Bonnevialle P, Mansat M, Durroux R, Devallet P, Rongières M
Service de Chirurgie orthopédique et traumatologique de Purpan, Toulouse.
Ann Chir Main. 1988;7(1):32-44. doi: 10.1016/s0753-9053(88)80067-x.
Twenty-nine patients were treated in the department of orthopedic surgery of Purpan (Toulouse), with thirty-five chondromata of the hand. Follow-up was over one year. Chondroma is a bone tumor predominantly of the left side, second ray of the hand and phalanx. Some multifocal cases have been observed. The diagnosis was made in half the cases through a pathological fracture. Chondroma is characterized by a diaphyseal or a metaphyso-diaphyseal lacuna, wearing away the cortical bone. Treatment consisted of curetting the tumor and filling the cavity with iliac cancellous bone graft. The clinical result was been excellent in 15 cases (60%), good in 6 cases (25%), with only some residual pain, and/or digital swelling. In two cases the finger was stiff, but functionally not disabling. In one case the stiffness was important and very disabling; after several recurrences it evolved into a chondrosarcoma.
图卢兹普尔潘骨科收治了29例手部有35处软骨瘤的患者。随访时间超过一年。软骨瘤是一种主要发生在手部左侧、第二掌骨和指骨的骨肿瘤。观察到一些多灶性病例。半数病例通过病理性骨折做出诊断。软骨瘤的特征是骨干或干骺端-骨干腔隙,侵蚀皮质骨。治疗包括刮除肿瘤并用髂骨松质骨移植填充腔隙。临床结果为15例(60%)极佳,6例(25%)良好,仅有一些残留疼痛和/或手指肿胀。2例手指僵硬,但功能未致残。1例僵硬严重且功能严重致残;经过几次复发后发展为软骨肉瘤。