1.A case of heterotopic pregnancy in a natural cycle: ultrasound diagnosis.
Chang Ho LEE ; Eun Kyeung BAEK ; Young Ju JEONG ; Kwan Sik KIM ; Young Ho JIN ; Chul Hee RHEU ; Jong Duk KIM
Korean Journal of Obstetrics and Gynecology 2002;45(3):533-
Heterotopic pregnancy in a natural cycle is rare case. This case occurs by one out of 30,000 cases of pregnancies. It is quite difficult to diagnose a heterotopic pregnancy clinically. But, recently, the availability of high-resolution sonography has improved the preoperative diagnosis rate. We present a case of spontaneous heterotopic pregnancy which was diagnosed pre-operatively by transvaginal ultrasound.
Diagnosis*
;
Pregnancy
;
Pregnancy, Heterotopic*
;
Ultrasonography*
2.Three Cases of Local Excision of Uterine Choriocarcinoma Lesion.
Nam Hee LEE ; Jin Hee SONG ; Mee Gyeong JEON ; Jeong Ju MOON ; Barbara H MARTIN ; Jeong Hae KIM
Korean Journal of Obstetrics and Gynecology 1997;40(8):1808-1813
In treating young women for gestational trophoblastic tumor ( G.T.T. ), all efforts are made to preserve fertility and hysterectomy is avoided unless absolutely essential. However, in some cases the operation may be lifesaving. During the last 20 years among the 310 cases of G.T.T. treated at Il Sin Christian Hospital, there were 3 cases in which hysterectomy was avoided by the excision of a localized uterine lesion thus preserving fertility.
Choriocarcinoma*
;
Female
;
Fertility
;
Humans
;
Hysterectomy
;
Pregnancy
;
Trophoblastic Neoplasms
3.Primary Ovarian Non-gestational Choriocarcinoma in a Young Woman.
Kwan Sik KIM ; Jung Hee KIM ; Myong Ja JUNG ; Byoung Chan OH
Korean Journal of Obstetrics and Gynecology 1997;40(8):1802-1807
Primary ovarian choriocarcinoma is an extremely rare germ cell neoplasm, and the prognosis is poor. Especially, the diagnosis of primary ovarian nongestational chori-ocarcinoma can be reliably established in a girl or innocent virgin. We report a case of primary ovarian, nongestational, pure choriocarcinoma in a 16-year-old woman. She died within 1 year after diagnosis in spite of the treatment with surgery and combin-ation chemotherapy.
Adolescent
;
Choriocarcinoma
;
Choriocarcinoma, Non-gestational*
;
Diagnosis
;
Drug Therapy
;
Female
;
Germ Cells
;
Humans
;
Pregnancy
;
Prognosis
4.A Case of Complete Response by Hormonal Therapy with Tamoxifen and Progesterone in Recurrent Endometrial Cancer to Metastasis to Lung.
Eun Ha CHOI ; Seung Joon LEE ; Chan Keum LEE ; Bong Ju LEE ; Chang Hong KIM ; Heung Gon KIM ; Ki Jung YOON
Korean Journal of Obstetrics and Gynecology 1997;40(8):1797-1801
Endometrial carcinoma has been the most common female pelvic malignancy in the U.S.A. Approximately one-fourth of patient treated for early endometrial cancer will develop reccure-nt disease. Kelly and Baker first descibed that the use of progestational agents for treatment of met- astatic endometrial cancer in 1961. Response of progesterone therapy in metastatic endometrial cancer is related to several factors. Higher response rates are observed in well differentiated tumors, longer disease free interval and tumors that positive for estrogen and progesterone re- ceptors. We experienced a case of complete response in recurrent endometrial cancer to metastasis to lung treated by tamoxifen and progesterone, we present this case with a brief review of lite- rature.
Endometrial Neoplasms*
;
Estrogens
;
Female
;
Humans
;
Lung*
;
Neoplasm Metastasis*
;
Progesterone*
;
Progestins
;
Tamoxifen*
5.A Case of Paget's Disease of the Vulva.
Chul SONG ; Sei Hyug IM ; Ji Yeong LEE ; Ho Sun CHOI ; Chang Soo PARK ; Hyung Seok KIM
Korean Journal of Obstetrics and Gynecology 1997;40(8):1794-1796
Sir James Paget described the first case of Paget's disease of the breast in 1874, and Du-breuilh, in 1901, reported the first case of extramammary Paget's disease of the vulva. Paget's disease of vulva is a rare intraepithelial neoplasm of uncertain histogenesis. Recently we expe-rienced a case of Paget's disease of the vulva that we present a brief review of literature.
Carcinoma in Situ
;
Paget Disease, Extramammary
;
Paget's Disease, Mammary
;
Vulva*
6.A Case of Low Grade Endometrial Stromal Sarcoma.
Seung Ok YANG ; Joung Kee PARK ; Gi Chul KANG ; Kyung Soo KIM ; Dong Jin KIM ; Kwang Soo KEE ; Hun Jung IM
Korean Journal of Obstetrics and Gynecology 1997;40(8):1788-1793
A low grade endometrial stromal sarcoma is a rare malignant tumor in woman. We experienced this infrequent malignant tumor in a 36 years old woman showing metas- tasis to both ovaries, omentum, rectum and mesenteric lymph nodes, and she was treated by total abdominal hysterectomy with bilateral salpingo-oophorectomy followed by VAC(vincristi n, actinomycin, cyclophoshamide) chemotherapy. The authors report this case with the clinicopathologic findings and brief review of literature.
