Imai N, Tanabe H, Hirose H, Shimokawa K
Department of Surgery, Kizawa Hospital, Minokamo, Japan.
Nihon Kyobu Geka Gakkai Zasshi. 1991 Mar;39(3):356-60.
Chondroblastomas are rare neoplasms, and comprise 0.5-1% of histologically proved primary bone tumors. We report a case of the tumor originating form the right 6th rib. The patient, a 15-year-old female, was admitted because the abnormal shadow was found on routine chest X-ray film. It was suspected to be the posterior mediastinal tumor based on the chest X-ray, CT and MRI. In surgery, the tumor was 4.0 x 4.0 x 2.5 cm in size and fixed on the rib, but not invasive to other tissue. The content was rough and soft granuloma like. Histological examination confirmed the diagnosis of chondroblastoma of the rib. The patient is doing well without symptoms of recurrence fifteen months after surgery.
软骨母细胞瘤是一种罕见的肿瘤,占组织学确诊的原发性骨肿瘤的0.5%-1%。我们报告一例起源于右第6肋骨的该肿瘤病例。患者为一名15岁女性,因常规胸部X线片发现异常阴影而入院。根据胸部X线、CT和MRI检查,怀疑为后纵隔肿瘤。手术中,肿瘤大小为4.0×4.0×2.5 cm,固定于肋骨,但未侵犯其他组织。内容物为粗糙、柔软的肉芽肿样。组织学检查确诊为肋骨软骨母细胞瘤。患者术后15个月情况良好,无复发症状。