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Metachronous Synovial Sarcoma After Treatment of Mixed Germ Cell Tumor in a Child with Complete Gonadal Dysgenesis

Patients with complete XY gonadal dysgenesis (GD) show a high predisposition to germ cell tumors (GCT). Patients with coexistence of GCT and GD have been reported previously. Here we present a 15-year-old girl with mixed GCT and GD who also developed an intra-abdominal synovial sarcoma one year afte...

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Autores principales: Karahan, Feryal, Çıtak, Elvan Çağlar, Yaman, Emel, Alakaya, Mehmet, Sağcan, Fatih, Yılmaz, Eda Bengi, Kuş, Funda, Gürses, İclal, Balcı, Yüksel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838380/
https://www.ncbi.nlm.nih.gov/pubmed/28836496
http://dx.doi.org/10.4274/jcrpe.4905
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author Karahan, Feryal
Çıtak, Elvan Çağlar
Yaman, Emel
Alakaya, Mehmet
Sağcan, Fatih
Yılmaz, Eda Bengi
Kuş, Funda
Gürses, İclal
Balcı, Yüksel
author_facet Karahan, Feryal
Çıtak, Elvan Çağlar
Yaman, Emel
Alakaya, Mehmet
Sağcan, Fatih
Yılmaz, Eda Bengi
Kuş, Funda
Gürses, İclal
Balcı, Yüksel
author_sort Karahan, Feryal
collection PubMed
description Patients with complete XY gonadal dysgenesis (GD) show a high predisposition to germ cell tumors (GCT). Patients with coexistence of GCT and GD have been reported previously. Here we present a 15-year-old girl with mixed GCT and GD who also developed an intra-abdominal synovial sarcoma one year after the treatment. This is the first report, to our knowledge, of synovial sarcoma associated with XY GD.
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spelling pubmed-58383802018-03-08 Metachronous Synovial Sarcoma After Treatment of Mixed Germ Cell Tumor in a Child with Complete Gonadal Dysgenesis Karahan, Feryal Çıtak, Elvan Çağlar Yaman, Emel Alakaya, Mehmet Sağcan, Fatih Yılmaz, Eda Bengi Kuş, Funda Gürses, İclal Balcı, Yüksel J Clin Res Pediatr Endocrinol Case Report Patients with complete XY gonadal dysgenesis (GD) show a high predisposition to germ cell tumors (GCT). Patients with coexistence of GCT and GD have been reported previously. Here we present a 15-year-old girl with mixed GCT and GD who also developed an intra-abdominal synovial sarcoma one year after the treatment. This is the first report, to our knowledge, of synovial sarcoma associated with XY GD. Galenos Publishing 2018-03 2018-02-26 /pmc/articles/PMC5838380/ /pubmed/28836496 http://dx.doi.org/10.4274/jcrpe.4905 Text en © Copyright 2018, Journal of Clinical Research in Pediatric Endocrinology, Published by Galenos Publishing. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Karahan, Feryal
Çıtak, Elvan Çağlar
Yaman, Emel
Alakaya, Mehmet
Sağcan, Fatih
Yılmaz, Eda Bengi
Kuş, Funda
Gürses, İclal
Balcı, Yüksel
Metachronous Synovial Sarcoma After Treatment of Mixed Germ Cell Tumor in a Child with Complete Gonadal Dysgenesis
title Metachronous Synovial Sarcoma After Treatment of Mixed Germ Cell Tumor in a Child with Complete Gonadal Dysgenesis
title_full Metachronous Synovial Sarcoma After Treatment of Mixed Germ Cell Tumor in a Child with Complete Gonadal Dysgenesis
title_fullStr Metachronous Synovial Sarcoma After Treatment of Mixed Germ Cell Tumor in a Child with Complete Gonadal Dysgenesis
title_full_unstemmed Metachronous Synovial Sarcoma After Treatment of Mixed Germ Cell Tumor in a Child with Complete Gonadal Dysgenesis
title_short Metachronous Synovial Sarcoma After Treatment of Mixed Germ Cell Tumor in a Child with Complete Gonadal Dysgenesis
title_sort metachronous synovial sarcoma after treatment of mixed germ cell tumor in a child with complete gonadal dysgenesis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838380/
https://www.ncbi.nlm.nih.gov/pubmed/28836496
http://dx.doi.org/10.4274/jcrpe.4905
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