Biswas Sugata Narayan, Chakraborty Partha Pratim, Gantait Kripasindhu, Bar Chittaranjan
Department of Medicine, Midnapore Medical College & Hospital, Midnapore, West Bengal, India.
Department of Dermatology & Venereology, Midnapore Medical College & Hospital, Midnapore, West Bengal, India.
BMJ Case Rep. 2016 Apr 18;2016:10.1136/bcr-2016-215192. doi: 10.1136/bcr-2016-215192.
A 52-year-old man presented with high-grade fever, headache and painful vesicular skin rash involving the upper trunk and upper extremities, 8 days after initiation of chemotherapy with azathioprine (50 mg/day), which had been prescribed for acral vitiligo. There was neither any history of preceding respiratory or gastrointestinal tract infection, nor was the patient known to have malignancy, drug hypersensitivity, inflammatory bowel disease, vasculitis or other autoimmune disease. Laboratory results revealed leucocytosis with neutrophilia and markedly elevated acute phase reactants. Antinuclear antibody, perinuclear and cytoplasmic antineutrophil cytoplasmic antibody were found negative. Punch biopsy from skin of the upper trunk revealed dense neutrophilic infiltration of dermis without signs of vasculitis, suggestive of Sweet's syndrome. In view of the temporal association with azathioprine and absence of an obvious alternative aetiology, provisional diagnosis of drug-induced bullous Sweet's syndrome was made. Azathioprine was discontinued and high-dose oral prednisolone initiated. The response was dramatic with resolution of skin lesions within 72 h without further recurrence at fourth week of follow-up.
一名52岁男性,在开始使用硫唑嘌呤(50毫克/天)进行化疗8天后,出现高热、头痛以及累及上躯干和上肢的疼痛性水疱性皮疹。硫唑嘌呤是因肢端白癜风而开具的。患者既无先前呼吸道或胃肠道感染史,也无恶性肿瘤、药物过敏、炎症性肠病、血管炎或其他自身免疫性疾病史。实验室检查结果显示白细胞增多伴中性粒细胞增多,急性期反应物显著升高。抗核抗体、核周型和胞质型抗中性粒细胞胞质抗体均为阴性。上躯干皮肤的打孔活检显示真皮有密集的中性粒细胞浸润,无血管炎迹象,提示为Sweet综合征。鉴于与硫唑嘌呤存在时间关联且无明显的其他病因,初步诊断为药物性大疱性Sweet综合征。停用硫唑嘌呤并开始使用大剂量口服泼尼松龙。反应显著,皮肤病变在72小时内消退,随访第四周无进一步复发。