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"Ovary"

Original Article

[English]
Malignant Ovarian Tumor in Children
Hye Ah Shin, Dae Yeon Kim, Minjeong Cho, Taehoon Kim, Seong Chul Kim, In Koo Kim
J Korean Assoc Pediatr Surg 2010;16(2):134-142.   Published online December 31, 2010
DOI: https://doi.org/10.13029/jkaps.2010.16.2.134

Malignant ovarian tumors in children are very rare, and consist of about 1% of all childhood malignant tumors. The purpose of this study is to examine the clinical characteristics, treatment, and prognosis for children with malignant ovarian tumors. We retrospectively reviewed the medical records of children under 15 years of age with malignant ovarian tumors who had been treated surgically at Asan Medical Center between 1989 and March 2009. There were 32 patients, ranged in age at surgery from 2 to 15 years (mean; 10.4 years). The median follow-up period was 64.7 months (from 1 month to 188 months). Pathologic diagnosis were; immature teratoma (n=10), mixed germ cell tumor (n=10), and dysgerminoma (n=6). Tumor stage was classified by the staging system of the International Federation of Gynecology and Obstetrics (FIGO). The number of patients in stage I, II, III, and IV were 24 (75%), 2 (6.2%), 4 (12.5%), and 2 (6.1%), respectively. The tumor recurred in 4 patients. Seven patients of group 1 did not receive postoperative adjuvant chemotherapy, and in three of them, the tumor recurred. Twenty-five patients (group 2) underwent postoperative adjuvant chemotherapy, and there was only one recurrence. One patient who did not receive postoperative adjuvant chemotherapy and expired 10 months after operation because of tumor recurrence and distant metastasis. The overall 5-year event free survival (EFS) was 84.2%: group 1 in 44.4%, and group 2 in 95.7%. Tumor recurrence was related to the postoperative adjuvant chemotherapy (p=0.004). In conclusion, proper surgical procedures with relevant postoperative adjuvant chemotherapy might improve clinical results in children with malignant ovarian tumors.

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Case Report

[English]
Laparoscopic Ovary Preserving Cystectomy for Benign Cystic Teratoma of the Ovary
Il Kyung Park, Woo Kyun Mok
J Korean Assoc Pediatr Surg 2006;12(1):41-46.   Published online June 30, 2006
DOI: https://doi.org/10.13029/jkaps.2006.12.1.41

Mature cystic teratoma, commonly called dermoid cyst, is the most common benign germ cell tumor of the ovary in children. Malignant transformation is rare, approximately 2%. As laparoscopic procedures are applied widely in pediatric surgery, a female chlid with a mature cystic teratoma may be an ideal candidate for laparoscopic surgery. Two children received laparoscopic operations successfuly for lower abdominal crises, twisted adnexa. There was no operative complication. Laparoscopic approach for ovarian lesions in infancy and childhood appears to be an effective and safe method for diagnosis as well as definitive therapy.

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Original Article

[English]
Case Series of Adolescent Ovarian Mucinous Cystadenocarcinoma, Single Center Experience
Cho, Ara , Yang, Hee-Beom , Kim, Hyun-Young
Adv Pediatr Surg 2021;27(2):46-53.
DOI: https://doi.org/10.13029/aps.2021.27.2.46
Purpose
Ovarian mucinous cystadenocarcinoma is rare in adolescent population and reports are scarce in Korea. The aim of this study was to identify the clinicopathologic features and prognosis of adolescent ovarian mucinous cystadenocarcinoma.
Methods
Adolescent patients who were diagnosed with ovarian mucinous cystadenocarcinoma between 2001 and 2012 in Seoul National University Children Hospital were included. We retrospectively reviewed medical records of demographics, preoperative evaluation, tumor characteristics, and prognosis of patients.
Results
Among 5 patients, none of them reported family history of cancer or underlying disease relevant to malignancy. The median follow-up period was 13.3 years. The mean age at the time of diagnosis was 15.4 years. The mean size of the tumor was 26 cm. Only one patient had neoadjuvant chemotherapy. All patients underwent surgical treatment. One patient underwent total abdominal hysterectomy and bilateral salpingo-oophorectomy for cytoreductive surgery and 4 patients underwent fertility sparing surgery. Three patients had platinum-based adjuvant chemotherapy. One patient suffered recurrence and eventual death and 4 patients are in disease free survival status.
Conclusion
Although ovarian mucinous cystadenocarcinoma in adolescent is rare, we should suspect the presence of it in case of adolescent intraabdominal large mass. As adolescent patients undergo fertility preserving surgery, serial and careful follow-up is necessary.
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