Gherman E
Z Orthop Ihre Grenzgeb. 1975 Oct;113(5):869-75.
Over 20 years 5 patients with dyschondroplasia (Ollier) have been seen in the department for Orthopedics and Traumatology at Cluj-Napoca (Romania). Three were male, two female. 4 came from large families. First signs appeared gradually in 3, in 2 spontaneous fractures drew the attention to the disease. Radiographycally there were the typical chondromas with a strong tendency towards ossification in the adult. Shortening and deformity is proportional to the growth of the chondromas. The cause is unknown. In one case a chondroma became sarcomatous. One arm had to be exarticulated. This patient had no recurrence after 14 years.
20多年来，克卢日-纳波卡（罗马尼亚）的骨科与创伤科诊治了5例软骨发育异常（奥利埃病）患者。其中男性3例，女性2例。4例来自大家庭。3例患者的首发症状逐渐出现，2例因自发性骨折而被发现患有此病。X线检查显示为典型的软骨瘤，在成人期有强烈的骨化倾向。肢体缩短和畸形与软骨瘤的生长成正比。病因不明。1例软骨瘤发生肉瘤变，不得不进行了肩关节离断术。该患者术后14年未复发。
