甲棘溶解性角化不良棘瘤的纵向赤甲。

IF 1.4 Q3 DERMATOLOGY Skin Appendage Disorders Pub Date : 2024-12-01 Epub Date: 2024-06-26 DOI:10.1159/000539465
Amal Chamli, Maryem Fazzeni, Imen Helal, Refka Frioui, Houda Hammami, Anissa Zaouak, Samy Fenniche
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引用次数: 0

摘要

简介:局灶性棘溶解性角化不良是一种独特的组织学模式,由Ackerman于1972年首次描述,包括表皮的局灶性基底上裂和表皮各级的角化不良细胞,并伴有角化过度和角化不全。1990年报道了首例甲下棘溶性角化不良性棘瘤(ADA)。这种趾下变异是非常罕见的。病例介绍:一个63岁的女性患者就诊纵向赤甲(LE)与远端骨关节溶解。皮肤镜检查显示LE伴少量碎片性出血,局部角化过度,游离边缘甲板变薄。组织病理学证实ADA的诊断。结论:ADA是一种罕见的肿瘤,可模拟多种炎症或肿瘤状况。据我们所知,这是文献中报道的第8例病例。这种不常见的实体可以模拟各种炎症或肿瘤状况。
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Acantholytic Dyskeratotic Acanthoma of the Nail Revealed by a Longitudinal Erythronychia.

Introduction: Focal acantholytic dyskeratosis is a distinctive histological pattern first described by Ackerman in 1972, consisting of focal suprabasal clefts in the epidermis and dyskeratotic cells at all levels of the epidermis with hyperkeratosis and parakeratosis. The first case of subungual acantholytic dyskeratosis acanthoma (ADA) was reported in 1990. This subungual variant is a very rare entity.

Case presentation: A 63-year-old female patient consulted for a longitudinal erythronychia (LE) associated with distal onycholysis. Dermoscopy showed LE with a few splinter hemorrhages, with localized hyperkeratosis and thinning of the nail plate at the free edge. Histopathology confirmed the diagnosis of ADA.

Conclusion: ADA is a rare tumor that could mimic various inflammatory or neoplastic conditions. To our knowledge, this is the eighth reported case in the literature. This uncommon entity could mimic various inflammatory or neoplastic conditions.

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CiteScore
2.00
自引率
10.00%
发文量
69
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