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.
To read this article in full you will need to make a payment
Purchase one-time access:
Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online accessOne-time access price info
- For academic or personal research use, select 'Academic and Personal'
- For corporate R&D use, select 'Corporate R&D Professionals'
Subscribe:
Subscribe to Journal of Pediatric and Adolescent GynecologyAlready a print subscriber? Claim online access
Already an online subscriber? Sign in
Register: Create an account
Institutional Access: Sign in to ScienceDirect