Adult
;
Dactinomycin
;
Drug Therapy
;
Female
;
Humans
;
Hysterectomy
;
Lymph Nodes
;
Omentum
;
Ovary
;
Rectum
;
Sarcoma, Endometrial Stromal*
7.A Case of Peritoneal Tuberculosis with Elevated Serum CA 125 Level.
Hye Kyung KWON ; Tae Lim JOO ; Soon Mi CHOI ; Kook LEE ; Kwan Sik LEE ; Nam Hoon CHO
Korean Journal of Obstetrics and Gynecology 1997;40(8):1783-1787
Peritoneal tuberculosis is a disease rarely seen nowadays. Its symptoms are easy fatigue, abdominal distension, intermittent abdominal pain and ascites. Its onset is insidious, which si-mulates symptoms of peritonitis or carcinomatosis. Peritoneal tuberculosis should be considered in the differential diagnosis when a Patient's symptoms and signs are ascites, ovarian tumor, vague abdominal pain and abdominal distension with high serum level of CA 125, an antigenic determinant of epithelial ovarian cancers. We have recently experienced a case of peritoneal tuberculosis with markedly elevated serum level of CA 125 in 54 year-old woman and report our case with a brief review of the literature.
Abdominal Pain
;
Ascites
;
Carcinoma
;
Diagnosis, Differential
;
Fatigue
;
Female
;
Humans
;
Middle Aged
;
Ovarian Neoplasms
;
Peritonitis
;
Peritonitis, Tuberculous*
8.4 Cases of Pelvic Actinomycoses.
Jeong Su KIM ; Chang Cho CHUNG ; Yong Hun CHEE ; Myung Choel SHIN ; Mi Hwa LEE ; Kyeong Sul LEE ; Jong Gun WON ; Dong Je CHO
Korean Journal of Obstetrics and Gynecology 1997;40(8):1763-1770
Actinomycoces is a gram positive, anaerobic, branching and non-acid fast bacterium which is a normal habitant of the skin, oral cavity, tonsil and gastrointestinal tract and its human infection is rare. Pelvic actinomycoses is frequently caused by Actinomycoces israel-ii. It is chronic, progressive, and more suppurative than granulomatous disease, and the symptoms are usually persistent and gradual, therefore the misdiagnosis and improper trea-tment are not uncommon. Actinomycoses is generally classified as cervicofacial, abdominal and thoracic type ac- cording to the site of the primary infection. Many actinomycotic pelvic infections in women used intrauterine device with long du- ration were reported, in contrast, others suggest that actinomycoces developed opportunistic infection irrespective of intrauterine device presence. We have experienced 4 cases of pelvic actinomycoses, one case with IUD(Lippes' loop) in a 47 year old woman, the other case with abdominal wall ctinomycoses in a 34 year old woman, the third case without IUD in a 41 year old woman, the fourth case with IUD(Cu-7) in a 37 year old woman and reported them with a review of literature.
Abdominal Wall
;
Actinomycosis*
;
Adult
;
Diagnostic Errors
;
Female
;
Gastrointestinal Tract
;
Humans
;
Intrauterine Devices
;
Middle Aged
;
Mouth
;
Opportunistic Infections
;
Palatine Tonsil
;
Pelvic Infection
;
Skin
9.A Case of Recurrent Fetal Cystic Hygroma with Polycystic Kidney.
Seong Hee KIM ; Ji Won SIN ; Hyeon Joo KIM ; Seong Sook SEO ; Hyeon Mi HA
Korean Journal of Obstetrics and Gynecology 1997;40(8):1756-1762
This is a case report of a cystic hygroma with polycystic kidney in a fetus which was suspected by ultrasonography and was confirmed by autopsy. Recently, we have experienced this case in 25-year old woman repeatedly and we report that with a brief review of relevant literature.
Adult
;
Autopsy
;
Female
;
Fetus
;
Humans
;
Lymphangioma, Cystic*
;
Polycystic Kidney Diseases*
;
Ultrasonography
10.A Case of Mayer-Rokitansky-Kster-Hayser Syndrom.
Kyoung Suk LEE ; Jeong Bae KANG ; Hong Bai KIM ; Keun Yong LEE ; Sung Won KANG
Korean Journal of Obstetrics and Gynecology 1997;40(8):1751-1755
A perplexing developmental error is 46,XX congenital absence of vagina ( Mayer-Rokitan-sky-Kster-Hauser syndrome, Mullerian dysgenesis, vaginal aplasia ). The Mayer-Rokitansky-Kster-Hauser syndrome refers to the climical entity consisting of primary amenorrhea associated with congenital absence of the vagina, 46,XX karyototype, a rudimentary uterus or complete absense, normal overian function and normal ovulation, normal female breast development, body proprotion and body hair, frequent association of renal, skeletal and other cpngenital anomalies. This syndrome results from agenesis of both Mllerian ducts or from a failure of the Mllerian ducts to estavlish a proper communication with that part of the vagina from the urogenital sinus. A case of mayer-Rokitansky-Kster-Hauser syndrom was reviewed briefly.
Amenorrhea
;
Breast
;
Female
;
Hair
;
Humans
;
Ovulation
;
Uterus
;
Vagina