Mesenchymal chondrosarcoma A cytogenetic, immunohistochemical and ultrastructural study

A case of mesenchymal chondrosarcoma was studied. The tumor was near-tetraploid and the clonal structural chromosomal abnormalities included add(7)(p13), add(22)(q13), markers, and double minutes. The ultrastructural and immunohistochemical findings were consistent with the diagnosis. Strong immunor...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Cancer genetics and cytogenetics 1995-08, Vol.83 (1), p.56-60
Hauptverfasser:	Dobin, Sheila M., Donner, Ludvik R., Speights, V.O.
Format:	Artikel
Sprache:	eng
Schlagworte:	Biological and medical sciences Bone Neoplasms - genetics Bone Neoplasms - pathology Bone Neoplasms - ultrastructure Chondrosarcoma, Mesenchymal - genetics Chondrosarcoma, Mesenchymal - pathology Chondrosarcoma, Mesenchymal - ultrastructure Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 7 Diseases of the osteoarticular system Humans Immunohistochemistry Infant Karyotyping Male Medical sciences Ploidies Tumors of striated muscle and skeleton
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Beschreibung
Zusammenfassung:	A case of mesenchymal chondrosarcoma was studied. The tumor was near-tetraploid and the clonal structural chromosomal abnormalities included add(7)(p13), add(22)(q13), markers, and double minutes. The ultrastructural and immunohistochemical findings were consistent with the diagnosis. Strong immunoreactivity for desmin was an unusual, not previously reported, feature of the neoplasm.
ISSN:	0165-4608 1873-4456
DOI:	10.1016/0165-4608(95)00031-3