ac levels ...
Chang Liu +6 more
wiley +1 more source
[A young man with intestinal polyposis and epistaxis]
, 2014 Contains fulltext : 137321.pdf (Publisher’s version ) (Closed access)BACKGROUND: Germline mutations in the SMAD4 gene lead to both juvenile polyposis syndrome and hereditary haemorrhagic telangiectasia (HHT). CASE DESCRIPTION: A 23-year-
Mager, J.J. +5 more
core