一名患有完全性性腺发育不全的儿童在混合性生殖细胞肿瘤治疗后发生异时性滑膜肉瘤。
Metachronous Synovial Sarcoma After Treatment of Mixed Germ Cell Tumor in a Child with Complete Gonadal Dysgenesis.
作者信息
Karahan Feryal, Citak Elvan Caglar, Yaman Emel, Alakaya Mehmet, Sağcan Fatih, Yılmaz Eda Bengi, Kuş Funda, Gürses İclal, Balcı Yüksel
机构信息
Mersin University Faculty of Medicine, Department of Pediatric Oncology, Mersin, Turkey.
Mersin University Faculty of Medicine, Department of Medical Oncology, Mersin, Turkey.
出版信息
J Clin Res Pediatr Endocrinol. 2018 Mar 1;10(1):87-90. doi: 10.4274/jcrpe.4905. Epub 2017 Aug 24.
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.
完全性XY性腺发育不全（GD）患者患生殖细胞肿瘤（GCT）的倾向很高。此前已有GCT与GD共存患者的报道。在此，我们报告一名15岁患有混合性GCT和GD的女孩，其在治疗一年后还发生了腹腔内滑膜肉瘤。据我们所知，这是首例与XY GD相关的滑膜肉瘤报告。
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