ArticleDiagnostic pathology2014
Solitary fibrous tumor - clinicopathologic, immunohistochemical and molecular analysis of 28 cases.
Article in Diagnostic pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.
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Who cites it
39 citing papers in PubMed, 116 citations in OpenAlex.
- Article
- Molecular genetic analysis of pulmonary benign metastasizing leiomyoma and intravenous leiomyomatosis: a comparative study using whole exome sequencing.Discover oncology · 2025Article
- Malignant Extrapleural Solitary Fibrous Tumor.Cureus · 2023Article
- An update on selected cutaneous (myo) fibroblastic mesenchymal tumors.Seminars in diagnostic pathology · 2023Review
- A giant breast malignant solitary fibrous tumor: A rare case report and brief review.Oncology letters · 2023Article
- Solitary fibrous tumor of the central nervous system invading and penetrating the skull: A case report.Oncology letters · 2023Article
- The Unique Spectrum ofThe application of clinical genetics · 2023Article
- Correction to: A case of a large solitary fibrous tumor in the thigh, displaying NAB2ex4-STAT6ex2 gene fusion.Skeletal radiology · 2022Article
- A case of a large solitary fibrous tumor in the thigh, displaying NAB2ex4-STAT6ex2 gene fusion.Skeletal radiology · 2021Article
- Solitary Fibrous Tumor of Internal Jugular Vein: An Extremely Rare Entity with Review of Literature.The Indian journal of radiology & imaging · 2021Article
- Aggressive Intraosseous Myofibroma of the Maxilla: Report of a Rare Case and Literature Review.Head and neck pathology · 2021Review
- Observational
- Atypical/malignant solitary fibrous tumor of the pancreas with spleen vein invasion: Case report and literature review.Medicine · 2020Review
- Recurrent Sinonasal CD34-Negative Malignant Solitary Fibrous Tumor Diagnosed on STAT6 Immunohistochemistry and NAB2-STAT6 Fusion.Head and neck pathology · 2020Article
- Liver metastasis and local recurrence of meningeal hemangiopericytoma: a case report.Translational cancer research · 2020Article
- Molecular changes in solitary fibrous tumor progression.Journal of molecular medicine (Berlin, Germany) · 2019Article
- Extremely rare case of intravascular solitary fibrous tumour in the inferior vena cava with review of the literature.Diagnostic pathology · 2019Review
- High p16 Expression Is Associated with Malignancy and Shorter Disease-Free Survival Time in Solitary Fibrous Tumor/Hemangiopericytoma.Journal of neurological surgery. Part B, Skull base · 2019Article
- Solitary fibrous tumour of the sigmoid colon mesentery.BMJ case reports · 2019Article
- Benign schwannoma of posterior mediastinum accompanied by bloody pleural effusion misdiagnosed as solitary fibrous tumor: A case report.Caspian journal of internal medicine · 2019Article
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Authors and funding
13 authors at 4 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundSolitary fibrous tumor is a mesenchymal tumor of fibroblastic type, which can affect any region of the body. Recently, a recurrent gene fusion NAB2-STAT6 has been identified as molecular hallmark. The NAB2-STAT6 fusion leads to EGR1 activation and transcriptional deregulation of EGR1-dependent target genes and is a driving event in initiation of SFT. In this study, we report the clinicopathologic and RT-PCR findings and evaluated expression of STAT6 and EGR1 protein in a cohort of 28 SFTs.
methods28 patients with a median age of 54 years were included with SFTs originating at different sites, most occurring in the lung and pleura (9, 32%), 5 in soft tissues of the lower extremities (18%) and 5 in the head and neck (18%). For detection of the NAB2-STAT6 fusion gene, RT-PCR was performed using RNA extracted from formalin-fixed and paraffin-embedded tissues. Immunohistochemistry was performed on all cases with antibodies against STAT6 and EGR1.
resultsAll patients were treated by surgery, 3 with adjuvant chemo- or radiotherapy. Follow-up data of 18 patients could be obtained of which 2 patients died of metastatic disease 13 months and 52 years after first diagnosis. Sixteen patients have no evidence of disease with a median follow up of 29.5 months (range 7 - 120 months). NAB2-STAT6 fusion transcripts were found in 19/28 cases (68%). The most common fusion was between NAB2 exon 4 and STAT6 exon 3 (11/19, 58%), mainly occurring in pleuropulmonary lesions. All cases showed strong nuclear expression of STAT6 (28/28, 100%) while EGR1 showed low-level variable nuclear expression in all samples, comparable with the EGR1 expression results of the control group.
conclusionsThe identification of the NAB2-STAT6 fusion in SFTs can provide important diagnostic information, especially in cases with aberrant morphology or when biopsy material is limited. STAT6 immunohistochemistry is another useful tool in diagnosing SFT. EGR1 immunohistochemistry indicates low-level protein expression in accordance with EGR1 activation due to distorted NAB2 activity. VIRTUAL SLIDES: The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/13000_2014_224.
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