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抗中性粒细胞胞浆抗体相关血管炎的皮肤表现:211例回顾性研究,重点关注临床病理相关性及抗中性粒细胞胞浆抗体状态

Cutaneous manifestations of ANCA-associated vasculitis: a retrospective review of 211 cases with emphasis on clinicopathologic correlation and ANCA status.

作者信息

Shakshouk Hadir, Gibson Lawrence E

机构信息

Department of Dermatology, Mayo Clinic, Rochester, MN, USA.

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.

出版信息

Int J Dermatol. 2023 Feb;62(2):231-238. doi: 10.1111/ijd.16214. Epub 2022 May 16.

Abstract

BACKGROUND

ANCA-associated vasculitis (AAV) may present a wide array of dermatological manifestations. Patients may remain ANCA negative, rendering diagnosis challenging for dermatologists if they depend heavily on ANCA testing to either confirm or rule out AAV.

OBJECTIVE

To compare clinical and histopathological features of AAV patients with skin lesions who are ANCA positive versus those who are ANCA negative.

METHODS

Retrospective review of medical charts to identify patients diagnosed with AAV by clinical and pathologic criteria who also had cutaneous manifestations.

RESULTS

Search revealed that 211 out of 932 (23%) patients had cutaneous manifestations. Of those, 40/211 (20%) patients had persistently ANCA-negative serology. Eosinophilic granulomatosis with polyangiitis (EGPA) comprised the largest cohort. Palpable purpura was the most prominent clinical feature. The most common histopathological feature was leukocytoclastic vasculitis (LCV) in 19 (29%) specimens, extravascular granuloma in 14 (22%), followed by perivascular infiltrate in 12 (18%), with eosinophils in nine. In the ANCA-negative subgroup, perivascular infiltrate was more common followed by LCV but without statistically significant difference.

CONCLUSIONS

Diagnosis of AAV should not be based on ANCA testing alone since a considerable number of patients with cutaneous lesions may be ANCA negative. The clinical or histopathologic findings of skin lesions in this study group did not vary based on ANCA status.

摘要

背景

抗中性粒细胞胞浆抗体相关性血管炎(AAV)可能有多种皮肤表现。患者可能抗中性粒细胞胞浆抗体呈阴性,如果皮肤科医生严重依赖抗中性粒细胞胞浆抗体检测来确诊或排除AAV,那么诊断将具有挑战性。

目的

比较抗中性粒细胞胞浆抗体阳性与抗中性粒细胞胞浆抗体阴性的有皮肤病变的AAV患者的临床和组织病理学特征。

方法

回顾性查阅病历,以确定根据临床和病理标准诊断为AAV且有皮肤表现的患者。

结果

检索发现932例患者中有211例(23%)有皮肤表现。其中,40/211例(20%)患者抗中性粒细胞胞浆抗体血清学持续阴性。嗜酸性肉芽肿性多血管炎(EGPA)患者队列最大。可触及性紫癜是最突出的临床特征。最常见的组织病理学特征是19例(29%)标本中有白细胞破碎性血管炎(LCV),14例(22%)有血管外肉芽肿,其次是12例(18%)有血管周围浸润,9例有嗜酸性粒细胞浸润。在抗中性粒细胞胞浆抗体阴性亚组中,血管周围浸润更常见,其次是LCV,但无统计学差异。

结论

AAV的诊断不应仅基于抗中性粒细胞胞浆抗体检测,因为相当一部分有皮肤病变的患者抗中性粒细胞胞浆抗体可能为阴性。本研究组皮肤病变的临床或组织病理学表现不因抗中性粒细胞胞浆抗体状态而异。

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