Department of Dermatology and Laboratory of Cell Biology, Ajou University School of Medicine, Yeongtong-Gu, Suwon, Korea.
Int J Dermatol. 2010 Feb;49(2):162-6. doi: 10.1111/j.1365-4632.2009.04209.x.
The histological findings associated with idiopathic guttate hypomelanosis (IGH) are hyperkeratosis, an atrophic epidermis, and flattened rete ridges. In addition, a decreased melanin content and reduced numbers of melanocytes are reported features. However, there are few recent studies that have been published on the histopathology of IGH and no comparative studies are available on the skin lesions and perilesional skin of patients with IGH.
The goals of this study were to identify the clinical and histopathological features of IGH and determine their correlation. We evaluated the clinical features and the histopathological differences between the skin lesions and the perilesional skin in patients with IGH.
A clinical survey was carried out on 47 patients with IGH. Specimens from skin lesions and perilesional skin were stained with hematoxylin-eosin, Fontana-Masson, MART-1, and NKI/beteb. We also studied the ultrastructure of four cases.
About 30% of the patients had their initial lesions prior to 20 years of age. The arm was the most commonly affected site (53%). Histologically, we found hyperkeratosis in 18 cases (38.3%), but epidermal atrophy was present in only five cases (10.6%), and flattened rete ridges in seven cases (14.9%) compared to the normal skin. Epidermal atrophy was more frequently found at nonsun-exposed areas. The IGH lesions demonstrated decreased melanin pigment and reduced numbers of melanocytes by NKI/beteb and MART-1. The ultrastructural evaluation showed degenerative melanocytes and decreased melanosomes. One specimen had normal melanocytes with decreased melanosomes.
Idiopathic guttate hypomelanosis is a disorder with multifactorial etiology; its pathogenesis may depend on various factors such as patient age and sun-exposure. Histopathologically, hyperkeratosis was frequently found; however, the other characteristic findings such as epidermal atrophy and flattened rete ridges were relatively rare.
特发性点状色素减退症(IGH)的组织学表现为角化过度、表皮萎缩和平坦的真皮乳头。此外,报道的特征还包括黑素含量减少和黑素细胞数量减少。然而,最近关于 IGH 组织病理学的研究很少,也没有关于 IGH 患者皮损和皮损周围皮肤的对比研究。
本研究旨在确定 IGH 的临床和组织病理学特征及其相关性。我们评估了 IGH 患者皮损和皮损周围皮肤的临床特征和组织病理学差异。
对 47 例 IGH 患者进行临床调查。皮损和皮损周围皮肤标本分别行苏木精-伊红、Fontana-Masson、MART-1 和 NKI/beteb 染色。我们还研究了 4 例的超微结构。
约 30%的患者在 20 岁之前出现首发皮损。手臂是最常见的受累部位(53%)。组织学上,我们发现 18 例(38.3%)有角化过度,但只有 5 例(10.6%)有表皮萎缩,7 例(14.9%)有平坦的真皮乳头,与正常皮肤相比。表皮萎缩在非暴露于阳光的部位更为常见。IGH 病变的 NKI/beteb 和 MART-1 显示黑素色素减少和黑素细胞数量减少。超微结构评估显示退行性黑素细胞和黑素小体减少。有一个标本的黑素细胞正常,但黑素小体减少。
特发性点状色素减退症是一种多因素病因的疾病;其发病机制可能取决于患者年龄和暴露于阳光等多种因素。组织病理学上,角化过度较为常见;然而,其他特征性表现,如表皮萎缩和平坦的真皮乳头,相对较少见。