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References in periodicals archive ?
Choroid plexus cells are neuroepithelial cells that line the intraventricular papillae and secrete cerebrospinal fluid (CSF).[1] Choroid plexus tumors (CPTs) are rare intracranial tumors that account for 2-5% of all pediatric brain cancers, to date, seldom reported.[2] According to the histological classification of the World Health Organization (WHO), CPTs can be divided into choroid plexus papilloma (CPP), atypical choroid plexus papilloma (aCPP), and choroid plexus carcinoma (CPC).[3] CPTs usually occur in children younger than 2 years, with about 10-20% of cases found in patients younger than 1 year.[4] The WHO classification of 2007 first mentioned aCPP, which carried at least a 5-fold increase in the risk of 5-year recurrence compared with CPP.
Tumor n Craniopharyngioma 8 Meningioma, grade I-II 59 Glioblastoma 60 Astrocytoma, grade I-II 35 Astrocytoma, grade III 7 Ependymoma, grade I-II 14 Ependymoma, grade III 3 Oligodendrogliomas, grade II 7 Oligodendrogliomas, grade III 1 Mixed glioma (oligoastrocytomas), grade III 3 Carcinoma (metastatic) 20 Medulloblastoma 18 Lymphoma 3 Schwannoma 3 Choroid plexus papilloma 6 Central neurocytoma 4 Primitive neuroectodermal tumor (PNET) 3 Atypical teratoid/rhabdoid tumor 4 Hypothalamic hamartoma 3 Table 4: Cases in which there were discrepancies between the frozen section report and the final diagnosis (based on permanent section).
According to cellular differentiation, number of mitosis and local invasion, choroid plexus neoplasms can be classified as choroid plexus papillomas or carcinomas (KOESTNER et al., 1999).
Choroid plexus papilloma of bilateral lateral ventricle.
(2) Misdiagnosis of this lesion on histopathology as oligodendroglioma and on imaging as meningioma, ependymoma, oligodendroglioma, choroid plexus papilloma have been reported.
The pre-operative differential diagnosis included glomus tumor (vagale or jugulare), meningioma, ELST, choroid plexus papilloma, and aneurysmal bone cyst.
Primary intracranial pigmented neoplasms are rare and include melanoma, melanocytoma, melanotic ependymoma, and subependymoma[1]; pigmented choroid plexus papilloma and carcinoma[2-5]; and melanotic astrocytoma.[6] Most of these lesions arise within or in close proximity to the ventricular system.
Common Posterior FOSSA Tumours Adults Children (Extra-axial>Intra-axial) (Intra-axial>Extra-axial) * Schwannoma * Primitive * Meningioma Neuroectodermal * Epidermoid Tumour (PNET), * Metastases Medulloblastoma * Haemangioblastoma * Astrocytoma * Choroid plexus papilloma * Ependymoma * Arachnoid cysts * Oligodendroglioma * Haemangioblastoma * Lymphoma * Atypical Teratoid Rhabdoid Tumour (ATRT) Since posterior fossa is a critical location with limited pace, even small tumours produce significant morbidity and ortality.
A variety of melanotic brain tumors have been described in the literature, including ependymoma, choroid plexus papilloma and carcinoma, medulloblastoma, medulloepithelioma, schwannoma, meningioma, melanocytoma, and melanoma.
was cerebellar neoplasm, frontal glioma, tuberculoma and choroid plexus papilloma. This study coincides with study of Patons.
Characterisation of X;17(q12q13) translocation breakpoints in a female patient with hypomelanosis of Ito and choroid plexus papilloma. Eur J Hum Genet.
Metastatic tumors and meningioma (07 cases each), Glioblastoma and pituitary adenoma (05 cases each) Astrocytoma (04 cases) and 1 case each of Gliosarcoma, Schwannoma, Medulloblastoma (PNET), undifferentiated carcinoma and choroid plexus papilloma.