abstract
Background: Ovarian germ cell tumors (OGCT) account for 2-5% of ovarian
malignancies, with an annual incidence of 1:100,000,
and typically occur in young women and adolescents.
The yolk sac tumor (YST) is the second most common subtype of OGCTs and
has an aggressive phenotype. Their rarity in
postmenopausal women has the potential to cause initial diagnostic
uncertainty
and lead to delayed or sub-optimal treatment. In
this article, we report two cases. The first case is a 67-year-old woman
with a pure YST and the second refers to a
59-year-old patient with YST with neuroendocrine differentiation. We
also review
and summarise the current literature.
Discussion:
YSTs in older women, either in association with ovarian epithelial
tumors
or without an identifiable epithelial precursor,
are a challenging clinical situation. The disease is aggressive and the
outcome
remains poor. Thirty-seven cases, including the two
reported in this article, have been described in the literature to
date.
12/ 37 described patients with malignant OGCTs died
within 8 months of diagnosis.
Conclusion: Ovarian cancer with a YST
component
in postmenopausal women has an aggressive behaviour
and adjuvant platinum-based chemotherapy should be considered.
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