"Choroid Plexus Neoplasms" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Benign or malignant tumors which arise from the choroid plexus of the ventricles of the brain. Papillomas (see PAPILLOMA, CHOROID PLEXUS) and carcinomas are the most common histologic subtypes, and tend to seed throughout the ventricular and subarachnoid spaces. Clinical features include headaches, ataxia and alterations of consciousness, primarily resulting from associated HYDROCEPHALUS. (From Devita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2072; J Neurosurg 1998 Mar;88(3):521-8)
| Descriptor ID |
D016545
|
| MeSH Number(s) |
C04.588.614.250.195.205.200 C10.228.140.211.280.300 C10.551.240.250.200.200
|
| Concept/Terms |
Choroid Plexus Neoplasms- Choroid Plexus Neoplasms
- Choroid Plexus Tumors
- Choroid Plexus Tumor
- Neoplasms, Choroid Plexus
- Choroid Plexus Neoplasm
- Neoplasm, Choroid Plexus
|
Below are MeSH descriptors whose meaning is more general than "Choroid Plexus Neoplasms".
Below are MeSH descriptors whose meaning is more specific than "Choroid Plexus Neoplasms".
This graph shows the total number of publications written about "Choroid Plexus Neoplasms" by people in this website by year, and whether "Choroid Plexus Neoplasms" was a major or minor topic of these publications.
To see the data from this visualization as text,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 3 | 0 | 3 |
| 1998 | 0 | 2 | 2 |
| 2000 | 1 | 0 | 1 |
| 2001 | 1 | 0 | 1 |
| 2005 | 1 | 0 | 1 |
| 2006 | 2 | 1 | 3 |
| 2009 | 2 | 0 | 2 |
| 2010 | 2 | 1 | 3 |
| 2011 | 1 | 1 | 2 |
| 2015 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 2 | 0 | 2 |
| 2018 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Choroid Plexus Neoplasms" by people in Profiles.
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Final results of the Choroid Plexus Tumor study CPT-SIOP-2000. J Neurooncol. 2022 Feb; 156(3):599-613.
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Pediatric choroid plexus carcinoma: Biologically and clinically in need of new perspectives. Pediatr Blood Cancer. 2018 07; 65(7):e27031.
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Successful Treatment of Recurrent Li-Fraumeni Syndrome-related Choroid Plexus Carcinoma. J Pediatr Hematol Oncol. 2017 11; 39(8):e473-e475.
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LC3A Silencing Hinders Aggresome Vimentin Cage Clearance in Primary Choroid Plexus Carcinoma. Sci Rep. 2017 08 14; 7(1):8022.
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NHERF1/EBP50 and NF2 as diagnostic markers for choroid plexus tumors. Acta Neuropathol Commun. 2016 05 27; 4(1):55.
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Choroid plexus carcinoma in children: the Head Start experience. Pediatr Blood Cancer. 2015 May; 62(5):784-9.
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Choroid plexus tumors in children: a population-based study. Pediatr Neurosurg. 2013; 49(6):331-8.
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Molecular characterization of choroid plexus tumors reveals novel clinically relevant subgroups. Clin Cancer Res. 2015 Jan 01; 21(1):184-92.
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Alternative lengthening of telomeres is enriched in, and impacts survival of TP53 mutant pediatric malignant brain tumors. Acta Neuropathol. 2014 Dec; 128(6):853-62.
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Defining and ranking effects of individual agents based on survival times of cancer patients treated with combination chemotherapies. Stat Med. 2011 Jul 10; 30(15):1777-94.