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Fatal hemorrhage from rupture of metastatic tumors rapidly developed after optimal primary surgery for ovarian angiosarcoma arising from a mature cystic teratoma

  • U Chul Ju1
  • Woo Dae Kang1
  • Seok Mo Kim1,*,

1Department of Obstetrics and Gynecology, Chonnam National University Medical School, Gwangju, Republic of Korea

DOI: 10.31083/j.ejgo.2020.04.5379 Vol.41,Issue 4,August 2020 pp.640-643

Submitted: 19 September 2019 Accepted: 28 October 2019

Published: 15 August 2020

*Corresponding Author(s): Seok Mo Kim E-mail: seokmo2001@hanmail.net

Abstract

Background: Primary ovarian angiosarcoma arising from a mature cystic teratoma is a very rare tumor, known to be very aggressive and respond poorly to chemotherapy. However, little information exists regarding the treatment of this disease. Case: Here, we report the first case of a teenage girl diagnosed with primary ovarian angiosarcoma arising from a mature cystic teratoma. The patient received no adjuvant treatment after primary surgery. Despite stage I disease, the patient presented with metastatic tumors within two months postoperatively. She died of a fatal hemorrhage presumed to occur in metastatic tumors after receiving delayed chemotherapy. Conclusion: Because primary ovarian angiosarcoma arising from a mature cystic teratoma can be found in young women, early diagnosis and proper treatment are essential. The tumors grow rapidly and are fragile enough to rupture, so it is reasonable to prescribe early adjuvant treatments after optimal debulking surgery before progression or recurrence. Treatment of the recurrent or metastatic tumors should be performed with caution because complications, such as severe bleeding, may arise from the hemorrhagic tumors.

Keywords

Primary ovarian angiosarcoma; Mature cystic teratoma; Young woman; Hemorrhage

Cite and Share

U Chul Ju,Woo Dae Kang, Seok Mo Kim. Fatal hemorrhage from rupture of metastatic tumors rapidly developed after optimal primary surgery for ovarian angiosarcoma arising from a mature cystic teratoma. European Journal of Gynaecological Oncology. 2020. 41(4);640-643.

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