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여아에서 발생된 Prune Belly Syndrome 1 례
박지홍,이명임,전우식,우연숙 대한산부인과학회 1994 Obstetrics & Gynecology Science Vol.37 No.7
저자들은 임신 28주에 조기양막파수로 조기분만하여 태아부검상 Prune belly syndrome으로 확진된 여아 1례를 경험하였기에 문헌고찰과 함께 보고하는 바이다. The prune belly syndrome is a rare compound fetal anomaly, characterized by congenital defect of abdominal muscles associated with urinary tract abnormalities and cryptorchidism. We experienced the compound fetal anomaly which was confirmed Prune Belly Syndrome by autopsy at the 28 weeks of gestation. So we present here with a brief review of references.
신면우,이향미,이명임,전우식,우연숙 대한산부인과학회 1994 Obstetrics & Gynecology Science Vol.37 No.6
22세 부인에서 우측 난소미분화배세포종으로 진단되어 우측난소난관 적출술과 좌측난소 부분절제술을 시행하고 4차례의 항암요법과 함께 주기적인 검사를 받아오던 난소 미분화 배세포종 1예를 경험하였기에 문헌적 고찰과 함께 보고하는 바이다. Dysgerminoma is the most common of all malignant germ cell tumors of the ovary, accounting for nearly 50% of all such tumors. Conservative treatment is indicated in the reproductive-age woman who wishes to preserve child-bearing capacity. Recently high dose cisplatin-based chemotherapy is highly effective in all cases of germ cell tumors, including dysgerminoma. We have experienced a case of dysgeminoma in 22 year old married woman. So we report this case with a brief review of its literatures.
신면우,최유덕,박지홍,이명임,전우식,우연숙 대한산부인과학회 1994 Obstetrics & Gynecology Science Vol.37 No.1
저자 등은 난소 미성숙기형종 1례를 경험하여 문헌고찰과 함께 보고하는 바이다. Immature teratoma of ovary is a type of malignant germ cell tumor, comprising less than 1% of ovarian tumors and 20% of malignant germ cell tumors. It has a specific age incidence, occurring most commonly in the first two decades of life and being almost none after menopause. Histopathologically, immature teratomas are composed of tissue derived from the three germ layers-ectoderm, mesoderm, and endoderm. Treatment consists of complete excision of tumor at early stage, followed by adjuntive combination chemotherapy. We had experienced a case of immature teratoma of the ovary, which presented, with a brief review of the literatures.
김득순,박흠례,이명임,전우식,우연숙 대한산부인과학회 1994 Obstetrics & Gynecology Science Vol.37 No.5
저자들은 최근 본원 산부인과에서 희귀하게 보고되는 난소 성기삭 종양과 유사한 자궁종양 1례를 경험하였기에 문헌고찰과 함께 보고하는 바이다. Uterine tumors with ovarian sex-cord like differentiation are composed predominantly or entirely of tubular epithelial-like structures. They wre probably of endometrial stromal differentiation because similar epithelial-like nests can be found in otherwise characteristic endometrial stromal tumors. Most of the patients in whom the tumors occurred were in the fifth decade of life. It has been suggested that the plexiform tumor is a type of epithelioid leiomyoma, but it also has some similarity to the uterine sex cord-like tumors, since both are composed of epithelial-like cords set within a fibrillar stroma. Because of the rarity of the tumor and its uncertain histogenesis, the case report of a patient with uterine tumor resembling ovarian sec-cord tumor is summarized and present with a brief review of its literature.