Ständer S, Rütten A, Metze D
Universitäts-Hautklinik der Westfälischen Wilhelms-Universität Münster.
Hautarzt. 2001 Jun;52(6):533-6. doi: 10.1007/s001050000114.
Familial dyskeratotic comedones is a rare autosomal dominant genodermatosis. In childhood or adolescence disseminated keratotic papules develop and gradually increase in number with time. The isolated papules show a central keratotic plug which tends to recur after extraction. Pruritus and occasional inflammation are the only symptoms. The lesions appear on the extremities, and less frequently on the trunk and the face. About half of the patients have a history of acne vulgaris. The histologic picture is highly characteristic and shows a deep invagination of an acantholytic and dyskeratotic epidermis with prominent cornification. Familial dyskeratotic comedones are generally refractory to any therapy. We report on two sisters with familial dyskeratotic comedones successfully treated by CO2-laser therapy.
家族性角化不良性粉刺是一种罕见的常染色体显性遗传性皮肤病。在儿童期或青春期,会出现播散性角化丘疹,且随着时间推移数量逐渐增多。孤立的丘疹有一个中央角化栓,拔除后容易复发。瘙痒和偶尔的炎症是仅有的症状。皮损出现在四肢,较少出现在躯干和面部。大约一半的患者有寻常痤疮病史。组织学表现具有高度特征性,显示棘层松解和角化不良的表皮有深凹陷,伴有明显的角化。家族性角化不良性粉刺通常对任何治疗都难治。我们报告了两例通过二氧化碳激光治疗成功治愈的家族性角化不良性粉刺姐妹。