Primary Intraocular Diffuse Large B-cell Lymphoma: Diagnostic Difficulties in Deep Retinal Infiltrations with Vitritis

被引:1
|
作者
Kapelko-Slowik, Katarzyna [1 ]
Urbaniak-Kujda, Donata [1 ,4 ]
Turno-Krecicka, Anna [2 ]
Potoczek, Stanislaw [1 ]
Dybko, Jaroslaw [1 ]
Biernat, Monika [1 ,3 ]
Slowik, Miroslaw [2 ]
机构
[1] Wroclaw Med Univ, Dept & Clin Hematol Blood Neoplast Disorders & Bo, 4 Pasteur St, PL-50367 Wroclaw, Poland
[2] Wroclaw Med Univ, Dept Ophthalmol, 4 Pasteur St, PL-50367 Wroclaw, Poland
[3] Wroclaw Med Univ, Dept Microbiol, 4 Pasteur St, PL-50367 Wroclaw, Poland
[4] Wroclaw Physiotherapy Coll, Wroclaw, Poland
关键词
Lymphoma; Vitritis; Retinal infiltration; Uveitis; Chemotherapy;
D O I
10.1007/s12288-015-0599-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose Primary intraocular lymphoma ( PIOL) is a rare malignancy with an aggressive clinical course. It is usually considered as a subset of primary central nervous system lymphoma. Differential diagnosis should include infectious and non-infectious aetiologies, particularly the common masqueraders sarcoidosis, tuberculosis, viral retinitis and syphilis. Patient The article presents a case of bilateral vitreo-retinal lymphoma manifesting as uveitis and vitritis resistant to corticosteroid therapy. The final diagnosis was based on a retinal biopsy. Results The patient was successfully treated with systemic and local therapy. Long-term complete remission ( CR) was reached. The relapse of diffuse large B-cell lymphoma was revealed in the frontal left lobe after 48 months of CR duration. Conclusion The diagnosis of PIOL is always very difficult. Cooperation of pathologists, ophthalmologists and hematologists is required for a quick and accurate diagnosis. Local and systemic treatment is needed to achieve CR, but the relapse rate remains very high.
引用
收藏
页码:S143 / S147
页数:5
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