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Castleman病伴蛛网膜下腔出血相关的脑动脉炎:两例报告

Cerebral angiitis associated with subarachnoid hemorrhage in Castleman's disease: report of two cases.

作者信息

Tanaka Jun, Fujita Atsushi, Hosoda Kohkichi, Kohmura Eiji

机构信息

Department of Neurosurgery, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe, 650-0017, Japan.

出版信息

BMC Neurol. 2016 May 4;16:60. doi: 10.1186/s12883-016-0585-4.

Abstract

BACKGROUND

Multicentric Castleman's disease (MCD) is characterized by a systemic lymphoproliferative disorder affecting systemic lymph nodes. Cerebrovascular involvements have rarely been reported, and to our knowledge, cerebral angiitis causing subarachnoid hemorrhage (SAH) in patients with Multicentric Castleman's disease (MCD) has not been previously described.

CASE PRESENTATION

We identified two cases of MCD with SAH who were receiving immunosuppressive therapy with low dose prednisolone. Both patients presented with sudden-onset headache and were diagnosed with cortical SAH in the sulci by a computed tomography scan. Digital subtraction angiography showed segmental stenosis in the peripheral area of the middle cerebral artery. In both cases, cerebral angiitis causing SAH induced by a systemic inflammatory condition and elevated levels of interleukin (IL) -6 were suspected and resolved over a period of several months.

CONCLUSION

Our cases highlight the clinical diversity of the potential causes of cerebral angiitis and expand the association of MCD and cortical SAH; however, cortical SAH patients have a more favorable outcome than aneurysmal SAH patients.

摘要

背景

多中心Castleman病(MCD)的特征是一种影响全身淋巴结的系统性淋巴增殖性疾病。脑血管受累情况鲜有报道,据我们所知,此前尚未描述过多中心Castleman病(MCD)患者发生导致蛛网膜下腔出血(SAH)的脑血管炎。

病例报告

我们发现两例患有SAH的MCD患者正在接受低剂量泼尼松龙免疫抑制治疗。两名患者均突发头痛,经计算机断层扫描诊断为脑沟皮质SAH。数字减影血管造影显示大脑中动脉周边区域节段性狭窄。在这两例病例中,均怀疑由全身炎症状态和白细胞介素(IL)-6水平升高引起的导致SAH的脑血管炎,并在数月内得到缓解。

结论

我们的病例突出了脑血管炎潜在病因的临床多样性,并扩展了MCD与皮质SAH之间的关联;然而,皮质SAH患者的预后比动脉瘤性SAH患者更有利。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b98c/4857415/e6c9b482c8ad/12883_2016_585_Fig1_HTML.jpg

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