Knipper J E, Hud J A, Cockerell C J
Department of Dermatology, University of Texas Southwestern Medical Center, Dallas 75235-9072.
Am J Dermatopathol. 1993 Feb;15(1):70-2. doi: 10.1097/00000372-199302000-00013.
A 57-year-old man developed hundreds of light brown, slightly atrophic papules, which were distributed diffusely over the back. Although clinically the lesions resembled seborrheic keratoses, histologic examination demonstrated changes of epidermolytic hyperkeratosis. The patient had neither a personal nor a family history of ichthyosiform disorders. The diagnosis of disseminated epidermolytic acanthoma was made in the context of the clinical, histologic, and historical features. Disseminated epidermolytic acanthoma is a rare condition that is readily diagnosable using clinicopathologic correlation; it is important to exclude it from other more serious conditions associated with epidermolytic hyperkeratosis.
一名57岁男性患者背部出现数百个浅棕色、轻度萎缩性丘疹,呈弥漫性分布。尽管这些损害在临床上类似脂溢性角化病,但组织学检查显示为表皮松解性角化过度改变。该患者既无鱼鳞病样疾病的个人史,也无家族史。根据临床、组织学及病史特点,诊断为播散性表皮松解性棘皮瘤。播散性表皮松解性棘皮瘤是一种罕见疾病,通过临床病理相关性检查易于诊断;将其与其他伴有表皮松解性角化过度的更严重疾病相鉴别很重要。