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Recurrent CIC-rearranged sarcoma of central nervous system: a clinicopathological case report
Shan Jiang1,2,3,4, Kay Ka-Wai Li5, Jingqi Hu1,2
1Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, China.
Abstract:
CIC-rearranged sarcoma (CRS) is a subgroup of small round blue cell tumors similar to Ewing's sarcoma but lacking the EWSR1 gene translocation. It is characterized by a CIC gene rearrangement on chromosome 19q13, with the most common partner gene being DUX4. In 2021, the WHO classification of central nervous system tumors (5th edition) introduced a new pathological classification for CRS based on bone and soft tissue tumor classifications, categorizing it as mesenchymal non-meningeal epithelial tumors. Primary CIC::DUX4 rearrangement sarcoma in the central nervous system is extremely rare, with no established standard treatment and a very poor prognosis. Herein, we present a case of intracranial CIC::DUX4 rearrangement diagnosed using DNA methylation classifiers and multiple omics diagnosis techniques. We also document the disease progression after chemoradiation therapy and subsequent in situ recurrence.
Insights
CIC-rearranged sarcoma (CRS) is a rare brain tumor lacking EWSR1 gene fusions. This case highlights diagnosis using advanced omics and methylation profiling, and its progression post-treatment.
Area of Science:
- Oncology
- Genetics
- Pathology
Background:
- CIC-rearranged sarcoma (CRS) is a rare small round blue cell tumor defined by CIC gene rearrangement, distinct from Ewing's sarcoma.
- CRS is now classified as a mesenchymal non-meningeal epithelial tumor under the 2021 WHO CNS tumor classification.
- Primary intracranial CIC::DUX4 rearrangement sarcoma is exceptionally rare, with limited treatment options and poor prognosis.
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