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Scoring Criteria for Autoimmune Bullous Diseases: Utility, Merits, and Demerits. 自身免疫性红斑疾病的评分标准:实用性、优点和缺点。
IF 1.9 Q3 DERMATOLOGY Pub Date : 2024-08-19 eCollection Date: 2024-09-01 DOI: 10.4103/idoj.idoj_611_23
Henry Tseng, Corey Stone, Dédée F Murrell

Background: Scoring systems play a crucial role in dermatology by providing objective measurements of disease severity, treatment efficacy, and outcome comparisons. In autoimmune blistering diseases (AIBDs), standardized scoring systems are essential for accurate evaluations; however, there is currently a lack of consensus on scoring methods.

Objective: This literature review explores scoring systems in AIBDs by tracing their development, addressing challenges, and highlighting their role in defining endpoints, regulatory considerations, and clinical trials.

Materials and methods: Existing scoring systems for AIBDs, such as the Pemphigus Disease Area Index, Autoimmune Bullous Skin Disorder Intensity Score, Pemphigus Oral Lesions Intensity Score, Oral Disease Severity Score, and Pemphigus Vulgaris Activity Score, are examined for their validity, reliability, and responsiveness. The Bullous Pemphigoid Disease Area Index for bullous pemphigoid is also discussed. The concept of minimal clinically important differences is explored to determine clinically significant improvements in disease severity.

Conclusion: This review provides a comprehensive understanding of the central role of scoring systems in dermatology and their implications for research and clinical practice in AIBDs.

背景:评分系统通过对疾病严重程度、治疗效果和结果比较进行客观测量,在皮肤病学中发挥着至关重要的作用。在自身免疫性水疱病(AIBDs)中,标准化评分系统对于准确评估至关重要;然而,目前在评分方法上还缺乏共识:本文献综述通过追溯AIBD评分系统的发展历程、探讨其面临的挑战以及强调其在终点定义、监管考虑和临床试验中的作用,对AIBD评分系统进行了探讨:研究了现有的AIBD评分系统,如丘疹性天疱疮疾病面积指数、自身免疫性大疱性皮肤病强度评分、丘疹性天疱疮口腔病变强度评分、口腔疾病严重程度评分和丘疹性天疱疮活动度评分,以了解其有效性、可靠性和响应性。此外,还讨论了针对大疱性类天疱疮的大疱性类天疱疮疾病面积指数。此外,还探讨了最小临床重要差异的概念,以确定疾病严重程度是否有显著的临床改善:本综述全面介绍了评分系统在皮肤病学中的核心作用及其对 AIBD 研究和临床实践的影响。
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引用次数: 0
A Comparative Study of the Efficacy of Intralesional Measles Mumps Rubella (MMR) Vaccine and Auto Implantation for the Treatment of Periungual and Palmoplantar Warts: A Randomized Controlled Trial. 麻疹腮腺炎风疹(MMR)疫苗鞘内注射与自动植入治疗掌周疣和掌跖疣疗效的比较研究:随机对照试验
IF 1.9 Q3 DERMATOLOGY Pub Date : 2024-08-16 eCollection Date: 2024-09-01 DOI: 10.4103/idoj.idoj_394_23
Ravindra Abusaria, Chinmai Yadav, Vinod Jain, Dilip Kachhawa, Pankaj Rao, Anand Lamoria

Background: Warts are benign epidermal proliferations, caused by infection of keratinocytes with human papillomavirus (HPV). Auto implantation and intralesional mumps, measles, and rubella (MMR) vaccine are novel methods of immunotherapy for treating periungual and palmoplantar warts. They act by stimulating the patient's immune system; this clears not only the local warts but also distant warts with lesser side effects.

Objective: We conducted this study to compare the efficacy and safety of both methods in treating periungual and palmoplantar warts.

Materials and methods: A total of 160 patients were randomly allocated into two groups of 80 patients. Group A was treated with 0.3 mL of intralesional MMR vaccine at an interval of 3 weeks or for a maximum of three sittings, and Group B was treated with auto implantation.

Results: At the end of therapy, the result was better in group A (MMR vaccine) as 86% of cases yielded an excellent response as compared to 71% in group B (auto implantation). The recurrence rate was 5% in group A and 4% in group B. There were no serious side effects in both groups with pain during injection (70%) in group A and swelling at the recipient site (8%) in group B being the most common side effect.

