Results 21 to 30 of about 2,713 (206)
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
Cirugía Laparoscópica en el Cáncer de Colon, en el Hospital Oncológico Solca Quito.
Introducción: La cirugía para el cáncer de colorrectal consiste en la resección en bloque del tumor y de ?12 ganglios linfáticos regionales, debe incluir la ligadura alta del vaso principal del segmento.
Miguel Rueda Mesías +2 more
doaj +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
Os registros de câncer de base populacional são uma fonte importante de casos para os estudos da epidemiologia e prevenção de câncer. O câncer colorretal é a segunda causa de morte por neoplasias em mulheres nos Estados Unidos. Weinberg et al8 através do
Nazira Mahayri +1 more
doaj +1 more source
Doença de Cowden ou síndrome dos hamartomas múltiplos [PDF]
Os autores descrevem um caso de doença de Cowden ou síndrome dos hamartomas múltiplos. Doença de transmissão autossômica dominante cuja tríade dermatológica clássica compõe-se de tricolemomas faciais múltiplos (hamartomas do infundíbulo folicular ...
Gerson Vettorato +3 more
doaj +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
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
Metástasis en pene de un adenocarcinoma del colon
Introducción: Entre las lesiones malignas que se describen, se encuentra el cáncer de pene. Esta entidad constituye del 2 al 5 % de los tumores urogenitales masculinos; la lesión metastásica es muy poco frecuente.
Raiza González Marshall +2 more
doaj
Anticancer potential of berberine: Molecular pathways and current clinical trial perspectives
Abstract Cancer is constantly rising mortality rates due to its late prognosis, poor management, and expensive treatment. Multi‐sectoral approaches for cancer management include hygienic practices, synthetic drug exploitation, radiation therapy, and diet modifications.
Muhammad Maaz +10 more
wiley +1 more source

