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Metachronous Synovial Sarcoma After Treatment of Mixed Germ Cell Tumor in a Child with Complete Gonadal Dysgenesis
Author(s) -
Feryal Karahan,
Elvan Çağlar Çıtak,
Emel Yaman,
Mehmet Alakaya,
Fatih Sağcan,
Eda Bengi Yılmaz,
Funda Kuş
Publication year - 2017
Publication title -
journal of clinical research in pediatric endocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.566
H-Index - 35
eISSN - 1308-5735
pISSN - 1308-5727
DOI - 10.4274/jcrpe.4905
Subject(s) - medicine , synovial sarcoma , gonadal dysgenesis , germ cell tumors , sarcoma , reticulum cell sarcoma , germ cell , girl , pathology , chemotherapy , genetics , gene , biology
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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