A CLINICO-PATHOLOGICAL ANALYSIS OF CHONDROBLASTOMA

Author:

Kumari Ragini1,Shankar Kunal2,Chaudhary Ajit Kumar3,Jana Debarshi4

Affiliation:

1. MBBS, M.D. (Patho.), Tutor, Department of Pathology, Darbhanga Medical College, Laheriasarai, Bihar.

2. MBBS, M.S. (Orthopaedics) [Hons.], Senior Resident, Department of Orthopaedics, Darbhanga Medical College & Hospital, Laheriasarai, Bihar.

3. MBBS, M.D. (Patho.), Professor and Head of Department, Department of Pathology, Darbhanga Medical College, Laheriasarai, Bihar.

4. Young Scientist (DST) Institute of Post-Graduate Medical Education and Research, A.J.C. Bose Road, Kolkata-700020, West Bengal, India.

Abstract

Objective: To determine the clinico-pathological and histological features of Chondroblastoma (CB). Place of study : Department of Pathology associated with Orthopaedics Department, Darbhanga Medical College and Hospital, Laheriasarai, Bihar. Methodology: The histological slides of all reported cases of CB were retrieved and reviewed for morphological features. Clinical features were noted from surgical pathology reports. Frequency of features was noted. Results: Sixty one cases of CB were identified. Pain was the most common presenting symptom. The age ranged from 10 to 38 years (mean 20 ± 1.98 years; M: F 2.5:1) with 61% patients in the second decade of life. Forty six cases occurred in long tubular bones; distal femur being most common site. Metaphysis, clavicle, temporal bone and metacarpal were also involved. Histologically, all CBs were composed of round to polygonal cells and scattered osteoclast-type multinucleated giant cells and majority had hemosiderin pigment. Chicken-wire calcifications and coarse calcifications were seen in 85% and 26% of cases respectively. A spindle cell component was seen in 54% of cases. ABC-like areas were seen in 10 cases. Mitosis ranged from 1 to 6/10 HPFs. Recurrence was seen in 2 cases. Recurrent tumor showed similar morphology when compared with the initial tumor. Conclusion: CB is a benign tumor but has potential for recurrence. Males are more affected, second decade is more common and distal femur is most common site. Metaphysis, clavicle, temporal bone and metacarpal were the rare sites of CB. Histological features predictive of recurrence were not separately identified.

Publisher

World Wide Journals

Reference23 articles.

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2. 2. Chandu de Silva MV, Reid R. Chondroblastoma: varied histologic appearance, potential diagnostic pitfalls, and clinicopathologic features associated with local recurrence. Ann Diag Pathol 2003; 7:205-13.

3. 3. Codman EA. Epiphyseal chondromatous giant cell tumors of the upper end of the humerus. Surg Gynec Obstet 1931; 52:543-8.

4. 4. Crim JR, Gold RH, Mirra JM, Gebhardt MC, Mankin HJ. Chondroblastoma of the femur with an aneurysmal bone cyst. Skeletal Radiol 1992; 21:403-5.

5. 5. Dahlin DC, Ivins JC. Benign chondroblastoma: a study of 125 cases. Cancer 1972; 30:401-13.

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