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Pure yolk sac tumor of ovary in an adult: a rare occurrence

  • M. Eslier1,*,
  • C. Blanc-Fournier2
  • F. Joly3
  • S. Martin-Françoise1

1The Gynecologic and Oncologic Surgery Department, Caen (France)

2The Anatomical Pathology and Cytology Department, Caen (France)

3The Department of Clinical Research Centre de Lutte contre le Cancer François Baclesse, Avenue du Général Harris, Caen (France)

DOI: 10.31083/j.ejgo.2020.02.5207 Vol.41,Issue 2,April 2020 pp.289-292

Published: 15 April 2020

*Corresponding Author(s): M. Eslier E-mail: maxime.eslier@hotmail.fr

Abstract

Background: Malignant ovarian germ cell tumors are relatively rare, making up less than 2-3 % of all ovarian malignancies. However, although they represent only a small fraction, they frequently affect young women of reproductive age. Malignant germ cell tumors are subdivided into dysgerminoma and non-dygerminomatous tumors. The most common types of non-dysgerminomatous tumors are yolk sac tumors (YSTs). Case Report: The authors present a case report of a 32-year-old woman with a history of gradual abdominal distention and an increased serum level of alpha-fetoprotein (AFP). She was diagnosed with a pure YST after removing her left ovary. Then, she was subsequently treated with adjuvant chemotherapy by four cycles of bleomycin, etoposide, and cisplatin after fertility-sparing surgery. Conclusion: This case report shows that older patients could have this tumor with no associated tumor.

Keywords

Yolk sac tumor; Endodermal sinus tumor; Ovarian cancer.

Cite and Share

M. Eslier,C. Blanc-Fournier,F. Joly,S. Martin-Françoise. Pure yolk sac tumor of ovary in an adult: a rare occurrence. European Journal of Gynaecological Oncology. 2020. 41(2);289-292.

References

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