Austin-Seymour M M, Donaldson S S, Egbert P R, McDougall I R, Kriss J P
Int J Radiat Oncol Biol Phys. 1985 Feb;11(2):371-9. doi: 10.1016/0360-3016(85)90160-9.
Thirty-two patients with orbital pseudotumor (18), reactive lymphoid hyperplasia (2), atypical lymphoid infiltrate (4) or malignant lymphoma (8) were treated in the Division of Radiation Therapy at Stanford University between January 1973 and May 1983. Of the 20 patients with pseudotumor or reactive lymphoid hyperplasia, 10 had unilateral lesions and 10 had bilateral lesions. Biopsy samples were obtained in 15 patients; in five patients with bilateral disease the diagnosis was made on the basis of computed tomography (CT) and clinical findings. The majority of patients were referred because of disease refractory to treatment with corticosteroids. The patients were given a mean dose of 2360 rad using complex, individualized megavoltage techniques including lens shielding. Radiotherapy was well tolerated with no significant acute or late complications. Fifteen patients had complete resolution of symptoms after treatment; five had continued symptoms. Of the 12 patients with malignant lymphoma or atypical lymphoid infiltrate, four had systemic lymphoma with orbital involvement and eight had orbital involvement only. The diagnosis was made by biopsy in all patients and immunophenotyping was done in six cases, of which 5 were monoclonal. Patients were evaluated with a chest radiograph, lymphogram or abdominal CT, bone marrow biopsy and orbital CT. A mean dose of 3625 rad was delivered to the orbit only. Most of the patients received complex megavoltage treatment using bolus. All patients in this group had a complete response and local control. There were no relapses in those with localized disease. Two patients developed cataracts. Carefully planned orbital radiotherapy provides local control without symptomatic sequelae for orbital masses ranging from pseudotumor to malignant lymphoma.
1973年1月至1983年5月期间,斯坦福大学放射治疗科对32例眼眶假瘤(18例)、反应性淋巴组织增生(2例)、非典型淋巴浸润(4例)或恶性淋巴瘤(8例)患者进行了治疗。在20例假瘤或反应性淋巴组织增生患者中,10例为单侧病变,10例为双侧病变。15例患者获取了活检样本;5例双侧病变患者的诊断基于计算机断层扫描(CT)和临床检查结果。大多数患者因对皮质类固醇治疗无效而前来就诊。采用包括晶状体屏蔽在内的复杂个体化兆伏级技术,患者平均接受了2360拉德的剂量。放疗耐受性良好,无明显急性或晚期并发症。15例患者治疗后症状完全缓解;5例仍有症状。在12例恶性淋巴瘤或非典型淋巴浸润患者中,4例为伴有眼眶受累的系统性淋巴瘤,8例仅眼眶受累。所有患者均通过活检确诊,6例进行了免疫表型分析,其中5例为单克隆性。患者接受了胸部X光、淋巴造影或腹部CT、骨髓活检和眼眶CT检查。仅对眼眶给予平均3625拉德的剂量。大多数患者采用加填充物的复杂兆伏级治疗。该组所有患者均有完全缓解和局部控制。局限性疾病患者无复发。2例患者出现白内障。精心规划的眼眶放疗可为从假瘤到恶性淋巴瘤的眼眶肿物提供局部控制且无后遗症。