SIMULTANEOUS INTERPHASE CYTOGENETIC ANALYSIS AND FLUORESCENCE IMMUNOPHENOTYPING OF DEDIFFERENTIATED CHONDROSARCOMA - IMPLICATIONS FOR HISTOPATHOGENESIS
Ja. Bridge et al., SIMULTANEOUS INTERPHASE CYTOGENETIC ANALYSIS AND FLUORESCENCE IMMUNOPHENOTYPING OF DEDIFFERENTIATED CHONDROSARCOMA - IMPLICATIONS FOR HISTOPATHOGENESIS, The American journal of pathology, 144(2), 1994, pp. 215-220
Cytogenetic analysis of four specimens (biopsy, definitive surgical, a
nd two separately occurring lung metastases) of a dedifferentiated cho
ndrosarcoma with a rhabdomyosarcomatous component revealed clonal kary
otypic abnormalities in each. Anomalies seen ill all specimens include
d a structurally aberrant chromosome 17 and extra copies of chromosome
s 5, 7, 12, and 20. The derivation of the chromosomally abnormal cells
was determined by a combined immunocytochemical/cytogenetic approach
that allowed simultaneous assessment of cytogenetic aberrations and im
munophenotypic features of individual cells. S-100 protein and desmin
antibodies were used to evaluate the chondrosarcomatous and rhabdomyos
arcomatous components, respectively. A chromosome 7-specific centromer
ic probe was used for determination of aneuploidy. In both specimens o
btained from the primary lesion, S-100 protein and desmin-positive and
-negative aneuploid cells were observed. These findings: 1) suggest th
at both the chondrocytic and rhabdomyoblastic cells arose from the sam
e abnormal clone, 2) support the theory of a common primitive mesenchy
mal cell progenitor with the ability to differentiate or express featu
res of more than one line of mesenchymal differentiation, and 3) indic
ate that the term dedifferentiated may be an inaccurate designation fo
r this neoplasm.