Conclusion: Both MMR and auto implantation had significant response rates. But MMR was faster and better.

背景:疣是表皮良性增生,由角质细胞感染人类乳头瘤病毒(HPV)引起。自体植入疗法和腮腺炎、麻疹和风疹(MMR)疫苗鞘内注射疗法是治疗毛周疣和掌跖疣的新型免疫疗法。它们通过刺激患者的免疫系统发挥作用,不仅能清除局部疣体,还能清除远处的疣体,而且副作用较小:我们开展了这项研究,以比较两种方法治疗毛周疣和掌跖疣的疗效和安全性:将 160 名患者随机分为两组,每组 80 人。A组采用0.3 mL麻风腮疫苗鞘内注射治疗,间隔3周或最多3次;B组采用自动植入治疗:治疗结束后,A 组(接种麻风腮疫苗)的疗效更好,86% 的病例获得了极佳反应,而 B 组(自动植入)只有 71%。两组均无严重副作用,最常见的副作用是注射时疼痛(A 组为 70%)和受体部位肿胀(B 组为 8%):结论:MMR 和自体脂肪植入术都有显著的反应率。结论:MMR 和自体脂肪移植都有明显的反应率,但 MMR 更快更好。
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引用次数: 0
A Retrospective Study of the Histopathological Spectrum of Erythema Nodosum Leprosum. 对结节性红斑组织病理学特征的回顾性研究
IF 1.9 Q3 DERMATOLOGY Pub Date : 2024-08-08 eCollection Date: 2024-09-01 DOI: 10.4103/idoj.idoj_952_23
Varniraj Patel, Rhea Ahuja, Sudheer K Arava, Sujay Khandpur, Neetu Bhari, Vishal Gupta, M Ramam

Background: There are no recent studies with a focus on the histopathology of erythema nodosum leprosum (ENL).

Objectives: To describe the histopathological spectrum of ENL.

Materials and methods: Digital records from the pathology department were searched, and 125 slides were included. The histopathologic findings were recorded using a pre-designed proforma.

Results: Several patterns were noted with the most common being a superficial and deep, perivascular and peri-appendageal, well-circumscribed dermal infiltrate that was seen in 70 (56.0%) biopsies. Other dermal patterns included a similar but loose infiltrate in 19 (15.2%) biopsies, diffuse dermal involvement in 9 (7.2%), top-heavy in 9 (7.2%), and bottom-heavy infiltrates in 12 (9.6%). Subcutaneous tissue was included in 107 biopsies. Extension of dermal infiltrates to the subcutis was noted in 71 (66.4%) biopsies and predominant involvement of the subcutis was noted in 6 (4.8%) biopsies, with lobular involvement in 60 (56.1%), septal involvement in 3 (2.8%), and septo-lobular involvement in 14 (13.1%). In 30 (28.0%) biopsies, the subcutaneous fat was uninvolved. The infiltrates contained neutrophils and foamy histiocytes in variable proportions, along with lymphocytes and plasma cells. Eosinophils were noted occasionally. Medium and/or small vessel vasculitis was noted in 11 (8.8%) biopsies. Fite-Faraco staining was available for 112 biopsies and revealed mainly fragmented and granular acid-fast bacilli (AFB) in 29 (25%) biopsies.

Limitations: Our study had a retrospective design; we could not compare the lesional age and clinical characteristics of patients with the histological features.

Conclusion: ENL is characterized by dermal infiltrates composed of foamy histiocytes and neutrophils in varying proportions arrayed in different dermal patterns. Extension of dermal infiltrates into the subcutis was frequent but absent in some. Predominant or exclusive involvement of the subcutis was rare. Vasculitis was noted in a small minority, while AFB were demonstrated in about a quarter of cases.

