 Hamartoma Syndrome, Multiple
"Hamartoma Syndrome, Multiple" 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.
A hereditary disease characterized by multiple ectodermal, mesodermal, and endodermal nevoid and neoplastic anomalies. Facial trichilemmomas and papillomatous papules of the oral mucosa are the most characteristic lesions. Individuals with this syndrome have a high risk of BREAST CANCER; THYROID CANCER; and ENDOMETRIAL CANCER. This syndrome is associated with mutations in the gene for PTEN PHOSPHATASE.
| Descriptor ID |
D006223
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| MeSH Number(s) |
C04.445.435 C04.651.435 C04.700.435 C16.320.700.435
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| Concept/Terms |
Hamartoma Syndrome, Multiple- Hamartoma Syndrome, Multiple
- Hamartoma Syndromes, Multiple
- Multiple Hamartoma Syndromes
- Syndrome, Multiple Hamartoma
- Syndromes, Multiple Hamartoma
- Multiple Hamartoma Syndrome
- Cowden's Disease
- Cowdens Disease
- Disease, Cowden's
- Cowden's Syndrome
- Cowdens Syndrome
- Syndrome, Cowden's
- Cowden Disease
- Disease, Cowden
- Cowden Syndrome
- Syndrome, Cowden
Bannayan-Riley-Ruvalcaba Syndrome- Bannayan-Riley-Ruvalcaba Syndrome
- Bannayan Riley Ruvalcaba Syndrome
- Syndrome, Bannayan-Riley-Ruvalcaba
- Bannayan-Zonana Syndrome
- Bannayan Zonana Syndrome
- Syndrome, Bannayan-Zonana
- Macrocephaly, Multiple Lipomas, and Hemangiomata
- Ruvalcaba-Myhre-Smith Syndrome
- Ruvalcaba Myhre Smith Syndrome
- Syndrome, Ruvalcaba-Myhre-Smith
- Myhre-Riley-Smith Syndrome
- Myhre Riley Smith Syndrome
- Syndrome, Myhre-Riley-Smith
- Riley-Smith Syndrome
- Riley Smith Syndrome
- Syndrome, Riley-Smith
- Ruvalcaba Syndrome
- Syndrome, Ruvalcaba
- Macrocephaly, Pseudopapilledema, And Multiple Hemangiomata
- Macrocephaly, Pseudopapilledema, and Multiple Hemangiomas
Lhermitte-Duclos Disease- Lhermitte-Duclos Disease
- Disease, Lhermitte-Duclos
- Lhermitte Duclos Disease
- Dysplastic Gangliocytoma of Cerebellum
- Cerebellum Dysplastic Gangliocytoma
- Cerebellum Dysplastic Gangliocytomas
- Dysplastic Gangliocytoma of the Cerebellum
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Below are MeSH descriptors whose meaning is more general than "Hamartoma Syndrome, Multiple".
- Diseases [C]
- Neoplasms [C04]
- Hamartoma [C04.445]
- Hamartoma Syndrome, Multiple [C04.445.435]
- Neoplasms, Multiple Primary [C04.651]
- Hamartoma Syndrome, Multiple [C04.651.435]
- Neoplastic Syndromes, Hereditary [C04.700]
- Hamartoma Syndrome, Multiple [C04.700.435]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Neoplastic Syndromes, Hereditary [C16.320.700]
- Hamartoma Syndrome, Multiple [C16.320.700.435]
Below are MeSH descriptors whose meaning is more specific than "Hamartoma Syndrome, Multiple".
This graph shows the total number of publications written about "Hamartoma Syndrome, Multiple" by people in UAMS Profiles by year, and whether "Hamartoma Syndrome, Multiple" 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 |
|---|
| 2021 | 1 | 0 | 1 | | 2015 | 2 | 0 | 2 | | 2012 | 3 | 0 | 3 | | 2011 | 1 | 0 | 1 | | 2010 | 3 | 0 | 3 | | 2008 | 2 | 0 | 2 |
To return to the timeline, click here.
Below are the most recent publications written about "Hamartoma Syndrome, Multiple" by people in Profiles over the past ten years.
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Baran JA, Tsai SD, Isaza A, Brodeur GM, MacFarland SP, Zelley K, Adams DM, Franco AT, Bauer AJ. The Clinical Spectrum of PTEN Hamartoma Tumor Syndrome: Exploring the Value of Thyroid Surveillance. Horm Res Paediatr. 2020; 93(11-12):634-642.
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Modi RM, Arnold CA, Stanich PP. Diffuse Esophageal Glycogenic Acanthosis and Colon Polyposis in a Patient With Cowden Syndrome. Clin Gastroenterol Hepatol. 2017 08; 15(8):e131-e132.
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Hagelstrom RT, Ford J, Reiser GM, Nelson M, Pickering DL, Althof PA, Sanger WG, Coccia PF. Breast Cancer and Non-Hodgkin Lymphoma in a Young Male with Cowden Syndrome. Pediatr Blood Cancer. 2016 Mar; 63(3):544-6.
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Shiver M, Hughes M, Naylor M, McLarney B, Stolle C, Shalin S, Gao L. A novel CYLD gene mutation and multiple basal cell carcinomas in a patient with Brooke-Spiegler syndrome. Clin Exp Dermatol. 2016 Jan; 41(1):98-100.
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