"Leiomyomatosis" 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 state of having multiple leiomyomas throughout the body. (Stedman, 25th ed)
| Descriptor ID |
D018231
|
| MeSH Number(s) |
C04.557.450.590.450.465
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Leiomyomatosis".
Below are MeSH descriptors whose meaning is more specific than "Leiomyomatosis".
This graph shows the total number of publications written about "Leiomyomatosis" by people in this website by year, and whether "Leiomyomatosis" 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 |
|---|
| 2013 | 1 | 0 | 1 |
| 2017 | 2 | 0 | 2 |
| 2018 | 2 | 1 | 3 |
| 2019 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Leiomyomatosis" by people in Profiles.
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An unusual case of inferior vena cava thrombosis: widening the differential diagnosis. Intern Emerg Med. 2020 06; 15(4):673-678.
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Diffuse Esophageal Leiomyomatosis in Pediatric Patients: A Systematic Review and Quality of Evidence Assessment. Eur J Pediatr Surg. 2019 Dec; 29(6):487-494.
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One-stage surgery for removal of intravascular leiomyomatosis extending to right ventricle. Medicine (Baltimore). 2018 Mar; 97(11):e0051.
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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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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.
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Disseminated cutaneous leiomyomatosis treated with oral amlodipine. Indian J Dermatol Venereol Leprol. 2013 Jan-Feb; 79(1):136.