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Published on: January 14, 2014
Pediatic intracranial synovial sarcoma: a case report.
Ming Liu1, Menglei Fan2, Dejiong Li3
1Department of Radiology, The Second People's Hospital of Guiyang (Jinyang Hospital), Guiyang, Guizhou, 550001, China. 120429414@qq.com.
Intracranial synovial sarcoma (SS) is rare. Magnetic resonance (MR) imaging reveals specific signs like the "triple signal sign" and "cobblestone sign," aiding diagnosis.
Area of Science:
- Neuroradiology
- Oncology
- Pathology
Background:
- Intracranial synovial sarcoma (SS) is an exceptionally rare primary brain tumor.
- Accurate preoperative diagnosis is crucial for effective management and surgical planning.
Purpose of the Study:
- To elucidate the characteristic MR imaging findings of intracranial synovial sarcoma.
- To enhance diagnostic accuracy for radiologists and neurosurgeons through case review and literature analysis.
Main Methods:
- Retrospective analysis of clinical data and MR imaging of a pathologically confirmed intracranial SS case.
- Review of relevant literature to identify common imaging features and potential misdiagnosis factors.
Main Results:
- MR imaging demonstrated a solid-cystic mass in the right frontal lobe.
- Key findings included T1WI isointensity, heterogeneous T2WI signal, elevated DWI signal, and uneven T1WI enhancement.
- Distinctive "triple signal sign" and "cobblestone sign" were observed.
Conclusions:
- Intracranial synovial sarcoma is a rare entity with specific, albeit uncommon, MR imaging features.
- Comprehensive MR examinations are valuable for differentiating SS from other intracranial lesions.
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