Rower J M, Carr R D, Lowney E D
Arch Dermatol. 1978 Jan;114(1):98-9.
Five cases of progressive cribriform and zosteriform hyperpigmentation are described. The following criteria were fulfilled: (1) uniformly tan cribriform macular pigmentation in a zosteriform distribution; (2) a histologic pattern that consisted of a mild increase in melanin pigment in the basal cell layer and complete absence of nevus cells; (3) no history of rash, injury, or inflammation to suggest postinflammatory hyperpigmentation; (4) onset well after birth with gradual extension; and (5) lack of other associated cutaneous or internal abnormalities. This appears to be a newly described entity, although it resembles a Becker's nevus without hypertrichosis or an typical café au lait spot. We believe that such progressive cribriform and zosteriform pigmentation is not uncommon.
本文描述了5例进行性筛状和带状色素沉着病例。符合以下标准:(1)呈带状分布的均匀棕褐色筛状斑状色素沉着;(2)组织学模式为基底细胞层黑色素轻度增加且无痣细胞;(3)无皮疹、损伤或炎症史提示炎症后色素沉着;(4)出生后很久发病且逐渐扩展;(5)无其他相关皮肤或内部异常。这似乎是一种新描述的疾病,尽管它类似于无多毛的贝克尔痣或典型的咖啡斑。我们认为这种进行性筛状和带状色素沉着并不罕见。