Chondroblastoma of bone
- 1 July 1992
- journal article
- Published by Springer Nature in Virchows Archiv
- Vol. 421 (4) , 355-366
- https://doi.org/10.1007/bf01660984
Abstract
The clinical and morphological findings of 53 chondroblastomas in the files of the Bone Tumour Registry of Westphalia are presented. The mean age of all patients was 19.2 years. The male-to-female ratio was 1.5∶1. Forty-two of the tumours (79.8%) were located in the long tubular bones and short tubular bones of the hands and were closely related to the growth plate. Six cases (11.3%) were found in the flat bones, 4 cases (7.5%) in the tarsal bones and 1 case (1.9%) in the craniofacial bones. The characteristic radiological feature of 44 investigated lesions was a mostly eccentric radiolucency with a geographic pattern of bone destruction and matrix calcifications. Periosteal reaction was evident in 9% of the cases. Most tumours demonstrate the typical morphological features of chondroblastoma, but 3 cases resembled a giant cell tumour. In 2 cases a haemangio-pericytomalike growth pattern was observed. Nine of the tumours had an aneurysmal bone cyst-like component. Vascular invasion was seen in 1 case. Immunohistochemically most cells in 30 of the cases and fetal chondroblasts in 3 cases were strongly positive with vimentin and S-100 protein. Collagen type II was positive in the chondroid matrix of the tumours and in fetal cartilage tissue; collagen type VI was present focally around individual tumour cells and was always seen in the chondroid matrix of the lesions and in fetal cartilage. These findings support the cartilaginous nature of these tumours. In paraffin sections, 46.6% of the cases revealed a distinct positive reaction of some tumour cells with the monoclonal cytokeratin antibody KL1 (molecular weight 55–57 kDa). Only 4 of them demonstrated a coexpression with the other monoclonal cytokeratin anti-body CK (clone MNF 116, molecular weight 45–56.5 kDa). In paraffin sections all fetal chondroblasts were negative with both cytokeratin antibodies. Frozen sections of 3 tumours showed a strong positive reaction with both cytokeratin antibodies in many chondroblasts, indicating an “aberrant” cytokeratin expression. Osteoclast-like giant cells stained positive with leucocyte-common antigen (LCA) and with the macrophage-associated antibody KP1, but were negative with the other macrophage-associated antibody MAC 387. Recurrence rate was 10.7%. The clinical course of all tumours was benign.Keywords
This publication has 61 references indexed in Scilit:
- THE CLASSIC: Epiphyseal Chondromatous Giant Cell Tumors of the Upper End of the HumerusClinical Orthopaedics and Related Research, 2006
- Cellular variant of extraskeletal myxoid chondrosarcoma of abdominal wall ? a case report with comparative immunohistochemical study on cartilaginous collagenous proteins in various myxoid mesenchymal tumorsZeitschrift für Krebsforschung und Klinische Onkologie, 1992
- Establishment from a human chondrosarcoma of a new immortal cell line with high tumorigenicity in vivo, which is able to form proteoglycan‐rich cartilage‐like nodules and to respond to insulin in vitroInternational Journal of Cancer, 1991
- Chondroblastoma of the RibPublished by Wolters Kluwer Health ,1990
- Immunohistochemistry of solid tumors Brief review of selected problemsAPMIS, 1990
- Late pulmonary metastases from chondroblastoma of the distal femur: A case reportActa Orthopaedica, 1990
- Immunohistochemical studies on the tissue localization of collagen types I, III, IV, V and VI in schwannomasVirchows Archiv B Cell Pathology Including Molecular Pathology, 1988
- Induction of cytokeratin expression in human mesenchymal cellsJournal of Cellular Physiology, 1987
- Type VI Collagen but not Type V Collagen is Present in CartilageCollagen and Related Research, 1984
- Immunoenzymatic labeling of monoclonal antibodies using immune complexes of alkaline phosphatase and monoclonal anti-alkaline phosphatase (APAAP complexes).Journal of Histochemistry & Cytochemistry, 1984