 Pinealoma
"Pinealoma" 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.
Neoplasms which originate from pineal parenchymal cells that tend to enlarge the gland and be locally invasive. The two major forms are pineocytoma and the more malignant pineoblastoma. Pineocytomas have moderate cellularity and tend to form rosette patterns. Pineoblastomas are highly cellular tumors containing small, poorly differentiated cells. These tumors occasionally seed the neuroaxis or cause obstructive HYDROCEPHALUS or Parinaud's syndrome. GERMINOMA; CARCINOMA, EMBRYONAL; GLIOMA; and other neoplasms may arise in the pineal region with germinoma being the most common pineal region tumor. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2064; Adams et al., Principles of Neurology, 6th ed, p670)
| Descriptor ID |
D010871
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| MeSH Number(s) |
C04.557.465.625.600.657 C04.557.470.670.657 C04.557.580.625.600.657 C04.588.614.250.195.766 C10.228.140.211.788 C10.551.240.250.625
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| Concept/Terms |
Pinealoma- Pinealoma
- Pinealomas
- Pineal Tumors
- Pineal Tumor
- Tumor, Pineal
- Tumors, Pineal
- Pineal Neoplasms
- Pineal Parenchymal Tumors
- Pineal Parenchymal Tumor
- Tumor, Pineal Parenchymal
- Tumors, Pineal Parenchymal
- Neoplasms, Pineal
- Neoplasm, Pineal
- Pineal Neoplasm
- Pineal Gland Tumor
- Pineal Gland Tumors
- Tumor, Pineal Gland
- Tumors, Pineal Gland
Mixed Pineocytoma-Pineoblastoma- Mixed Pineocytoma-Pineoblastoma
- Mixed Pineocytoma Pineoblastoma
- Mixed Pineocytoma-Pineoblastomas
- Pineocytoma-Pineoblastoma, Mixed
- Pineocytoma-Pineoblastomas, Mixed
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Below are MeSH descriptors whose meaning is more general than "Pinealoma".
Below are MeSH descriptors whose meaning is more specific than "Pinealoma".
This graph shows the total number of publications written about "Pinealoma" by people in this website by year, and whether "Pinealoma" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2010 | 1 | 0 | 1 | | 2017 | 1 | 0 | 1 | | 2021 | 1 | 0 | 1 | | 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Pinealoma" by people in Profiles.
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Malik N, Samples DC, Finneran MM, Graber S, Dorris K, Norris G, Foreman NK, Hankinson TC, Handler MH. Pediatric pineal region masses: a single-center experience over 25?years. Childs Nerv Syst. 2023 09; 39(9):2307-2316.
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Kunigelis KE, Kleinschmidt-DeMasters BK, Youssef AS, Lillehei KO, Ormond DR. Clinical Features of Pineal Parenchymal Tumors of Intermediate Differentiation (PPTID): A Single-Institution Series. World Neurosurg. 2021 11; 155:e229-e235.
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Kamihara J, Bourdeaut F, Foulkes WD, Molenaar JJ, Moss? YP, Nakagawara A, Parareda A, Scollon SR, Schneider KW, Skalet AH, States LJ, Walsh MF, Diller LR, Brodeur GM. Retinoblastoma and Neuroblastoma Predisposition and Surveillance. Clin Cancer Res. 2017 07 01; 23(13):e98-e106.
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Mittal VA, Karlsgodt K, Zinberg J, Cannon TD, Bearden CE. Identification and treatment of a pineal region tumor in an adolescent with prodromal psychotic symptoms. Am J Psychiatry. 2010 Sep; 167(9):1033-7.
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Li G, Mitra S, Karamchandani J, Edwards MS, Wong AJ. Pineal parenchymal tumor of intermediate differentiation: clinicopathological report and analysis of epidermal growth factor receptor variant III expression. Neurosurgery. 2010 May; 66(5):963-8; discussion 968.
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Apuzzo ML, Petrovich Z, Luxton G, Jepson JH, Cohen D, Breeze RE. Interstitial radiobrachytherapy of malignant cerebral neoplasms: rationale, methodology, prospects. Neurol Res. 1987 Jun; 9(2):91-100.
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