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Leithner, A; Weinhaeusel, A; Zeitlhofer, P; Koch, H; Radl, R; Windhager, R; Beham, A; Haas, OA.
Evidence of a polyclonal nature of myositis ossificans.
Virchows Arch. 2005; 446(4):438-441
Doi: 10.1007/s00428-004-1169-z
Web of Science
PubMed
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- Führende Autor*innen der Med Uni Graz
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Leithner Andreas
- Co-Autor*innen der Med Uni Graz
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Beham Alfred
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Koch Horst
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Radl Roman
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Windhager Reinhard
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- Abstract:
- Myositis ossificans is a localized, self-limiting, reparative lesion that is composed of reactive hypercellular fibrous tissue and bone. Although it is clearly a benign lesion, its clinical, radiological, and histological appearance may sometimes mimic a malignant tumor. Whether myositis ossificans represents a monoclonal or polyclonal hyperplastic proliferation is not yet known. To address this question, we therefore extracted DNA from the respective paraffin-embedded tumor tissues of nine women with a median age of 50 years at diagnosis (range: 20-84 years) and studied the X inactivation pattern by means of methylation-sensitive polymerase chain reaction and primers that target the polymorphic CGG trinucleotide repeat of the FMR1 gene. The fact that we did not detect any skewing of the X inactivation pattern in the five successfully analyzed cases corroborates the notion that myositis ossificans results from a polyclonal proliferation and confirms that it is a reactive, reparative process. Analysis of the X inactivation pattern may, thus, supplement the differential diagnostic work-up of cases with an uncertain histology, at least in the informative proportion of female patients.
- Find related publications in this database (using NLM MeSH Indexing)
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Adult -
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Aged -
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Aged, 80 and over -
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Cell Proliferation -
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Clone Cells - pathology
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DNA Methylation - pathology
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Diagnosis, Differential - pathology
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Dosage Compensation, Genetic - pathology
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Female - pathology
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Humans - pathology
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Middle Aged - pathology
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Myositis Ossificans - genetics
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Sarcoma - diagnosis
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Soft Tissue Neoplasms - diagnosis
- Find related publications in this database (Keywords)
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myositis ossificans
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DNA methylation
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X inactivation
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polymerase chain reaction
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FMR1