Voulgarelis M, Dafni U G, Isenberg D A, Moutsopoulos H M
National University of Athens, Greece.
Arthritis Rheum. 1999 Aug;42(8):1765-72. doi: 10.1002/1529-0131(199908)42:8<1765::AID-ANR28>3.0.CO;2-V.
Several reports have noted an increased incidence of malignant lymphoma in patients with Sjögren's syndrome (SS). Each case series has consisted of a limited number of patients with malignant non-Hodgkin's lymphoma (MNHL). In this report, we describe the disease characteristics, the clinical course, and the evolution in 33 patients followed up in 9 European medical centers.
The pool of MNHL patients from participating centers in a European Concerted Action on SS were analyzed. We report on the disease characteristics, its evolution, prognosis, current treatment practices, and survival.
The MNHLs in this study were primarily situated in the marginal zone (48.5%), with the manifestations mostly extranodal (78.8%) and most often identified in the salivary glands (54.6%). Lymphadenopathy (65.6%), skin vasculitis (33.3%), peripheral nerve involvement (24.2%), low-grade fever (25.0%), anemia (48.1%), and lymphopenia (78.6%) were observed significantly more frequently than in the general SS population. Patients with high-to-intermediate grade lymphoma had significantly worse survival (P = 0.041). The presence of B symptoms (fever, night sweats, and weight loss) and a large tumor diameter (>7 cm) were additional independent risk factors for death.
The novel observations of this study were those related to the type of MNHL, the survival prognosis, and the very high frequency of skin vasculitis, peripheral nerve involvement, anemia, and lymphopenia. Some of the previously reported results on extranodal manifestations were confirmed.
多项报告指出,干燥综合征(SS)患者中恶性淋巴瘤的发病率有所增加。每个病例系列所包含的恶性非霍奇金淋巴瘤(MNHL)患者数量有限。在本报告中,我们描述了9个欧洲医学中心随访的33例患者的疾病特征、临床病程及病情演变。
对欧洲干燥综合征联合行动参与中心的MNHL患者群体进行分析。我们报告疾病特征、病情演变、预后、当前治疗方法及生存率。
本研究中的MNHL主要位于边缘区(48.5%),表现多为结外(78.8%),最常出现在唾液腺(54.6%)。与一般SS人群相比,淋巴结病(65.6%)、皮肤血管炎(33.3%)、周围神经受累(24.2%)、低热(25.0%)、贫血(48.1%)和淋巴细胞减少(78.6%)的发生率明显更高。高中度淋巴瘤患者的生存率明显更差(P = 0.041)。B症状(发热、盗汗和体重减轻)和大肿瘤直径(>7 cm)是另外的独立死亡危险因素。
本研究的新发现涉及MNHL的类型、生存预后以及皮肤血管炎、周围神经受累、贫血和淋巴细胞减少的高发生率。先前报道的一些关于结外表现的结果得到了证实。