Rare Tumors (Apr 2013)

Primary ovary choriocarcinoma: individual DNA polymorphic analysis as a strategy to confirm diagnosis and treatment

  • Fernando Nalesso,
  • Maria Del Pilar Estevez Diz,
  • Cristina Anton,
  • Tiago Kenji Takahashi,
  • Vanessa Dionisio Cantagalli,
  • Gilka F. Gattàs,
  • Pedro Exman

DOI
https://doi.org/10.4081/rt.2013.e24
Journal volume & issue
Vol. 5, no. 2
pp. e24 – e24

Abstract

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Primary choriocarcinoma of the ovary is rare. Furthermore, this tumor can arise from gestational tissue or pure germ cells of the ovary, with the latter resulting in non-gestational choriocarcinoma. While the clinical characteristics and histology of both tumor types are identical, differentiation of these tumors is necessary for effective treatment. One strategy for the differentiation of these tumors types is to assay for the presence of paternal DNA. Accordingly, in the present case, a patient with primary choriocarcinoma of the ovary with a non-gestational origin was confirmed by DNA analysis. The patient subsequently exhibited an excellent response to chemotherapy, and following surgery, achieved complete remission. A pathological analysis of surgical specimens further confirmed the absence of tumor.

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