Nakashima Hiroaki, Imagama Shiro, Ito Zenya, Ando Kei, Kobayashi Kazuyoshi, Ukai Junichi, Muramoto Akio, Shinjyo Ryuichi, Matsumoto Tomohiro, Yamauchi Ippei, Satou Akira, Ishiguro Naoki
Department of Orthopedic Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Department of Orthopedic Surgery, Yokkaichi Municipal Hospital, Yokkaichi, Japan.
Nagoya J Med Sci. 2014 Aug;76(3-4):349-54.
The central nervous system, in particular the spinal cord, is a rare site for primary lymphoma occurrence, with very few published cases. We report an extremely rare primary lymphoma in the cauda equina in a single case with literature review. An immunocompetent 59-year-old male, who complained of progressive low back and bilateral leg pain for 7 months, was studied. Magnetic resonance imaging (MRI) revealed an intradural space-occupying lesion from T12 to S1, poorly demarcated to the normal cauda equina. The intradural lesion showed T1 low intensity, T2 low isointensity, and marked homogeneous enhancement with gadolinium-diethylenetriaminepentaacetic acid on MRI. We performed spinal tap to obtain additional information about the intradural lesion. Large-sized atypical lymphoid cells were found during pathological examination. Fluorodeoxyglucose accumulation was found only in the lumbar area, which corresponded with the MRI findings, and the primary lymphoma site was defined as the cauda equina area. For further detailed pathological diagnosis, we performed surgical biopsy of the cauda equina. Morphological and immunohistochemical assessment made a diagnosis of diffuse large B-cell lymphoma of the cauda equina. The patient received radiotherapy to the lumbosacral area (50 Gy) and methotrexate (MTX) therapy after surgery. The patient was able to walk without help after the therapies. Follow-up MRI performed 1 year after biopsy showed remission of the lesion. MRI and spinal tap were effective tools for the early definitive diagnosis of cauda equina lymphoma. Combined treatment with radiotherapy and MTX should be performed as early as possible.
中枢神经系统,尤其是脊髓,是原发性淋巴瘤罕见的发病部位,仅有极少的病例报道。我们报告一例极其罕见的马尾原发性淋巴瘤病例,并进行文献复习。研究对象为一名59岁免疫功能正常的男性,他主诉下腰部及双侧腿部进行性疼痛7个月。磁共振成像(MRI)显示从T12至S1水平存在硬膜内占位性病变,与正常马尾界限不清。该硬膜内病变在MRI上表现为T1低信号、T2等低信号,注射钆喷酸葡胺后呈明显均匀强化。我们进行了腰椎穿刺以获取有关硬膜内病变的更多信息。病理检查发现大量非典型淋巴细胞。仅在腰椎区域发现氟脱氧葡萄糖聚集,这与MRI表现相符,原发性淋巴瘤部位确定为马尾区域。为进一步明确病理诊断,我们对马尾进行了手术活检。形态学和免疫组化评估诊断为马尾弥漫性大B细胞淋巴瘤。患者术后接受了腰骶部放疗(50 Gy)及甲氨蝶呤(MTX)治疗。治疗后患者能够独立行走。活检后1年进行的随访MRI显示病变缓解。MRI和腰椎穿刺是早期明确诊断马尾淋巴瘤的有效工具。应尽早进行放疗和MTX联合治疗。