TY - JOUR
T1 - Optic nerve seeding of atypical meningiomas presenting with subacute visual loss
T2 - 2 case reports with genetic characterization
AU - Kitamura, Yohei
AU - Akiyama, Takenori
AU - Sasaki, Hikaru
AU - Hayashi, Yuichiro
AU - Yoshida, Kazunari
PY - 2013/8
Y1 - 2013/8
N2 - Meningiomas rarely cause CSF dissemination, and CSF seeding to the optic nerve (ON) is extremely rare. This is the first report of 2 cases of atypical meningioma with subacute visual loss due to ON seeding. The authors present the genetic characteristics of these atypical meningiomas with CSF dissemination. The patient in Case 1 was a 36-year-old woman with a 1.5-cm mass within the left ON, and the patient in Case 2 was a 70-year-old woman with a 0.9-cm mass around the right ON. Both individuals had undergone multiple surgeries for primary lesions and local recurrent lesions. They presented with subacute visual loss, and both tumors were completely resected. The pathological diagnosis was atypical meningioma with high MIB-1 indices and p53-positive cell ratios in each case. Comparative genomic hybridization showed significant chromosomal copy number alterations similar to the results of previous surgeries, confirming that the tumors were disseminated lesions. The present findings suggest that genetic characteristics, such as 1p and 10qcen-23 losses and 17q and 20 gains, shared by the 2 cases might be associated with CSF dissemination of meningiomas.
AB - Meningiomas rarely cause CSF dissemination, and CSF seeding to the optic nerve (ON) is extremely rare. This is the first report of 2 cases of atypical meningioma with subacute visual loss due to ON seeding. The authors present the genetic characteristics of these atypical meningiomas with CSF dissemination. The patient in Case 1 was a 36-year-old woman with a 1.5-cm mass within the left ON, and the patient in Case 2 was a 70-year-old woman with a 0.9-cm mass around the right ON. Both individuals had undergone multiple surgeries for primary lesions and local recurrent lesions. They presented with subacute visual loss, and both tumors were completely resected. The pathological diagnosis was atypical meningioma with high MIB-1 indices and p53-positive cell ratios in each case. Comparative genomic hybridization showed significant chromosomal copy number alterations similar to the results of previous surgeries, confirming that the tumors were disseminated lesions. The present findings suggest that genetic characteristics, such as 1p and 10qcen-23 losses and 17q and 20 gains, shared by the 2 cases might be associated with CSF dissemination of meningiomas.
KW - Atypical meningioma
KW - Cerebrospinal fluid seeding
KW - Comparative genomic hybridization
KW - Dissemination
KW - Oncology
KW - Optic nerve
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UR - http://www.scopus.com/inward/citedby.url?scp=84881165848&partnerID=8YFLogxK
U2 - 10.3171/2013.1.JNS121533
DO - 10.3171/2013.1.JNS121533
M3 - Article
C2 - 23432529
AN - SCOPUS:84881165848
SN - 0022-3085
VL - 119
SP - 494
EP - 498
JO - Journal of neurosurgery
JF - Journal of neurosurgery
IS - 2
ER -