IIntroduction: Central neurocytoma is a tumor of neuronal origin that should be taken into consideration in the differential diagnosis of intraventricular neoplasms. Reports of neurocytomas with an extraventricular localization are rare: to our knowledge, the case described here is the first in which a neurocytoma developed within the ventricles but also invaded the brain stem. Case report: The authors describe the unusual case of a 5-year-old boy with an intraventricular neurocytoma presenting with massive involvement of the basal nuclei and the brain stem. The patient underwent first biopsy and then surgery for ventricular-peritoneal shunting and partial removal of the tumor. Histology showed the tumor to be a typical neurocytoma with Mib-1 <2%. The postoperative course was uneventful. At 3 years' follow-up, the patient's clinical condition is stable and there are no signs of disease progression. Discussion: The literature is reviewed and the characteristics of this unusual tumor are discussed.
Intraventricular neurocytoma with massive brain stem involvement in a 5-year-old child / Lenzi, J., Frati, A., Raco, A., Pichierri, A., Giangaspero, F., Salvati, M., Delfini, R.. - In: CHILDS NERVOUS SYSTEM. - ISSN 0256-7040. - STAMPA. - 22:1(2006), pp. 95-98. [10.1007/s00381-004-1092-2]
Intraventricular neurocytoma with massive brain stem involvement in a 5-year-old child
LENZI, JACOPO;FRATI, ALESSANDRO;RACO, Antonino;PICHIERRI, ANGELO;GIANGASPERO, FELICE;SALVATI, Maurizio;DELFINI, Roberto
2006
Abstract
IIntroduction: Central neurocytoma is a tumor of neuronal origin that should be taken into consideration in the differential diagnosis of intraventricular neoplasms. Reports of neurocytomas with an extraventricular localization are rare: to our knowledge, the case described here is the first in which a neurocytoma developed within the ventricles but also invaded the brain stem. Case report: The authors describe the unusual case of a 5-year-old boy with an intraventricular neurocytoma presenting with massive involvement of the basal nuclei and the brain stem. The patient underwent first biopsy and then surgery for ventricular-peritoneal shunting and partial removal of the tumor. Histology showed the tumor to be a typical neurocytoma with Mib-1 <2%. The postoperative course was uneventful. At 3 years' follow-up, the patient's clinical condition is stable and there are no signs of disease progression. Discussion: The literature is reviewed and the characteristics of this unusual tumor are discussed.| File | Dimensione | Formato | |
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