Gunawan Hendra, Zulfan Zulfan
Department of Dermatology and Venereology, Faculty of Medicine, Universitas Padjadjaran, Dr. Hasan Sadikin Hospital, Bandung, Indonesia.
Clin Cosmet Investig Dermatol. 2024 Jul 22;17:1687-1693. doi: 10.2147/CCID.S464192. eCollection 2024.
Wells' syndrome is a rare inflammatory skin disease characterized by pruritic erythematous lesions and cutaneous edema, often accompanied by eosinophilia. Parasitic infestations, such as toxocariasis and strongyloidiasis, can serve as triggers. However, Wells' syndrome associated with toxocariasis and strongyloidiasis has not been reported previously in Indonesia. Herein, we present a case of a 27-year-old male with a chief complaint of recurrent, pruritic, and painful erythematous rash on the right lower leg for 6 months, accompanied by fever and diarrhea. Physical examination showed cutaneous edema with erythematous macules and bullae on the affected leg. Peripheral blood eosinophilia was noted, and the histopathological analysis demonstrated flame figures, confirming the diagnosis of Wells' syndrome. A stool culture identified , confirming strongyloidiasis, and serological testing was positive for toxocariasis immunoglobulin G antibodies. The patient was treated with albendazole 400 mg twice daily for 3 weeks resulted in clinical improvement observed by the 14th day. The diverse clinical features of Wells' syndrome present a challenge to clinicians in making an accurate diagnosis, which typically hinges on histopathological assessment and identifying flame figures. Therefore, clinicopathological correlation is important to establish an accurate diagnosis.
韦尔斯综合征是一种罕见的炎症性皮肤病,其特征为瘙痒性红斑性皮损和皮肤水肿,常伴有嗜酸性粒细胞增多。寄生虫感染,如弓蛔虫病和类圆线虫病,可作为触发因素。然而,印度尼西亚此前尚未报道过与弓蛔虫病和类圆线虫病相关的韦尔斯综合征。在此,我们报告一例27岁男性病例,其主要症状为右小腿反复出现瘙痒性疼痛性红斑皮疹6个月,伴有发热和腹泻。体格检查发现患侧腿部有皮肤水肿,伴有红斑和大疱。外周血嗜酸性粒细胞增多,组织病理学分析显示有火焰状图形,确诊为韦尔斯综合征。粪便培养发现 ,确诊为类圆线虫病,血清学检测弓蛔虫病免疫球蛋白G抗体呈阳性。患者接受阿苯达唑400毫克每日两次,共3周治疗,第14天时临床症状有所改善。韦尔斯综合征多样的临床特征给临床医生做出准确诊断带来挑战,准确诊断通常取决于组织病理学评估和识别火焰状图形。因此,临床病理相关性对于准确诊断很重要。