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Eye Tumors in Childhood as First Sign of Tumor Predisposition Syndromes: Insights from an Observational Study Conducted in Germany and Austria

SIMPLE SUMMARY: Eye tumors in children are very rare. In Europe, these eye tumors are nearly always diagnosed early and cure rates are high. However, eye tumors in childhood often occur as the first sign of a genetic tumor predisposition syndrome. This study collected data of children with malignant...

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Autores principales: Reschke, Madlen, Biewald, Eva, Bronstein, Leo, Brecht, Ines B., Dittner-Moormann, Sabine, Driever, Frank, Ebinger, Martin, Fleischhack, Gudrun, Grabow, Desiree, Geismar, Dirk, Göricke, Sophia, Guberina, Maja, Le Guin, Claudia H. D., Kiefer, Tobias, Kratz, Christian P., Metz, Klaus, Müller, Bert, Ryl, Tatsiana, Schlamann, Marc, Schlüter, Sabrina, Schönberger, Stefan, Schulte, Johannes H., Sirin, Selma, Süsskind, Daniela, Timmermann, Beate, Ting, Saskia, Wackernagel, Werner, Wieland, Regina, Zenker, Martin, Zeschnigk, Michael, Reinhardt, Dirk, Eggert, Angelika, Ritter-Sovinz, Petra, Lohmann, Dietmar R., Bornfeld, Norbert, Bechrakis, Nikolaos, Ketteler, Petra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8070790/
https://www.ncbi.nlm.nih.gov/pubmed/33919815
http://dx.doi.org/10.3390/cancers13081876
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author Reschke, Madlen
Biewald, Eva
Bronstein, Leo
Brecht, Ines B.
Dittner-Moormann, Sabine
Driever, Frank
Ebinger, Martin
Fleischhack, Gudrun
Grabow, Desiree
Geismar, Dirk
Göricke, Sophia
Guberina, Maja
Le Guin, Claudia H. D.
Kiefer, Tobias
Kratz, Christian P.
Metz, Klaus
Müller, Bert
Ryl, Tatsiana
Schlamann, Marc
Schlüter, Sabrina
Schönberger, Stefan
Schulte, Johannes H.
Sirin, Selma
Süsskind, Daniela
Timmermann, Beate
Ting, Saskia
Wackernagel, Werner
Wieland, Regina
Zenker, Martin
Zeschnigk, Michael
Reinhardt, Dirk
Eggert, Angelika
Ritter-Sovinz, Petra
Lohmann, Dietmar R.
Bornfeld, Norbert
Bechrakis, Nikolaos
Ketteler, Petra
author_facet Reschke, Madlen
Biewald, Eva
Bronstein, Leo
Brecht, Ines B.
Dittner-Moormann, Sabine
Driever, Frank
Ebinger, Martin
Fleischhack, Gudrun
Grabow, Desiree
Geismar, Dirk
Göricke, Sophia
Guberina, Maja
Le Guin, Claudia H. D.
Kiefer, Tobias
Kratz, Christian P.
Metz, Klaus
Müller, Bert
Ryl, Tatsiana
Schlamann, Marc
Schlüter, Sabrina
Schönberger, Stefan
Schulte, Johannes H.
Sirin, Selma
Süsskind, Daniela
Timmermann, Beate
Ting, Saskia
Wackernagel, Werner
Wieland, Regina
Zenker, Martin
Zeschnigk, Michael
Reinhardt, Dirk
Eggert, Angelika
Ritter-Sovinz, Petra
Lohmann, Dietmar R.
Bornfeld, Norbert
Bechrakis, Nikolaos
Ketteler, Petra
author_sort Reschke, Madlen
collection PubMed
description SIMPLE SUMMARY: Eye tumors in children are very rare. In Europe, these eye tumors are nearly always diagnosed early and cure rates are high. However, eye tumors in childhood often occur as the first sign of a genetic tumor predisposition syndrome. This study collected data of children with malignant eye tumors diagnosed in five years in Germany and Austria to learn about the association of eye tumors in childhood with tumor predisposition syndrome. The study recruited 300 children with malignant eye tumors in childhood. In the here-presented cohort, more than 40% of eye tumors were associated with rare tumor predisposition syndromes. For this reason, all children with eye tumors and their families should receive genetic counseling for a tumor predisposition syndrome. Children with a genetic predisposition to cancer should receive a tailored surveillance, including detailed history, physical examination and, if indicated, imaging to screen for other cancers later in life. ABSTRACT: Retinoblastoma and other eye tumors in childhood are rare diseases. Many eye tumors are the first signs of a genetic tumor predisposition syndrome and the affected children carry a higher risk of developing other cancers later in life. Clinical and genetic data of all children with eye tumors diagnosed between 2013–2018 in Germany and Austria were collected in a multicenter prospective observational study. In five years, 300 children were recruited into the study: 287 with retinoblastoma, 7 uveal melanoma, 3 ciliary body medulloepithelioma, 2 retinal astrocytoma, 1 meningioma of the optic nerve extending into the eye. Heritable retinoblastoma was diagnosed in 44% of children with retinoblastoma. One child with meningioma of the optic nerve extending into the eye was diagnosed with neurofibromatosis 2. No pathogenic constitutional variant in DICER1 was detected in a child with medulloepithelioma while two children did not receive genetic analysis. Because of the known association with tumor predisposition syndromes, genetic counseling should be offered to all children with eye tumors. Children with a genetic predisposition to cancer should receive a tailored surveillance including detailed history, physical examinations and, if indicated, imaging to screen for other cancer. Early detection of cancers may reduce mortality.
