Corticotroph Pituitary Carcinoma in a Patient With Lynch Syndrome (LS) and Pituitary Tumors in a Nationwide LS Cohort.

Bengtsson, Daniel; Joost, Patrick; Aravidis, Christos; Askmalm Stenmark, Marie; Backman, Ann-Sofie; Melin, Beatrice; von Salomé, Jenny; Zagoras, Theofanis; Gebre-Medhin, Samuel; Burman, Pia

Bengtsson, Daniel; Joost, Patrick; Aravidis, Christos; Askmalm Stenmark, Marie; Backman, Ann-Sofie; Melin, Beatrice; von Salomé, Jenny; Zagoras, Theofanis; Gebre-Medhin, Samuel; Burman, Pia.

Afiliação

Bengtsson D; Department of Clinical and Experimental Medicine, Linköping University, 58183 Linköping, Sweden.
Joost P; Department of Internal Medicine, Kalmar County Hospital, 39185 Kalmar, Sweden.
Aravidis C; Department of Oncology and Pathology, Institute of Clinical Sciences, Lund University, 22184 Lund, Sweden.
Askmalm Stenmark M; Department of Immunology, Genetics and Pathology, Uppsala University, 75185 Uppsala, Sweden.
Backman AS; Division of Clinical Genetics, Department of Clinical and Experimental Medicine, Linköping University, 58185 Linköping, Sweden.
Melin B; Department of Clinical Genetics, Office for Medical Services, 22184 Lund, Sweden.
von Salomé J; Division of Clinical Genetics, Department of Laboratory Medicine, Lund University, 22184 Lund, Sweden.
Zagoras T; Centrum for Digestive Diseases, Karolinska University Hospital, Solna, 17176 Stockholm, Sweden.
Gebre-Medhin S; Institution of Medicine, Karolinska Institutet, Solna, 17176 Stockholm, Sweden.
Burman P; Department of Radiation Sciences, Oncology, Umeå University, 90187 Umeå, Sweden.

J Clin Endocrinol Metab ; 102(11): 3928-3932, 2017 11 01.

Article em En | MEDLINE | ID: mdl-28938458

Assuntos

Carcinoma/patologia; Neoplasias Colorretais Hereditárias sem Polipose/patologia; Neoplasias Hipofisárias/patologia; Carcinoma/genética; Estudos de Coortes; Neoplasias Colorretais Hereditárias sem Polipose/genética; Corticotrofos/patologia; Reparo de Erro de Pareamento de DNA/genética; Mutação em Linhagem Germinativa; Humanos; Neoplasias Hepáticas/genética; Neoplasias Hepáticas/secundário; Masculino; Pessoa de Meia-Idade; Neoplasias Hipofisárias/genética; Sistema de Registros; Suécia

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article

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