Neoplastic Syndromes, Hereditary
"Neoplastic Syndromes, Hereditary" 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.
The condition of a pattern of malignancies within a family, but not every individual's necessarily having the same neoplasm. Characteristically the tumor tends to occur at an earlier than average age, individuals may have more than one primary tumor, the tumors may be multicentric, usually more than 25 percent of the individuals in direct lineal descent from the proband are affected, and the cancer predisposition in these families behaves as an autosomal dominant trait with about 60 percent penetrance.
| Descriptor ID |
D009386
|
| MeSH Number(s) |
C04.700 C16.320.700
|
| Concept/Terms |
Neoplastic Syndromes, Hereditary- Neoplastic Syndromes, Hereditary
- Hereditary Neoplastic Syndromes
- Hereditary Neoplastic Syndrome
- Neoplastic Syndrome, Hereditary
- Syndrome, Hereditary Neoplastic
- Syndromes, Hereditary Neoplastic
- Hereditary Cancer Syndromes
- Cancer Syndrome, Hereditary
- Hereditary Cancer Syndrome
- Syndrome, Hereditary Cancer
- Syndromes, Hereditary Cancer
- Cancer Syndromes, Hereditary
|
Below are MeSH descriptors whose meaning is more general than "Neoplastic Syndromes, Hereditary".
Below are MeSH descriptors whose meaning is more specific than "Neoplastic Syndromes, Hereditary".
This graph shows the total number of publications written about "Neoplastic Syndromes, Hereditary" by people in this website by year, and whether "Neoplastic Syndromes, Hereditary" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2005 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2017 | 3 | 0 | 3 |
| 2018 | 2 | 2 | 4 |
| 2019 | 2 | 1 | 3 |
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Below are the most recent publications written about "Neoplastic Syndromes, Hereditary" by people in Profiles.
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BAP1 Tumour Predisposition Syndrome: A New Mutation in One Family. Acta Derm Venereol. 2019 10 01; 99(11):1045-1046.
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Radiologist's Primer on Imaging of Common Hereditary Cancer Syndromes. Radiographics. 2019 May-Jun; 39(3):759-778.
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Modeling malignancies using induced pluripotent stem cells: from chronic myeloid leukemia to hereditary cancers. Exp Hematol. 2019 03; 71:61-67.
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Dermatoscopy of Vascular Lesions. Dermatol Clin. 2018 Oct; 36(4):389-395.
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Cancer prevention by aspirin in children with Constitutional Mismatch Repair Deficiency (CMMRD). Eur J Hum Genet. 2018 10; 26(10):1417-1423.
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[Updates and interpretation on NCCN clinical practice guidelines for gastric cancer 2017 version 5]. Zhonghua Wei Chang Wai Ke Za Zhi. 2018 Feb 25; 21(2):160-164.
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Imaging findings of hereditary renal tumors, a review of what the radiologist should know. Eur J Radiol. 2018 Apr; 101:8-16.
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Hereditary leiomyomatosis and renal cell cancer syndrome: An update and review. J Am Acad Dermatol. 2017 Jul; 77(1):149-158.
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Consensus statement for the treatment of infantile haemangiomas with propranolol. Australas J Dermatol. 2017 May; 58(2):155-159.
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Review of hereditary leiomyomatosis renal cell carcinoma with focus on clinical and pathobiological aspects of renal tumors. Pol J Pathol. 2017; 68(4):284-290.