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spelling pubmed-80707902021-04-26 Eye Tumors in Childhood as First Sign of Tumor Predisposition Syndromes: Insights from an Observational Study Conducted in Germany and Austria Reschke, Madlen Biewald, Eva Bronstein, Leo Brecht, Ines B. Dittner-Moormann, Sabine Driever, Frank Ebinger, Martin Fleischhack, Gudrun Grabow, Desiree Geismar, Dirk Göricke, Sophia Guberina, Maja Le Guin, Claudia H. D. Kiefer, Tobias Kratz, Christian P. Metz, Klaus Müller, Bert Ryl, Tatsiana Schlamann, Marc Schlüter, Sabrina Schönberger, Stefan Schulte, Johannes H. Sirin, Selma Süsskind, Daniela Timmermann, Beate Ting, Saskia Wackernagel, Werner Wieland, Regina Zenker, Martin Zeschnigk, Michael Reinhardt, Dirk Eggert, Angelika Ritter-Sovinz, Petra Lohmann, Dietmar R. Bornfeld, Norbert Bechrakis, Nikolaos Ketteler, Petra Cancers (Basel) Article SIMPLE SUMMARY: Eye tumors in children are very rare. In Europe, these eye tumors are nearly always diagnosed early and cure rates are high. However, eye tumors in childhood often occur as the first sign of a genetic tumor predisposition syndrome. This study collected data of children with malignant eye tumors diagnosed in five years in Germany and Austria to learn about the association of eye tumors in childhood with tumor predisposition syndrome. The study recruited 300 children with malignant eye tumors in childhood. In the here-presented cohort, more than 40% of eye tumors were associated with rare tumor predisposition syndromes. For this reason, all children with eye tumors and their families should receive genetic counseling for a tumor predisposition syndrome. Children with a genetic predisposition to cancer should receive a tailored surveillance, including detailed history, physical examination and, if indicated, imaging to screen for other cancers later in life. ABSTRACT: Retinoblastoma and other eye tumors in childhood are rare diseases. Many eye tumors are the first signs of a genetic tumor predisposition syndrome and the affected children carry a higher risk of developing other cancers later in life. Clinical and genetic data of all children with eye tumors diagnosed between 2013–2018 in Germany and Austria were collected in a multicenter prospective observational study. In five years, 300 children were recruited into the study: 287 with retinoblastoma, 7 uveal melanoma, 3 ciliary body medulloepithelioma, 2 retinal astrocytoma, 1 meningioma of the optic nerve extending into the eye. Heritable retinoblastoma was diagnosed in 44% of children with retinoblastoma. One child with meningioma of the optic nerve extending into the eye was diagnosed with neurofibromatosis 2. No pathogenic constitutional variant in DICER1 was detected in a child with medulloepithelioma while two children did not receive genetic analysis. Because of the known association with tumor predisposition syndromes, genetic counseling should be offered to all children with eye tumors. Children with a genetic predisposition to cancer should receive a tailored surveillance including detailed history, physical examinations and, if indicated, imaging to screen for other cancer. Early detection of cancers may reduce mortality. MDPI 2021-04-14 /pmc/articles/PMC8070790/ /pubmed/33919815 http://dx.doi.org/10.3390/cancers13081876 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Reschke, Madlen
Biewald, Eva
Bronstein, Leo
Brecht, Ines B.
Dittner-Moormann, Sabine
Driever, Frank
Ebinger, Martin
Fleischhack, Gudrun
Grabow, Desiree
Geismar, Dirk
Göricke, Sophia
Guberina, Maja
Le Guin, Claudia H. D.
Kiefer, Tobias
Kratz, Christian P.
Metz, Klaus
Müller, Bert
Ryl, Tatsiana
Schlamann, Marc
Schlüter, Sabrina
Schönberger, Stefan
Schulte, Johannes H.
Sirin, Selma
Süsskind, Daniela
Timmermann, Beate
Ting, Saskia
Wackernagel, Werner
Wieland, Regina
Zenker, Martin
Zeschnigk, Michael
Reinhardt, Dirk
Eggert, Angelika
Ritter-Sovinz, Petra
Lohmann, Dietmar R.
Bornfeld, Norbert
Bechrakis, Nikolaos
Ketteler, Petra
Eye Tumors in Childhood as First Sign of Tumor Predisposition Syndromes: Insights from an Observational Study Conducted in Germany and Austria
title Eye Tumors in Childhood as First Sign of Tumor Predisposition Syndromes: Insights from an Observational Study Conducted in Germany and Austria
title_full Eye Tumors in Childhood as First Sign of Tumor Predisposition Syndromes: Insights from an Observational Study Conducted in Germany and Austria
title_fullStr Eye Tumors in Childhood as First Sign of Tumor Predisposition Syndromes: Insights from an Observational Study Conducted in Germany and Austria
title_full_unstemmed Eye Tumors in Childhood as First Sign of Tumor Predisposition Syndromes: Insights from an Observational Study Conducted in Germany and Austria
title_short Eye Tumors in Childhood as First Sign of Tumor Predisposition Syndromes: Insights from an Observational Study Conducted in Germany and Austria
title_sort eye tumors in childhood as first sign of tumor predisposition syndromes: insights from an observational study conducted in germany and austria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8070790/
https://www.ncbi.nlm.nih.gov/pubmed/33919815
http://dx.doi.org/10.3390/cancers13081876
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