Retroperitoneal Fibrosis
"Retroperitoneal Fibrosis" 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 slowly progressive condition of unknown etiology, characterized by deposition of fibrous tissue in the retroperitoneal space compressing the ureters, great vessels, bile duct, and other structures. When associated with abdominal aortic aneurysm, it may be called chronic periaortitis or inflammatory perianeurysmal fibrosis.
Descriptor ID |
D012185
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MeSH Number(s) |
C23.550.355.700
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Concept/Terms |
Retroperitoneal Fibrosis- Retroperitoneal Fibrosis
- Fibroses, Retroperitoneal
- Fibrosis, Retroperitoneal
- Retroperitoneal Fibroses
- Ormond's Disease
- Disease, Ormond's
- Idiopathic Retroperitoneal Fibrosis
- Ormond Disease
- Disease, Ormond
Periaortitis, Chronic- Periaortitis, Chronic
- Chronic Periaortitides
- Chronic Periaortitis
- Periaortitides, Chronic
- Fibrosis, Perianeurysmal Inflammatory
- Perianeurysmal Inflammatory Fibrosis
- Inflammatory Perianeurysmal Fibrosis
- Perianeurysmal Fibrosis, Inflammatory
- Fibrosis, Inflammatory Perianeurysmal
- Inflammatory Fibrosis, Perianeurysmal
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Below are MeSH descriptors whose meaning is more general than "Retroperitoneal Fibrosis".
Below are MeSH descriptors whose meaning is more specific than "Retroperitoneal Fibrosis".
This graph shows the total number of publications written about "Retroperitoneal Fibrosis" by people in UAMS Profiles by year, and whether "Retroperitoneal Fibrosis" 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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2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Retroperitoneal Fibrosis" by people in Profiles over the past ten years.
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Akhtar I, Shenoy V, Khan M, Saad AG. Large Tumefactive IgG4-related Disease: Histologic, Cytologic, and Immunohistochemical Features of a Very Unusual Case. Appl Immunohistochem Mol Morphol. 2020 03; 28(3):e21-e25.
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