Chondroma of soft parts

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Abstract

The clinical and pathological features of 104 cases of chondroma of soft parts are presented. The tumor occurred predominately in the third and fourth decades, was slightly more common in male (61%) than in female patients, and affected chiefly the soft tissues of the hand (64%) and feet (20%). The presenting symptom was usually a slowly and insidiously growing mass, occasionally causing tenderness or pain. Nearly always the tumor was well demarcated and lobulated and measured between 1 and 2 cm in greatest diameter. Microscopically, most of the tumors were composed of adult‐type hyaline cartilage, undergoing calcification in a large percentage of cases. In addition, histologic variants with giant cell proliferation and chondroblastic activity could be distinguished. Despite the slight cellular pleomorphism and the plump appearance of many cartilage cells in the chondroblastic variants, there was no evidence that these tumors behaved differently from the tumors composed predominately of adult‐type hyaline cartilage. Of the 56 patients with follow‐up information (median follow‐up period, 5.7 years) 44 were alive and well with no evidence of recurrence in the follow‐up period. In 10 patients the tumor had recurred once. Multiple recurrences or metastatic lesions were not observed. Two patients died of unrelated cause. Complete local excision appears to be the treatment of choice. Copyright © 1978 American Cancer Society

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APA

Chung, E. B., & Enzinger, F. M. (1978). Chondroma of soft parts. Cancer, 41(4), 1414–1424. https://doi.org/10.1002/1097-0142(197804)41:4<1414::AID-CNCR2820410429>3.0.CO;2-O

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