Works matching Cowden syndrome and cancer

Results: 120

Cowden Syndrome Diagnosed by Bilateral Breast Cancer with Lhermitte-Duclos Disease: A Case Report.

Published in:

Case Reports in Oncology, 2020, v. 13, n. 1, p. 419, doi. 10.1159/000506979

By:

Morisaki, Tamami;
Kashiwagi, Shinichiro;
Kouhashi, Rika;
Yabumoto, Akimichi;
Asano, Yuka;
Takashima, Tsutomu;
Hirakawa, Kosei;
Ohira, Masaichi

Publication type:

Article

Hereditary breast cancer associated with Cowden syndrome-related PTEN mutation with Lhermitte-Duclos disease.

Published in:

Surgical Case Reports, 2017, v. 3, n. 1, p. 1, doi. 10.1186/s40792-017-0355-6

By:

Kimura, Fuyo;
Ueda, Ai;
Sato, Eiichi;
Akimoto, Jiro;
Kaise, Hiroshi;
Yamada, Kimito;
Hosonaga, Mari;
Kawai, Yuko;
Teraoka, Saeko;
Okazaki, Miki;
Ishikawa, Takashi

Publication type:

Article

PTEN in colorectal cancer: a report on two Cowden syndrome patients.

Published in:

Clinical Genetics, 2012, v. 81, n. 6, p. 555, doi. 10.1111/j.1399-0004.2011.01639.x

By:

Kersseboom, R;
Dubbink, HJ;
Corver, WE;
van Tilburg, AJP;
Poley, JW;
van Leerdam, ME;
Atmodimedjo, PN;
van de Laar, IMBH;
Collée, JM;
Dinjens, WNM;
Morreau, H;
Wagner, A

Publication type:

Article

Endometrial cancer in a 14-year-old girl with Cowden syndrome: A case report.

Published in:

Journal of Obstetrics & Gynaecology Research, 2013, v. 39, n. 4, p. 876, doi. 10.1111/j.1447-0756.2012.02052.x

By:

Baker, William David;
Soisson, Andrew Patrick;
Dodson, Mark Kane

Publication type:

Article

A progressive and refractory case of breast cancer with Cowden syndrome.

Published in:

2022

By:

Sueta, Aiko;
Takeno, Masako;
Goto-Yamaguchi, Lisa;
Tomiguchi, Mai;
Inao, Toko;
Yamamoto-Ibusuki, Mutsuko;
Yamamoto, Yutaka

Publication type:

Case Study

Breast Cancer in Cowden Syndrome: Manifestation of a Familial Cancer Syndrome.

Published in:

Clinical Journal of Oncology Nursing, 2010, v. 14, n. 1, p. 33, doi. 10.1188/10.CJON.33-35

By:

Erickson, Janetlynne;
Lyon, Debra E.

Publication type:

Article

A Case of Cowden Syndrome with Bilateral Breast Cancer: Invasive Carcinoma of No Special Type and Pure Cribriform Carcinoma.

Published in:

Iranian Journal of Radiology, 2020, v. 17, n. 1, p. 1, doi. 10.5812/iranjradiol.91951

By:

Yoo Kyeong Seo;
Go Eun Yang;
Taek Geun Ohk

Publication type:

Article

KILLIN Gene Discovery Stirs Up Research on Cowden Syndrome Cancers.

Published in:

JNCI: Journal of the National Cancer Institute, 2011, v. 103, n. 5, p. 362, doi. 10.1093/jnci/djr055

By:

Schmidt, Charlie

Publication type:

Article

Managing the risk of cancer in Cowden syndrome: a case report.

Published in:

Journal of Medical Case Reports, 2012, v. 6, n. 1, p. 225, doi. 10.1186/1752-1947-6-225

By:

Hammami, Sonia;
Berriche, Olfa;
Ali, Hichem Belhadj;
Hellara, Olfa;
Ansar, Farooq;
Mahjoub, Silvia

Publication type:

Article

A Patient with Transverse Colon Cancer Complicated by Cowden Syndrome Administered FOLFOXIRI + Bevacizumab Therapy.

