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Pulse Therapy in Rituximab Era: A Retrospective Study of 124 Patients of Pemphigus from a Tertiary Care Center of South Rajasthan 利妥昔单抗时代的脉冲疗法:南拉贾斯坦邦一家三级医疗中心 124 例丘疹性荨麻疹患者的回顾性研究
Pub Date : 2024-07-01 DOI: 10.4103/cdr.cdr_21_23
A. Mittal, Rini Makhija, M. Meena, Manisha Balai, Lalit Kumar Gupta, S. Mehta
Pemphigus is a potentially life-threatening autoimmune blistering disease which characteristically affects skin and mucosae. Pulse therapy for the treatment of pemphigus has been in vogue for several years and considered better than conventional corticosteroids. This study was conducted to evaluate the efficacy and safety of pulse therapy in pemphigus patients treated over a period of 10 years. This retrospective study was based on medical records of Pemphigus patients treated at Department of Dermatology from January 2008 to December 2017. Diagnosis of pemphigus was made on clinical ground, Tzanck smear and histopathology of skin/mucous membrane lesions. Patients were put on DCP/DAP depending on the completion of family. A total of 124 patients were included in the study. Age of patients ranged from 18 years to 72 years with mean of 41.21±12.71 years. Amongst 124 patients, 114 (92%) had pemphigus vulgaris and 10 (8%) had pemphigus foliaceous. 89 patients received DCP and 35 patients received DAP therapy. Number of pulses received by patients in phase I ranged from 4 to 27, average being 8.16±4.63. 106 patients completed the phase I of which 83 completed the phase II. 54 patients had successfully completed phase III of which 22 are currently in phase IV and 28 patients have completed their five year follow up period and considered as cured. Pulse therapy is a cheap and easily available mode of therapy in treatment of pemphigus in India even in the present era of modern molecules like Rituximab. With pulse therapy, it is now possible to induce and maintain remission, and achieve cure, provided the patients strictly adhere to the prescribed schedule.
丘疹性荨麻疹是一种可能危及生命的自身免疫性水疱病,主要影响皮肤和黏膜。治疗丘疹性荨麻疹的脉冲疗法已流行数年,被认为优于传统的皮质类固醇激素。 这项研究旨在评估脉冲疗法在治疗丘疹性荨麻疹患者 10 年间的疗效和安全性。 这项回顾性研究基于 2008 年 1 月至 2017 年 12 月期间在皮肤科接受治疗的丘疹性荨麻疹患者的病历。丘疹性荨麻疹的诊断依据是临床依据、Tzanck涂片和皮肤/粘膜病变的组织病理学。患者根据家庭情况接受DCP/DAP治疗。 研究共纳入了 124 名患者。患者年龄从 18 岁到 72 岁不等,平均年龄为(41.21±12.71)岁。124 名患者中,114 人(92%)患有寻常型丘疹性荨麻疹,10 人(8%)患有叶状丘疹性荨麻疹。89 名患者接受了 DCP 治疗,35 名患者接受了 DAP 治疗。第一阶段患者接受的脉冲数从 4 到 27 不等,平均为 8.16±4.63。106 名患者完成了第一阶段的治疗,其中 83 名患者完成了第二阶段的治疗。54 名患者成功完成了第三阶段的治疗,其中 22 名患者目前处于第四阶段,28 名患者完成了五年的随访,被视为治愈。 在印度,脉冲疗法是治疗丘疹性荨麻疹的一种既便宜又容易获得的治疗模式,即使在利妥昔单抗等现代分子的时代也是如此。现在,只要患者严格遵守规定的时间表,脉冲疗法就有可能诱导和维持缓解,并达到治愈的目的。
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引用次数: 0
Clinical and Onychoscopic Nail Findings in Preschool Children: An Observational Study 学龄前儿童的临床和趾甲镜检查结果:观察研究
Pub Date : 2024-07-01 DOI: 10.4103/cdr.cdr_56_23
Ekalavya Bilkhiwal, Arun C Inamadar, Ajit B Janagond
Nail examination plays a critical role in dermatologic conditions. Children with nail changes involve fewer physician consultations. Nail signs in early childhood can indicate the presence of a syndrome or underlying systemic disorder. The aim of the study was to investigate the frequency of nail findings in patients under 5 years of age. The study involved 368 pediatric patients under the age of 5 years. It was an observational study conducted in dermatology, obstetrics and gynecology, and pediatric departments. A Dermlite handyscope FFH2 (×10 zoom) was used to magnify visible nail changes during a comprehensive nail examination. Out of 368 cases, 213 were male and 155 were female. The average age of the patients was 22.74 months (range: 0–60). Nail findings were observed in 130 (35.3%) patients. In the study, single nail changes were observed in 123 (33.42%), whereas multiple nail changes were seen in 5 (1.35%) patients. The most common clinical nail finding was white striations in 60 (16.3%) cases, followed by punctate leukonychia in 21 (5.7%), onychoschizia in 13 (3.5%), pseudohypertrophy of the hallux in 12 (3.3%), koilonychia in 7 (1.9%), Beau’s lines in 3 (0.8%), and subungual hematoma in 3 (0.8%) cases. Median canaliform nail dystrophy, Muehrcke’s lines, onychophagia, and pitting were found in only one case each (0.3%). Physiological nail findings were more prevalent than pathological ones. The use of an onychoscope facilitated a more precise identification of nail changes by highlighting their features.
