"Fibroma" 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 benign tumor of fibrous or fully developed connective tissue.
| Descriptor ID |
D005350
|
| MeSH Number(s) |
C04.557.450.565.590.340
|
| Concept/Terms |
Myxofibroma- Myxofibroma
- Myxofibromas
- Fibromyxoma
- Fibromyxomas
|
Below are MeSH descriptors whose meaning is more general than "Fibroma".
Below are MeSH descriptors whose meaning is more specific than "Fibroma".
This graph shows the total number of publications written about "Fibroma" by people in this website by year, and whether "Fibroma" 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 |
|---|
| 1998 | 0 | 1 | 1 |
| 2000 | 0 | 1 | 1 |
| 2004 | 2 | 0 | 2 |
| 2005 | 1 | 0 | 1 |
| 2008 | 2 | 0 | 2 |
| 2009 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2011 | 1 | 1 | 2 |
| 2012 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2014 | 2 | 0 | 2 |
| 2015 | 2 | 0 | 2 |
| 2016 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Fibroma" by people in Profiles.
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A novel case of malignant ossifying fibromyxoid tumor with a BCOR internal tandem duplication in a child. Pediatr Blood Cancer. 2023 03; 70(3):e29972.
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Pleomorphic fibroma and dermal atypical lipomatous tumor: are they related? J Cutan Pathol. 2013 Apr; 40(4):379-84.
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Miscellaneous tumour-like lesions of the ovary: cross-sectional imaging review. Br J Radiol. 2012 May; 85(1013):477-86.
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Juvenile juxtacortical chondromyxoid fibroma of bone: a case report. Hum Pathol. 2008 Jun; 39(6):960-5.
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Beta-catenin mutations do not contribute to cardiac fibroma pathogenesis. Pediatr Dev Pathol. 2008 Jul-Aug; 11(4):291-4.
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Expression of Birt-Hogg-Dub? gene mRNA in normal and neoplastic human tissues. Mod Pathol. 2004 Aug; 17(8):998-1011.
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Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis. Am J Hum Genet. 2003 Oct; 73(4):791-800.
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The gene for juvenile hyaline fibromatosis maps to chromosome 4q21. Am J Hum Genet. 2002 Oct; 71(4):975-80.
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Solitary fibrous tumors of soft tissue. A clinicopathologic and immunohistochemical study of 12 cases. Am J Surg Pathol. 1995 Nov; 19(11):1257-66.
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Pseudosarcomatous fibromyxoid tumor of the urinary bladder and prostate: immunohistochemical, ultrastructural, and DNA flow cytometric analyses of nine cases. Hum Pathol. 1993 Nov; 24(11):1203-10.