DiMaio D J, Cohen P R
Department of Pathology, University of Texas--Houston Medical School, 77030, USA.
J Am Acad Dermatol. 1998 Feb;38(2 Pt 1):243-7. doi: 10.1016/s0190-9622(98)70599-7.
Focal acantholytic dyskeratosis is a distinctive histologic pattern characterized by (1) suprabasilar clefts around preserved papillae, (2) acantholytic and dyskeratotic cells at all levels of the epidermis, and (3) hyperkeratosis and parakeratosis. These histologic changes have been observed as an incidental finding in a variety of skin lesions.
Our purpose was to identify the lesions associated with incidental focal acantholytic dyskeratosis.
Eight specimens containing incidental focal acantholytic dyskeratosis were retrospectively evaluated, and the published literature describing lesions with incidental focal acantholytic dyskeratosis was reviewed.
The ages of the eight patients ranged from 29 to 53 years. Incidental focal acantholytic dyskeratosis was seen in nevi with architectural disorder (four lesions), scars (two lesions), a ruptured follicle (one lesion), and a seborrheic keratosis (one lesion). Incidental focal acantholytic dyskeratosis was either present in the "clinically normal-appearing" skin adjacent to the lesion (five lesions) or within the lesion (three lesions). Twenty-one additional cases of incidental focal acantholytic dyskeratosis have previously been reported.
Incidental focal acantholytic dyskeratosis has been described in benign and malignant epithelial lesions, fibrohistiocytic lesions, inflammatory lesions, melanocytic lesions, and miscellaneous lesions. This pathologic change was observed either within the actual lesion or in the immediately adjacent epithelium. The cause of this clinically benign, microscopically intriguing condition remains to be determined.
局灶性棘层松解性角化不良是一种独特的组织学模式,其特征为:(1)围绕保留乳头的基底上裂隙;(2)表皮各层均有棘层松解和角化不良细胞;(3)角化过度和不全角化。这些组织学改变在多种皮肤病变中作为偶然发现被观察到。
我们的目的是确定与偶然局灶性棘层松解性角化不良相关的病变。
回顾性评估8例含有偶然局灶性棘层松解性角化不良的标本,并复习已发表的描述有偶然局灶性棘层松解性角化不良病变的文献。
8例患者年龄在29至53岁之间。偶然局灶性棘层松解性角化不良见于结构紊乱的痣(4个病变)、瘢痕(2个病变)、破裂的毛囊(1个病变)和脂溢性角化病(1个病变)。偶然局灶性棘层松解性角化不良要么存在于病变旁“临床外观正常”的皮肤中(5个病变),要么存在于病变内(3个病变)。此前已报道另外21例偶然局灶性棘层松解性角化不良病例。
偶然局灶性棘层松解性角化不良已在良性和恶性上皮病变、纤维组织细胞病变、炎症性病变、黑素细胞病变及其他病变中被描述。这种病理改变在实际病变内或紧邻的上皮中被观察到。这种临床良性但显微镜下引人关注的情况的病因仍有待确定。