Pleomorphic xanthoastrocytoma associated with von Recklinghausen neurofibromatosis.

OZEK, MEMET; SAV, A; PAMIR, Mustafa; OZER, AF; OZEK, E; ERZEN, C

doi:10.1007/bf00301935

Pleomorphic xanthoastrocytoma associated with von Recklinghausen neurofibromatosis.

OZEK M., SAV A., PAMIR M. N., OZER A., OZEK E., ERZEN C.

Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, cilt.9, sa.1, ss.39-42, 1993 (SCI-Expanded, Scopus)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 9 Sayı: 1
Basım Tarihi: 1993
Doi Numarası: 10.1007/bf00301935
Dergi Adı: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Sayfa Sayıları: ss.39-42
Anahtar Kelimeler: PLEOMORPHIC XANTHOASTROCYTOMA, BENIGN GLIOMA, GLIAL FIBRILLARY ACIDIC PROTEIN, VONRECKLINGHAUSEN NEUROFIBROMATOSIS, YOUNG SUBJECTS, GLIOMA
Acıbadem Mehmet Ali Aydınlar Üniversitesi Adresli: Evet

Özet

The authors present a case of pleomorphic xanthoastrocytoma that occurred in a 14-year-old boy with von Recklinghausen's neurofibromatosis. The circumscribed turmor with a cystic component was located in the medial right temporal lobe. The designation of pleomorphic xanthoastrocytoma has been suggested for this neoplasm on the basis of its unique histological features. These include positive glial fibrillary acidic protein staining.