指甲检查在皮肤病中起着至关重要的作用。有指甲变化的儿童就诊次数较少。幼儿期的指甲症状可能预示着存在某种综合征或潜在的全身性疾病。 这项研究的目的是调查 5 岁以下患者出现指甲病变的频率。 这项研究涉及 368 名 5 岁以下的儿科患者。这是一项在皮肤科、妇产科和儿科进行的观察性研究。在进行全面指甲检查时,使用 Dermlite handyscope FFH2(×10 变焦)放大可见的指甲变化。 在 368 例患者中,男性 213 例,女性 155 例。患者的平均年龄为 22.74 个月(0-60 个月)。有 130 名患者(35.3%)发现了指甲病变。研究发现,123 例(33.42%)患者的指甲出现单个病变,5 例(1.35%)患者的指甲出现多个病变。临床上最常见的指甲病变是白色条纹(60 例,占 16.3%),其次是点状白斑(21 例,占 5.7%)、甲沟炎(13 例,占 3.5%)、假性甲沟炎(12 例,占 3.3%)、甲沟炎(7 例,占 1.9%)、博氏线(3 例,占 0.8%)和甲下血肿(3 例,占 0.8%)。中线管状甲营养不良、Muehrcke's 纹、糜烂性甲沟炎和点状甲沟炎各仅发现一例(0.3%)。 生理性指甲病变比病理性指甲病变更常见。使用甲状镜可以突出指甲变化的特征,从而更准确地识别指甲变化。
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引用次数: 0
Scleredema in a Young Child: Response to Systemic Steroids 幼儿巩膜水肿:对全身性类固醇的反应
Pub Date : 2024-07-01 DOI: 10.4103/cdr.cdr_70_23
S. Murthy, Ullas Biradar, C. Raghuveer, Lakshmipathi Y Pattar
Scleredema is an uncommon fibromucinous connective tissue disease occurring frequently in adults but rarely in children. It is most commonly seen in postinfectious settings or linked to hematological disorders or diabetes. A 5-year-old male child presented with induration and thickening of the skin over the extremities, face, and neck. Clinical and histological features were consistent with scleredema. Various treatment modalities are available for scleredema. The patient responded well to systemic steroids. This case is being reported for its rare occurrence in young children.
巩膜水肿是一种不常见的纤维黏液结缔组织病,常发于成人,但很少发生在儿童身上。它最常见于感染后或与血液病或糖尿病有关。一名 5 岁男童四肢、面部和颈部皮肤出现压痕和增厚。临床和组织学特征与巩膜水肿一致。巩膜水肿有多种治疗方法。患者对全身性类固醇治疗反应良好。本病例因罕见于幼儿而被报道。
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引用次数: 0
Cydnidae Pigmentation: A Dermoscopic Case Series 蝶形花科色素沉着:皮肤镜病例系列
Pub Date : 2024-07-01 DOI: 10.4103/cdr.cdr_106_23
Shipra Agrawal, Shilpi Sharma
Insects can cause a variety of dermatological problems ranging from asymptomatic cutaneous pigmentation to life threatening anaphylaxis. The pigmentation caused by burrowing bug, is oval to bizarre in shape, brown-black in colour, seen mainly over exposed areas. There are handful of case reports describing the dermoscopic features of Cydnidae pigmentation. We have tried to summarise all the literature available on clinical and dermoscopic details of Cydnidae pigmentation.
