1.A Case of Dysgerminoma Incidentally Found after Pelviscopic Ovarian Surgery.
Seo Yeong PARK ; Sang Young RYU ; Noh Hyun PARK ; Yong Sang SONG ; Soon Beom KANG ; Hyo Pyo LEE
Korean Journal of Obstetrics and Gynecology 1997;40(12):2885-2891
No abstract available.
Dysgerminoma*
2.A Case of Dysgerminoma.
Dong Won KIM ; Hye Young CHUNG ; Seung Il KIM ; Young Hyun KWACK
Journal of the Korean Pediatric Society 1984;27(10):1018-1021
No abstract available.
Dysgerminoma*
3.A case of dysgerminoma in combination with mature solid teratoma.
Sung Jin HWANG ; Soo Nyung KIM ; In Jae CHO ; Doo Ho KIM
Korean Journal of Obstetrics and Gynecology 1993;36(7):3214-3220
No abstract available.
Dysgerminoma*
;
Teratoma*
4.8 cases of dysgerminoma of the ovary.
O Soon NAH ; Jong Chan LEE ; Sang Yoon PARK ; Je Ho LEE ; Eui Don LEE ; Kyung Hee LEE ; Kee Bok PARK
Korean Journal of Obstetrics and Gynecology 1993;36(8):3326-3333
No abstract available.
Dysgerminoma*
;
Female
;
Ovary*
5.Torsion and ruptured dysgerminoma of ovary in pregnancy.
Chang Kyo LIM ; Hye Young KIM ; Jang Yeoun KWON ; Dae Hyun KIM ; Mi Yeoun CHO
Korean Journal of Obstetrics and Gynecology 1992;35(2):292-296
No abstract available.
Dysgerminoma*
;
Female
;
Ovary*
;
Pregnancy*
6.A successful spontaneous pregnancy after surgery and chemotherapy in a patient with recurrent dysgerminoma: A case report
Amor Mae M. Pasigon ; Jimmy A. Billod
Philippine Journal of Obstetrics and Gynecology 2022;46(3):136-140
Dysgerminoma comprises 3%–5% among ovarian malignancies, mostly seen in adolescent and early adult women. The recurrence rate is approximately 10%–20%, occurring within 2 years of diagnosis, and has been reported that more than 75% occur in the 1st year. A 19‑year‑old nulligravid initially presented with severe abdominal pain, who underwent emergency exploratory laparotomy and left salpingo‑oophorectomy, whose histopathologic result revealed dysgerminoma, Stage IC2. Recurrence of dysgerminoma was noted on the contralateral ovary 10 months after for which she had undergone another surgery for wedge resection of the right ovarian mass and complete surgical staging. She received adjuvant chemotherapy without complications. Despite two consecutive surgeries and chemotherapy, she had conceived naturally and her pregnancy was carried to term with no complications and delivered to a live baby girl by normal spontaneous delivery. This case is a proof of how fertility‑sparing surgeries and chemotherapy in dysgerminoma can successfully preserve reproductive functions for future conceptions.
Chemotherapy, Adjuvant
;
Dysgerminoma
;
Pregnancy
;
Recurrence
7.Swyer syndrome presenting as dysgerminoma: A case report
Silima Tarenia ; Sujaya Chattopadhyay ; Niladri Das ; Deep Hathi ; Arjun Baidya ; Puranjoy Chakrabarty ; Nilanjan Sengupta ; Soumik Goswami
Journal of the ASEAN Federation of Endocrine Societies 2023;38(1):108-113
Complete gonadal dysgenesis with 46,XY karyotype is a clinical condition characterized by the absence of testicular tissue but typical Mullerian structures in a phenotypically female individual. The condition presents as primary amenorrhoea or delayed puberty. Eventually, malignant neoplasms may arise. We report a case of a 16-year-old patient with Swyer syndrome presenting with primary amenorrhoea and with previous diagnosis four years earlier of a malignant dysgerminoma in the right ovary.
Swyer syndrome
;
dysgerminoma
;
gonadal dysgenesis
8.Diagnosis and treament of ovarian germ cell tumors
Journal Ho Chi Minh Medical 2003;7(4):207-215
In 5 years (1994-1998), 168 patients with ovarian germ cell tumors were diagnosed and treated in HCM city Cancer Hospital. Ovarian germ cell tumor is a rare disease. These tumors were often detected in early stage (61.2% in stage I, among them 39.6% in stage IA). The tumor marker AFP plays an important role in diagnosis and follow-up the disease. AFP was positive in 60% cases of malignant germ cell tumors, among them 55.6% were immature teratomas, and AFP was negative in dysgerminoma. The rate of teratomas was highest: 53%, rate of dysgerminoma: 19%, endodermal sinus tumor 14.9%, embryonal carcinoma 9.5% and mixed forms 3.6%. It’s necessary to emphasize the role of preservative surgery in the treatment of these tumors
Ovarian Neoplasms
;
alpha-Fetoproteins
;
Dysgerminoma
;
diagnosis
;
therapeutics
;
9.A Case of Coincidental Gonadoblastoma and Dysgerminoma in 45X/47XYY Mosaic Turner Variant.
Seung Chul KIM ; Seung Sup PARK ; Ki Hyung KIM ; Do Yoon PARK ; Man Soo YOON
Korean Journal of Obstetrics and Gynecology 2005;48(7):1805-1810
45X/47XYY mosaicism is a very rare sex chromosomal disorder with limited clinical information. We experienced an unusual mosaic syndrome in a 16-year old woman with a phenotypic female, short stature, and immature secondary sexual characteristics. We performed both gonadectomy and found a gonadoblastoma in one gonad and dysgerminoma in another gonad.
Adolescent
;
Chromosome Disorders
;
Dysgerminoma*
;
Female
;
Gonadoblastoma*
;
Gonads
;
Humans
;
Mosaicism