[表现为单侧内耳道病变的原发性中枢神经系统淋巴瘤:病例报告]。

Q4 Medicine Clinical Neurology Pub Date : 2024-05-24 Epub Date: 2024-04-25 DOI:10.5692/clinicalneurol.cn-001939
Rie Tohge, Masaaki Iwase, Takayuki Kondo
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引用次数: 0

摘要

一名 61 岁的男子右耳听力下降并蹒跚行走 7 个月,虽然之前的核磁共振成像评估显示有轻微异常,但他被诊断为突发性耳聋。随访期间,他出现了听力减退、右面神经麻痹、右下颌疼痛、右侧颞部疼痛和小脑共济失调。入院时脑脊液检查显示葡萄糖浓度降低,可溶性白细胞介素-2受体(sIL-2R)水平升高,而血清sIL-2R水平在正常范围内。脑部核磁共振成像显示,一个肿胀的造影剂增强病灶从右侧内耳道延伸至小脑中部。镓-67(67Ga)单光子发射计算机断层扫描(SPECT-CT)显示病变部位有异常聚集。肿瘤切除后进行病理分析,诊断为原发性中枢神经系统淋巴瘤。在本病例中,核磁共振成像和 67Ga SPECT-CT 的特征与前庭裂隙瘤的特征截然不同。此外,脑脊液中 sIL-2R 的升高而非血清中的升高有助于鉴别诊断。
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[Primary central nervous system lymphoma presenting as a unilateral internal auditory canal lesion: a case report].

A 61-year-old man with right hearing loss and staggering for seven months was diagnosed with sudden deafness although previous evaluation with MRI indicated minor abnormal findings. During follow-up, he developed hypogeusia, right facial nerve palsy, pain in right mandible, right-sided temporal pain, and cerebellar ataxia. Cerebrospinal fluid examination at admission revealed reduced glucose concentration and elevated soluble interleukin-2 receptor (sIL-2R) level, whereas serum sIL-2R level was within the normal range. Brain MRI showed a swollen contrast-enhanced lesion extending from the right internal auditory canal to the middle cerebellar peduncle. Gallium-67 (67Ga) single-photon emission-computed tomography-computed tomography (SPECT-CT) revealed abnormal accumulation at the lesion site. Pathologic analysis of the tumor after resection led to the diagnosis of primary central nervous system lymphoma. In the present case, the MRI and 67Ga SPECT-CT characteristics were distinct from those of vestibular schwannoma. In addition, elevation of sIL-2R in the cerebrospinal fluid but not in serum was useful for differential diagnosis.

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来源期刊
Clinical Neurology
Clinical Neurology Medicine-Neurology (clinical)
CiteScore
0.30
自引率
0.00%
发文量
147
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