Published in:

2023

By:

Takehara, Kazuhiro;
Ishizaki, Yoichi;
Nagakari, Kunihiko;
Ohuchi, Masakazu;
Fukunaga, Masaki;
Sakamoto, Kazuhiro

Publication type:

Case Study

Differential expression of novel naturally occurring splice variants of PTEN and their functional consequences in Cowden syndrome and sporadic breast cancer.

Published in:

Human Molecular Genetics, 2006, v. 15, n. 5, p. 777, doi. 10.1093/hmg/ddi492

By:

Agrawal, Shipra;
Eng, Charis

Publication type:

Article

Germline alterations in RASAL1 in Cowden syndrome patients presenting with follicular thyroid cancer and in individuals with apparently sporadic epithelial thyroid cancer.

Published in:

2014

By:

Ngeow, Joanne;
Ni, Ying;
Tohme, Rita;
Song Chen, Fu;
Bebek, Gurkan;
Eng, Charis

Publication type:

journal article

Incidence and clinical characteristics of thyroid cancer in prospective series of individuals with Cowden and Cowden-like syndrome characterized by germline PTEN, SDH, or KLLN alterations.

Published in:

2011

By:

Ngeow, Joanne;
Mester, Jessica;
Rybicki, Lisa A;
Ni, Ying;
Milas, Mira;
Eng, Charis

Publication type:

journal article

Cowden syndrome: presenting as advanced breast cancer in a young woman with macrocephaly.

Published in:

Internal Medicine Journal, 2012, v. 42, n. 10, p. 1160, doi. 10.1111/j.1445-5994.2012.02874.x

By:

Winter, H.;
Mcewen, A.

Publication type:

Article

Germline PTEN, SDHB-D, and KLLN alterations in endometrial cancer patients with Cowden and Cowden-like syndromes: An international, multicenter, prospective study.

Published in:

Cancer (0008543X), 2015, v. 121, n. 5, p. 688, doi. 10.1002/cncr.29106

By:

Mahdi, Haider;
Mester, Jessica L.;
Nizialek, Emily A.;
Ngeow, Joanne;
Michener, Chad;
Eng, Charis

Publication type:

Article

StatBite Lifetime Risk of Selected Cancers for People With Cowden Syndrome.

Published in:: JNCI: Journal of the National Cancer Institute, 2011, v. 103, n. 5, p. 363, doi. 10.1093/jnci/djr065
Publication type:: Article

Therapeutic Implications of PTEN Loss in Patients with Cowden Syndrome and Renal Cell Cancer.

Published in:

Surgery, Gastroenterology & Oncology, 2023, v. 28, n. 3, p. 136, doi. 10.21614/sgo-588

By:

Lanzafame, Katia;
Inzerilli, Nicola;
Carciotto, Rosaria;
Longhitano, Claudio;
Stella, Stefania;
Salvatore, Lo Bianco;
Rossi, Lorenzo;
Vigneri, Paolo

Publication type:

Article

Cowden syndrome: a major indication for extensive cancer surveillance.

Published in:

Medical Oncology, 2012, v. 29, n. 2, p. 1365, doi. 10.1007/s12032-011-9896-x

By:

Tutluer, Seda;
Tanriover, Mine;
Guven, Gulay

Publication type:

Article

Breast Cancer and Non-Hodgkin Lymphoma in a Young Male with Cowden Syndrome.

Published in:

2016

By:

Hagelstrom, Robert Tanner;
Ford, James;
Reiser, Gwendolyn M.;
Nelson, Marilu;
Pickering, Diane L.;
Althof, Pamela A.;
Sanger, Warren G.;
Coccia, Peter F.

Publication type:

journal article

Cowden syndrome: Recognizing and managing a not-so-rare hereditary cancer syndrome.

