Patients with germline DICER1 mutations are at increased risk of developing a wide
range of relatively rare tumors. In the female genital tract, DICER1 mutations are
associated with embryonal rhabdomyosarcoma of the uterine cervix and ovarian sex cordstromal
tumors. Primary embryonal rhabdomyosarcoma of the uterine corpus is exceedingly rare,
and there is limited information about its clinicopathological features in the literature.
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