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Pathology of choroid plexus papillomas: A review

Clinical Neurology and Neurosurgery, 1998
Choroid plexus papillomas (CPPs) are rare, usually slow growing neoplasms. Their biological behaviour cannot be predicted in an individual case. Furthermore, the neuropathological diagnosis of these neoplasms is occasionally difficult because light and ...
Leonello Tacconi, M L Rossi
exaly   +2 more sources

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Pediatric choroid plexus neoplasms

International Journal of Radiation Oncology*Biology*Physics, 1998
Choroid plexus tumors (CPT) are rare childhood neoplasms. The relatively small number of reported cases and the controversies surrounding the clinical and pathological classification of these tumors have made it difficult to define a standard of care for these patients. Our intention is to contribute to the body of knowledge of these tumors and further
E, Chow, D A, Reardon, A B, Shah, J J, Jenkins, J, Langston, R L, Heideman, R A, Sanford, L E, Kun, T E, Merchant   +8 more
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Choroid Plexus Neoplasms

The American Journal of Surgical Pathology, 1986
Choroid plexus neoplasms account for less than 1% of all intracranial tumors, with papillomas (CPPs) more frequent than carcinomas (CPCs). Immunocytochemical characterization of these neoplasms has been limited. Glial fibrillary acidic protein (GFAP), S100 protein, and keratin have been variably demonstrated by others.
C M, Coffin, M R, Wick, J T, Braun, L P, Dehner   +3 more
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Choroid Plexus Neoplasms

, 2009
Christine E. Fuller, Sonia Narendra, Ioana Tolocica   +2 more
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THE NEURORADIOLOGY OF CHILDHOOD CHOROID PLEXUS NEOPLASMS

American Journal of Roentgenology, 1973
The features of 14 cases of choroid plexus neoplasms from the Hospital for Sick Children, Toronto, are presented, and similar available data from 130 previously reported cases in children are tabulated.In any neuroradiologic practice, choroid plexus papillomas and carcinomas are rarely encountered.
J R, Thompson, D C, Harwood-Nash, C R, Fitz   +2 more
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Choroid plexus papillomas

British Journal of Neurosurgery, 1994
Choroid plexus papillomas (CPPs) are rare neoplasms accounting for less than 1% of all intracranial tumours. We present our experience with 13 consecutive cases managed by us between 1981 and 1991. There were eight children and five adults. Five patients
D Rout, Arun Kumar Gupta, V V Radhakrishnan   +2 more
exaly   +2 more sources

Ultrasonic diagnosis of a choroid plexus neoplasm in a child

The British Journal of Radiology, 1984
Choroid plexus neoplasms arise from the epithelial cells of the choroid plexus of the brain and can occur wherever choroid plexus is found within the cranial cavity. Although relatively uncommon, these tumours are usually benign and are often accessible to surgical removal. It is therefore of paramount importance that their presence be recognised early
P S, Reddy, S R, Wild, G M, Hendry
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Childhood choroid plexus neoplasms

European Journal of Pediatrics, 1983
Fourteen children less than 2 years old with choroid plexus papilloma (CPP) were studied. Of these patients nine had the tumor in the lateral ventricles (LV), three in the fourth ventricle (4th V), one in the third ventricle (3rd V) and one in the third and left lateral ventricle (LLV).
I, Pascual-Castroviejo, F, Villarejo, A, Perez-Higueras, C, Morales, S I, Pascual-Pascual   +4 more
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NEOPLASM OF THE CHOROID PLEXUS

American Journal of Diseases of Children, 1934
Neoplasms of the brain in infancy undoubtedly occur with greater frequency than reports of their discovery would suggest. Because of the readiness with which their symptomatology may be confused with that of gastro-intestinal dysfunction, particularly projectile vomiting, uncomplicated by a lesion of the nervous system, recognition of the presence of ...
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Pediatric choroid plexus neoplasms: MR, CT, and pathologic correlation.

Radiology, 1989
Choroid plexus papillomas are rare, constituting approximately 0.5% of all intracranial neoplasms. Four benign choroid plexus papillomas and one choroid plexus carcinoma were retrospectively reviewed in patients aged 4-20 months who had been examined with magnetic resonance (MR) imaging with a field strength of 0.5 T or 1.0 T and with computed ...
T L, Coates, D B, Hinshaw, N, Peckman, J R, Thompson, A N, Hasso, B A, Holshouser, D S, Knierim   +6 more
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