Cancer overturned: Endometrioma mimicking granulosa cell tumor and the importance of FOXL2 analysis
ConclusionsA somatic missense mutation in the FOXL2 gene is a sensitive molecular marker for AGCT. Mutation analysis can help distinguish malignant from benign pathology to provide appropriate treatment and disease surveillance.
Source: Gynecologic Oncology Reports - Category: OBGYN Source Type: research
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