昆虫可引起各种皮肤病,从无症状的皮肤色素沉着到危及生命的过敏性休克。钻地虫引起的色素沉着呈椭圆形至怪异形,呈棕黑色,主要出现在暴露部位。描述穴盘蝽色素沉着皮肤镜特征的病例报告屈指可数。我们试图总结所有关于恙虫病的临床和皮肤镜细节的文献。
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引用次数: 0
An Unusual Case Report of Iatrogenic Metrorrhagia and Hematochezia Following Itraconazole 伊曲康唑引起的先天性月经过多和血崩的罕见病例报告
Pub Date : 2024-07-01 DOI: 10.4103/cdr.cdr_25_23
Yashaswi Rai
Itraconazole is an effective triazole antimycotic drug that has a desirable pharmacokinetic profile to combat various fungal pathogens. It acts by inhibiting ergosterol biosynthesis in fungal cell membranes. Itraconazole is not totally selective toward Cytochrome P450 family 3 subfamily A member 4 (CYP450 3A4), but exhibits the most potent inhibition of CYP450 3A4. Thus, these drugs interfere with CYP450 3A4 proteins expressed in the liver, intestine, kidney, adrenals, ovary, and testis. We present a case report of metrorrhagia and hematochezia following intake of itraconazole, a commonly used azole drug against dermatophytic infection. This article strongly highlights eliciting menstrual history and gynecological- and surgical-related problems before prescribing itraconazole. Also, to be aware of the vaginal bleeding being the unusual side effects of itraconazole.
伊曲康唑是一种有效的三唑类抗真菌药物,具有理想的药代动力学特征,可用于抗击各种真菌病原体。它通过抑制真菌细胞膜上麦角甾醇的生物合成发挥作用。伊曲康唑对细胞色素 P450 家族 3 亚家族 A 成员 4(CYP450 3A4)没有完全的选择性,但对 CYP450 3A4 的抑制作用最强。因此,这些药物会干扰在肝、肠、肾、肾上腺、卵巢和睾丸中表达的 CYP450 3A4 蛋白。我们报告了一例服用伊曲康唑(一种常用的抗皮癣菌感染的唑类药物)后出现月经过多和血崩的病例。本文着重强调,在开具伊曲康唑处方前,应了解月经史以及妇科和外科相关问题。此外,还要注意阴道出血是伊曲康唑的异常副作用。
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引用次数: 0
Topical Tacrolimus and Pimecrolimus in Dermatology: An Overview 皮肤科外用他克莫司和吡美莫司:概述
Pub Date : 2024-07-01 DOI: 10.4103/cdr.cdr_121_23
A. Bubna
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引用次数: 0
Mucocutaneous Manifestations among Patients with Malignancies at a Tertiary Care Center in Maharashtra: A Cross-Sectional Study 马哈拉施特拉邦一家三级医疗中心恶性肿瘤患者的皮肤黏膜表现:一项横断面研究
Pub Date : 2024-07-01 DOI: 10.4103/cdr.cdr_84_22
S. Kachare, V. Belgaumkar, S. Pradhan
Malignant disorders are a leading cause of mortality and morbidity. Cutaneous manifestations may be presenting features of internal malignancies, leading to diagnosis of occult tumors, while others may occur as adverse reactions to therapeutic modalities. To classify cutaneous manifestations among patients with malignant disorders, document their clinical profile, and analyze them with respect to age, gender, type of malignancy, and treatment. One hundred twenty patients with proven malignancy presenting with mucocutaneous lesions were enrolled in the cross-sectional study. On the basis of history, clinical examination, investigations and skin biopsy, the lesions were classified as (1) Primary cutaneous malignancy, (2) Cutaneous metastasis, (3) Paraneoplastic syndromes, (4) Mucocutaneous manifestations not related to malignancies, (5) Adverse effects secondary to treatment modalities. One hundred twenty patients comprised 70 females (58.3%) and 50 males (41.7%). They were categorized as primary cutaneous malignancy (20.2%), hematological malignancies (15%), solid organ malignancy (50.9%), and gastrointestinal malignancies (5%). HIV seropositivity was seen in two patients (1.6%). Maximum belonged to Category 5 (60, 50%), of which 52 (86.7%) were adverse effects of chemotherapy with single patient showing radiation dermatitis and one patient in Category 3 (0.8%). Eleven patients showed cutaneous metastasis (9.1%), predominantly carcinoma breast. Clinically, primary cutaneous malignancies often presented as ulceronodular growths with squamous cell carcinoma being the most common histopathological type (30%). Anagen effluvium was the most common (35%) manifestation overall and in solid organ malignancies followed by melanonychia (16, 13.33%), cutaneous xerosis (9, 7.5%), and mucocutaneous hyperpigmentation (23, 19.16%). Mucocutaneous manifestations need prompt attention to facilitate timely diagnosis and improved outcomes.
