Clevy C, Brajon D, Combes E, Benzaquen M, Dales J-P, Koeppel M-C, Berbis P
Service de dermatologie, hôpital Nord, chemin des Bourrely, 13015 Marseille, France.
Service de dermatologie, hôpital Nord, chemin des Bourrely, 13015 Marseille, France.
Ann Dermatol Venereol. 2017 May;144(5):349-355. doi: 10.1016/j.annder.2015.06.026. Epub 2017 Mar 18.
The infectious causes of cutaneous vasculitis are well known and include streptococcal infections among others. Cases resulting from parasitic infection are less frequent. Scabies, which is currently on the increase, has only been reported in a few isolated cases. Herein, we report two noteworthy cases of profuse scabies complicated by cutaneous vasculitis.
Case 1: a 90-year-old woman, residing in a nursing home, was admitted to our dermatology department complaining of pruritus, present for one month, predominantly on the inside of the thighs and on the buttocks, associated with purpuric lesions on the lower limbs. A skin biopsy revealed leukocytoclastic vasculitis. A diagnosis of scabies was based on severe pruritus and hypereosinophilia and was confirmed by microscopic examination of the parasitology sample and the skin biopsy sample. Despite thorough investigation, no other cause of vasculitis could be found. Complete regression of the skin lesions was achieved with scabies treatment only, without any specific treatment for the vasculitis. Case 2: a 74-year-old man, living in a nursing home, was hospitalized for purpuric papules on the lower limbs, present for one month. Physical examination revealed linear patterns in the interdigital spaces associated with scabies evident on dermoscopic examination. The skin biopsy revealed signs of vasculitis. As in our first case, no aetiology of vasculitis was found and a favorable outcome was achieved by means of scabies treatment alone with no specific treatment for vasculitis.
Both of our patients presented scabies and vasculitis. In view of the absence of other causes of vasculitis and of the complete regression of lesions due to vasculitis without recurrence achieved with the scabies treatment alone, a diagnosis was made of scabietic vasculitis, probably as a result of cutaneous hypersensitivity reaction to humeral mediators.
皮肤血管炎的感染性病因众所周知,包括链球菌感染等。由寄生虫感染引起的病例较少见。目前呈上升趋势的疥疮仅在少数孤立病例中有报道。在此,我们报告两例值得关注的大量疥疮并发皮肤血管炎的病例。
病例1:一名90岁女性,居住在养老院,因瘙痒一个月入住我院皮肤科,瘙痒主要位于大腿内侧和臀部,伴有下肢紫癜性皮损。皮肤活检显示白细胞破碎性血管炎。疥疮的诊断基于严重瘙痒和嗜酸性粒细胞增多,并通过寄生虫学样本和皮肤活检样本的显微镜检查得以证实。尽管进行了全面检查,但未发现血管炎的其他病因。仅通过疥疮治疗,皮肤病变完全消退,未对血管炎进行任何特殊治疗。病例2:一名74岁男性,居住在养老院,因下肢紫癜性丘疹一个月入院。体格检查发现指间间隙有线性图案,皮肤镜检查显示有明显的疥疮。皮肤活检显示血管炎迹象。与我们的首例病例一样,未发现血管炎的病因,仅通过疥疮治疗取得了良好效果,未对血管炎进行特殊治疗。
我们的两名患者均表现为疥疮和血管炎。鉴于不存在血管炎的其他病因,且仅通过疥疮治疗血管炎病变完全消退且未复发,诊断为疥疮性血管炎,可能是由于对体液介质的皮肤过敏反应所致。