Published in:

Journal of Surgical Oncology, 2015, v. 111, n. 1, p. 125, doi. 10.1002/jso.23735

By:

Mester, Jessica;
Eng, Charis

Publication type:

Article

Occult Breast Cancer due to Multiple Calcified Hamartomas in a Patient with Cowden Syndrome.

Published in:

Case Reports in Radiology, 2012, p. 1, doi. 10.1155/2012/638725

By:

García, E. B. Gómez;
Lobbes, M. B. I.;
van de Vijver, K.;
Keymeulen, K.;
van der Ent, F.;
Yntema, H. G.;
Tjan-Heijnen, V. C.;
Boetes, C.

Publication type:

Article

Cowden Syndrome Presenting as Breast Cancer: Imaging and Clinical Features.

Published in:

Korean Journal of Radiology, 2014, v. 15, n. 5, p. 586, doi. 10.3348/kjr.2014.15.5.586

By:

Mirinae Seo;
Nariya Cho;
Hye Shin Ahn;
Hyeong-Gon Moon

Publication type:

Article

Cancer risk and genotype–phenotype correlation in Japanese patients with Cowden syndrome.

Published in:

International Journal of Clinical Oncology, 2022, v. 27, n. 4, p. 639, doi. 10.1007/s10147-022-02116-w

By:

Teramae, Satoshi;
Muguruma, Naoki;
Okamoto, Koichi;
Oseto, Kumiko;
Nishikawa, Ryutaro;
Tanoue, Takayuki;
Hirata, Keiji;
Yanai, Shunichi;
Matsumoto, Takayuki;
Shimizu, Seiji;
Miwa, Jun;
Sasaki, Yu;
Yashima, Kazuo;
Ohnuma, Hiroyuki;
Sato, Yasushi;
Kitayama, Yoshitaka;
Ohda, Yoshio;
Yamauchi, Atsushi;
Sanomura, Yoji;
Tanaka, Kumiko

Publication type:

Article

Screening for germline phosphatase and tensin homolog-mutations in suspected Cowden syndrome and Cowden syndrome-like families among uterine cancer patients.

Published in:

Oncology Letters, 2015, v. 9, n. 4, p. 1782, doi. 10.3892/ol.2015.2890

By:

TZORTZATOS, GERASIMOS;
ARAVIDIS, CHRISTOS;
LINDBLOM, ANNIKA;
MINTS, MIRIAM;
THAM, EMMA

Publication type:

Article

Unexpected cancer-predisposition gene variants in Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome patients without underlying germline PTEN mutations.

Published in:

PLoS Genetics, 2018, v. 14, n. 3, p. 1, doi. 10.1371/journal.pgen.1007352

By:

Yehia, Lamis;
Ni, Ying;
Sesock, Kaitlin;
Niazi, Farshad;
Fletcher, Benjamin;
Chen, Hannah JinLian;
LaFramboise, Thomas;
Eng, Charis

Publication type:

Article

Germline SDHx variants modify breast and thyroid cancer risks in Cowden and Cowden-like syndrome via FAD/NAD-dependant destabilization of p53.

Published in:

Human Molecular Genetics, 2012, v. 21, n. 2, p. 300, doi. 10.1093/hmg/ddr459

By:

Ni, Ying;
He, Xin;
Chen, Jinlian;
Moline, Jessica;
Mester, Jessica;
Orloff, Mohammed S.;
Ringel, Matthew D.;
Eng, Charis

Publication type:

Article

Gastric adenocarcinoma and proximal polyposis of the stomach: diagnosis and clinical perspectives.

Published in:

Clinical & Experimental Gastroenterology, 2018, v. 11, p. 447, doi. 10.2147/CEG.S163227

By:

Rudloff, Udo

Publication type:

Article

Similarities of cutaneous and breast pathology in Cowden's Syndrome.

Published in:

Experimental Dermatology, 1998, v. 7, n. 6, p. 380, doi. 10.1111/j.1600-0625.1998.tb00338.x

By:

Schrager, Carolina A.;
Schneider, Douglas;
Gruener, Alexandra C.;
Tsou, Hui C.;
Peacocke, Monica

Publication type:

Article

PTEN breast cancer susceptibility: a matter of dose.

