Cocaine-induced pyoderma gangrenosum with negative anti-neutrophil cytoplasmic antibodies: A case report

Q3 Medicine
R. Lim, Nicole A. Negbenebor, E. Lin, Sara D. Ragi, L. Robinson-Bostom, Cathy M Massoud
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引用次数: 0

Abstract

Cutaneous pyoderma gangrenosum (PG) is an ulcerating autoinflammatory neutrophilic dermatosis often associated with inflammatory bowel disease, hematologic diseases, or arthritis. PG secondary to systemic medications is less commonly reported. PG is a diagnosis of exclusion that requires investigation of other causes of cutaneous ulcers prior to final diagnosis. We herein describe a case of cocaine-induced PG with atypical features (recurrent ulcerations limited to the lower extremities and perinuclear anti-neutrophil cytoplasmic antibody negativity) following years of abstinence from cocaine. PG is a rare autoinflammatory neutrophilic dermatosis and a diagnosis of exclusion because of its nonspecific clinical presentation. Drug-induced PG is less common but presents an opportunity to further research the pathogenesis of PG. This unusual case reinforces that drug-induced PG may have non-classical features and may serve as an indicator of past or present substance abuse, allowing for patient education and counseling.
抗中性粒细胞胞浆抗体阴性的可卡因诱发坏疽性脓皮病1例
坏疽性皮肤脓皮病(PG)是一种溃疡性自身炎症性中性粒细胞皮肤病,常与炎症性肠病、血液病或关节炎有关。继发于全身性药物治疗的PG报道较少。PG是一种排除性诊断,需要在最终诊断前对皮肤溃疡的其他原因进行调查。我们在此报告一例可卡因诱导的PG,其不典型特征(复发性溃疡局限于下肢,核周抗中性粒细胞细胞质抗体阴性)是在多年戒除可卡因后发生的。PG是一种罕见的自身炎症性中性粒细胞性皮肤病,由于其非特异性临床表现而被排除。药物性PG不太常见,但为进一步研究PG的发病机制提供了机会。这一不寻常的病例强化了药物性PG可能具有非经典特征,可以作为过去或现在药物滥用的指标,允许患者接受教育和咨询。
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来源期刊
CiteScore
1.20
自引率
0.00%
发文量
2950
审稿时长
12 weeks
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