Li Yuchen, Nie Ruxiao, Cao Xianwei, Wan Chuan
Department of Dermatology, The First Affiliated Hospital of Nanchang University, Nanchang, People's Republic of China.
Clin Cosmet Investig Dermatol. 2023 Jan 10;16:67-70. doi: 10.2147/CCID.S393841. eCollection 2023.
Eosinophilic pustular folliculitis (EPF) is a rare, chronic, non-infectious inflammatory skin disease. Although the pathogenesis of EPF is unknown, eosinophilic pustular folliculitis may be associated with human immunodeficiency virus (HIV) infection, malignancies or syphilis. Here, we report the first case of EPF associated with syphilis, indicating that syphilis and EPF are correlated with T-helper type 2 immune responses. A 48-year-old man gradually developed erythema and pustules on the face, neck. Physical examination revealed multiple infiltrative red patches and plaques on the face, neck with tiny pustules. Skin biopsy results revealed that the dermal follicular sebaceous gland unit was infiltrated by a large number of neutrophils and eosinophils, forming eosinophilic microabscesses. Therefore, the patient was diagnosed with EPF associated with syphilis and received drug treatment. After the treatment, the pustules markedly decreased, leaving behind pigmentation. Furthermore, the patient is still being followed up.
嗜酸性脓疱性毛囊炎(EPF)是一种罕见的慢性非感染性炎症性皮肤病。尽管EPF的发病机制尚不清楚,但嗜酸性脓疱性毛囊炎可能与人类免疫缺陷病毒(HIV)感染、恶性肿瘤或梅毒有关。在此,我们报告首例与梅毒相关的EPF病例,表明梅毒和EPF与2型辅助性T细胞免疫反应相关。一名48岁男性面部、颈部逐渐出现红斑和脓疱。体格检查发现面部、颈部有多个浸润性红色斑块和斑片,伴有微小脓疱。皮肤活检结果显示真皮毛囊皮脂腺单位有大量中性粒细胞和嗜酸性粒细胞浸润,形成嗜酸性微脓肿。因此,该患者被诊断为与梅毒相关的EPF并接受了药物治疗。治疗后,脓疱明显减少,遗留色素沉着。此外,该患者仍在接受随访。