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累及中枢神经系统的 Erdheim-Chester 病,伴椎动脉被膜独特表现。

Erdheim-Chester Disease Involving the Central Nervous System with the Unique Appearance of a Coated Vertebral Artery.

作者信息

Suzuki Hime, Wanibuchi Masahiko, Komatsu Katsuya, Akiyama Yukinori, Mikami Takeshi, Sugita Shintaro, Hasegawa Tadashi, Kaya Mitsunori, Takada Kohichi, Mikuni Nobuhiro

机构信息

Department of Neurosurgery, Sapporo Medical University School of Medicine, Hokkaido, Japan.

Department of Surgical Pathology, Sapporo Medical University School of Medicine, Hokkaido, Japan.

出版信息

NMC Case Rep J. 2016 Aug 29;3(4):125-128. doi: 10.2176/nmccrj.cr.2015-0331. eCollection 2016 Oct.

Abstract

Erdheim-Chester disease (ECD) is a rare non-Langerhans cell histiocytosis. It is characterized by multiple xanthogranulomatous masses throughout the body, predominantly in the tibia. One of the characteristic radiological findings of the lesions associated with ECD is a "coated artery," which is often observed in the aorta. Although approximately one-fourth of ECD cases involve the central nervous system (CNS), an intracranial-coated artery has only been reported in four cases. We report a case of ECD that involves the CNS and has the unique appearance of a coated vertebral artery (VA). These tumors entirely encase the bilateral VAs without stenosis and are attached to the dura. Cranial magnetic resonance imaging also showed multiple extra-axial tumors in the cavernous sinus, the frontal convexity, and the orbital cavity. Further investigation revealed additional extracranial lesions around the cervical carotid artery, at the bilateral tibia, and at the elbow joint. A biopsy of the cervical and tibial lesions confirmed ECD. Steroid therapy resulted in a month-long improvement of preoperative symptoms. However, the patient's condition gradually progressed and he died of pneumonia 1 year after ECD diagnosis. The encasement of the intracranial artery by the tumor without stenosis and the dural attachment suggest ECD, which requires whole body investigation.

摘要

厄尔德海姆-切斯特病(ECD)是一种罕见的非朗格汉斯细胞组织细胞增多症。其特征是全身多处出现黄色瘤样肿块,主要位于胫骨。与ECD相关的病变的特征性影像学表现之一是“包绕动脉”,常在主动脉中观察到。尽管约四分之一的ECD病例累及中枢神经系统(CNS),但颅内包绕动脉仅在4例中被报道过。我们报告1例累及CNS且具有包绕椎动脉(VA)独特表现的ECD病例。这些肿瘤完全包绕双侧VA而无狭窄,并附着于硬脑膜。头颅磁共振成像还显示海绵窦、额叶凸面和眶腔内有多个轴外肿瘤。进一步检查发现颈总动脉周围、双侧胫骨和肘关节处还有颅外病变。颈段和胫骨病变的活检证实为ECD。类固醇治疗使术前症状改善了1个月。然而,患者病情逐渐进展,在ECD诊断1年后死于肺炎。肿瘤无狭窄地包绕颅内动脉且附着于硬脑膜提示为ECD,这需要进行全身检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a7c/5386163/df12eac83027/nmccrj-3-125-g001.jpg

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