A clinicopathological review of 23 patients (mean age, 67 years; range, 42-85 years) with chondrosarcoma of the bones of the hand was done. The mean follow up was 8.5 years. Eleven patients presented with a progressive painless swelling, 26% having had symptoms for over 10 years. The proximal phalanx was the commonest site. Initial clinical misdiagnosis as ganglion, bursa, gout, rheumatoid arthritis and a cyst occurred in five patients. Radiologically most lesions showed bone expansion, cortical destruction and soft-tissue extension. The majority was of high histologic grade (Evan's grade 2 & 3) with extensive myxoid areas. Five out of eight patients who were originally treated by curettage or excision had local recurrences compared to none treated by ray resection or amputation of phalanx (P=0.002). None had metastases. The low risk of metastases despite the high histologic grade indicates that chondrosarcomas of the hand behave differently from chondrosarcomas elsewhere.

The lateral surgical approach to the proximal femur potentially damages the nerve supply to the vastus lateralis (VL) muscle. This study describes the detailed anatomy of the nerve supply to the VL muscle based on dissection of ten cadaveric lower limbs. In all specimens, a single nerve trunk arose from the femoral nerve, which is most subsequently divided into two main divisions. These divisions gave two branches each. These branches coursed from anteriorly and proximally to posteriorly and distally within the muscle. When the muscle was reflected anteriorly from its attachment to the linea aspera, there was no damage to its innervation. Splitting of the VL in the midlateral line of the femur, however, resulted in denervation of the posterior half of the muscle. Precise knowledge of the nerve supply to the VL will help avoid iatrogenic denervation of the muscle in surgical procedures at the proximal femur through the lateral approach.

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Chondrosarcoma (CHS) is a rare malignant neoplasm of the jaws. Based on the morphologic features alone, a correct diagnosis of CHS may be difficult. Therefore, correlation of radiological and clinicopathological features are mandatory for the diagnosis of CHS. A case of CHS of the maxilla is reported. A brief discussion on the etiopathogenesis, radiologic and histologic presentation of the tumor and the treatment modalities of this unusual tumor is discussed.