Indian Journal of Pathology and Microbiology (Jan 2018)

Primary intrauterine dysgerminoma in a pregnant woman: A rare case report

  • Mojgan Akbarzadeh-Jahromi,
  • Fatemeh Sari Aslani,
  • Fatemesadat Najib,
  • Shahla Hosseini

DOI
https://doi.org/10.4103/IJPM.IJPM_598_17
Journal volume & issue
Vol. 61, no. 4
pp. 590 – 592

Abstract

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Primary extraovarian dysgerminoma is very rare. Nearly all reported uterine germ cell tumors are nondysgerminoma. Herein, we reported a primary intrauterine dysgerminoma. A 21-year-old pregnant woman G2 L1 with a gestational age of 33 weeks referred to an obstetric ward with a chief complaint of labor pain and membrane rupture. Ultrasonography showed a large hypoechoic lobulated area adjacent to the lower part of her uterus. She underwent an operation and a huge mass was detected in her uterus, which was extended to her pelvic floor. Histopathological and immunohistochemical examinations were consistent with dysgerminoma.

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