Nomura K, Hashimoto I, Takahashi G, Ito M
Department of Dermatology, Aomori Prefectural Central Hospital, Higashi-Tsukurimichi 2-1-1, Aomori 030-0913, Japan.
Am J Dermatopathol. 2001 Jun;23(3):227-31. doi: 10.1097/00000372-200106000-00012.
Atrichia with papular lesions is a rare inherited skin disorder characterized by congenital atrichia with numerous papules. We describe a 27-year-old woman with atrichia, who had numerous papules on her scalp, nape, and axillae. Histologically, many keratinous cysts were seen in the middermis of a skin specimen from the nape. Electron microscopy showed that the developing keratinocytes in the walls of some cysts were rich in glycogen granules and had epidermoid keratinization with formation of keratohyaline granules and that laminated bodies were formed before keratinization. Langerhans cells were often seen in the walls of the cysts. In addition, a broad glassy vitreous layer surrounded the cyst wall. From these findings, it was suggested that the cystic lesions might have originated from immature or incomplete hair follicles. In particular, the structure of the cyst wall corresponded well to infundibular and/or isthmal portions of the outer root sheath of the hair follicle.
丘疹性秃发是一种罕见的遗传性皮肤病,其特征为先天性秃发并伴有大量丘疹。我们描述了一名27岁的秃发女性,其头皮、颈部和腋窝有大量丘疹。组织学上,从颈部获取的皮肤标本的中真皮层可见许多角质囊肿。电子显微镜显示,一些囊肿壁内正在发育的角质形成细胞富含糖原颗粒,具有表皮样角化,形成透明角质颗粒,且在角化前形成板层小体。囊肿壁内常可见朗格汉斯细胞。此外,囊肿壁周围有一层宽阔的玻璃样玻璃体层。根据这些发现,提示囊性病变可能起源于不成熟或不完全的毛囊。特别是,囊肿壁的结构与毛囊外根鞘的漏斗部和/或峡部非常吻合。