Mudroch Steven M, Rohan Craig, Conger Nicholas G, Lindholm David A
Department of Medicine, Wright-Patterson Medical Center, Wright-Patterson Air Force Base, USA.
Department of Medicine, Wright State University, Dayton, USA.
Cureus. 2020 Sep 9;12(9):e10330. doi: 10.7759/cureus.10330.
Acute febrile neutrophilic dermatosis, or Sweet syndrome, is a rare disorder associated with medications, underlying malignancy, or systemic inflammatory conditions. We present the case of a 71-year-old male living with well-controlled human immunodeficiency virus (HIV) on antiretroviral therapy, who presented with multiple painful, pseudo-vesicular, almost-necrotic appearing papules on his bilateral palms in the setting of constitutional symptoms and altered mental status. Biopsy of his palmar lesions revealed a dense, diffuse, dermal neutrophilic infiltrate consistent with Sweet syndrome. Infectious, rheumatologic, and oncologic work-up was negative. He was treated initially with intravenous immunoglobulin, prednisone, and dapsone; and he was continued on suppressive dapsone. He responded well clinically, but he relapsed multiple times in the setting of medication non-adherence before his ultimate diagnosis with sarcoidosis. A review of the literature of persons living with HIV and diagnosed with Sweet syndrome reveals no clear clinical association between the two despite plausible pathologic mechanisms. Patients living with HIV who are diagnosed with Sweet syndrome should be evaluated thoroughly for potential etiologies; the search for the underlying etiology of Sweet syndrome should go beyond their diagnosis of HIV.
急性发热性嗜中性皮病,即斯威特综合征,是一种与药物、潜在恶性肿瘤或全身性炎症性疾病相关的罕见病症。我们报告了一例71岁男性病例,该患者接受抗逆转录病毒治疗,其人类免疫缺陷病毒(HIV)病情得到良好控制,在出现全身症状和精神状态改变的情况下,双侧手掌出现多个疼痛性、假水疱性、几乎呈坏死样的丘疹。对其手掌病变进行活检,结果显示密集、弥漫性的真皮嗜中性粒细胞浸润,符合斯威特综合征。感染性、风湿性和肿瘤学检查均为阴性。他最初接受静脉注射免疫球蛋白、泼尼松和氨苯砜治疗;之后继续使用氨苯砜进行抑制性治疗。他在临床上反应良好,但在最终诊断为结节病之前,因未坚持服药多次复发。对已诊断为斯威特综合征的HIV感染者的文献回顾显示,尽管存在合理的病理机制,但两者之间没有明确的临床关联。被诊断为斯威特综合征的HIV感染者应全面评估潜在病因;对斯威特综合征潜在病因的排查不应局限于HIV诊断。