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Published on: September 12, 2019
Primary vaginal extraosseous Ewing sarcoma/primitive neuroectodermal tumor with cranial metastasis
Chi-Man Yip1, Shu-Shong Hsu, Nai-Jen Chang
1Division of Neurosurgery, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan, R.O.C. yip_chiman@yahoo.com
Journal of the Chinese Medical Association : JCMA
|June 23, 2009
Summary
Extraosseous Ewing sarcoma, a rare soft tissue cancer, can occur in the female genital tract. This case highlights a vaginal tumor metastasizing to the scalp, successfully treated with surgery, radiation, and chemotherapy.
Area of Science:
- Oncology
- Pathology
Background:
- Extraosseous Ewing sarcoma (EES) is part of the Ewing sarcoma/primitive neuroectodermal tumor (PNET) family.
- EES commonly affects soft tissues in children and young adults but rarely involves the female genital tract.
Observation:
- A rare case of vaginal EES/PNET is presented.
- The tumor metastasized to the right frontoparietal scalp, skull, and dura.
- Microscopic examination revealed similar features in both primary vaginal and metastatic head tumors.
Findings:
- The patient underwent surgical resection of both tumors.
- Adjuvant radiotherapy and chemotherapy were administered post-surgery.
- A favorable clinical outcome was achieved following the multimodal treatment approach.
Implications:
- This case underscores the possibility of vaginal EES/PNET, even in rare instances.
- It emphasizes the importance of considering EES/PNET in the differential diagnosis of soft tissue tumors in this location.
- The successful treatment outcome suggests that aggressive multimodal therapy can be effective for metastatic EES/PNET.
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