Zhou Qiao-Lin, Li Zhao-Kun, Xu Fang, Liang Xiao-Gong, Wang Xing-Biao, Su Jing, Tang Yu-Feng
Department of Hematology, Mianyang Central Hospital, School of Medicine, University of Electronic Science and Technology of China, Mianyang 621000, Sichuan Province, China.
Department of Neurology, Mianyang Central Hospital, School of Medicine, University of Electronic Science and Technology of China, Mianyang 621000, Sichuan Province, China.
World J Clin Cases. 2022 Sep 16;10(26):9502-9509. doi: 10.12998/wjcc.v10.i26.9502.
Central nervous system (CNS) lesions and peripheral neuropathy are rare among patients with non-Hodgkin's lymphoma (NHL). Lymphomatous infiltration or local oppression usually accounts for CNS or peripheral nerve lesions. The incidence of peripheral neuropathy was 5%. Guillain-Barré syndrome (GBS) is rare and may occur in less than 0.3% of patients with NHL. Hemophagocytic syndrome (HPS) is a rare complication of NHL. It has been reported that 1% of patients with hematological malignancies develop HPS. Diffuse large B-cell lymphoma (DLBCL) combined with GBS has been reported in 10 cases.
We report the case of a 53-year-old man who was initially hospitalized because of abnormal feelings in the lower limbs and urinary incontinence. He was finally diagnosed with DLBCL combined with GBS and HPS after 16 d, which was earlier than previously reported. Immunoglobulin pulse therapy, dexamethasone, and etoposide were immediately administered. The neurological symptoms did not improve, but cytopenia was relieved. However, GBS-related clinical symptoms were relieved partially after one cycle of rituximab - cyclophosphamide, hydroxydaunorubicin, vincristine, and prednisone (R-CHOP) chemotherapy and disappeared after six cycles of R-CHOP.
GBS and HPS heralding the diagnosis of Epstein-Barr virus DLBCL are rare. Herein, we report a rare case of DLBCL combined with GBS and HPS, and share our clinical experience. Traditional therapies may be effective if GBS occurs before lymphoma is diagnosed. Rapid diagnosis and treatment of DLBCL are crucial.
中枢神经系统(CNS)病变和周围神经病变在非霍奇金淋巴瘤(NHL)患者中较为罕见。淋巴瘤浸润或局部压迫通常是中枢神经系统或周围神经病变的原因。周围神经病变的发生率为5%。吉兰-巴雷综合征(GBS)罕见,在NHL患者中的发生率可能低于0.3%。噬血细胞综合征(HPS)是NHL的一种罕见并发症。据报道,1%的血液系统恶性肿瘤患者会发生HPS。已有10例弥漫性大B细胞淋巴瘤(DLBCL)合并GBS的病例报道。
我们报告一例53岁男性患者,最初因下肢感觉异常和尿失禁入院。16天后最终诊断为DLBCL合并GBS和HPS,这比之前报道的时间更早。立即给予免疫球蛋白冲击治疗、地塞米松和依托泊苷。神经症状未改善,但血细胞减少得到缓解。然而,在接受一个周期的利妥昔单抗-环磷酰胺、羟基柔红霉素、长春新碱和泼尼松(R-CHOP)化疗后,GBS相关临床症状部分缓解,六个周期的R-CHOP化疗后症状消失。
以爱泼斯坦-巴尔病毒DLBCL诊断为先兆的GBS和HPS罕见。在此,我们报告一例罕见的DLBCL合并GBS和HPS病例,并分享我们的临床经验。如果GBS在淋巴瘤诊断之前发生,传统治疗可能有效。DLBCL的快速诊断和治疗至关重要。