无全身性疾病的中性荨麻疹性皮肤病:病例报告

IF 2.3 Q2 DERMATOLOGY Dermatology Reports Pub Date : 2024-01-30 DOI:10.4081/dr.2024.9756
Sukaina Al Haddad, Abdulrahman Alfawzan, Maisa A Alfalah, Manea Alharbi
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引用次数: 0

摘要

嗜中性荨麻疹性皮肤病(NUD)是一种不常见的疾病,人们对其了解不多。我们报告了一名 24 岁女性患者的病例,她患有持续性瘙痒和疼痛的荨麻疹斑块,对常规治疗无效。从组织病理学角度看,该病表现为血管周围和间质中性粒细胞浸润,伴有白细胞增生,但无血管炎或皮肤水肿的证据,与中性粒细胞性荨麻疹皮肤病一致。为排除潜在的自身免疫性疾病、自身炎症和门静脉系统疾病而进行的进一步检查结果均为阴性。此外,患者的皮肤糜烂对秋水仙碱和达泊松等多种治疗方法均无效,但对白细胞介素-1受体拮抗剂 Anakinra 的治疗有明显反应。根据文献综述,本文报告的病例是第二例具有 NUD 临床和病理特征但无全身性疾病的病例,也是第一例对秋水仙碱和地松治疗耐药,但对 Anakinra 有充分反应的 NUD 病例。
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Neutrophilic urticarial dermatosis without systemic disease: case report
Neutrophilic urticarial dermatosis (NUD) is an uncommon and not well understood disease. We report a 24-year-old female with persistent present with pruritic and painful urticarial plaques unresponsive to convential treatment. Histopathologically, it demonstrates a perivascular and interstitial neutrophilic infiltrate with leukocytoclasia without evidence of vasculitis or dermal edema consistent with neutrophilic urticarial dermatosis. Further investigations to rule out underlying autoimmune, autoinflammatory and gentic systemic disease were negative. Furthermore, the cutaneous eruption was resistant to multiple therapeutic interventions including colchicine and dapsone treatment, and show significant response to treatment with anakinra, interleukin-1 receptor antagonist. Based on literature review, the case reported here is the second case with clinical and pathologic features of NUD without systemic disease and the first case of NUD that showed resistant to colchicine and dapsone treatment, with adequate response to anakinra.
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来源期刊
Dermatology Reports
Dermatology Reports DERMATOLOGY-
CiteScore
1.40
自引率
0.00%
发文量
74
审稿时长
10 weeks
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