Results 31 to 40 of about 82,723 (215)
Background Hereditary adenomatous polyposis syndromes, including familial adenomatous polyposis and other rare adenomatous polyposis syndromes, increase the lifetime risk of colorectal and other cancers.
G. Zaffaroni +38 more
semanticscholar +1 more source
Introduction. Chronic rhinosinusitis is a disease that occurs everywhere, characterized by inflammation of the mucous membrane of the paranasal sinuses and nasal cavity.
I. I. Chernushevich +4 more
doaj +1 more source
Efficacy of Benralizumab in severe asthma in real life and focus on nasal polyposis.
INTRODUCTION Severe asthma occurs in 5-10% of asthmatic patients, with nasal polyposis as one of the most frequent comorbidity. Benralizumab was recently marketed, thus we could analyse its effects in real-life in severe asthma, and compare the effects ...
D. Bagnasco +20 more
semanticscholar +1 more source
SummaryA review of 313 cases of nasal polyposis indicates that there is a high incidence of recurrence in this disease. Other nasal pathology affects a significant number of these patients. Simple surgical removal of the polypi by a transnasal route is the common mode of treatment.
openaire +2 more sources
Familial Adenomatous Polyposis (FAP) and Other Polyposis Syndromes
There have been significant advances in our knowledge about the molecular changes that precede and accompany the development of inherited predispositions to colorectal cancer.
Scott Rodney J
doaj +1 more source
Danish guidelines for management of non-APC-associated hereditary polyposis syndromes
Hereditary Polyposis Syndromes are a group of rare, inherited syndromes characterized by the presence of histopathologically specific or numerous intestinal polyps and an increased risk of cancer. Some polyposis syndromes have been known for decades, but
Anne Marie Jelsig +9 more
doaj +1 more source
Familial Adenomatous Polyposis Syndrome: An Update and Review of Extraintestinal Manifestations.
CONTEXT.— Familial adenomatous polyposis (FAP) is a rare genetic disorder with autosomal dominant inheritance, defined by numerous adenomatous polyps, which inevitably progress to colorectal carcinoma unless detected and managed early.
P. Dinarvand +7 more
semanticscholar +1 more source
Colorectal malakoplakia in a child presenting as multiple polyposis coli
Malakoplakia of the gastrointestinal tract is a rare chronic inflammatory disorder, usually affecting the descending colon, sigmoid colon and rectum. It is commonly seen in adults. Only few cases have been reported in children.
Meena N Jadhav +3 more
doaj +1 more source
NTHL1 tumor syndrome is an autosomal recessive rare disease caused by biallelic inactivating variants in the NTHL1 gene and which presents a broad tumor spectrum.
Carla Pinto +20 more
doaj +1 more source

