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伴有 TS-HDS、FGFR-3 或 Plexin D1 抗体的小纤维神经病中小血管炎或滤泡周围炎。

Small-Vessel Vasculitis or Perifolliculitis in Small-Fiber Neuropathy With TS-HDS, FGFR-3, or Plexin D1 Antibodies.

机构信息

Department of Neurology, Henry Ford Health, Detroit, MI.

Department of Neurology, Honor Health, Phoenix, AZ; and.

出版信息

J Clin Neuromuscul Dis. 2024 Dec 1;26(2):63-69. doi: 10.1097/CND.0000000000000492.

Abstract

INTRODUCTION

Small-fiber neuropathy (SFN) is highly prevalent but often idiopathic. TS-HDS, FGFR-3, and Plexin D1 autoantibodies (seropositive) may be present in more than 40% of idiopathic cases. Another autoimmune biomarker is a non-length-dependent (NLD) skin biopsy pattern. Our goal was to demonstrate that small-vessel vasculitis and perifolliculitis (inflammation) on skin biopsies are additional biomarkers.

METHODS

All pure SFN skin biopsy reports were reviewed for inflammation, and their charts were examined for other relevant history.

RESULTS

Seven of 80 patients with pure SFN had inflammation (8.8%); 5 patients were female (71%) and 2 were male (29%); average age was 45 (16-67). All 7 patients with inflammation were seropositive (100%, P = 0.0495), and 6 patients (86%) had either NLD inflammation or NLD pathology (P = 0.0003).

DISCUSSION

Inflammation is present only in a small portion of punch biopsies, but may be another autoimmune SFN biomarker. It is strongly associated with seropositivity and NLD-pathology. Further studies are likely indicated to assess inflammation pathophysiology and immunotherapy responsiveness.

摘要

简介

小纤维神经病(SFN)患病率很高,但通常是特发性的。在超过 40%的特发性病例中可能存在 TS-HDS、FGFR-3 和 Plexin D1 自身抗体(血清阳性)。另一种自身免疫生物标志物是非长度依赖性(NLD)皮肤活检模式。我们的目标是证明小血管血管炎和毛囊周围炎(皮肤活检中的炎症)是其他生物标志物。

方法

回顾了所有 80 例单纯 SFN 皮肤活检报告中是否存在炎症,并检查了他们的图表以了解其他相关病史。

结果

80 例单纯 SFN 患者中有 7 例(8.8%)存在炎症;5 例为女性(71%),2 例为男性(29%);平均年龄为 45 岁(16-67 岁)。所有 7 例有炎症的患者均为血清阳性(100%,P = 0.0495),且 6 例(86%)患者存在 NLD 炎症或 NLD 病理学(P = 0.0003)。

讨论

炎症仅存在于一小部分打孔活检中,但可能是另一种自身免疫性 SFN 生物标志物。它与血清阳性和 NLD-病理学密切相关。可能需要进一步研究来评估炎症的病理生理学和免疫治疗反应。

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