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Dergiler / Journal of Clinical Research in Pediatric Endocrinology / 2018 / Cilt: 10 - Sayı: 1

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

Feryal KARAHAN
ELVAN ÇAĞLAR ÇITAK
Emel YAMAN
Mehmet ALAKAYA
Fatih SAĞCAN
Eda Bengi YILMAZ
Funda KUŞ
İCLAL GÜRSES
YÜKSEL BALCI
Sayfa
87–90
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

This is the first report, to our knowledge, of synovial sarcoma associated with XY GD.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Patients with complete XY gonadal dysgenesis (GD) show a high predisposition to germ cell tumors (GCT).
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Temel Bulgular & Veri:Here we present a 15-year-old girl with mixed GCT and GD who also developed an intraabdominal synovial sarcoma one year after the treatment.
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Sonuç & Katkı:This is the first report, to our knowledge, of synovial sarcoma associated with XY GD.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Özet

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 intraabdominal 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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Bu Makaleye Atıf Yap

KARAHAN, F., ÇITAK, E. Ç., YAMAN, E., ALAKAYA, M., SAĞCAN, F., YILMAZ, E. B., KUŞ, F., GÜRSES, İ., BALCI, Y. (2018). Metachronous Synovial Sarcoma After Treatment of Mixed Germ Cell Tumor in a Child with Complete Gonadal Dysgenesis. Journal of Clinical Research in Pediatric Endocrinology, Cilt: 10 - Sayı: 1, 87–90. https://ajindex.com/articles/202522

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Kaynakça (13)

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