Abstract
Leydig cell tumors account for 3% of testicular tumors and have never been reported after treatment for Ewing's sarcoma. We report the unusual occurrence of a patient who developed a Leydig cell tumor of the testis 18 years after successful treatment for Ewing's sarcoma. Additional monitoring for second malignancies may become appropriate as long-term survival continues to improve for patients with Ewing's sarcoma.
Original language | English (US) |
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Pages (from-to) | 1008-1010 |
Number of pages | 3 |
Journal | Pediatric Blood and Cancer |
Volume | 49 |
Issue number | 7 |
DOIs | |
State | Published - Dec 2007 |
Externally published | Yes |
Keywords
- Ewing's sarcoma
- Leydig cell tumor
- Secondary malignancy
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Hematology
- Oncology