Clinical and epidemiological characteristics of children with germ cell tumors: A single center experience in a developing country

Germ cell tumor (GCT) is a rare malignancy accounting for 2-3% of all pediatric tumors. The overall survival rate of children and adolescents with GCT is more than 80% after adopting combined therapy. The aim of this study is to review clinical presentation, management, and outcome in a single-cent...

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Main Authors: Sonay İncesoy-Özdemir, Ulya Ertem, Gürses Şahin, Ceyhun Bozkurt, Nazmiye Yüksek, Ayşe Ceyda Ören, Eda Balkaya, Afra Alkan
Format: Article
Language:English
Published: Hacettepe University Institute of Child Health 2017-08-01
Series:The Turkish Journal of Pediatrics
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Online Access:https://turkjpediatr.org/article/view/1008
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author Sonay İncesoy-Özdemir
Ulya Ertem
Gürses Şahin
Ceyhun Bozkurt
Nazmiye Yüksek
Ayşe Ceyda Ören
Eda Balkaya
Afra Alkan
author_facet Sonay İncesoy-Özdemir
Ulya Ertem
Gürses Şahin
Ceyhun Bozkurt
Nazmiye Yüksek
Ayşe Ceyda Ören
Eda Balkaya
Afra Alkan
author_sort Sonay İncesoy-Özdemir
collection DOAJ
description Germ cell tumor (GCT) is a rare malignancy accounting for 2-3% of all pediatric tumors. The overall survival rate of children and adolescents with GCT is more than 80% after adopting combined therapy. The aim of this study is to review clinical presentation, management, and outcome in a single-center series with extracranial GCT. Clinical characteristics, pathologic presentations, and survival outcomes of 101 children with GCT, treated at our hospital from 1988 to 2011, were analyzed. Sixty-two of patients were female and 39 of them were male. Fifty-eight (57%) patients had gonadal tumor (24 testicular, 34 ovarian), 43 (43%) extragonadal. Histologically, teratomas were found most frequently (26 mature, 10 immature), followed by yolk sac tumors (n: 33), mixed malignant tumors (n: 13), embryonal carcinoma (n: 10), disgerminoma (n: 8) and seminoma (n: 1). Twenty-six patients were diagnosed as mature teratoma and we excluded them in the evaluation of staging and survival. Five-year overall and relaps-free survival were 80.3% (mean follow-up time: 215.8 months) and 73.4% (mean follow-up time: 176.2 months), respectively. Five-year survival rates were 93.2% and 90.2% in malign GCTs diagnosed after 1999.
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spelling doaj-art-c0e04a919ab041fa9b3701b6a810a5dc2025-08-20T02:01:51ZengHacettepe University Institute of Child HealthThe Turkish Journal of Pediatrics0041-43012791-64212017-08-0159410.24953/turkjped.2017.04.007Clinical and epidemiological characteristics of children with germ cell tumors: A single center experience in a developing countrySonay İncesoy-Özdemir0Ulya Ertem1Gürses Şahin2Ceyhun Bozkurt3Nazmiye Yüksek4Ayşe Ceyda Ören5Eda Balkaya6Afra Alkan7Departments of Pediatric Oncology, Yıldırım Beyazıt University, Ankara, Turkey.Department of Pediatric Oncology, Dr. Sami Ulus Children's Hospital, Ankara, Turkey.Department of Pediatric Oncology, Dr. Sami Ulus Children's Hospital, Ankara, Turkey.Department of Pediatric Oncology, Dr. Sami Ulus Children's Hospital, Ankara, Turkey.Department of Pediatric Oncology, Zonguldak Karaelmas University, Zonguldak, Turkey.Department of Pediatric Oncology, Dr. Sami Ulus Children's Hospital, Ankara, Turkey.Department of Pediatric Oncology, Dr. Sami Ulus Children's Hospital, Ankara, Turkey.Departments of Biostatistics, Yıldırım Beyazıt University, Ankara, Turkey. Germ cell tumor (GCT) is a rare malignancy accounting for 2-3% of all pediatric tumors. The overall survival rate of children and adolescents with GCT is more than 80% after adopting combined therapy. The aim of this study is to review clinical presentation, management, and outcome in a single-center series with extracranial GCT. Clinical characteristics, pathologic presentations, and survival outcomes of 101 children with GCT, treated at our hospital from 1988 to 2011, were analyzed. Sixty-two of patients were female and 39 of them were male. Fifty-eight (57%) patients had gonadal tumor (24 testicular, 34 ovarian), 43 (43%) extragonadal. Histologically, teratomas were found most frequently (26 mature, 10 immature), followed by yolk sac tumors (n: 33), mixed malignant tumors (n: 13), embryonal carcinoma (n: 10), disgerminoma (n: 8) and seminoma (n: 1). Twenty-six patients were diagnosed as mature teratoma and we excluded them in the evaluation of staging and survival. Five-year overall and relaps-free survival were 80.3% (mean follow-up time: 215.8 months) and 73.4% (mean follow-up time: 176.2 months), respectively. Five-year survival rates were 93.2% and 90.2% in malign GCTs diagnosed after 1999. https://turkjpediatr.org/article/view/1008childrengerm cell tumorsurvivaltreatment
spellingShingle Sonay İncesoy-Özdemir
Ulya Ertem
Gürses Şahin
Ceyhun Bozkurt
Nazmiye Yüksek
Ayşe Ceyda Ören
Eda Balkaya
Afra Alkan
Clinical and epidemiological characteristics of children with germ cell tumors: A single center experience in a developing country
The Turkish Journal of Pediatrics
children
germ cell tumor
survival
treatment
title Clinical and epidemiological characteristics of children with germ cell tumors: A single center experience in a developing country
title_full Clinical and epidemiological characteristics of children with germ cell tumors: A single center experience in a developing country
title_fullStr Clinical and epidemiological characteristics of children with germ cell tumors: A single center experience in a developing country
title_full_unstemmed Clinical and epidemiological characteristics of children with germ cell tumors: A single center experience in a developing country
title_short Clinical and epidemiological characteristics of children with germ cell tumors: A single center experience in a developing country
title_sort clinical and epidemiological characteristics of children with germ cell tumors a single center experience in a developing country
topic children
germ cell tumor
survival
treatment
url https://turkjpediatr.org/article/view/1008
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