糠疹青苔状的;在纳杰夫的16名伊拉克病人的临床和组织学评价的病例系列

Dr. Muhsin Aldhalimi, Mais Alsalihi
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摘要

背景:地衣样糠疹是一种罕见的丘疹鳞状疾病,病因不明。临床谱包括急性溃疡性变异体,急性地衣样松疹和变异体,慢性非溃疡性地衣样松疹(PLC)。第三种,更为罕见和侵袭性的形式,热性溃疡性糜烂性Mucha-Habermann病(FUMHD)也会发生。苔藓样糠疹通常是良性的,具有慢性病程,最终在数月至数年内自然消退。目的:本研究旨在评估纳杰夫Al-Sader医疗城近五年来患者的地衣样糠疹的临床和组织学情况。患者和方法:这是2017年1月至2021年11月期间在纳杰夫回顾性研究的病例系列。根据病历和在线档案对16例临床和组织学PL患者进行评估。对其石蜡包埋切片进行组织病理学检查并进行统计学分析。结果:对16例地衣样糠疹患者进行了评价;PLC比PLEVA更常见(14:2)。主要发生在人生第二个十年(37.5%)。诊断时年龄5 ~ 41岁,平均±SD为20.1±9.9岁,PLC(21.4±9.7)岁高于PLEVA(11±7)岁。女性在PLC中多于男性(9:5),因为只有两个报告的PLEVA病例是男性。皮肤光型III是IV型的两倍(11:5)。城镇患者多于农村患者。发病高峰为2020年(31.25%),其次为2021年(18.75%)。然而,临床和组织病理学特征是经典的,可与已发表的文献相媲美。结论:PL多见于青壮年;PLC以女性为主,PLEVA以男性为主。患有皮肤光型III型的患者城市多于农村。
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Pityriasis Lichenoides; A Case Series With Clinical And Histological Evaluation In A Sample Of Sixteen Iraqi Patients In Najaf
Background: Pityriasis lichenoides is an uncommon papulosquamous disorder of an unknown etiology. The clinical spectrum consists of an acute ulcerative variant, pityriasis lichenoides et varioliformis acuta (PLEVA), and a chronic, non-ulcerative variant, pityriasis lichenoides chronica (PLC). A third, much more rare and aggressive form, febrile ulceronecrotic Mucha–Habermann disease (FUMHD), also occurs. Pityriasis Lichenoides is often benign, with a chronic course and with eventual spontaneous resolution over months to years. Objectives: The current study aims to evaluate the pityriasis lichenoides among patients attending Al-Sader medical city, Najaf, in the last five years, clinically and histologically. Patients and method: This is a case series performed retrospectively over the period from January 2017 through November 2021, in Najaf. Sixteen patients with clinical and histological PL were evaluated according to their medical records and online archives. A histopathological revision of their paraffin-embedded sections was also performed and statistically analyzed. Results: Sixteen patients with pityriasis lichenoides were evaluated; PLC was more common than PLEVA (14:2). PL mainly affects people in the second decade of life (37.5%). The age at the time of diagnosis ranged from 5 to 41 years, with a mean ±SD of 20.1± 9.9 years, which was higher for PLC (21.4±9.7) years than for PLEVA (11±7) years. Females outnumber males in PLC (9:5) as the only two reported cases of PLEVA were males. The skin phototype III was double that of type IV (11:5). More urban patients than rural patients were presented. The cases peak was in 2020 (31.25%), followed by 2021 (18.75). However, the clinical and histopathological features were classic and comparable to the published literature. Conclusion:  PL is a disease predominant among young adults; more females were affected by PLC, while males were predominantly affected by PLEVA. More patients, who were more urban than rural, with skin phototype III were affected.  
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