Kopp Sandra A, High Whitney A, Green Justin J
University of Medicine and Dentistry of New Jersey--Robert Wood Johnson Medical School at Camden, NJ, USA.
Skinmed. 2012 Jul-Aug;10(4):254-6.
A 44-year-old woman with a medical history of chronic pain syndrome presented with a 3-day history of a painful "rash" that started on her face and spread to her legs. Further history revealed that she recently started a new medication, varenicline, 7 weeks prior to admission and had a long-standing history of intranasal cocaine use. Review of systems was significant for rhinitis, nasal congestion, joint pain, and a febrile episode 2 days prior to admission. Physical examination revealed centrally violaceous, tender, stellate, and retiform purpuric patches and plaques on her extremities, nasal dorsum, and cheeks. Approximately 1.0-centimeter tender purpuric nodules were noted on her bilateral second proximal interphalangeal joints. She was afebrile. Initial laboratory data revealed a mild leukopenia, normal serum urea nitrogen and creatinine without hematuria, and an elevated erythrocyte sedimentation rate. Further analysis showed a normal complement level, negative antinuclear antibody, human immunodeficiency virus, rapid plasma reagin, and hepatitis panel. Trace cryoglobenemia and a positive anti-streptolysin O were noted, along with a positive antineutrophil cytoplasmic antibody (c-ANCA) (> 8.0 U) and perinuclear antineutrophil cytoplasmic antibodies, or p-ANCA (1.5 U). The hypercoagulable workup was negative. A skin biopsy taken from the left thigh was consistent with leukocytoclastic vasculitis. After several weeks of high-dose oral prednisone taper, the patient's symptoms improved, but flared upon discontinuation. On follow-up, she admitted to frequent relapses of cocaine abuse and had developed tender purpuric plaques on her nose, ears, and extremities, some with ulcerations (Figure 1 and Figure 2). She also had significant edema and joint pain that limited her ambulation. Further evaluation revealed normal chest x-ray results; however, computed tomography of her sinuses demonstrated thickened maxillary sinuses consistent with subacute/ chronic sinusitis. She also developed hematuria. Mass spectrometry analysis ofhair and urine samples tested positive for cocaine and levamisole. A presumptive diagnosis of levamisole-induced Wegener's vasculitis was made. She was restarted on high-dose prednisone and methotrexate with improvement and advised to discontinue cocaine use, so as to avoid exposure to both substances.
一名有慢性疼痛综合征病史的44岁女性,出现了一种疼痛性“皮疹”,病程3天,始于面部,蔓延至腿部。进一步询问病史发现,她在入院前7周开始服用一种新药——伐尼克兰,并且有长期鼻内使用可卡因的病史。系统回顾显示,她有鼻炎、鼻充血、关节疼痛,入院前两天有发热发作。体格检查发现其四肢、鼻背和脸颊有中央呈紫色、压痛、星状和网状的紫癜斑和斑块。双侧第二近端指间关节处可见约1.0厘米压痛性紫癜结节。她无发热。初始实验室检查数据显示轻度白细胞减少,血清尿素氮和肌酐正常,无血尿,红细胞沉降率升高。进一步分析显示补体水平正常,抗核抗体、人类免疫缺陷病毒、快速血浆反应素和肝炎指标均为阴性。发现微量冷球蛋白血症和抗链球菌溶血素O阳性,同时抗中性粒细胞胞浆抗体(c-ANCA)(>8.0 U)和核周抗中性粒细胞胞浆抗体(p-ANCA)(1.5 U)阳性。高凝检查为阴性。从左大腿取的皮肤活检结果符合白细胞破碎性血管炎。经过数周大剂量口服泼尼松逐渐减量治疗后,患者症状有所改善,但停药后病情复发。随访时,她承认频繁复发可卡因滥用问题,鼻子、耳朵和四肢出现了压痛性紫癜斑块,有些伴有溃疡(图1和图2)。她还出现了明显的水肿和关节疼痛,限制了她的活动能力。进一步评估显示胸部X线检查结果正常;然而,鼻窦计算机断层扫描显示上颌窦增厚,符合亚急性/慢性鼻窦炎。她还出现了血尿。头发和尿液样本的质谱分析显示可卡因和左旋咪唑检测呈阳性。初步诊断为左旋咪唑诱发的韦格纳肉芽肿性血管炎。她重新开始使用大剂量泼尼松和甲氨蝶呤,病情有所改善,并被建议停止使用可卡因,以避免接触这两种物质。