Journals / Turkish Journal of Cancer / 2001 / Cilt: 31 - Sayı: 4

Seminoma arising in androgen insensitivity syndrome (testicular feminization syndrome): A case report

Pages
168–171
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Primary removal of the mass and postoperative radiotherapy were treatment of choice for the patient.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Androgen insensitivity (testicular feminization) syndrome is a rare inherited form of male pseudohermaphroditism that occurs in phenotypically normal woman with male karyotype (XY).
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Key Findings & Data:The undescended testis may go into malignant transformation.
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Conclusion & Impact:Primary removal of the mass and postoperative radiotherapy were treatment of choice for the patient.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Psödohermafroditizm · Radyoterapi · Androjen duyarsızlığı sendromu

Abstract

Androgen insensitivity (testicular feminization) syndrome is a rare inherited form of male pseudohermaphroditism that occurs in phenotypically normal woman with male karyotype (XY). The undescended testis may go into malignant transformation. The androgen insensitivity syndrome with malignant testicular disorder is very rare. A thirty-one year old female was admitted to the hospital with the complaint of primary amenorrhea. Clinical and laboratory investigation revealed testicular feminization syndrome with seminoma developed from intraabdominal undescended testis. Primary removal of the mass and postoperative radiotherapy were treatment of choice for the patient.

Özet

Seminoma arising in androgen insensitivity syndrome (testicular feminization syndrome): A case report

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Cite This Article

ZORLU, A. F., CENGİZ, M., GÜRKAYNAK, M., YILDIZ, F., ATAHAN, İ. L. (2001). Seminoma arising in androgen insensitivity syndrome (testicular feminization syndrome): A case report. Turkish Journal of Cancer, Cilt: 31 - Sayı: 4, 168–171. https://ajindex.com/articles/368429

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