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Published on: July 29, 2013
Meningioma mimicking an intraparenchymal cystic tumor
Tomoaki Tamada1, Rei Enatsu1, Noriaki Kikuchi2
1Department of Neurosurgery, Sapporo Medical University School of Medicine, Sapporo, Japan.
Abstract:
Meningiomas rarely exhibit cystic lesions with mural nodules, and may be misdiagnosed as intraparenchymal cystic tumors. We herein present a 64-year-old woman with a cystic lesion and enhancing mural nodule in the left temporal lobe accompanied by peritumoral brain edema. Differential diagnoses included low-grade gliomas, hemangioblastoma, and cystic meningioma. Gross total resection of the tumor was achieved through a temporal surgical approach. Intraoperative findings showed that the tumor was an extraparenchymal tumor. The cyst was covered by an extraparenchymal thin membrane and the cystic fluid was yellowish in color. The final result of the pathological examination was microcystic meningioma, WHO grade I. Although intraparenchymal tumors, such as hemangioblastoma, ganglioglioma, pilocytic astrocytoma, and pleomorphic xanthoastrocytoma, commonly display this MRI pattern, meningioma needs to be included in the differential diagnosis.
Insights
Cystic meningiomas with mural nodules are rare and can mimic intraparenchymal tumors. This case highlights the importance of considering meningioma in the differential diagnosis for such brain lesions.
Area of Science:
- Neurosurgery
- Neuropathology
- Neuroradiology
Background:
- Meningiomas are typically dural-based tumors, but cystic variants with mural nodules are uncommon.
- These rare presentations can be mistaken for intraparenchymal cystic neoplasms on imaging.
- Accurate preoperative diagnosis is crucial for appropriate surgical planning and patient management.
Observation:
- A 64-year-old woman presented with a left temporal lobe cystic lesion and enhancing mural nodule, associated with peritumoral brain edema.
- Initial differential diagnoses included low-grade gliomas and hemangioblastoma.
- Intraoperative findings confirmed an extraparenchymal tumor with a thin membrane and yellowish cystic fluid.
Findings:
- Pathological examination confirmed the diagnosis of microcystic meningioma, WHO grade I.
- The imaging characteristics mimicked those of intraparenchymal tumors like hemangioblastoma and pleomorphic xanthoastrocytoma.
- Gross total resection was successfully achieved via a temporal surgical approach.
Implications:
- This case underscores the necessity of including meningioma in the differential diagnosis for cystic brain lesions with mural nodules.
- Recognizing this rare presentation can prevent misdiagnosis and guide neurosurgical interventions.
- Further awareness of cystic meningioma subtypes can improve diagnostic accuracy in neuro-oncology.
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