Published in:

Ecancermedicalscience, 2010, v. 4, p. 1, doi. 10.3332/ecancer.2010.192

By:

Alimonti, A.

Publication type:

Article

Familial cancer among consecutive uterine cancer patients in Sweden.

Published in:

Hereditary Cancer in Clinical Practice, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1897-4287-12-14

By:

Tzortzatos, Gerasimos;
Wersäll, Ofra;
Danielsson, Kristina Gemzell;
Lindblom, Annika;
Tham, Emma;
Mints, Miriam

Publication type:

Article

Cowden syndrome: Oral presentations of a paraneoplastic syndrome. Case report and review of the literature.

Published in:

2017

By:

Tariq, Snober;
Katz, Joseph

Publication type:

Case Study

PTEN Hamartoma Tumor Syndrome/Cowden Syndrome: Genomics, Oncogenesis, and Imaging Review for Associated Lesions and Malignancy.

Published in:

Cancers, 2021, v. 13, n. 13, p. 3120, doi. 10.3390/cancers13133120

By:

Dragoo, David D.;
Taher, Ahmed;
Wong, Vincenzo K.;
Elsaiey, Ahmed;
Consul, Nikita;
Mahmoud, Hagar S.;
Mujtaba, Bilal;
Stanietzky, Nir;
Elsayes, Khaled M.

Publication type:

Article

Challenges in Managing Patients with Hereditary Cancer at Gynecological Services.

Published in:

Obstetrics & Gynecology International, 2019, p. 1, doi. 10.1155/2019/4365754

By:

Ueda, Mako;
Tsubamoto, Hiroshi;
Kashima-Morii, Mina;
Torii, Yoshitaka;
Kamihigashi, Mariko;
Wakimoto, Yu;
Nakagomi, Nami;
Hashimoto-Tamaoki, Tomoko;
Sawai, Hideaki;
Shibahara, Hiroaki

Publication type:

Article

Dysphagia and Neck Swelling in a Case of Undiagnosed Lhermitte-Duclos Disease and Cowden Syndrome.

Published in:

Case Reports in Oncological Medicine, 2015, v. 2015, p. 1, doi. 10.1155/2015/546297

By:

Hu, Zishuo Ian;
Bangiyev, Lev;
Seidman, Roberta J.;
Cohen, Jules A.

Publication type:

Article

Cowden Syndrome.

Published in:

Journal of Genetic Counseling, 1997, v. 6, n. 2, p. 181, doi. 10.1023/A:1025664119494

By:

Eng, Charis

Publication type:

Article

Hereditary gynecologic tumors and precision cancer medicine.

Published in:

Journal of Obstetrics & Gynaecology Research, 2022, v. 48, n. 5, p. 1076, doi. 10.1111/jog.15197

By:

Ogawa, Chikako;
Hirasawa, Akira;
Ida, Naoyuki;
Nakamura, Keiichiro;
Masuyama, Hisashi

Publication type:

Article

O-11 A rare cause of thyroid cancer - Li Fraumeni 2 syndrome.

Published in:

JCEM Case Reports, 2024, v. 2, p. 1, doi. 10.1210/jcemcr/luad146.061

By:

Talaibekova, Sezim;
Saygili, Emre Sedar;
Karakiliç, Ersen

Publication type:

Article

Selected syndromes of hamartomatous polyposis of the gastrointestinal tract – clinical and genetic aspects.

Published in:

Nowotwory, 2022, v. 72, n. 2, p. 131, doi. 10.5603/NJO.2022.0019

By:

Pytrus, Tomasz;
Pesz, Karolina;
Kofla-Dłubacz, Anna;
Stawarski, Andrzej;
Gil, Justyna

Publication type:

Article

Systemic Treatment Strategies for Patients with Hereditary Breast Cancer Syndromes.

