Dellagi K, Micheau C, Estelin R, Genin J
Ann Otolaryngol Chir Cervicofac. 1985;102(7):537-41.
A patient with a nasal chondroma and Ollier's disease treated at the Institut Gustave-Roussy, Villejuif, had a long past medical history of over 10 years, starting with a nasal lesion diagnosed as a myxoma. Follow up clinical and radiologic examinations failed to detect recurrences. The discovery, ten years after excision of tumor, of multiple skeletal enchondromas raised the hypothesis of Ollier's disease, this being responsible for the myxoid chondroma of the nasal cavities. A past medical history of surgery to the left lower limb presenting a valgus deformity, and of a left suborbital angioma treated by curietherapy confirmed the diagnosis of Ollier's disease and suggested that of a Maffuci syndrome. Prognosis of the disease is dominated by the risk of onset of chondrosarcoma.
一位在维勒瑞夫古斯塔夫 - 鲁西研究所接受治疗的患有鼻软骨瘤和奥利尔病的患者,有超过10年的漫长既往病史,最初是被诊断为黏液瘤的鼻部病变。后续的临床和放射学检查未发现复发情况。在肿瘤切除十年后发现多个骨骼内生软骨瘤,这引发了奥利尔病的假说,即其导致了鼻腔的黏液样软骨瘤。既往有左下肢手术史,伴有外翻畸形,以及曾接受镭疗法治疗的左眶下血管瘤,这些证实了奥利尔病的诊断,并提示可能患有马富西综合征。该疾病的预后主要受软骨肉瘤发病风险的影响。