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AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
These two synchronous tumours, made this case rare and interesting.
📌 3 Key Takeaways
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Objective & Hypothesis:Swyer syndrome or 46 XY gonadal dysgenesis is characterized by a female phenotype with streak gonads and normal female external genitalia and complicated by the frequent occurrence of germ cell tumors.
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Key Findings & Data:A 15 year-old female with clitoris hypertrophy and pelvic mass was found to have a gonadoblastoma in the left ovary and dysgerminoma in the right ovary.
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Conclusion & Impact:These two synchronous tumours, made this case rare and interesting.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Swyer syndrome or 46 XY gonadal dysgenesis is characterized by a female phenotype with streak gonads and normal female external genitalia and complicated by the frequent occurrence of germ cell tumors. Gonadoblastoma and dysgermi¬noma are the most frequently reported malignancies. A 15 year-old female with clitoris hypertrophy and pelvic mass was found to have a gonadoblastoma in the left ovary and dysgerminoma in the right ovary. Her karyotype was 46 XY. These two synchronous tumours, made this case rare and interesting.
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Cite This Article
ÇETİNGÜL, N., VERGİN, C., KAVAKLI, K., KÖPRÜBAŞI, F., DARCAN, Ş., ÖZTOP, S., BALIK, E., ERHAN, Y., NİŞLİ, G. (1996). A patient with Swyer sydrome presenting with gonadoblastoma and dysgerminoma. Medical Journal of Ege University, Cilt: 6 - Sayı: 3, 87–89. https://ajindex.com/articles/283157