Familial Cancer

Novel candidates in early-onset familial colorectal cancer

Anne M. L. Jansen, Pradipta Ghosh, Tikam C. Dakal, Thomas P. Slavin, C. Richard Boland, Ajay Goel

MLH1 promoter hypermethylation: are you absolutely sure about the absence of MLH1 germline mutation? About a new case

Caroline Kientz, Fabienne Prieur, Alix Clemenson, Marie-Odile Joly, Marie-Laure Stachowicz, Jessie Auclair, Valéry Attignon, Renaud Schiappa, Qing Wang

A unique case of two somatic APC mutations in an early onset cribriform-morular variant of papillary thyroid carcinoma and overview of the literature

M. D. Aydemirli, K. van der Tuin, F. J. Hes, A. M. W. van den Ouweland, T. van Wezel, E. Kapiteijn, H. Morreau

Long-term positive psychological outcomes in an Australian pancreatic cancer screening program

R. S. O’Neill, B. Meiser, S. Emmanuel, D. B. Williams, A. Stoita

Neurofibromatosis type 2 discordance in monozygous twins

S. Amico, P. Smith, S. Tobi, M. Perry, A. Wallace, D. G. Evans

Clear cell chondrosarcoma in Von Hippel-Lindau disease

Koen M. A. Dreijerink, Rachel S. van Leeuwaarde, Wenzel M. Hackeng, Rachel H. Giles, Wendy W. J. de Leng, Paul C. Jutte, Albert J. H. Suurmeijer, Bernadette P. M. van Nesselrooij, Lodewijk A. A. Brosens

Radiotherapy-induced malignancies in breast cancer patients with TP53 pathogenic germline variants (Li–Fraumeni syndrome)

Vanessa Petry, Renata Colombo Bonadio, Allyne Queiroz Carneiro Cagnacci, Luiz Antonio Leite Senna, Roberta do Nascimento Galvão Campos, Guilherme Cutait Cotti, Paulo M. Hoff, Maria Candida Barisson Villares Fragoso, Maria del Pilar Estevez-Diz

Renal cell carcinoma in young FH mutation carriers: case series and review of the literature

J. A. Hol, M. C. J. Jongmans, A. S. Littooij, R. R. de Krijger, R. P. Kuiper, J. J. T. van Harssel, A. Mensenkamp, M. Simons, G. A. M. Tytgat, M. M. van den Heuvel-Eibrink, M. van Grotel

‘We don’t know for sure’: discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultations

Niki M. Medendorp, Marij A. Hillen, Pomme E. A. van Maarschalkerweerd, Cora M. Aalfs, Margreet G. E. M. Ausems, Senno Verhoef, Lizet E. van der Kolk, Lieke P. V. Berger, Marijke R. Wevers, Anja Wagner, Barbara A. H. Caanen, Anne M. Stiggelbout, Ellen M. A. Smets

Abstracts of the 4th meeting of the European Hereditary Tumour Group, Barcelona, Spain, October 17–19th, 2019