背景:最近还没有以麻风结节性红斑(ENL)的组织病理学为重点的研究:描述ENL的组织病理学特征:搜索病理科的数字记录,共纳入 125 张切片。使用预先设计的脓疱病表格记录组织病理学结果:结果:活组织病理结果显示了多种模式,其中最常见的是浅层和深层、血管周围和腱膜周围、环状真皮浸润,见于 70 例(56.0%)活组织病理切片。其他真皮形态包括 19 例(15.2%)活检中出现的类似但松散的浸润、9 例(7.2%)活检中出现的弥漫性真皮受累、9 例(7.2%)活检中出现的顶部重型浸润和 12 例(9.6%)活检中出现的底部重型浸润。107例活检中包括皮下组织。71份活检样本(66.4%)发现真皮浸润扩展至皮下,6份活检样本(4.8%)发现皮下主要受累,60份活检样本(56.1%)发现小叶受累,3份活检样本(2.8%)发现隔膜受累,14份活检样本(13.1%)发现隔叶受累。在 30 例(28.0%)活检中,皮下脂肪未受累。浸润中含有不同比例的中性粒细胞和泡沫组织细胞,以及淋巴细胞和浆细胞。偶尔会发现嗜酸性粒细胞。11例(8.8%)活检中发现了中血管和/或小血管炎。112份活检样本进行了Fite-Faraco染色,结果显示29份(25%)活检样本中的酸性无菌杆菌(AFB)主要呈碎片状和颗粒状:局限性:我们的研究采用回顾性设计,无法将患者的病变年龄和临床特征与组织学特征进行比较:ENL的特征是由泡沫组织细胞和中性粒细胞组成的真皮浸润,其比例不一,排列成不同的真皮形态。真皮浸润常扩展至皮下,但有些病例则没有皮下浸润。皮下主要或完全受累的情况很少见。少数病例出现血管炎,而约四分之一的病例显示出嗜酸性粒细胞。
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引用次数: 0
Blaschkoidal Lesion Over the Buttock in a Young Woman. 一名年轻女性臀部的布拉什克样皮损
IF 1.9 Q3 DERMATOLOGY Pub Date : 2024-08-08 eCollection Date: 2024-09-01 DOI: 10.4103/idoj.idoj_953_23
Hitaishi Mehta, Anish Thind, Debajyoti Chatterjee, Anuradha Bishnoi
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引用次数: 0
Intertriginous Xanthomas: Clues to Homozygous Familial Hypercholesterolemia. 三叉黄瘤:家族性高胆固醇血症的线索。
IF 1.9 Q3 DERMATOLOGY Pub Date : 2024-08-08 eCollection Date: 2024-09-01 DOI: 10.4103/idoj.idoj_60_24
Nikhil Mehta, Gouri Anand, Anamika Choudhary, Somesh Gupta
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引用次数: 0
Dermoscopic Features of Dermatitis Cruris Pustulosa et Atrophicans: A Retrospective Study from a Tertiary Care Center in South India. 脓疱性皮炎和萎缩性皮炎的皮肤镜特征:印度南部一家三级医疗中心的回顾性研究。
IF 1.9 Q3 DERMATOLOGY Pub Date : 2024-08-08 eCollection Date: 2024-09-01 DOI: 10.4103/idoj.idoj_855_23
Kanmani Indra Couppoussamy, Rajendra Devanda

Background: Dermatitis cruris pustulosa et atrophicans (DCPA) is a chronic superficial folliculitis that can cause scarring alopecia if left untreated. Hardly any studies are there describing the dermoscopic features of DCPA. Dermoscopy can be a useful tool for diagnosing DCPA in addition to clinical and histopathological features and for differentiating other conditions like superficial folliculitis, folliculitis decalvans, and pseudofolliculitis.

Aims/objectives: The aim of this retrospective study was to describe the dermoscopic features of 30 patients with DCPA at a tertiary care center in South India.

Materials and methods: A retrospective study of clinical and biopsy-proven cases of DCPA at a tertiary care center in South India.

Results: Thirty patients of DCPA of skin phototype IV or V were studied. Male preponderance of DCPA was noted in our study. Lower extremities 28 (93.3%) and upper extremities 2 (6.7%) were the common sites of involvement. The most common findings noted in dermoscopy were follicular-based pustules in 30 (100%) patients, follicular white structureless area in 16 (53.3%), perifollicular collarette of scales in 12 (40%), diffuse background dotted blood vessels in 12 (40%), and the absence of follicular orifices in 12 (40%). Other findings were yellow or hemorrhagic scales, perifollicular linear white lines, broken hair, and perifollicular dotted blood vessels. Pigmentary patterns observed were dark brown pigmentation, blue-grey globules, blue-grey dots, and accentuation of the pigmentary network.

