Published online Sep 26, 2020. doi: 10.12998/wjcc.v8.i18.4272
Peer-review started: April 13, 2020
First decision: July 25, 2020
Revised: August 4, 2020
Accepted: August 20, 2020
Article in press: August 20, 2020
Published online: September 26, 2020
Processing time: 161 Days and 18.5 Hours
Lymphoplasmacyte-rich meningioma (LPRM) is one of the rarest variants of meningioma and is classified as grade I (benign) tumor. It is characterized by abundant infiltrates of lymphocytes and plasma cells. Here, we report an extremely rare case of LPRM with an atypical imaging finding of multiple cysts around a solid mass.
The patient was a 36-year-old man with intermittent headache, dizziness, and vomiting for 2 years. Computed tomography and magnetic resonance imaging presented a cystic solid mass in the right frontal lobe with heavy peritumoral edema and obvious contrast enhancement. The patient was treated with right frontotemporal craniotomy, and gross total resection of the tumor was achieved without adjuvant therapy. There was no clinical or neuroradiological evidence of recurrent or residual tumor for 3 years after initial surgery.
LPRM is one of the rarest variants of meningioma. Although, the mass of this case had common features, multiple cysts with nonuniform size and thin wall around the solid part are uncommon imaging finding, increasing the rate of misdiagnosis. The definitive diagnosis of LPRM relies on histopathological findings.
Core Tip: Lymphoplasmacyte-rich meningioma (LPRM) is one of the rarest variants of meningioma. A case of LPRM is presented here with atypical imaging finding of multiple cysts around a solid mass, which has been reported even more rarely. In computed tomography and magnetic resonance imaging findings, the mass had common features: An irregular shape, unclear boundary with neighboring brain tissue, heavy peritumoral brain edema, significant enhancement of the solid part, and dural tail sign. Multiple cysts with nonuniform size and thin wall around the solid part are uncommon imaging finding, increasing the rate of misdiagnosis. The definitive diagnosis of LPRM relies on histopathological findings.