Distinct clinical and genetic mutation characteristics in sporadic and Lynch syndrome-associated endometrial cancer in a Chinese population.
Sign Up to like & getrecommendations! Published in 2021 at "Cancer epidemiology"
DOI: 10.1016/j.canep.2021.101934
Abstract: BACKGROUND The diagnosis of Lynch syndrome-associated endometrial cancer patients is significant for early warning of their relatives. The purpose of this study was to provide diagnostic indicators of Lynch syndrome-associated endometrial cancer by screening the… read more here.
Keywords: syndrome associated; associated endometrial; endometrial cancer; cancer ... See more keywords
Ultrasonographic appearance of the endometrium after saline infusion in women presenting with PRM-associated endometrial changes, due to the use of ulipristal acetate
Sign Up to like & getrecommendations! Published in 2022 at "Journal of Obstetrics and Gynaecology"
DOI: 10.1080/01443615.2022.2111516
Abstract: Abstract Ulipristal acetate (UPA), used for the treatment in women with symptomatic fibroids, is associated with endometrial changes visualised on ultrasound as thickening up to more than 16 mm in approximately 10% of the patients. Is… read more here.
Keywords: intrauterine pathology; pathology; treatment; ulipristal acetate ... See more keywords
First report of granulosa cell tumour associated with an endometrial adenoma in a crossbreed cow in Portugal
Sign Up to like & getrecommendations! Published in 2018 at "Journal of the Hellenic Veterinary Medical Society"
DOI: 10.12681/jhvms.18889
Abstract: A 12.5 year-old female crossbred cow without clinical signs at ante mortem inspection was slaughtered. The post-mortem inspection revealed poor carcass condition, interstitial nephritis and generalized lymphadenitis. The reproductive tract presented an unilateral and highly… read more here.
Keywords: cell tumour; adenoma; granulosa cell; endometrial adenoma ... See more keywords
Lynch Syndrome-Associated Endometrial Cancer With Combined EPCAM-MSH2 Deletion: A Case Report
Sign Up to like & getrecommendations! Published in 2022 at "Frontiers in Oncology"
DOI: 10.3389/fonc.2022.856452
Abstract: Background Lynch syndrome (LS), an autosomal dominant disorder, is characterized by germline pathogenic variants in DNA mismatch repair (MMR) genes like MSH2. EPCAM deletions cause a minority (3%) of LS cases. However, there are only… read more here.
Keywords: endometrial cancer; msh2; lynch syndrome; case ... See more keywords