Neoplasms, Connective and Soft Tissue
"Neoplasms, Connective and Soft Tissue" 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.
Neoplasms developing from some structure of the connective and subcutaneous tissue. The concept does not refer to neoplasms located in connective or soft tissue.
Below are MeSH descriptors whose meaning is more general than "Neoplasms, Connective and Soft Tissue".
Below are MeSH descriptors whose meaning is more specific than "Neoplasms, Connective and Soft Tissue".
This graph shows the total number of publications written about "Neoplasms, Connective and Soft Tissue" by people in Harvard Catalyst Profiles by year, and whether "Neoplasms, Connective and Soft Tissue" 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 |
|---|
| 2008 | 1 | 0 | 1 |
| 2012 | 2 | 0 | 2 |
| 2015 | 1 | 0 | 1 |
| 2016 | 0 | 2 | 2 |
| 2017 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2019 | 1 | 0 | 1 |
| 2020 | 2 | 1 | 3 |
| 2022 | 3 | 0 | 3 |
| 2023 | 2 | 0 | 2 |
Below are the most recent publications written about "Neoplasms, Connective and Soft Tissue" by people in Profiles.
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FGFR1 gene fusions in a subset of pediatric mesenchymal tumors: Expanding the genetic spectrum of tumors sharing histologic overlap with infantile fibrosarcoma and "NTRK-rearranged" spindle cell neoplasms. Genes Chromosomes Cancer. 2023 11; 62(11):641-647.
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A Clinicopathologic and Molecular Characterization of Uterine Sarcomas Classified as Malignant PEComa. Am J Surg Pathol. 2023 05 01; 47(5):535-546.
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A case of FN1-fused calcified chondroid mesenchymal neoplasm of the hand with novel FGFR3 partner gene. Genes Chromosomes Cancer. 2023 04; 62(4):237-241.
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Distinctive Nested Glomoid Neoplasm: Clinicopathologic Analysis of 20 Cases of a Mesenchymal Neoplasm With Frequent GLI1 Alterations and Indolent Behavior. Am J Surg Pathol. 2023 01 01; 47(1):12-24.
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Mesenchymal neoplasms with NTRK and other kinase gene alterations. Histopathology. 2022 Jan; 80(1):4-18.
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Perivascular epithelioid cell tumors (PEComa) of the gynecologic tract. Genes Chromosomes Cancer. 2021 03; 60(3):168-179.
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Long-term Outcomes for Extraskeletal Myxoid Chondrosarcoma: A SEER Database Analysis. Cancer Epidemiol Biomarkers Prev. 2020 11; 29(11):2351-2357.
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Mesenchymal tumors of the gastrointestinal tract with NTRK rearrangements: a clinicopathological, immunophenotypic, and molecular study of eight cases, emphasizing their distinction from gastrointestinal stromal tumor (GIST). Mod Pathol. 2021 01; 34(1):95-103.
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Expanding the Spectrum of Pediatric NTRK-rearranged Mesenchymal Tumors. Am J Surg Pathol. 2019 04; 43(4):435-445.
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Molecular and Clinicopathologic Heterogeneity of Intracranial Tumors Mimicking Extraskeletal Myxoid Chondrosarcoma. J Neuropathol Exp Neurol. 2018 08 01; 77(8):727-735.