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Lumbosacral nerve root lesion with malignant lymphoma

机译:腰ac神经根病变伴恶性淋巴瘤

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A 66-year old man presented with a one-year history of progressive pain and weakness in his left leg. Neurological examination showed severeparesis, muscle atrophy, areflexia of the left leg, and dysesthesia and hypoesthesia in L5, S1, S2 dermatome, all of which suggested a lumbosacralpolyradiculopathy. Routine hematological examinations were within normal limits. Cerebrospinal fluid examination showed an elevated protein level(83 mg/dl) with slight pleocytosis (13 cells/mm 3). Cytological analysis of the cerebrospinal fluid showed no malignancy. Needle electromyographyshowed diffuse signs of denervation of the nerves related to L5 and S1 nerve roots. Enhanced computed tomography presented an intrapelvictumor-like lesion [Figure 1]a and [Figure 1]b. The lesion seemed to protrude to the pelvis through the anterior sacral foramina. Lumbosacralmagnetic resonance imaging (MRI) revealed a left-side dominant swelling in L5, S1, and S2 nerve roots [Figure 1]c. Sagittal [Figure 1]d andcoronal [Figure 1]e T1-weighted MRI image showed a distinct gadolinium-enhancement of the left lumbosacral nerve roots. Initial whole-bodyexamination revealed no other lesions. He received intravenous immunoglobulin and steroid therapy after a tentative diagnosis of chronicinflammatory demyelinating polyradiculoneuropathy had been made. Leg pain was temporarily relieved, although leg weakness and muscle atrophynever recovered. Soluble interleukin-2 receptor was elevated to 2070 U/ml. Finally, a repeated cytological examination of the cerebrospinal fluidand random skin biopsy revealed large atypical cells positive for CD 20 and he was diagnosed as having a diffuse large B-cell lymphoma.Malignant lymphoma is a common disease and an occasional cranial nerve infiltration has been described.[1] However, infiltration of the peripheralnervous system by the lymphoma cells, termed as “neurolymphomatosis,” is a rare presentation of the disease.
机译:一名66岁的男性患者有一年的左腿进行性疼痛和无力史。神经系统检查显示L5,S1,S2皮刀严重的轻瘫,肌肉萎缩,左腿反射消失以及感觉异常和感觉减退,所有这些均提示腰s多神经根病。常规血液学检查均在正常范围内。脑脊液检查显示蛋白水平升高(83 mg / dl),并有轻微的胞吞作用(13细胞/ mm 3)。脑脊液的细胞学分析未见恶性。针状肌电图显示与L5和S1神经根相关的神经神经支配的弥漫征象。增强型计算机断层扫描显示骨盆腔内样病变[图1] a和[图1] b。病变似乎通过前孔突出到骨盆。腰ac磁共振成像(MRI)显示L5,S1和S2神经根左侧显性肿胀[图1] c。矢状位[图1] d和冠状位[图1] e T1加权MRI图像显示左腰s神经根有明显的g增强。最初的全身检查未发现其他病变。在初步诊断为慢性炎症性脱髓鞘性多发性神经根病后,他接受了静脉注射免疫球蛋白和类固醇治疗。尽管腿部无力和肌肉萎缩没有恢复,但暂时缓解了腿部疼痛。可溶性白介素2受体升高至2070 U / ml。最后,对脑脊液进行了反复的细胞学检查并进行了随机皮肤活检,发现CD 20呈阳性的非典型大细胞,并被诊断为弥漫性大B细胞淋巴瘤。恶性淋巴瘤是一种常见疾病,偶见颅神经浸润。 。[1]然而,淋巴瘤细胞浸润周围神经系统,称为“神经营养不良症”,是该病的罕见表现。

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