Jordan Karin, Grothey Axel, Grothe Wilfried, Kegel Thomas, Wolf Hans-Heinrich, Schmoll Hans-Joachim
Internal Medicine IV, Hematology/Oncology, Martin-Luther-University Halle/Wittenberg, Halle/Saale, Germany.
Eur J Haematol. 2005 Mar;74(3):263-6. doi: 10.1111/j.1600-0609.2004.00367.x.
Lymphomatoid granulomatosis is a rare Epstein-Barr virus (EBV)-positive-B-cell lymphoproliferative disorder. Treatment options include corticosteroids, antiviral therapy, interferon-alpha and chemotherapy. However, long-term prognosis is poor and no therapeutic standard has been established yet. In a 21-year-old woman, a biopsy of mediastinal mass revealed lymphomatoid granulomatosis. Combined therapy with valganciclovir and interferon-alpha proved ineffective. In view of the CD20 expression of the tumor cells, monotherapy with rituximab was intiated. After 3 months a complete remission was achieved. Rituximab was continued for another 6 months with subsequent consolidation radiotherapy. This is the first report of an enduring complete remission (20 months) of a non-CNS lymphomatoid granulomatosis treated with rituximab.
淋巴瘤样肉芽肿病是一种罕见的爱泼斯坦-巴尔病毒(EBV)阳性B细胞淋巴增殖性疾病。治疗选择包括皮质类固醇、抗病毒治疗、α干扰素和化疗。然而,长期预后较差,尚未确立治疗标准。在一名21岁女性中,纵隔肿块活检显示为淋巴瘤样肉芽肿病。缬更昔洛韦与α干扰素联合治疗无效。鉴于肿瘤细胞的CD20表达,开始使用利妥昔单抗单药治疗。3个月后实现完全缓解。利妥昔单抗继续使用6个月,随后进行巩固放疗。这是首例关于利妥昔单抗治疗非中枢神经系统淋巴瘤样肉芽肿病获得持久完全缓解(20个月)的报告。