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Choroid plexus papillomas in infancy and childhood

✍ Scribed by A. Spallone; F. S. Pastore; R. Giuffre; B. Guidetti


Publisher
Springer
Year
1990
Tongue
English
Weight
683 KB
Volume
6
Category
Article
ISSN
0256-7040

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✦ Synopsis


The present study deals with 15 cases of choroid plexus papilloma, out of approximately 500 cases of brain tumors observed in children up to 16 years old. Several features are considered, including clinical symptoms and signs--mostly related to increased intracranial pressure--radiological diagnosis, pathology and surgical treatment, and results. Surgery may be radical in most cases, with the exception of histologically malignant papillomas. The management results are usually satisfactory. An adequate choice of surgical approach is mandatory and surgical technique should be meticulous, also in order to avoid the risk of intraoperative tumoral seeding.


πŸ“œ SIMILAR VOLUMES


Chromosome aberrations in choroid plexus
✍ Michael J. Donovan; Eduardo J. Yunis; Umberto Degirolami; Jonathan A. Fletcher; πŸ“‚ Article πŸ“… 1994 πŸ› John Wiley and Sons 🌐 English βš– 770 KB

## Abstract Karyotypic data on choroid plexus papillomas are scarce and, to date, have revealed no consistent aberrations. We karyotyped a choroid plexus papilloma which was characterized by a stemline of 52,XX, + 7, + 11, + 12, + 12, + 15, + 18. Additional copies of chromosomes 16, 17, and 20 were