Histiocytoma, Malignant Fibrous
"Histiocytoma, Malignant Fibrous" 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 most commonly diagnosed soft tissue sarcoma. It is a neoplasm with a fibrohistiocytic appearance found chiefly in later adult life, with peak incidence in the 7th decade.
MeSH Number(s)
C04.557.450.565.590.425.360
C04.557.450.795.400
Concept/Terms
Histiocytoma, Malignant Fibrous- Histiocytoma, Malignant Fibrous
- Fibrous Histiocytoma, Malignant
- Fibrous Histiocytomas, Malignant
- Histiocytomas, Malignant Fibrous
- Malignant Fibrous Histiocytomas
- Malignant Fibrohistiocytic Tumors
- Fibrohistiocytic Tumor, Malignant
- Fibrohistiocytic Tumors, Malignant
- Malignant Fibrohistiocytic Tumor
- Tumor, Malignant Fibrohistiocytic
- Tumors, Malignant Fibrohistiocytic
- Malignant Fibrous Histiocytoma
Below are MeSH descriptors whose meaning is more general than "Histiocytoma, Malignant Fibrous".
Below are MeSH descriptors whose meaning is more specific than "Histiocytoma, Malignant Fibrous".
This graph shows the total number of publications written about "Histiocytoma, Malignant Fibrous" by people in Harvard Catalyst Profiles by year, and whether "Histiocytoma, Malignant Fibrous" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2005 | 1 | 0 | 1 |
| 2006 | 1 | 0 | 1 |
| 2007 | 2 | 0 | 2 |
| 2008 | 3 | 2 | 5 |
| 2009 | 2 | 0 | 2 |
| 2010 | 2 | 2 | 4 |
| 2011 | 2 | 1 | 3 |
| 2012 | 1 | 1 | 2 |
| 2013 | 1 | 0 | 1 |
| 2014 | 2 | 1 | 3 |
| 2017 | 0 | 1 | 1 |
| 2019 | 1 | 1 | 2 |
Below are the most recent publications written about "Histiocytoma, Malignant Fibrous" by people in Profiles.
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Intracranial Myxoid Mesenchymal Tumor with Rare EWSR1-CREM Translocation. Pediatr Neurosurg. 2019; 54(5):347-353.
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Atypical central neurocytoma with novel EWSR1-ATF1 fusion and MUTYH mutation detected by next-generation sequencing. BMJ Case Rep. 2019 Jan 14; 12(1).
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ALK Expression in Angiomatoid Fibrous Histiocytoma: A Potential Diagnostic Pitfall. Am J Surg Pathol. 2019 01; 43(1):93-101.
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Intracranial myxoid mesenchymal tumors with EWSR1-CREB family gene fusions: myxoid variant of angiomatoid fibrous histiocytoma or novel entity? Brain Pathol. 2018 03; 28(2):183-191.
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Characterization of metastatic angiomatoid fibrous histiocytoma. J Pediatr Hematol Oncol. 2015 May; 37(4):e268-71.
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Surgery for Li Fraumeni syndrome: pushing the limits of surgical oncology. Am J Clin Oncol. 2015 Feb; 38(1):98-102.
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Prognostic significance of treatment-induced pathologic necrosis in extremity and truncal soft tissue sarcoma after neoadjuvant chemoradiotherapy. Cancer. 2014 Dec 01; 120(23):3676-82.
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Myxoid variant of so-called angiomatoid "malignant fibrous histiocytoma": clinicopathologic characterization in a series of 21 cases. Am J Surg Pathol. 2014 Jun; 38(6):816-23.
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DNA copy number changes in tumors within the spectrum of cellular, atypical, and metastasizing fibrous histiocytoma. J Am Acad Dermatol. 2014 Aug; 71(2):256-63.
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The extended fleur-de-lis latissimus dorsi flap: a novel flap and approach for coverage of lower back defects. J Plast Reconstr Aesthet Surg. 2013 Dec; 66(12):1811-3.