"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
|
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
|
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
|
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 |
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1995 | 1 | 0 | 1 |
1997 | 1 | 0 | 1 |
1999 | 0 | 1 | 1 |
2002 | 0 | 1 | 1 |
2004 | 1 | 0 | 1 |
2007 | 1 | 1 | 2 |
2008 | 1 | 0 | 1 |
2010 | 2 | 0 | 2 |
2011 | 2 | 1 | 3 |
2012 | 1 | 0 | 1 |
2014 | 2 | 0 | 2 |
2015 | 1 | 0 | 1 |
2017 | 1 | 0 | 1 |
2019 | 1 | 0 | 1 |
2020 | 1 | 0 | 1 |
2021 | 1 | 0 | 1 |
2022 | 2 | 0 | 2 |
2024 | 1 | 1 | 2 |
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click here.
Below are the most recent publications written about "Pinealoma" by people in Profiles.
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Papillary tumor of the pineal region: analysis of DNA methylation profiles and clinical outcomes in 76 cases. Acta Neuropathol Commun. 2024 Jul 16; 12(1):117.
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The occipital interhemispheric transtentorial approach in infants and toddlers: efficacy and complications. Childs Nerv Syst. 2024 Aug; 40(8):2367-2372.
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Long term outcomes following surgery for pineal region tumors. J Neurooncol. 2022 Feb; 156(3):491-498.
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Metastases in the Pineal Region: A Systematic Review of Clinical Features, Management Strategies, and Survival Outcomes. World Neurosurg. 2022 Mar; 159:156-167.e2.
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Pearls & Oy-sters: Primary Pineal Melanoma With Leptomeningeal Carcinomatosis. Neurology. 2021 08 03; 97(5):248-250.
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Case 3: Polyuria and Polydipsia in an 11-year-old Boy. Pediatr Rev. 2020 05; 41(5):252-255.
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Risk-adapted therapy and biological heterogeneity in pineoblastoma: integrated clinico-pathological analysis from the prospective, multi-center SJMB03 and SJYC07 trials. Acta Neuropathol. 2020 02; 139(2):259-271.
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Retinoblastoma and Neuroblastoma Predisposition and Surveillance. Clin Cancer Res. 2017 07 01; 23(13):e98-e106.
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Outcomes After Surgery and Radiotherapy for Papillary Tumor of the Pineal Region. World Neurosurg. 2015 Jul; 84(1):76-81.
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Clinical outcomes and patterns of failure in pineoblastoma: a 30-year, single-institution retrospective review. World Neurosurg. 2014 Dec; 82(6):1232-41.