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视神经脊髓炎谱系疾病伴肺腺癌和导管内乳头状黏液性肿瘤。

Neuromyelitis optica spectrum disorder with lung adenocarcinoma and intraductal papillary mucinous neoplasm.

机构信息

Department of Neurology, Fourth Affiliated Hospital, School of Medicine, Zhejiang University, No. N1, Shangcheng Avenue, Yiwu, 322000, China.

Department of Neurology, Second Affiliated Hospital, School of Medicine, Zhejiang University, 88 Jiefang Road, Hangzhou, 310009, China.

出版信息

Mult Scler Relat Disord. 2019 Jul;32:77-80. doi: 10.1016/j.msard.2019.04.031. Epub 2019 May 3.

Abstract

Few cases reported the coexistence of tumors and neuromyelitis optica spectrum disorder (NMOSD), which is generally considered idiopathic. Here we describe a 61-year-old woman who developed anti-aquaporin-4 IgG positive myelitis with a pathologically-diagnosed lung adenocarcinoma and a radiologically-diagnosed intraductal papillary mucinous neoplasm. With corticosteroids and immunoglobulin in the acute phase and surgical resection of the lung adenocarcinoma, the patient recovered substantially. This case highlights the need for tumor screening in patients with NMOSD, especially those over 50 years old.

摘要

鲜有肿瘤合并视神经脊髓炎谱系疾病(NMOSD)的病例报告,NMOSD 一般被认为是特发性疾病。本研究报道了 1 例 61 岁女性,发生抗水通道蛋白 4(AQP4)抗体阳性的脊髓炎,经病理诊断为肺腺癌,影像学诊断为导管内乳头状黏液瘤。经急性期使用糖皮质激素和免疫球蛋白治疗以及肺腺癌的手术切除后,患者基本康复。该病例强调了 NMOSD 患者,尤其是 50 岁以上患者进行肿瘤筛查的必要性。

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