Psoriasis neurodermiformis, verrucous psoriasis, and psoriasiform keratosis: A clinicopathological evaluation

N. Patil, A. Bubna
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Abstract

Background: Psoriasis neurodermiformis (PN) and verrucous psoriasis (VP) are two distinct forms of psoriasis characterized by thickened plaques, whose proper description in most dermatologic texts is still lacking. Psoriasiform keratosis (PK) is a recently described clinical entity characterized by a solitary keratotic plaque whose microscopic findings simulate psoriasis. Aim: To compare and evaluate the clinical and histological profile of PN, VP and PK, and systematically characterize each of them. Settings and Design: This was a prospective, descriptive study done on a total of 51 patients, who were diagnosed with PN, VP and PK based on certain clinical criteria. The study was done at a teaching hospital in eastern India. Methods and Materials: The study was carried out on a total of 51 patients presenting with thickened psoriasiform plaques, who visited our outpatient department, over a period of 9 months. They were then carefully evaluated clinically (along with their demographic profile), followed by meticulous microscopic assessment. Each biopsy specimen was then categorically evaluated to enable a precise diagnostic conclusion. Statistical Analysis: As all values in our study were qualitative, they were expressed as numeric values and percentages. Results: Out of 51 patients, 18 were diagnosed as PN, 19 with VP and 14 with PK. PN demonstrated an equal gender distribution, whereas in VP and PK a male preponderance was apparent. History of past/present psoriasis was positive in only one patient diagnosed with VP. Intensity of pruritus was marked in 88.88%, 21.05% and 14.28% of patients with PN, VP and PK respectively. Dorsa of feet was the commonest site of involvement in PN and VP. In PK, the shin was the predominating site. VP presented clinically as mammillated, verrucous and crateriform phenotypes. PN and PK however, demonstrated single clinical patterns. Microscopically, none of the specimens satisfied all the 7 epidermal criteria set forth by Ackerman. In each slide Trozak’s histologic psoriasiform numeric score was >10. Conclusion: PN, VP and PK are certainly not as rare as previously considered. Mammillated VP closely mimics PN clinically. Crateriform VP is an extremely rare phenotypic expression encountered. Histological findings of papillomatosis, buttressing and anastomosing rete ridges and a dense dermal lymphocytic infiltrate point more in favor toward VP. Detecting solitary keratotic plaques with a psoriasiform histology should allow clinicians to consider the possibility of PK.
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牛皮癣神经性真皮样病,疣状牛皮癣和牛皮癣状角化病:临床病理评价
背景:神经性真皮样银屑病(PN)和疣状银屑病(VP)是两种不同形式的银屑病,其特征是斑块增厚,在大多数皮肤病学文献中仍然缺乏适当的描述。牛皮癣状角化病(PK)是最近描述的一种临床实体,其特征是孤立的角化斑块,其显微镜检查结果与牛皮癣相似。目的:比较和评价PN、VP和PK的临床和组织学特征,并对其进行系统表征。背景和设计:这是一项前瞻性描述性研究,共对51例患者进行了研究,这些患者根据一定的临床标准被诊断为PN, VP和PK。这项研究是在印度东部的一家教学医院进行的。方法与材料:本研究共对51例以增厚的牛皮癣样斑块就诊的门诊患者进行了为期9个月的研究。然后对他们进行仔细的临床评估(连同他们的人口统计资料),然后进行细致的显微镜评估。然后对每个活检标本进行分类评估,以获得准确的诊断结论。统计分析:由于本研究的所有数值均为定性,故均以数值和百分比表示。结果:51例患者中,PN 18例,VP 19例,PK 14例,PN的性别分布相同,而VP和PK的男性优势明显。过去/现在牛皮癣的历史是阳性的,只有一个患者诊断为副总裁。PN、VP和PK患者瘙痒程度分别为88.88%、21.05%和14.28%。足背是PN和VP最常见的受累部位。在PK中,胫骨是主要部位。VP临床表现为乳头状、疣状和样型。然而,PN和PK表现出单一的临床模式。显微镜下,没有一个标本符合Ackerman提出的所有7个表皮标准。在每张幻灯片中,Trozak的组织学银屑病数值评分>10。结论:PN、VP和PK并不像以前认为的那样罕见。乳头状VP在临床上与PN非常相似。样型VP是一种极为罕见的表型表达。组织学表现为乳头状瘤状病变,网状隆起和吻合,真皮淋巴细胞浸润点密集,更倾向于VP。检测具有牛皮癣样组织学的孤立性角化斑块应允许临床医生考虑PK的可能性。
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