• Medientyp: E-Artikel
  • Titel: Chondrosarcoma with Target-Like Chondrocytes: Update on Molecular Profiling and Specific Morphological Features
  • Beteiligte: Povýšil, Ctibor; Hojný, J.; Kaňa, M.
  • Erschienen: Charles University in Prague, Karolinum Press, 2022
  • Erschienen in: Folia Biologica, 68 (2022) 3, Seite 112-124
  • Sprache: Englisch
  • DOI: 10.14712/fb2022068030112
  • ISSN: 0015-5500; 2533-7602
  • Schlagwörter: Cell Biology ; Developmental Biology ; Genetics ; Molecular Biology ; General Medicine ; Immunology ; Biochemistry
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  • Beschreibung: <jats:p>This is the first histological and molecular analysis of two chondrosarcomas with target-like chondrocytes that were compared with a group of conventional chondrosarcomas and enchondromas. The unique histological feature of target-like chondrocytes is the presence of unusual hypertrophic eosinophilic APAS-positive perichondrocytic rings (baskets). In the sections stained with Safranin O/Fast green, the outer part of the ring was blue and the material in the lacunar space stained orange, similarly to intercellular regions. Immunohistoche­mical examination showed strong positivity for vimentin, factor XIIIa, cyclin D1, osteonectin, B-cell lymphoma 2 apoptosis regulator (Bcl-2), p53 and p16. The S-100 protein was positive in 25 % of neoplastic cells. Antibodies against GFAP, D2-40 (podoplanin), CD99, CKAE1.3 and CD10 exhibited weak focal positivity. Pericellular rings/baskets contained type VI collagen in their peripheral part, in contrast to the type II collagen in intercellular interterritorial spaces. Ultra­structural examination revealed that pericellular rings contained an intralacunar component composed of microfibrils with abundant admixture of aggregates of dense amorphous non-fibrillar material. The outer extralacunar zone was made up of a layer of condensed thin collagen fibrils with admixture of non-fibrillar dense material. NGS sequencing identified a fusion transcript involving fibronectin 1 (FN1) and fibroblast growth factor receptor 2 (FGFR2) at the RNA level. At the DNA level, no significant va­riant was revealed except for the presumably germ­line variant in the <jats:italic>SPTA1</jats:italic> gene. </jats:p><jats:p> Erratum to this article was published in: Folia Biologica, 2022, 68, (5-6): 211–211. <jats:ext-link xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="uri" xlink:href="https://doi.org/10.14712/fb2022068050211">https://doi.org/10.14712/fb2022068050211</jats:ext-link></jats:p>
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