TY - JOUR
T1 - Psammomatous Cavernous Malformation Presenting as Drug-Resistant Epilepsy
T2 - Case Illustration and Review of Literature
AU - Sharma, Kanika
AU - Kalakoti, Piyush
AU - Shaughnessy, John E.
AU - De La Cruz, Nestor
AU - Dossani, Rimal H.
AU - Zhu, Peimin
AU - Gonzalez-Toledo, Eduardo
AU - Ledbetter, Christina
AU - Pinskton, James B.
AU - Nanda, Anil
AU - Riel-Romero, Rosario Maria
AU - Minagar, Alireza
AU - Notarianni, Christina
AU - Sun, Hai
N1 - Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2016/9/1
Y1 - 2016/9/1
N2 - Background Psammoma bodies (PBs) are whorled, laminated hyaline spherules containing calcium deposits. Intracranially, the presence of PBs is associated with variants of meningioma and pituitary lesions, as well as aging choroid plexus. Limited information exists on their presence in vascular malformation. Results In this report, we describe a case of an adolescent male with drug-resistant epilepsy that was surgically managed at our regional epilepsy center. The epileptogenic focus was determined to be emanating from an indolent right insular lesion. Histopathologic evaluation showed the abundance of intravascular and perivascular PBs. Immunohistochemical evaluation confirmed the vascular origin using vascular markers. The unusual presence of PBs in a vascular lesion was unanticipated. Conclusions Based on our case, we present the clinicoradiologic characteristics, supplemented with intraoperative findings, for this unusual lesion. In addition, because of the unusual presence of PBs in vascular lesions, we provide the findings of a systematic literature review to show the association of PBs with intracranial vascular lesions.
AB - Background Psammoma bodies (PBs) are whorled, laminated hyaline spherules containing calcium deposits. Intracranially, the presence of PBs is associated with variants of meningioma and pituitary lesions, as well as aging choroid plexus. Limited information exists on their presence in vascular malformation. Results In this report, we describe a case of an adolescent male with drug-resistant epilepsy that was surgically managed at our regional epilepsy center. The epileptogenic focus was determined to be emanating from an indolent right insular lesion. Histopathologic evaluation showed the abundance of intravascular and perivascular PBs. Immunohistochemical evaluation confirmed the vascular origin using vascular markers. The unusual presence of PBs in a vascular lesion was unanticipated. Conclusions Based on our case, we present the clinicoradiologic characteristics, supplemented with intraoperative findings, for this unusual lesion. In addition, because of the unusual presence of PBs in vascular lesions, we provide the findings of a systematic literature review to show the association of PBs with intracranial vascular lesions.
KW - Cavernoma
KW - Drug-resistant epilepsy
KW - Electrocorticography
KW - Psammoma
KW - Vascular malformation
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U2 - 10.1016/j.wneu.2016.05.093
DO - 10.1016/j.wneu.2016.05.093
M3 - Review article
C2 - 27283183
AN - SCOPUS:84976878683
SN - 1878-8750
VL - 93
SP - 120
EP - 126
JO - World Neurosurgery
JF - World Neurosurgery
ER -