恶性疾病是导致死亡和发病的主要原因。皮肤表现可能是内部恶性肿瘤的表现特征,从而导致隐匿性肿瘤的诊断,而其他皮肤表现则可能是治疗方法的不良反应。 对恶性疾病患者的皮肤表现进行分类,记录其临床特征,并根据年龄、性别、恶性肿瘤类型和治疗方法进行分析。 这项横断面研究选取了 120 名经证实患有恶性肿瘤并伴有粘膜病变的患者。根据病史、临床检查、检验和皮肤活检结果,这些病变被分为:(1)原发性皮肤恶性肿瘤;(2)皮肤转移;(3)副肿瘤综合征;(4)与恶性肿瘤无关的皮肤黏膜表现;(5)继发于治疗方法的不良反应。 120 名患者中有 70 名女性(58.3%)和 50 名男性(41.7%)。他们被分为原发性皮肤恶性肿瘤(20.2%)、血液恶性肿瘤(15%)、实体器官恶性肿瘤(50.9%)和胃肠道恶性肿瘤(5%)。两名患者(1.6%)出现艾滋病毒血清阳性。第 5 类患者最多(60 例,50%),其中 52 例(86.7%)为化疗不良反应,一名患者出现放射性皮炎,一名患者为第 3 类(0.8%)。11 名患者出现皮肤转移(9.1%),主要是乳腺癌。临床上,原发性皮肤恶性肿瘤通常表现为溃疡性生长,鳞状细胞癌是最常见的组织病理学类型(30%)。脱发是最常见的表现(35%),在实体器官恶性肿瘤中也是如此,其次是黑斑(16,13.33%)、皮肤干燥症(9,7.5%)和粘膜色素沉着(23,19.16%)。 粘膜表现需要及时关注,以便及时诊断和改善预后。
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引用次数: 0
Reactive Infectious Mucocutaneous Eruption with Extensive Cutaneous Involvement 反应性传染性粘膜皮肤破溃伴大面积皮肤受累
Pub Date : 2024-07-01 DOI: 10.4103/cdr.cdr_109_23
Zeynoire Anderson, A. Fotouhi, S. Tolliver, Darius Mehregan
Recently, there has been discussion to reclassify pediatric Stevens–Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) as drug-induced epidermal necrolysis (DEN), separating it from infectious etiologies and redefining pediatric mucocutaneous eruptions as either reactive infectious mucocutaneous eruption (RIME) or DEN. In this report, we describe a previously healthy 4-year-old girl with rapidly progressive mucocutaneous blistering involving four mucosal membranes and 37.5% of total body surface area (BSA) following a prodromal rhinovirus and enterovirus infection. The symptoms occurred in the absence of an inciting medication and improved with only supportive care. This case illustrates a rare occurrence of RIME with TEN-like BSA involvement, prompting a review of the literature exploring the relationship between BSA involvement in RIME and its influence on patient outcomes. Findings support the proposed reclassification of SJS/TEN as DEN and postinfectious mucocutaneous eruptions as RIME.
最近,有人讨论将小儿史蒂文斯-约翰逊综合征/毒性表皮坏死症(SJS/TEN)重新归类为药物诱发表皮坏死症(DEN),将其与感染性病因分开,并将小儿粘膜糜烂重新定义为反应性感染性粘膜糜烂(RIME)或DEN。在本报告中,我们描述了一名原本健康的 4 岁女孩,在鼻病毒和肠道病毒感染前驱症状出现后,她的粘膜水疱迅速进展,累及四层粘膜,占体表总面积(BSA)的 37.5%。这些症状是在没有使用诱发药物的情况下出现的,并且仅通过支持性护理就得到了改善。该病例说明了一种罕见的 RIME,即 TEN 样 BSA 受累,这促使人们对文献进行回顾,探讨 RIME 中 BSA 受累之间的关系及其对患者预后的影响。研究结果支持将 SJS/TEN 重新分类为 DEN 和将感染后粘膜糜烂重新分类为 RIME 的建议。
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引用次数: 0
Curious Case of Swelling over the Back: A Case Report of Sebaceous Cell Carcinoma in a Patient of Airborne Contact Dermatitis 背部肿胀的奇特病例:空气接触性皮炎患者皮脂腺细胞癌病例报告
Pub Date : 2024-07-01 DOI: 10.4103/cdr.cdr_123_23
Sonia Jain, Sangeeta Galui, Pratiksha Sonkusale
Sebaceous carcinoma is a rare variety of malignant tumor involving sebaceous glands. Compared to its ocular counterpart, the extraocular variant is even more rare, accounting for only one-fourth of all cases. It is a great mimicker of a plethora of benign and malignant tumors, hence often misdiagnosed. Surgical excision is the preferred mode of treatment in most cases. Here, we present the case of a 72-year-old male with airborne-contact dermatitis who was initially misdiagnosed with acrochordon, which was later found to be a case of sebaceous carcinoma on histopathology. There is a paucity of literature regarding sebaceous gland carcinomas located outside the head-and-neck region, which makes this case even more interesting.
