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Tumors of the Choroid Plexus in Children
Neurosurgery, 1989 Abstract Primary neoplasms of the choroid plexus in children are surgically treatable, and the encouraging results of surgical removal, even for carcinoma, justify an aggressive surgical approach, Forty cases operated on over a span of 45 years have been reviewed in detail, including a rereading of all microscopic slides.
R G, Ellenbogen +2 more
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Journal of Neuro-Oncology, 2007 Background Choroid plexus carcinomas (CPC) are rare brain tumors with a dismal prognosis. Although the role of surgery has been well established, the question of whether chemotherapy improves the prognosis is still under discussion.
Brigitte Wrede
exaly +2 more sources
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Microscopy Research and Technique, 2000
Choroid plexus tumors are rare intraventricular papillary neoplasms derived from choroid plexus epithelium, which account for only between 0.4-0.6% of all intracranial and 2-3% of pediatric neoplasms. Plexus papillomas outnumber choroid plexus carcinomas by a ratio of 5:1 and around 80% of choroid plexus carcinomas arise in children.
C H, Rickert, W, Paulus
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Choroid plexus tumors are rare intraventricular papillary neoplasms derived from choroid plexus epithelium, which account for only between 0.4-0.6% of all intracranial and 2-3% of pediatric neoplasms. Plexus papillomas outnumber choroid plexus carcinomas by a ratio of 5:1 and around 80% of choroid plexus carcinomas arise in children.
C H, Rickert, W, Paulus
openaire +2 more sources
Revista de neurologia, 2001
Tumors of the choroid plexus are rare tumors of neuro ectodermal origin, accounting for less 1% of intracranial tumors in all ages. Most cases present in children less than 2 years of age. These tumors have been classified according to histopathological criteria into papilloma and carcinoma.We review the epidemiological, clinical, neuropathological ...
M, Gelabert-González +4 more
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Tumors of the choroid plexus are rare tumors of neuro ectodermal origin, accounting for less 1% of intracranial tumors in all ages. Most cases present in children less than 2 years of age. These tumors have been classified according to histopathological criteria into papilloma and carcinoma.We review the epidemiological, clinical, neuropathological ...
M, Gelabert-González +4 more
openaire +3 more sources
2019
Derived from choroid plexus epithelium and vascularized by choroidal arteries, choroid plexus tumors (CPTs) are primary intraventricular brain tumors of neuroectodermal origin with a papillary pattern resembling nonneoplastic choroid plexus. CPTs include both benign choroid plexus papilloma (CPP) and malignant choroid plexus carcinoma (CPC), as well as
Serge Weis +6 more
+4 more sources
Derived from choroid plexus epithelium and vascularized by choroidal arteries, choroid plexus tumors (CPTs) are primary intraventricular brain tumors of neuroectodermal origin with a papillary pattern resembling nonneoplastic choroid plexus. CPTs include both benign choroid plexus papilloma (CPP) and malignant choroid plexus carcinoma (CPC), as well as
Serge Weis +6 more
+4 more sources
Choroid Plexus Tumors in the Dog
Journal of the American Veterinary Medical Association, 1980SUMMARY Clinical and necropsy records for nine dogs with tumors of the choroid plexus were reviewed. In seven of the dogs, the tumors were on the left side of the fourth ventricle. All of the dogs were males, ranging in age from 13 months to 9 years. Upper motor neuron tetraparesis and positional nystagmus were the most common neurologic signs.
F A, Zaki, L A, Nafe
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2020
Choroid plexus tumors are rare intracranial tumors which account for only 0.4–0.6% of all brain tumors. These are intraventricular papillary neoplasms derived from choroid plexus epithelium and range from well-differentiated choroid plexus papillomas (CPP WHO grade I) to highly aggressive choroid plexus carcinomas (WHO grade III), with rare ...
Daniel H. Fulkerson +3 more
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Choroid plexus tumors are rare intracranial tumors which account for only 0.4–0.6% of all brain tumors. These are intraventricular papillary neoplasms derived from choroid plexus epithelium and range from well-differentiated choroid plexus papillomas (CPP WHO grade I) to highly aggressive choroid plexus carcinomas (WHO grade III), with rare ...
Daniel H. Fulkerson +3 more
openaire +2 more sources