Lynchin oireyhtymän syöpää ehkäisevä seuranta muuttuu geenikohtaiseksi

Mecklin, Jukka-Pekka

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Mecklin, J.-P. (2020). Lynchin oireyhtymän syöpää ehkäisevä seuranta muuttuu geenikohtaiseksi. Duodecim, 137(17), 1867-1869. https://www.duodecimlehti.fi/lehti/2020/17/duo15749

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Duodecim

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Mecklin, Jukka-Pekka

Date

2020

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Asetyylisalisyylihapon tehosta vakuuttavaa näyttöä ja rokote kehitteillä

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Kustannus Oy Duodecim

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0301-8989

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Jukka-Pekka Mecklin: Apuraha (Syöpäsäätiö, VTR, J&A Erkon Säätiö)

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Except where otherwise noted, this item's license is described as In Copyright

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Risk-Reducing Gynecological Surgery in Lynch Syndrome : Results of an International Survey from the Prospective Lynch Syndrome Database

Dominguez-Valentin, Mev; Seppälä, Toni T.; Engel, Christoph; Aretz, Stefan; Macrae, Finlay; Winship, Ingrid; Capella, Gabriel; Thomas, Huw; Hovig, Eivind; Nielsen, Maartje; Sijmons, Rolf H.; Bertario, Lucio; Bonanni, Bernardo; Tibiletti, Maria G.; Cavestro, Giulia M.; Mints, Miriam; Gluck, Nathan; Katz, Lior; Heinimann, Karl; Vaccaro, Carlos A.; Green, Kate; Lalloo, Fiona; Hill, James; Schmiegel, Wolff; Vangala, Deepak; Perne, Claudia; Strauß, Hans-Georg; Tecklenburg, Johanna; Holinski-Feder, Elke; Steinke-Lange, Verena; Mecklin, Jukka-Pekka; Plazzer, John-Paul; Pineda, Marta; Navarro, Matilde; Vidal, Joan B.; Kariv, Revital; Rosner, Guy; Piñero, Tamara A.; Gonzalez, María L.; Kalfayan, Pablo; Sampson, Julian R.; Ryan, Neil A. J.; Evans, D. G.; Møller, Pål; Crosbie, Emma J. (MDPI, 2020)

Purpose: To survey risk-reducing hysterectomy and bilateral salpingo-oophorectomy (BSO) practice and advice regarding hormone replacement therapy (HRT) in women with Lynch syndrome. Methods: We conducted a survey in 31 ...
The “unnatural” history of colorectal cancer in Lynch syndrome : lessons from colonoscopy surveillance

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Individuals with Lynch syndrome (LS), one of the most common inherited cancer syndromes, are at increased risk of developing malignancies, in particular colorectal cancer (CRC). Regular colonoscopy with polypectomy is ...
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Lynch syndrome (LS) is one of the most prevalent hereditary cancer syndromes in man and accounts for some 3% of unselected patients with colorectal or endometrial cancer and 10–15% of those with DNA mismatch repair ...
Detection of a major Lynch Syndrome-causing MLH1 founder variant in a large-scale genotyped cohort

Sipilä, Lauri J.; Aavikko, Mervi; Ravantti, Janne; Martin, Samantha; Kuopio, Teijo; Lahtinen, Laura; FinnGen; Peltomäki, Päivi; Mecklin, Jukka-Pekka; Aaltonen, Lauri A.; Seppälä, Toni T. (Springer, 2024)

Some 50% of Finnish Lynch Syndrome (LS) cases are caused by a founder variant in MLH1, in which the entire exon 16 has been lost due to an Alu-mediated recombination event. We piloted detecting the variant in FinnGen, a ...
Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment : a report from the prospective Lynch syndrome database

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Background The Prospective Lynch Syndrome Database (PLSD) collates information on carriers of pathogenic or likely pathogenic MMR variants (path_MMR) who are receiving medical follow-up, including colonoscopy surveillance, ...

Lynchin oireyhtymän syöpää ehkäisevä seuranta muuttuu geenikohtaiseksi

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