An 11-year-old girl was admitted with a 3-year history of decreasing hearing and headache, occasional vomiting and poor school performance of 8 months duration. Neurologically she showed signs of a cerebellopontine angle mass. This was confirmed by CT scan, which showed an enhancing lesion in the right cerebellopontine angle. The lesion was totally removed, with excellent results. Histologically the tumor appeared to be a choroid plexus papilloma. Choroid plexus papillomas of thr cerebellopontine angle are extremely rare in children

Spallone, A., Pastore, F.s., Hagi Mao, M. (1986). Choroid plexus papillomas of the cerebellopontine angle in a child. ITALIAN JOURNAL OF NEUROLOGICAL SCIENCES, 7, 613-616 [10.1007/BF02341477].

Choroid plexus papillomas of the cerebellopontine angle in a child

SPALLONE, ALDO;PASTORE, FRANCESCO SAVERIO;
1986-12-01

Abstract

An 11-year-old girl was admitted with a 3-year history of decreasing hearing and headache, occasional vomiting and poor school performance of 8 months duration. Neurologically she showed signs of a cerebellopontine angle mass. This was confirmed by CT scan, which showed an enhancing lesion in the right cerebellopontine angle. The lesion was totally removed, with excellent results. Histologically the tumor appeared to be a choroid plexus papilloma. Choroid plexus papillomas of thr cerebellopontine angle are extremely rare in children
dic-1986
Pubblicato
Rilevanza nazionale
Articolo
Esperti anonimi
Settore MED/27 - NEUROCHIRURGIA
English
Choroid plexus papilloma, cerebellopontine angle, CT scanning, children
Spallone, A., Pastore, F.s., Hagi Mao, M. (1986). Choroid plexus papillomas of the cerebellopontine angle in a child. ITALIAN JOURNAL OF NEUROLOGICAL SCIENCES, 7, 613-616 [10.1007/BF02341477].
Spallone, A; Pastore, Fs; Hagi Mao, M
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/72867
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