B-Cell Lymphoma Intramedullary Tumor: Case Report and Systematic Review.

Daniel Gregório Gonsalves, Paulo Eduardo Albuquerque Zito Raffa, Gabriela Gerenutti de Sousa, Melissa Esposito Gomes Rigueiral, Iracema Araújo Estevão, Cesar Cozar Pacheco, Roger Thomaz Rotta Medeiros, Paulo Roberto Franceschini, Paulo Henrique Pires de Aguiar
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Abstract

Intramedullary tumors represent the major cause of spinal cord injuries, and its symptoms include pain and weakness. Progressive weakness may concomitantly occur in the upper and lower limbs, along with lack of balance, spine tenderness, sensory loss, trophic changes of extremity, hyperreflexia, and clonus. The study protocol was in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) guidelines. A systematic search of the MEDLINE electronic database was performed to identify the studies reporting the clinical features of children and adults who presented with an intramedullary lymphoma. Twenty-one studies were included, reporting 25 cases. Manuscripts were excluded if the full-text article was not available, original data were not reported (e.g., review articles), or if the main disease was not intramedullary lymphoma. A structured data extraction form was employed to standardize the identification and retrieval of data from manuscripts. To enlighten the discussion, a case is also presented. An 82-year-old woman with Fitzpatrick skin type II, diagnosed and treated for non-Hodgkin's lymphoma 7 years ago, was admitted with mental confusion and memory loss for the past 2 months-evolving with recurring falls from her own height. One day before admission, she displayed Brown-Séquard syndrome. An expansive lesion from C2 to C4 in the cervical spinal cord was found and a hypersignal spinal cord adjacent was described at the bulb medullary transition to the C6-C7 level. A primary spinal cord tumor was considered, as well as a melanoma metastasis, due to the lesion's flame pattern. The patient presented a partial recovery of symptoms and a reduction of the spinal cord edema after being empirically treated with corticosteroids, but the lesion maintained its extent. Subsequently, a large diffuse B-cell lymphoma with nongerminal center was found in open body biopsy, infiltrating neural tissue. The main objective of the present study is to report a surgical case treated for a large diffuse B-cell lymphoma, in addition to presenting the results of a systematic review of primary intramedullary spinal cord lymphoma.

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b细胞淋巴瘤髓内肿瘤:1例报告及系统回顾。
髓内肿瘤是脊髓损伤的主要原因,其症状包括疼痛和虚弱。进行性无力可同时发生在上肢和下肢,并伴有缺乏平衡、脊柱压痛、感觉丧失、四肢营养改变、反射亢进和冠状胬肉。研究方案符合系统评价和荟萃分析首选报告项目(PRISMA)指南。对MEDLINE电子数据库进行系统搜索,以确定报告髓内淋巴瘤儿童和成人临床特征的研究。纳入21项研究,报告了25例病例。如果没有全文文章,原始数据没有报道(例如,综述文章),或者主要疾病不是髓内淋巴瘤,则排除稿件。采用结构化数据提取表对稿件数据的识别和检索进行标准化。为了启发讨论,还提出了一个案例。一名82岁的菲茨帕特里克皮肤II型女性,7年前被诊断为非霍奇金淋巴瘤并接受治疗,在过去的2个月里因精神混乱和记忆丧失而入院,并伴有反复从自己的高度跌落。入院前一天,她表现出布朗-萨梅夸德综合症。在颈脊髓中发现从C2到C4的扩张性病变,在球髓过渡到C6-C7水平处发现高信号脊髓。原发性脊髓肿瘤,以及黑色素瘤转移,由于病变的火焰模式被认为。经经验性皮质类固醇治疗后,患者症状部分恢复,脊髓水肿减轻,但病变程度维持原状。随后,在开体活检中发现一个具有非生殖中心的大弥漫性b细胞淋巴瘤,浸润神经组织。本研究的主要目的是报道一例手术治疗大弥漫性b细胞淋巴瘤的病例,并对原发性髓内脊髓淋巴瘤进行系统回顾。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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