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배광범(KB Bai),서광태(KT Suh),한영란(YR Han),정동건(DG Chung),신명우(MW Shin) 대한산부인과학회 1988 Obstetrics & Gynecology Science Vol.31 No.5
19세의 ㅈ은 여성의 자궁경부에서 기원한 1례를 경험하였기에 문헌적 고찰과 함께 보고하는 바이다. Embryonal rhabdomyosarcoma, more commonly called sarcoma botryoides, is the most common malignant tumor arsing from the infant vagina. Eighty-five percent of these tumors arise in girls under 5 years of age. a fewer appear after menarche ; however, a greater percentage of tumors developing in this age group arise in the uterine cervix than arise in the vagina. We present a case of botryoid embryonal rhabdomyosacoma arising from uterine cervix with a review of a literatures.
강순범,한영란,박소현,임문환,유영철,노정래 대한산부인과학회 1991 Obstetrics & Gynecology Science Vol.34 No.3
A case of endocervical stromal sarcoma is presented. The patient was 29 years old, and presented with profuse vaginal discharge and passage of a piece of tissue from vagina. DCB showed roughly suggestive findings of embryonal rhabdomyosarcoma. During following up for rebiopsy, pelvic examination revealed exophytic polypoid cervical mass. The polyp was excised and histologic examination revealed spindle cell sarcoma. A radical hysterectomy with bilateral salpingo-oophorectomy, partial vaginectomy and pelvic lymph node dissection was performed. Histopathologic examination of the uterus and cervix revealed endocervical stromal sarcoma.
임신중 정신질환의 치료를 위하여 전기충격요법을 받았던 산모 2 예
김승욱,신희철,윤보현,한영란,송현진,박소현,임문환 대한산부인과학회 1990 Obstetrics & Gynecology Science Vol.33 No.2
정신질환이 동반된 두 임산부에게 정신질환의 치료를 위하여 임신도중에 전기충격요법을 시행한 후 만삭 때 정상태아를 분만한 예를 2예 경험하였기에 문헌고찰과 더불어 보고하는 바이다. The effect of electroconvulsive therapy on the psychotic pregnant woman have not been prospectively evaluated. But the current case reports in other countries support the relative safety of electroconvulsive therapy in pregnancy when the patient is carefully selected and monitored, and electroconvulsive therapy has a minimal effect, if any, on the fetus. We report two cases of psychotic women who were given electroconvulsive therapy during pregnancy and delivered full-term, developmentally normal babies.
김종혁,박노현,이진용,한영란,박소현,임문환 대한산부인과학회 1991 Obstetrics & Gynecology Science Vol.34 No.2
본 병원 산부인과에서 흉수와 복수를 동반한 16×13×9.5 cm 크기의 우측 난소섬유 난포막종양을 수술제거함으로써 흉부 X-선상 흉수가 완전히 소실되었고 수술 후 9개월째에도 흉수 및 복수가 재발한 증거가 없었던 Meigs' syndrome 1례를 경험하였기에 이를 보고하는 바이다. Meigs' syndrome is characterized by the pleural effusion and ascites in association with nonmetastaic pelvic tumors in women. The pleural effusion is most commonly right sided, may be exudate or transudate, and is thought to develop from movement of ascitic fluid across the diaphragm. Both the ascites and pleural fluid dramatically resolve following removal of the pelvic tumor. A case of Meigs' syndrome associated with fibrothecoma is presented with a brief review of literatures.