皮脂腺癌是一种罕见的皮脂腺恶性肿瘤。与眼部肿瘤相比,眼外肿瘤更为罕见,仅占所有病例的四分之一。皮脂腺瘤可与多种良性和恶性肿瘤相似,因此经常被误诊。手术切除是大多数病例的首选治疗方式。在此,我们介绍一例 72 岁男性患者的病例,他患有空气接触性皮炎,最初被误诊为尖锐湿疣,后来经组织病理学检查发现是皮脂腺癌。关于头颈部以外的皮脂腺癌的文献很少,因此这个病例更加有趣。
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引用次数: 0
Role of Serum IFN-γ and IL-10 as Predictive Biomarkers of Vitiligo Disease Activity: A Case-Control Study 血清 IFN-γ 和 IL-10 作为白癜风疾病活动性预测生物标志物的作用:病例对照研究
Pub Date : 2024-07-01 DOI: 10.4103/cdr.cdr_1_23
Karishma Desai, H. Yadalla
IFNγ is a pleiotropic cytokine and through the regulation of immunologically relevant genes, they coordinate a wide range of cellular programs.[1] As a potent pro-inflammatory cytokine, it plays a pivotal role to induce depigmentation in vitiligo. In this study, we aim to assess the role of IFNγ in the activity, duration and extent of the disease and the antagonistic action of IL-10 is also assessed in vitiligo. A case-control study was conducted with 100 study participants with 50 cases clinically diagnosed as Vitiligo and 50 controls. All patients underwent complete evaluation with detailed demographic parameters, history and physical examination. The severity of the disease was assessed clinically by Vitiligo Area Scoring Index (VASI) and Vitiligo Disease Activity Score (VIDA). And blood investigations done were IFN-γ and IL-10. We observed significantly higher levels of serum IFNγ levels in the patient group when compared with those of the normal controls (p=0.002) and showed a positive correlation with the activity and severity of the disease with a significant VASI (p=0.05) and VIDA score (p=<0.001). The mean serum IL-10 (p<0.001) in patients with vitiligo was significantly lower than that in the control group. This study showed significantly high serum levels of IFN-γ and correspondingly low levels of IL-10. New strategies, such as the combination of IFNγ blockade with inhibition of other signalling pathways, may further improve IFNγ targeted immunotherapy of the disease.
IFNγ是一种多效细胞因子,通过调控免疫相关基因,它们能协调多种细胞程序[1]。作为一种强效促炎细胞因子,IFNγ在诱导白癜风患者色素脱失方面发挥着关键作用。在本研究中,我们旨在评估 IFNγ 在疾病的活动、持续时间和程度中的作用,同时评估 IL-10 在白癜风中的拮抗作用。 这项病例对照研究有 100 名参与者参加,其中 50 例经临床诊断为白癜风,50 例为对照组。所有患者都接受了全面的评估,包括详细的人口统计学参数、病史和体格检查。临床上通过白癜风面积评分指数(VASI)和白癜风疾病活动度评分(VIDA)来评估疾病的严重程度。血液检查包括 IFN-γ 和 IL-10。 我们观察到,与正常对照组相比,患者组的血清 IFNγ 水平明显较高(p=0.002),并且与疾病的活动性和严重程度呈正相关,VASI(p=0.05)和 VIDA 评分(p=<0.001)显著。白癜风患者的平均血清IL-10(p<0.001)明显低于对照组。 这项研究显示,IFN-γ 的血清水平明显较高,而 IL-10 的水平则相应较低。IFN-γ阻断与其他信号通路抑制相结合等新策略可能会进一步改善该疾病的IFN-γ靶向免疫疗法。
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引用次数: 0
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Clinical Dermatology Review
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