"Lynch Syndrome II" 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.
Hereditary nonpolyposis colorectal neoplasms associated with other malignancies, more commonly of ovarian or uterine origin. When also associated with SEBACEOUS GLAND NEOPLASMS, it is called MUIR-TORRE SYNDROME.
| Descriptor ID |
D055847
|
| MeSH Number(s) |
C04.700.250.500 C16.320.700.250.500
|
| Concept/Terms |
Lynch Syndrome II- Lynch Syndrome II
- Lynch cancer family syndrome 2
- Lynch Cancer Family Syndrome II
- Colon Cancer, Familial Nonpolyposis, Type 2
- Colorectal Cancer, Hereditary Nonpolyposis, Type 2
|
Below are MeSH descriptors whose meaning is more general than "Lynch Syndrome II".
Below are MeSH descriptors whose meaning is more specific than "Lynch Syndrome II".
This graph shows the total number of publications written about "Lynch Syndrome II" by people in this website by year, and whether "Lynch Syndrome II" was a major or minor topic of these publications.
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Below are the most recent publications written about "Lynch Syndrome II" by people in Profiles.
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Neuroendocrine-type prostatic adenocarcinoma with microsatellite instability in a patient with lynch syndrome. Int J Surg Pathol. 2010 Dec; 18(6):550-3.