Deteriorating neurological symptoms of Degos disease despite the treatment with eculizumab and beraprost: A case report with detailed radiological findings

IF 0.4 Q4 CLINICAL NEUROLOGY Neurology and Clinical Neuroscience Pub Date : 2024-02-25 DOI:10.1111/ncn3.12801
Yamato Nakamura, Masanori Sawamura, Tatsuhiko Miyazaki, Aya Muramatsu, Makoto Suzuki, Hiroaki Yagi, Akinobu Hori, Yusuke Katsuyama, Hidefumi Yoshida, Kang Kim, Hiroshi Yamada, Ryosuke Takahashi, K. Harada
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引用次数: 0

Abstract

Degos disease is a rare vasculopathy with a poor prognosis. Here, we report a case of a 17‐year‐old Japanese male with Degos disease who exhibited progressive deterioration of neurological symptoms despite treatment with eculizumab and beraprost. We also report detailed radiological findings including brain magnetic resonance imaging and perfusion computed tomography, and hereby suggest the importance of the perfusion study in detecting early changes associated with Degos disease.
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尽管使用了依库珠单抗和贝前列素,德戈斯病的神经症状仍在恶化:附详细放射学检查结果的病例报告
Degos 病是一种罕见的血管病变,预后不良。在此,我们报告了一例患有 Degos 病的 17 岁日本男性患者,尽管他接受了依库珠单抗和贝前列素的治疗,但其神经症状仍呈进行性恶化。我们还报告了详细的放射学检查结果,包括脑磁共振成像和灌注计算机断层扫描,并在此提出灌注检查在检测与 Degos 病相关的早期病变方面的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
0.80
自引率
0.00%
发文量
76
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