Luo Han, Li Shanshan, Liu Bo
Department of Neurology, Shenzhen Longhua District Central Hospital, Shenzhen, Guangdong, China.
Medicine (Baltimore). 2024 Dec 27;103(52):e41097. doi: 10.1097/MD.0000000000041097.
High-grade B-cell lymphoma is highly malignant and progresses rapidly, often being at the intermediate or advanced stage with poor prognosis when detected. This disease involves the central nervous system in 9% to 45% of cases, while peripheral nerve injury is relatively rare.
A 42-year-old male was admitted to the hospital due to recurrent peripheral facial paralysis lasting for 8 months and weakness in both lower extremities lasting for 1 month. No other symptoms and signs were apparent.
Fluorescence in situ hybridization showed the following results: IgH/Bcl2 t(14:18)(q32;q21) chromosomal translocation: negative; Bc16 gene translocation: positive; and Myc(8;q24) chromosomal translocation: positive. The clonal gene rearrangement test for B-cell lymphoma was positive, and the clonal gene rearrangement test for T-cell lymphoma was negative.The patient was diagnosed with high-grade B-cell lymphoma.
The treatment plan included chemotherapy, targeted drug therapy, biological therapy, immunotherapy, etc.
The patient who was followed up for 1 and 3 years had stable conditions and was able to take care of himself, with an mRS score of 1. Five years after the initial diagnosis, the patient experienced recurrence and systemic metastasis of high-grade B-cell lymphoma, ultimately dying from multiple organ failure.
Lymphoma manifests mainly as progressive impairment of multiple cranial nerves or recurrent alternating peripheral nerve injury complicated with elevated protein concentrations in cerebrospinal fluid; it can be easily misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy. Performing lymph node biopsy for high-grade B-cell lymphoma as early as possible helps detect lymphoma in the early stage.
高级别B细胞淋巴瘤恶性程度高,进展迅速,确诊时多处于中晚期,预后较差。该疾病9%至45%的病例累及中枢神经系统,而周围神经损伤相对少见。
一名42岁男性因反复周围性面瘫8个月、双下肢无力1个月入院。无其他明显症状和体征。
荧光原位杂交结果显示:IgH/Bcl2 t(14:18)(q32;q21)染色体易位:阴性;Bc16基因易位:阳性;Myc(8;q24)染色体易位:阳性。B细胞淋巴瘤克隆基因重排检测阳性,T细胞淋巴瘤克隆基因重排检测阴性。患者被诊断为高级别B细胞淋巴瘤。
治疗方案包括化疗、靶向药物治疗、生物治疗、免疫治疗等。
随访1年和3年的患者病情稳定,能够自理,改良Rankin量表评分为1分。初诊5年后,患者出现高级别B细胞淋巴瘤复发及全身转移,最终死于多器官功能衰竭。
淋巴瘤主要表现为多组脑神经进行性损害或反复交替性周围神经损伤并伴有脑脊液蛋白浓度升高;易误诊为慢性炎症性脱髓鞘性多发性神经根神经病。尽早对高级别B细胞淋巴瘤进行淋巴结活检有助于早期发现淋巴瘤。