Results 21 to 30 of about 20,569 (202)
Abstract Lynch syndrome (LS) is the most common hereditary colorectal cancer syndrome, caused by a germline pathogenic variant in one of the mismatch repair (MMR) genes. Among these, MSH6‐associated LS represents a distinct subtype with unique molecular and clinical characteristics.
Salwa Ben Yahia +4 more
wiley +1 more source
Objetivo: Investigar o perfil epidemiológico das internações hospitalares por neoplasia maligna de cólon no Brasil, no período de 2009 a 2024. Métodos: Estudo ecológico de perfil epidemiológico realizado no Brasil entre 2009 e 2024, com dados do SIH/SUS (
Jasmine Truppel Simas
doaj +1 more source
Neoplasia Neuroendocrina - No Neuroendocrina de Colon (MINEN): Unificando Conceptos
Las neoplasias neuroendócrinas representan un 1% de todas las neoplasias malignas del tubo digestivo, de las cuales, el 14-20% corresponden al colon y solo el 1 a 3% a neoplasias rectales. El 85% de las neoplasias colónicas son carcinomas neuroendocrinos pobremente diferenciados que contienen un componente no-neuroendocrino en el 25-40% de los casos ...
Rocio Soledad Perez Dominguez +3 more
openaire +1 more source
ABSTRACT Lynch syndrome (LS) is the most common hereditary colorectal cancer (CRC) syndrome and is characterized by an accelerated adenoma‐carcinoma sequence, a relatively higher prevalence of flat and subtle CRC precursor lesions, and exceptionally high adenoma miss rates despite intensive colonoscopy surveillance.
Robert Hüneburg +3 more
wiley +1 more source
Colorectal cancer screening reduces disease burden, but the comparative performance of screening strategies remains unclear. This population‐based study shows that the tandem strategy (positive results from both questionnaire‐based risk assessment and fecal immunochemical testing) substantially improved the detection rates of colorectal cancer and ...
Ruyue Liu +5 more
wiley +1 more source
ABSTRACT Colorectal cancer (CRC) remains a leading cause of cancer‐related morbidity and mortality worldwide yet is largely preventable through effective screening and surveillance. While most CRC cases are sporadic, a substantial proportion occur in individuals at increased risk due to hereditary cancer syndromes or family history who require tailored
Ophir Gilad +5 more
wiley +1 more source
A case report of Peutz–Jeghers syndrome in a child with Crohn's disease
Abstract Peutz–Jeghers syndrome (PJS) is a rare genetic disorder characterized by hamartomatous polyps and mucocutaneous hyperpigmented freckles, whereas Crohn's disease (CD) is a condition characterized by chronic intestinal inflammation. Here, we present a rare case report of an 11‐year‐old male who presented with both CD and PJS.
Hasala Rannulu +5 more
wiley +1 more source
Racional Atualmente existem dúvidas quanto ao método ideal de rastreio e vigilância para o câncer colorretal. A retossigmoidoscopia é preconizada, já que é barata, eficaz e causa pouco desconforto, mas não pode diagnosticar tumores do cólon ...
Frank Shigueo NAKAO +2 more
doaj +1 more source
A case report of non‐syndromic colonic ganglioneuroma in a patient with juvenile polyposis
Abstract Colonic ganglioneuromas in children are rare, particularly without associated hereditary syndromes like multiple endocrine neoplasia (MEN2B), neurofibromatosis type 1(NF1), or Phosphatase and tensin homolog hamartoma tumor syndrome (PHTS). We report a 12‐year‐old male with a history of juvenile polyposis syndrome (JPS) and segmental colonic ...
Holly Coffey +2 more
wiley +1 more source
Introducción: El cáncer colorrectal es una de las neoplasias de mayor morbilidad y mortalidad a escala mundial. En Cuba ocupa la tercera causa de muerte por tumores malignos.
Raquel Onoria Cayon Poyeaux +4 more
doaj

