Nishiyama N, Nakatani S, Inoue K, Katoh T, Kinoshita H
Department of Surgery, Kita Citizen's Hospital of Osaka City, Japan.
Jpn J Thorac Cardiovasc Surg. 2000 Mar;48(3):180-3. doi: 10.1007/BF03218117.
Malignant lymphoma originating in the bone is rare and is now recognized as being an independent clinicopathologic entity known as primary lymphoma of bone. A 60-year-old man complaining of right chest and back pain consulted our hospital for further examination. Chest X-ray and computed tomogram revealed osteolysis and a surrounding soft tissue mass in the sixth right rib. An ultrasonically-guided needle biopsy of the tumor was performed, and histologic examination indicated the dense proliferation of similar-sized atypical cells with nucleoli and an irregular nuclear border. A diagnosis of diffuse, medium-sized non-Hodgkin's lymphoma, B-cell type was made. En block resection of the tumor and chest wall was performed. Macroscopically, the tumor measured 7.5 x 4.8 x 3.0 cm in diameter, and the histologic findings were similar to those of the preoperative needle biopsy. Unfortunately, postoperative treatment with radiation therapy and chemotherapy was ultimately unsuccessful, and a local recurrence and metastatic lesions appeared in the stomach and para-aortic abdominal lymph nodes 7 months after the first symptom appeared. The patient died 3 months later. Surgery was chosen as the initial therapy as it was considered that a rib resection would not result in serious respiratory compromise and the complete resection of the tumor would be superior to radiation therapy for local control. Some authors have reported that the surgical resection of a primary lymphoma of the bone originating in a rib can yield a good prognosis. However, it is a systemic disease and a more effective therapeutic strategy should be developed.
原发于骨的恶性淋巴瘤较为罕见,目前被认为是一种独立的临床病理实体,即骨原发性淋巴瘤。一名60岁男性因右胸及背部疼痛前来我院进一步检查。胸部X线和计算机断层扫描显示右侧第六肋骨骨质溶解及周围软组织肿块。对肿瘤进行了超声引导下针吸活检,组织学检查显示大小相似的非典型细胞密集增殖,有核仁且核边界不规则。诊断为弥漫性、中等大小B细胞型非霍奇金淋巴瘤。对肿瘤及胸壁进行了整块切除。肉眼观察,肿瘤直径为7.5×4.8×3.0 cm,组织学表现与术前针吸活检相似。不幸的是,术后放疗和化疗最终未成功,在出现首发症状7个月后,胃部及腹主动脉旁淋巴结出现局部复发和转移病灶。患者3个月后死亡。选择手术作为初始治疗方法,因为认为肋骨切除不会导致严重的呼吸功能损害,且肿瘤的完整切除在局部控制方面优于放疗。一些作者报告称,起源于肋骨的骨原发性淋巴瘤手术切除可获得良好预后。然而,它是一种全身性疾病,应制定更有效的治疗策略。