Borroni G, Brazzelli V, Vignati G, Zaccone C, Vignoli G P, Rabbiosi G
Department of Human and Hereditary Pathology, University of Pavia, Italy.
Am J Dermatopathol. 1992 Aug;14(4):304-9. doi: 10.1097/00000372-199208000-00003.
Acrodermatitis enteropathica (AE) is an autosomic recessive disorder affecting early infancy. Two cases of infantile AE with low plasma zinc levels are reported in which unusually prominent bullous and vesicobullous lesions were seen on the hands and feet, in addition to the more typical erythematous and scaly patches. Both psoriasiform and bullous lesions responded dramatically to oral zinc-sulfate supplementation. The histopathologic features of the bullous lesions of AE have not previously been fully examined. Histologically, the bullous lesions were characterized by intraepidermal vacuolar changes with massive ballooning, leading to intraepidermal vesiculation and blistering, with prominent epidermal necrosis and with no acantholysis. The bullous lesions did not arise on erythematous patchy lesions, but developed ex novo on unaffected skin. The histopathologic differential diagnosis with other bullous conditions is discussed.
肠病性肢端皮炎(AE)是一种影响婴幼儿的常染色体隐性疾病。本文报告了两例血浆锌水平低的婴儿AE病例,除了更典型的红斑和鳞屑斑外,在手足部位还出现了异常突出的大疱和水疱大疱性损害。银屑病样损害和大疱性损害对口服硫酸锌补充剂均有显著反应。此前尚未对AE大疱性损害的组织病理学特征进行全面研究。组织学上,大疱性损害的特征为表皮内空泡改变伴大量气球样变,导致表皮内水疱形成和大疱形成,伴有明显的表皮坏死且无棘层松解。大疱性损害并非发生于红斑性斑片状损害上,而是在未受累皮肤上新发出现。本文还讨论了与其他大疱性疾病的组织病理学鉴别诊断。