Chordoid Meningioma: The Rarest Subtype of Grade II Meningioma
Author Information
Author(s): Muacevic Alexander, Adler John R, Valerio Jose, Santiago Rea Noe, Zumaeta Jorge, Rey Martinez Luis
Primary Institution: Palmetto General Hospital, Hialeah, USA
Conclusion
Chordoid meningiomas are rare tumors that require early detection and complete resection to minimize recurrence risk.
Supporting Evidence
- Chordoid meningiomas account for only a small percentage of all meningiomas.
- Complete resection is crucial to minimize the risk of recurrence.
- The patient achieved full motor recovery after surgery.
Takeaway
Chordoid meningiomas are very rare brain tumors that can cause weakness and need to be completely removed to help the patient feel better.
Methodology
The case involved imaging, corticosteroid treatment, embolization, and complete tumor resection.
Limitations
The findings are based on a single case report, limiting generalizability.
Participant Demographics
A 44-year-old female with a history of hypertension, hyperlipidemia, type 2 diabetes mellitus, and schizophrenia.
Digital Object Identifier (DOI)
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