Orbital Pseudotumor

被引:55
作者
Mendenhall, William M. [1 ]
Lessner, Alan M. [2 ]
机构
[1] Univ Florida, Coll Med, Dept Radiat Oncol, Gainesville, FL USA
[2] Univ Florida, Coll Med, Dept Ophthalmol, Gainesville, FL 32610 USA
来源
AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS | 2010年 / 33卷 / 03期
关键词
orbital pseudotumor; review; CLINICAL-FEATURES; INFLAMMATORY PSEUDOTUMOR; RADIOTHERAPY; MYOSITIS; TUMORS; MANAGEMENT; OUTCOMES; THERAPY; DISEASE;
D O I
10.1097/COC.0b013e3181a07567
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Orbital pseudotumor is a benign condition that accounts for approximately 10% of all orbital mass lesions. Any part of the orbit may be involved. The etiology is unknown. The presentation may be either acute or subacute. Patients may present with a palpable mass, a swollen eyelid, congestion, pain, diminished ocular motility, and/or decreased visual acuity. Approximately, 25% of patients present with bilateral disease. A modest proportion of patients experience resolution of their symptoms without treatment. Biopsy is indicated for those who do not respond to, or relapse after, first-line therapy. Oral corticosteroids are the initial treatment and approximately 80% of patients respond. Roughly half of those who respond to corticosteriods relapse. Second-line therapy consists of either low-dose radiotherapy (20-30 Gy at 2 Gy per fraction), cytotoxic chemotherapy, or immunosuppressive agents. Radiotherapy results in long-term local control rates of 50% or higher. Limited lesions may be successfully resected. A small subset of patients may experience inexorable progression to a fixed, painful, sightless eye and require orbital exenteration.
引用
收藏
页码:304 / 306
页数:3
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