http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
임산모에 동반된 염전 및 파열상을 보인 난소미분화배세포종 1 예
임창교(CK Lim),김혜영(HY Kim),권장연(JY Kwon),김대현(TH Kim),조미연(MY Cho) 대한산부인과학회 1992 Obstetrics & Gynecology Science Vol.35 No.2
Dysgerminoma is the most common malignant germ cell tumor of the ovary, accounting for approximately 3∼5% of all ovarian malignancies. However, disgerminoma complicating pregnancy is not very uncommon. Furthermore, torsion and ruptured dysgerminoma in pregnancy is rare complication during the third trimester of pregnancy. We have experienced a case of torsion and ruptured dysgerminoma of ovary which occurred at 34 weeks gestation in a 26 year old woman. So we report this case with a brief review of literature.
이영인(YI Lee),엄기명(KM Um),권장연(JY Kwon),한상원(SW Han),차동수(DS Cha),김대현(TH Kim),조미연(MY Cho) 대한산부인과학회 1992 Obstetrics & Gynecology Science Vol.35 No.10
Papillary serous carcinoma of the peritoneum, though biologically and histologically similar to papillary serous carcinoma of the ovary and malignant mesothelioma, is a distinct clinicopathologic entity and should be classificed as a distinct carcinoma separate from the other two for the differences in the response to therapentic intravention and prognosis. We have experienced a case of papillary serous carcinoma of the peritoneum and it is presented with brief review.
Asphyxiating Thoracic Dysplasia 1 예
정동원(DW Jung),양경무(KM Yang),황인성(IS Hwang),김명철(MC Kim),조미연(MY Cho),김동진(DJ Kim) 대한산부인과학회 1997 Obstetrics & Gynecology Science Vol.40 No.10
Asphyxiating thoracic dysplasia(ATD;Jeunes`s syndrome) is a rare variety of short limb dwarfism. It is characterized by an extremely small thorax when compared to the ab-dominal circumference, which frequently results in respiratory distress. Other anomalies as-sociated with Jeune`s syndrome are pelvic bone malformations and renal dysplasia. It was first described and namely by Jeune et al. in 1954. Jeune`s syndrome is an autosomal rece-ssive trait and has a 25% recurrence risk. These patients died at early age due to respirat-ory insufficiency. Death due to uremia has occurred in number of children surviving infan-cy, following progressive renal failure, hypertension and hepatic failure. About 50 cases have been reported in the world literature. We experienced a case of small thorax with short limb dwarfism on antenatal ultraso- und examination and then the baby was delivered by cesarean section. The diagnosis was confirmed to Asphyxiating thoracic dysplasia by clinical features, radiological findings and pathological findings. We reported a case of Asphyxiating thoracic dysplasia with review of literatures.
구재석(JS Koo),차동수(DS Cha),한상원(SW Han),조미연(MY Cho) 대한산부인과학회 1996 Obstetrics & Gynecology Science Vol.39 No.6
Malignant Mixed Mullerian tumor(MMMT) is an uncommon tumor containing epithelial and mesenchymal components. According to stromal element, it is divided to homologous type and heterologous type. MMMT is highly malignant and the prognosis is poor due to frequent metastasis and recurrence. The disease is usually advanced when diagnosed. We experienced two case of MMMT(a case received irradiation for the rectal cancer 7 years prior to the diagnosis of tumor). So we report above cases with brief review of literature.
박찬호(CH Park),한상원(SW Han),최종환(JW Choi),차동수(DS Cha),조미연(MY Cho) 대한산부인과학회 1996 Obstetrics & Gynecology Science Vol.39 No.3
Anticoagulant therapy has an established place in the treatment and prophylaxis of a wide variety of thromboembolic problem. Advances in medicine and surgery have introduced anticoagulant therapy to younger patients, including women in their active menstrual years. Although hemorrhage into visceral organs compplicating anticoagulant therapy does not seem common, the possibility of ovarian hemorrhage must be considered in the menstruating female who is receiving anticoagulant therapy and who presents with sign and symptoms of intraperitoneal bleeding. Lack of awareness of the complication may result in delay in making a correct diagnosis and instituting appropriate therapy. We experienced one case of ovarian hematoma in patient receiving anticoagulant therapy, and report this case with a brief review of the concerned literatures.
자궁근종의 경피적 혈관색전술 후 경험한 자궁근종괴사 1 예
홍민(M Hong),김일한(IH Kim),한혁동(HD Han),김영주(YK Kim),송지선(JS Song),조미연(MY Cho) 대한산부인과학회 1999 Obstetrics & Gynecology Science Vol.42 No.4
Uterine fibroids are the most common benign tumor of the female genital tract. Traditional therapy for symptomatic fibroids has been either myomectomy or hysterectomy, depending on whether futhur fertility is desire. A promised new alternative therapy-embolization of the uterine arteries- is now available. A 29 year-old woman was diagnosed of uterine fibroid by ultrasonogram and other techniques. We have experienced one case of uterine fibroid necrosis after transarterial embolization. Now we report a case of uterine artery embolization for treatment of uterine fibriods with a brief review.
오준환(JH Oh),김명철(MC Kim),박기환(KH Park),최종환(JW Choi),양석우(SW Yang),조미연(MY Cho) 대한산부인과학회 1998 Obstetrics & Gynecology Science Vol.41 No.10
The amniotic band syndrome is a collection of fetal malformation associated with mesodermic fibrous bands that appear to entangle or entrap various fetal parts in utero, leading to deformation, malformation, or disruption. In about one third of cases, craniofacial deformities associated with amniotic band. Excencephaly is a precursor of anencephaly in which a large amount of brain tissue is present despite the absence of the calvaria. In exencephaly, destruction and disorganization of the developing brain ultimately result in the development of the anencephaly. We had experienced a case of exencephaly at early midtrimester by the amniotic band and presented with a brief review of literature.
최종환(JW Choi),김명철(MC Kim),오준환(JH Oh),박기환(KH Park),송지선(JS Song),조미연(MY Cho) 대한산부인과학회 1998 Obstetrics & Gynecology Science Vol.41 No.10
Nonimmunologic hydrops fetalis may be caused by a variety of conditions. Chorioangioma is the most common primary benign tumor of the placenta, occuring in 1% of all pregnancy. Most of the tumors are not clinically significant until they exceed 5 cm in diameter. These larger placental chorioangioma have been associated with adverse perinatal and maternal outcomes such as polyhydramnios, premature labor, pregnancy induced hypertention, fetal hydrops, fetal disseminated intravascular coagulopathy, fetal anemia and etc. We report a prenatal diagnosis of nonimmune hydrops fetalis as a consequence of large placental chorioangioma at 24 weeks of gestation in 40-year-old multiparous woman with a brief review of related literatures.