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一位患有干燥综合征和视神经脊髓炎谱系障碍的患者出现大脑大动脉可逆性狭窄。

Reversible stenosis of large cerebral arteries in a patient with combined Sjögren's syndrome and neuromyelitis optica spectrum disorder.

作者信息

Ii Yuichiro, Shindo Akihiro, Sasaki Ryogen, Naito Yutaka, Tanaka Keiko, Kuzuhara Shigeki

机构信息

Department of Neurology, Mie University Graduate School of Medicine, 2-174, Edobashi, Tsu, Mie 514-8507, Japan.

出版信息

Rheumatol Int. 2008 Oct;28(12):1277-80. doi: 10.1007/s00296-008-0611-y. Epub 2008 May 21.

Abstract

We report a 49-year-old woman with neuromyelitis optica (NMO) spectrum disorder coexisting with Sjögren's syndrome (SS). She presented with acute brainstem symptoms and transverse myelitis. Brain MRI showed focal high signal intensity lesions in the hypothalamus and the pontine tegmentum on T2-weighted and FLAIR images. MRA revealed stenotic changes of the bilateral middle cerebral artery (MCA), posterior cerebral arteries (PCA) and basilar artery (BA). Spinal MRI revealed hyperintense lesions within the cord extending from the T4 to the T6 level on the T2-weighted image. The patient fulfilled the clinical criteria of primary SS. In addition, anti-AQP4 antibody which is highly specific for NMO was detected in the serum at the acute phase. The patient excellently responded to IVIg while methylprednisolon pulse therapy was not effective. Follow-up MRA displayed complete resolution of the stenosis of the MCA, PCA and BA.

摘要

我们报告了一名49岁患有视神经脊髓炎谱系障碍(NMO)并伴有干燥综合征(SS)的女性。她出现了急性脑干症状和横贯性脊髓炎。脑部MRI在T2加权和液体衰减反转恢复(FLAIR)图像上显示下丘脑和脑桥被盖有局灶性高信号强度病变。磁共振血管造影(MRA)显示双侧大脑中动脉(MCA)、大脑后动脉(PCA)和基底动脉(BA)有狭窄改变。脊髓MRI在T2加权图像上显示脊髓内从T4到T6水平有高信号病变。该患者符合原发性SS的临床标准。此外,急性期血清中检测到对NMO高度特异的抗水通道蛋白4(AQP4)抗体。患者对静脉注射免疫球蛋白(IVIg)反应良好,而甲泼尼龙冲击疗法无效。随访MRA显示MCA、PCA和BA的狭窄完全消退。

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