Stoof T J, Starink T M, Nieboer C
Department of Dermatology, Free University Hospital, Amsterdam, The Netherlands.
J Am Acad Dermatol. 1989 May;20(5 Pt 2):924-7. doi: 10.1016/s0190-9622(89)70110-9.
We describe the case of a 38-year-old woman with adult-onset porokeratotic eccrine ostial and dermal duct nevus. The patient had a 9-year history of multiple keratotic papules and comedo-like pits on the medial border of the left foot. Light- and electron microscopic studies showed multiple cornoid lamella-like parakeratotic columns, which invariably were associated with hyperplastic eccrine ostia and distal sweat ducts. It is concluded that this entity, the first reported case of adult-onset porokeratotic eccrine ostial and dermal duct nevus, is a variant of the congenital form described previously by Abell and Read and by Aloi and Pippione.
我们描述了一例38岁成年发病的汗孔角化性小汗腺开口和真皮导管痣女性患者。患者左足内侧缘有多个角化性丘疹和粉刺样凹陷,病史长达9年。光镜和电镜研究显示多个鸡眼样板层样不全角化柱,这些柱状物总是与增生的小汗腺开口和远端汗腺导管相关。结论是,该病例作为首例成年发病的汗孔角化性小汗腺开口和真皮导管痣,是先前由阿贝尔和里德以及阿洛伊和皮皮奥内描述的先天性形式的一种变体。