Limitations: The limitations of the study were the retrospective nature of the study, the small sample size, and the lack of a comparison group.

Conclusion: The predominant dermoscopic features observed in our patients were follicular-based pustules, follicular white structureless areas, perifollicular collarette of scales, diffuse background dotted blood vessels, and the absence of follicular orifices. Vascular and pigmentary patterns were less commonly noted.

背景:脓疱性皮炎和萎缩性皮炎(DCPA)是一种慢性浅表性毛囊炎,如不及时治疗可导致瘢痕性脱发。目前几乎没有研究描述 DCPA 的皮肤镜特征。除了临床和组织病理学特征外,皮肤镜还是诊断 DCPA 的有用工具,可用于区分浅表毛囊炎、脱屑性毛囊炎和假性毛囊炎等其他疾病:这项回顾性研究旨在描述南印度一家三级医疗中心的 30 名 DCPA 患者的皮肤镜特征:对印度南部一家三级医疗中心的 DCPA 临床和活检证实病例进行回顾性研究:研究了30例皮肤光型为IV型或V型的DCPA患者。我们的研究发现,DCPA 患者中男性居多。常见受累部位为下肢 28 例(93.3%)和上肢 2 例(6.7%)。皮肤镜检查中最常见的发现是,30 名患者(100%)出现毛囊性脓疱,16 名患者(53.3%)出现毛囊白色无结构区,12 名患者(40%)出现毛囊周围鳞屑丘疹,12 名患者(40%)出现弥漫性背景点状血管,12 名患者(40%)没有毛囊口。其他发现有黄色或出血性鳞屑、毛囊周围线状白线、断发和毛囊周围点状血管。观察到的色素模式有黑褐色色素沉着、蓝灰色球状色素沉着、蓝灰色点状色素沉着和色素网络加重:该研究的局限性在于研究的回顾性、样本量小以及缺乏对比组:我们在患者身上观察到的主要皮肤镜特征是以毛囊为基础的脓疱、毛囊白色无结构区、毛囊周围鳞屑丘疹、弥漫性背景点状血管以及无毛囊口。血管和色素斑较少见。
{"title":"Dermoscopic Features of Dermatitis Cruris Pustulosa et Atrophicans: A Retrospective Study from a Tertiary Care Center in South India.","authors":"Kanmani Indra Couppoussamy, Rajendra Devanda","doi":"10.4103/idoj.idoj_855_23","DOIUrl":"10.4103/idoj.idoj_855_23","url":null,"abstract":"<p><strong>Background: </strong>Dermatitis cruris pustulosa et atrophicans (DCPA) is a chronic superficial folliculitis that can cause scarring alopecia if left untreated. Hardly any studies are there describing the dermoscopic features of DCPA. Dermoscopy can be a useful tool for diagnosing DCPA in addition to clinical and histopathological features and for differentiating other conditions like superficial folliculitis, folliculitis decalvans, and pseudofolliculitis.</p><p><strong>Aims/objectives: </strong>The aim of this retrospective study was to describe the dermoscopic features of 30 patients with DCPA at a tertiary care center in South India.</p><p><strong>Materials and methods: </strong>A retrospective study of clinical and biopsy-proven cases of DCPA at a tertiary care center in South India.</p><p><strong>Results: </strong>Thirty patients of DCPA of skin phototype IV or V were studied. Male preponderance of DCPA was noted in our study. Lower extremities 28 (93.3%) and upper extremities 2 (6.7%) were the common sites of involvement. The most common findings noted in dermoscopy were follicular-based pustules in 30 (100%) patients, follicular white structureless area in 16 (53.3%), perifollicular collarette of scales in 12 (40%), diffuse background dotted blood vessels in 12 (40%), and the absence of follicular orifices in 12 (40%). Other findings were yellow or hemorrhagic scales, perifollicular linear white lines, broken hair, and perifollicular dotted blood vessels. Pigmentary patterns observed were dark brown pigmentation, blue-grey globules, blue-grey dots, and accentuation of the pigmentary network.</p><p><strong>Limitations: </strong>The limitations of the study were the retrospective nature of the study, the small sample size, and the lack of a comparison group.</p><p><strong>Conclusion: </strong>The predominant dermoscopic features observed in our patients were follicular-based pustules, follicular white structureless areas, perifollicular collarette of scales, diffuse background dotted blood vessels, and the absence of follicular orifices. Vascular and pigmentary patterns were less commonly noted.</p>","PeriodicalId":13335,"journal":{"name":"Indian Dermatology Online Journal","volume":null,"pages":null},"PeriodicalIF":1.9,"publicationDate":"2024-08-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11444451/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142365120","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