Published in:

Oncologist, 2017, v. 22, n. 6, p. 655, doi. 10.1634/theoncologist.2016-0430

By:

Parkes, Amanda;
Arun, Banu K.;
Litton, Jennifer K.

Publication type:

Article

Lhermitte-Duclos Disease: A Rare Entity With Typical Histology but Ambiguous Histogenesis.

Published in:

International Journal of Surgical Pathology, 2024, v. 32, n. 6, p. 1113, doi. 10.1177/10668969231215816

By:

Rajeswarie, R. T.;
Mallik, Dattatraya;
Gopal, Swaroop

Publication type:

Article

KLLN-mediated DNA damage-induced apoptosis is associated with regulation of p53 phosphorylation and acetylation in breast cancer cells.

Published in:

Cell Death Discovery, 2018, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41420-018-0094-x

By:

Sankunny, Madhav;
Eng, Charis

Publication type:

Article

KLLN-mediated DNA damage-induced apoptosis is associated with regulation of p53 phosphorylation and acetylation in breast cancer cells.

Published in:

Cell Death Discovery, 2018, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41420-018-0094-x

By:

Sankunny, Madhav;
Eng, Charis

Publication type:

Article

Diagnosis program in the endometrial cancer.

Published in:

2017

By:

Bohîlțea, Roxana Elena;
Baroș, Andrei-Alexandru;
Ţurcan, Natalia;
Cîrstoiu, Monica Mihaela

Publication type:

Abstract

Susceptibility to Breast Cancer: Hereditary Syndromes and Low Penetrance Genes.

Published in:

Breast Disease, 2007, v. 27, n. 1, p. 21

By:

Peshkin, Beth N.;
Nusbaum, Rachel;
Vogel, Kristen J.;
Ready, Kaylene

Publication type:

Article

Coexisting lipomatous meningioma and glioblastoma in Cowden syndrome: A unique tumor association.

Published in:

Neuropathology, 2023, v. 43, n. 1, p. 110, doi. 10.1111/neup.12858

By:

Prieto, Ruth;
Hofecker, Verena;
Corbacho, Cesáreo

Publication type:

Article

When is molecular genetic testing for colorectal cancer indicated?

Published in:

Journal of Gastroenterology & Hepatology, 2002, v. 17, n. 4, p. 389, doi. 10.1046/j.1440-1746.2002.02727.x

By:

BARBARA, LEGGETT

Publication type:

Article

KLLN epigenotype-phenotype associations in Cowden syndrome.

Published in:

European Journal of Human Genetics, 2015, v. 23, n. 11, p. 1538, doi. 10.1038/ejhg.2015.8

By:

Nizialek, Emily A;
Mester, Jessica L;
Dhiman, Vineet K;
Smiraglia, Dominic J;
Eng, Charis

Publication type:

Article

Where Birt-Hogg-Dubé meets Cowden Syndrome: mirrored genetic defects in two cases of syndromic oncocytic tumours.

Published in:

European Journal of Human Genetics, 2013, v. 21, n. 10, p. 1169, doi. 10.1038/ejhg.2013.8

By:

Pradella, Laura Maria;
Lang, Martin;
Kurelac, Ivana;
Mariani, Elisa;
Guerra, Flora;
Zuntini, Roberta;
Tallini, Giovanni;
MacKay, Alan;
Reis-Filho, Jorge S;
Seri, Marco;
Turchetti, Daniela;
Gasparre, Giuseppe

Publication type:

Article

PTEN hamartoma tumor syndromes.

Published in:

European Journal of Human Genetics, 2008, v. 16, n. 11, p. 1289, doi. 10.1038/ejhg.2008.162

By:

Blumenthal, Gideon M.;
Dennis, Phillip A.

Publication type:

Article

Detection of functional PTEN lipid phosphatase protein and enzyme activity in squamous cell carcinomas of the head and neck, despite loss of heterozygosity at this locus.

Published in:

2001

By:

Snaddon, J;
Parkinson, E K;
Craft, J A;
Bartholomew, C;
Fulton, R

Publication type:

journal article