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与特发性毛细血管渗漏综合征相关的广泛性白质脑病:一例伴有神经病理学表现的病例报告

Extensive leukoencephalopathy associated with idiopathic capillary leak syndrome: report of a case with neuropathology.

作者信息

Ohira Junichiro, Yoshimura Hajime, Takanashi Masashi, Yamashita Daisuke, Hara Shigeo, Ueno Yuji, Hattori Nobutaka, Kawamoto Michi, Kohara Nobuo

机构信息

Department of Neurology, Kyoto University Hospital, 606-8507, 54 Kawaharacho, Shogoin, Sakyo-ku, Kyoto, Japan.

Department of Neurology, Kobe City Medical Center General Hospital, 650-0047, 2-1-1 Minatojima-Minamimachi, Chuou-ku, Kobe, Hyogo, Japan.

出版信息

Neurol Sci. 2021 May;42(5):2095-2098. doi: 10.1007/s10072-020-05000-5. Epub 2021 Jan 7.

Abstract

INTRODUCTION

Idiopathic systemic capillary leak syndrome (ISCLS) is a rare cryptogenic disorder characterized by recurrent hemoconcentration, hypoalbuminemia, edema, and hypotension due to extravascular fluid leakage. This is the first report that details uncommon extensive leukoencephalopathy caused by ISCLS upon a neuropathological investigation.

CASE REPORT

A 68-year-old female had recurrent episodes of hemoconcentration, hypoalbuminemia, and generalized edema and was diagnosed with ISCLS. After 9 years, brain magnetic resonance imaging (MRI) incidentally revealed extensive leukoencephalopathy without neurological deficits. Thorough examinations ruled out other disorders, and the cerebral involvement due to ISCLS was finally diagnosed. Three years later, she developed an acute-onset coma and status epilepticus together with hypotension and hemoconcentration, which were compatible with ISCLS recurrence. Electroencephalogram and MRI were correlated with a seizure arising from the left hemisphere. Extensive leukoencephalopathy did not show notable changes for 3 years. Although treatment for ISCLS recurrence temporally improved hemoconcentration and consciousness, consciousness worsened again by marked edema of the left hemisphere, and she died of cerebral herniation. A brain autopsy revealed straggly perivascular plasma leakage around the small vessels of the deep white matter, which supported that the leukoencephalopathy was caused by ISCLS. Widespread myelin pallor and decreased axonal density with sparse astrogliosis and microgliosis were observed in the cerebral white matter and corresponded with a chronic change in the MRI.

CONCLUSION

Current radiological and pathological observations revealed that frequent perivascular leakages could cause chronic leukoencephalopathy, were linked with the development of systemic capillary leakage in ISCLS, and provided insights into the mysterious pathophysiology.

摘要

引言

特发性系统性毛细血管渗漏综合征(ISCLS)是一种罕见的隐源性疾病,其特征为因血管外液体渗漏导致反复出现血液浓缩、低白蛋白血症、水肿和低血压。这是首份在神经病理学调查中详细描述由ISCLS引起的罕见广泛性白质脑病的报告。

病例报告

一名68岁女性反复出现血液浓缩、低白蛋白血症和全身性水肿,被诊断为ISCLS。9年后,脑部磁共振成像(MRI)偶然发现广泛性白质脑病但无神经功能缺损。全面检查排除了其他疾病,最终确诊为ISCLS所致的脑部病变。三年后,她出现急性昏迷和癫痫持续状态,同时伴有低血压和血液浓缩,这与ISCLS复发相符。脑电图和MRI显示癫痫发作源于左半球。广泛性白质脑病3年内未出现明显变化。尽管对ISCLS复发的治疗暂时改善了血液浓缩和意识,但因左半球明显水肿意识再次恶化,她死于脑疝。脑部尸检显示深部白质小血管周围有散在的血管周围血浆渗漏,这支持白质脑病是由ISCLS引起的。在脑白质中观察到广泛的髓鞘苍白、轴突密度降低,伴有稀疏的星形胶质细胞增生和小胶质细胞增生,这与MRI的慢性变化相符。

结论

目前的放射学和病理学观察表明,频繁的血管周围渗漏可导致慢性白质脑病,与ISCLS中系统性毛细血管渗漏的发生有关,并为其神秘的病理生理学提供了见解。

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