Clear Cell Ependymoma of the Temporal Lobe in a Child: A Case Report

2007 ◽  
Vol 44 (1) ◽  
pp. 79-84 ◽  
Author(s):  
Hakan Seyithanoglu ◽  
Feyza Karagoz Guzey ◽  
Erhan Emel ◽  
Ibrahim Alatas ◽  
Arsal Acarbas ◽  
...  
2005 ◽  
Vol 8 (3) ◽  
pp. 386-390 ◽  
Author(s):  
Angelica Oviedo ◽  
Dachling Pang ◽  
John Zovickian ◽  
Matthew Smith

Clear cell meningioma (CCM) is a rare variant of meningioma. Only 17 cases have been previously reported in children. Although it has bland cytologic features, it has a higher rate of recurrence than does conventional meningioma. This variant has been reported in sites such as spinal/intradural (lumbar and thoracic), cerebellopontine angle, and supratentorial. The differential diagnosis of CCM includes microcystic meningioma, hemangioblastoma, and clear cell ependymoma. The characteristic histology and immunohistochemistry leads to the diagnosis. We present a case of a 7-year-old boy with a CCM of the cauda equina and a review of pediatric CCM.


2007 ◽  
Vol 31 (3) ◽  
pp. 241-247 ◽  
Author(s):  
Ji Hoon Kim ◽  
Byung-Kyu Cho ◽  
In-One Kim ◽  
Sung-Hye Park

Neurosurgery ◽  
2000 ◽  
Vol 47 (6) ◽  
pp. 1434-1434 ◽  
Author(s):  
Hiroyoshi Akutsu ◽  
Yasushi Shibata ◽  
Masao Okazaki ◽  
Akio Hyodo ◽  
Akira Matsumura

Neurosurgery ◽  
2000 ◽  
Vol 47 (6) ◽  
pp. 1434-1434 ◽  
Author(s):  
Hiroyoshi Akutsu ◽  
Yasushi Shibata ◽  
Masao Okazaki ◽  
Akio Hyodo ◽  
Akira Matsumura

ABSTRACT OBJECTIVE AND IMPORTANCE Clear cell ependymoma of the spinal cord has not been reported in the literature, although ependymoma in the cerebral and cerebellar hemispheres has been described. We present the first case report of this rare histological type of ependymoma arising in the cervical spinal cord and emphasize the importance of recognizing this histological entity. CLINICAL PRESENTATION A 42-year-old woman presented with numbness in both upper limbs and spastic gait. Magnetic resonance imaging revealed an intramedullary tumor at the C6–T1 level with syringomyelia. INTERVENTION The tumor was totally removed. Histological analysis revealed that the tumor was composed of round cells with perinuclear halos similar to those observed in oligodendroglioma. However, we diagnosed clear cell ependymoma because these tumor cells exhibited epithelial features and ependymal rosettes under light microscopic examination. CONCLUSION Histological diagnosis was crucial to our determining whether to perform postoperative adjuvant therapy in this patient. Neurosurgeons should be aware of the possibility of this histological entity among intramedullary spinal cord tumors.


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