An Unusual Case of Mpox Presenting with an Eschar-Like Lesion Over the Neck 一个罕见的颈部炭疽病例
IF 1.9 Q3 DERMATOLOGY Pub Date : 2024-07-24 DOI: 10.4103/idoj.idoj_757_23
Sindhu C. Bhaskaramenon, T. Anish, R. Sivaprasad, Sandhya George, Bindu Sudarsanan, Shubin Chenayil, Shinas Babu
{"title":"An Unusual Case of Mpox Presenting with an Eschar-Like Lesion Over the Neck","authors":"Sindhu C. Bhaskaramenon, T. Anish, R. Sivaprasad, Sandhya George, Bindu Sudarsanan, Shubin Chenayil, Shinas Babu","doi":"10.4103/idoj.idoj_757_23","DOIUrl":"https://doi.org/10.4103/idoj.idoj_757_23","url":null,"abstract":"","PeriodicalId":13335,"journal":{"name":"Indian Dermatology Online Journal","volume":null,"pages":null},"PeriodicalIF":1.9,"publicationDate":"2024-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141806969","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Primary Cutaneous Mucormycosis in Association with Diabetes Mellitus: A Rare Case 糖尿病合并原发性皮肤黏液瘤病:一个罕见病例
IF 1.9 Q3 DERMATOLOGY Pub Date : 2024-07-22 DOI: 10.4103/idoj.idoj_902_23
V. Mendiratta, Damini Verma, Anjali Birla, Divya Jyoti, Smita Singh
{"title":"Primary Cutaneous Mucormycosis in Association with Diabetes Mellitus: A Rare Case","authors":"V. Mendiratta, Damini Verma, Anjali Birla, Divya Jyoti, Smita Singh","doi":"10.4103/idoj.idoj_902_23","DOIUrl":"https://doi.org/10.4103/idoj.idoj_902_23","url":null,"abstract":"","PeriodicalId":13335,"journal":{"name":"Indian Dermatology Online Journal","volume":null,"pages":null},"PeriodicalIF":1.9,"publicationDate":"2024-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141817086","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Pigmented Nodule on Leg in a Child 儿童腿上的色素结节
IF 1.9 Q3 DERMATOLOGY Pub Date : 2024-07-22 DOI: 10.4103/idoj.idoj_942_23
H. Mehta, Divya Bhatia, U. Saikia, Keshavmurthy Vinay, Sunil Dogra
{"title":"A Pigmented Nodule on Leg in a Child","authors":"H. Mehta, Divya Bhatia, U. Saikia, Keshavmurthy Vinay, Sunil Dogra","doi":"10.4103/idoj.idoj_942_23","DOIUrl":"https://doi.org/10.4103/idoj.idoj_942_23","url":null,"abstract":"","PeriodicalId":13335,"journal":{"name":"Indian Dermatology Online Journal","volume":null,"pages":null},"PeriodicalIF":1.9,"publicationDate":"2024-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141815701","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Repigmentation of Vitiligo Universalis after Starting Antitubercular Therapy 开始抗结核治疗后泛发性白癜风的色素再形成
IF 1.9 Q3 DERMATOLOGY Pub Date : 2024-07-22 DOI: 10.4103/idoj.idoj_923_23
Prakhar Srivastava, Prachi Srivastava, Niti Khunger
{"title":"Repigmentation of Vitiligo Universalis after Starting Antitubercular Therapy","authors":"Prakhar Srivastava, Prachi Srivastava, Niti Khunger","doi":"10.4103/idoj.idoj_923_23","DOIUrl":"https://doi.org/10.4103/idoj.idoj_923_23","url":null,"abstract":"","PeriodicalId":13335,"journal":{"name":"Indian Dermatology Online Journal","volume":null,"pages":null},"PeriodicalIF":1.9,"publicationDate":"2024-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141815832","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Indian Dermatology Online Journal
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