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Sertoli-Leydig Cell tumor , Poorly Differentiated의 1 례
이근영,강성원,이의열,이예교 대한산부인과학회 1991 Obstetrics & Gynecology Science Vol.34 No.6
저자 등은 poorly differentiated cell type의 sertoli-leydig cell tumor를 가진 22세 미혼여성에서 남성화현상이 나타나지 않으면서, highly malignant clinical progression을 나타내는 1례를 경험하였기에 간단한 문헌과 함께 보고하는 바이다. The Sertoli-Leydig cell tumor is a gonadal tumor of sex-cord type, similar to that seen in the various phase of testicular development in the male. This tumor account for less than 0.4% of all ovarian tumor, exhibit a wider range of patterns and cell types than any other ovarian neoplasms, sometimes resulting in inappropriate therapy. This case has been presented of a 22 years old female who has a stage Ia Setoli-Leydig cell tumor with poorly differentiated. She died about two months after unilateral salpingo-oophorectomy, because of rapid malignant progression with multiple metastasis including retroperitoneal lymph nodes. We present this case with the brief review of literatures.