Alorainy May, Alshaya Mohammed, Al-Rikabi Ammar, Ayesh Mohammed, Alsaif Fahad
College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Saudi Commission for Health Specialties, Riyadh, Saudi Arabia.
Case Rep Dermatol. 2017 Dec 18;9(3):259-264. doi: 10.1159/000485370. eCollection 2017 Sep-Dec.
Acrodermatitis continua of Hallopeau (ACH) is an uncommon inflammatory disease manifesting as sterile pustular eruption of the fingers and toes. The disease is of a chronic relapsing nature and is often refractory to treatment. With longstanding disease, osteitis with consequent bone resorption of the underlying phalanges can occur, leading to disability. While the incidence of ACH is rare in children, complications like osteolysis have not been reported previously in this age group. In this paper, we report the case of an 8-year-old boy with severe ACH complicated by bone resorption.
哈洛佩奥连续性肢端皮炎（ACH）是一种罕见的炎症性疾病，表现为手指和脚趾的无菌性脓疱疹。该疾病具有慢性复发性，且常常难以治疗。随着病情长期发展，可发生骨质炎，进而导致其下方指骨的骨质吸收，最终导致残疾。虽然ACH在儿童中的发病率很低，但此前尚未有该年龄组发生骨质溶解等并发症的报道。在本文中，我们报告了一例患有严重ACH并伴有骨质吸收的8岁男孩的病例。
