Kudo T, Okada K, Hirano Y, Sageshima M
Department of Orthopaedics, Akita University School of Medicine, Japan.
Tohoku J Exp Med. 2001 Aug;194(4):251-7. doi: 10.1620/tjem.194.251.
Chondroblastoma of the metacarpal bone has been extremely rare and only seven cases have been reported in the English literature. Here we reported the eighth case of a chondroblastoma that developed on the first metacarpal bone of the right hand of a 21-year-old man. Radiographs showed an expansile osteolytic lesion with a multilocular appearance. In MR images, the lesion showed low intensity in T1 and high intensity in T2-weighted images with multiple fluid-fluid levels, which are findings resembling those of an aneurysmal bone cyst. From the pathological findings, however, it was recognized as a chondroblastoma with aneurysmal bone cyst-like change. Good clinical results was obtained by the subtotal resection of the metacarpal bone with a columnar-shaped iliac bone graft.
掌骨软骨母细胞瘤极为罕见,英文文献中仅报道过7例。在此,我们报告第8例软骨母细胞瘤,该病例发生于一名21岁男性右手的第一掌骨。X线片显示为一膨胀性溶骨性病变,呈多房状。在磁共振成像(MR)中,病变在T1加权像上呈低信号,在T2加权像上呈高信号,并伴有多个液-液平面,这些表现类似于骨囊肿。然而,根据病理结果,其被诊断为具有骨囊肿样改变的软骨母细胞瘤。通过第一掌骨次全切除并柱状髂骨植骨,获得了良好的临床效果。