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Case reports highlight unique recurrence patterns in adult-type ovarian granulosa cell tumors, suggesting importance of tailored surveillance strategies.
Adult-type ovarian granulosa cell tumors are rare low-grade malignancies characterized by late recurrence and atypical clinical manifestations. This study reports two cases of recurrent adult-type ovarian granulosa cell tumor with distinct timelines and anatomical sites, including one case with two postoperative recurrences. We analyze their imaging features, surgical management, histopathology, postoperative follow-up, and review relevant literature. These cases highlight the importance of long-term follow-up and raise awareness of rare recurrence sites, emphasizing the diagnostic value of imaging and the need for individualized surveillance strategies in adult-type ovarian granulosa cell tumor patients.
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Wang et al. (2025) studied this question.
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