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Regression of a pigmented Spitzoid lesion in an adolescent. 青少年色素样Spitzoid病变的消退。
IF 1.2 Q4 DERMATOLOGY Pub Date : 2023-03-01
Maruša Jerše, Liljana Mervic
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引用次数: 0
Regression of a pigmented Spitzoid lesion in an adolescent. 青少年色素样Spitzoid病变的消退。
IF 1.2 Q4 DERMATOLOGY Pub Date : 2023-03-01 DOI: 10.15570/actaapa.2023.8
Maruša Jerše, Liljana Mervic
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引用次数: 0
Serum survivin in acne versus post-acne scarring and the possible effect of isotretinoin therapy on its level. 痤疮患者血清生存素与痤疮后瘢痕形成及异维甲酸治疗对其水平的可能影响。
IF 1.2 Q4 DERMATOLOGY Pub Date : 2023-03-01
Tarek Mahmoud Hussein, Nourane Tawfik Abdelsalam Tawfik, Mennatullah Mohamed Abbas Abd-Rabboh, Alsayeda Alsayed Ahmad Taha

Introduction: Acne vulgaris is a common chronic inflammatory disorder of the pilosebaceous unit. Survivin is an apoptosis inhibitor protein, and it contributes crucially to cell cycle regulation. This study measures the serum level of survivin in acne and post-acne scarring patients, and assesses the possible effect of isotretinoin therapy on its level.

Methods: Sixty participants, including 40 acne patients (Group IA, IB), and 20 age- and sex-matched controls (Group II) were included. Group IA included 20 patients with active moderate-to-severe acne without scarring, and this group was further prescribed oral isotretinoin therapy for 3 months. Group IB included 20 patients with post-acne scarring of a duration not more than 6 months, without evident active acne lesions. Serum survivin levels were measured in the three groups using an enzyme-linked immunosorbent assay.

Results: There was a statistically significant higher serum survivin level in the acne scar group, followed by the active acne group, than in controls. In addition, there was a statistically significant reduction in survivin levels after treatment, and it was positively correlated with a reduction in the global acne grading system (GAGS) in the active acne group.

Conclusions: Survivin may play a role in the evolution of acne and acne scarring, and it could be a possible target for isotretinoin therapy.

寻常痤疮是一种常见的毛囊皮脂腺单位慢性炎症性疾病。Survivin是一种细胞凋亡抑制蛋白,在细胞周期调控中起着重要作用。本研究测量了痤疮和痤疮后瘢痕患者的血清survivin水平,并评估异维甲酸治疗对其水平的可能影响。方法:60例受试者,包括40例痤疮患者(IA组,IB组)和20例年龄和性别匹配的对照组(II组)。IA组包括20例无瘢痕形成的中重度活动性痤疮患者,该组进一步给予口服异维甲酸治疗3个月。IB组包括20例持续时间不超过6个月的痤疮后瘢痕形成患者,无明显的活动性痤疮病变。采用酶联免疫吸附法测定三组患者血清survivin水平。结果:痤疮瘢痕组和活动性痤疮组血清survivin水平均高于对照组,差异有统计学意义。此外,治疗后的survivin水平有统计学意义的降低,并且与活动性痤疮组整体痤疮分级系统(GAGS)的降低呈正相关。结论:Survivin可能在痤疮和痤疮瘢痕形成过程中发挥作用,可能是异维甲酸治疗的靶点。
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引用次数: 0
Dermoscopy: the ultimate tool for diagnosis of nail psoriasis? A review of the diagnostic utility of dermoscopy in nail psoriasis. 皮肤镜检查:指甲银屑病的终极诊断工具?皮肤镜检查在甲癣诊断中的应用综述。
IF 1.2 Q4 DERMATOLOGY Pub Date : 2023-03-01
Ahu Yorulmaz

Dermoscopy is a highly practical noninvasive diagnostic tool. Several dermoscopic algorithms have been proposed in the evaluation of skin diseases, which allow clinicians not only to identify and make differential diagnosis, but also to determine the treatment choices in challenging clinical circumstances. Over the years, we have witnessed a rapid increase in the utilization of dermoscopy in the assessment of nail disorders. However, to assess the diagnostic utility of dermoscopy in inflammatory nail diseases, current evidence is insufficient. Nail psoriasis is a significant challenge because of the difficulties in its diagnosis. Detection of nail involvement is of utmost importance in psoriasis because it is highly associated with arthritis, which is an indication for systemic treatment. Dermoscopy holds promise as a potential tool in the diagnosis of nail psoriasis, capable of providing characteristic clinical findings without any delay and discomfort. This review summarizes current evidence regarding the unique dermoscopic features of nail psoriasis. It addresses whether dermoscopy may serve as the gold-standard diagnostic tool, excluding the necessity of histopathological examination for the ultimate diagnosis of nail psoriasis.

皮肤镜检查是一种非常实用的非侵入性诊断工具。几种皮肤镜算法已被提出用于评估皮肤病,使临床医生不仅可以识别和做出鉴别诊断,而且还可以在具有挑战性的临床情况下确定治疗选择。多年来,我们目睹了皮肤镜在指甲疾病评估中的应用迅速增加。然而,评估皮肤镜在炎性指甲疾病中的诊断效用,目前的证据是不足的。指甲牛皮癣是一个重大的挑战,因为它的诊断困难。检测指甲受累是最重要的银屑病,因为它是高度相关的关节炎,这是一个系统治疗的指征。皮肤镜检查有望作为诊断甲牛皮癣的潜在工具,能够提供特征性的临床表现,没有任何延迟和不适。这篇综述总结了目前关于指甲牛皮癣独特的皮肤镜特征的证据。它讨论了皮肤镜检查是否可以作为金标准诊断工具,排除了最终诊断指甲牛皮癣的组织病理学检查的必要性。
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引用次数: 0
Trigeminal trophic syndrome, a rare and often overlooked cause of facial ulceration: a case report and literature review. 三叉神经营养综合征,一个罕见的和经常被忽视的原因面部溃疡:一个病例报告和文献复习。
IF 1.2 Q4 DERMATOLOGY Pub Date : 2023-03-01
Laura Đorđević Betetto, Vid Bajuk

Trigeminal trophic syndrome (TTS) is an uncommon and relatively unknown cause of facial ulceration that occurs after damage to the trigeminal nerve. It characteristically involves non-healing facial ulceration(s) with accompanying anesthesia, paresthesia, and dysesthesia along the distribution of a trigeminal dermatome. The ulcerations are believed to be self-induced in response to paresthesia. The disease is most common in middle-aged women, manifesting as a unilateral crescent-shaped ulceration on the ala nasi, with sparing of the nasal tip. The diagnosis is clinical and mostly based on exclusion of other possible causes of facial ulcerations, with emphasis on neoplasms, infection-associated vasculitis, and factitial disorders. There are no specific histological or laboratory signs. There is no standard treatment protocol; however, a number of different successful strategies have been reported, including pharmaceutical and surgical interventions, transcutaneous nerve stimulation, and simple occlusion dressings. Due to the self-inflicted nature of this disorder, the cornerstone of management is patient education with behavioral modification. Here, we report a case of TTS following herpes zoster ophthalmicus and review the current literature on this subject.

三叉神经营养综合征(TTS)是一种罕见且相对未知的原因,发生在三叉神经损伤后的面部溃疡。它的特征包括伴有麻醉、感觉异常和沿三叉皮节分布的感觉不良的面部溃疡。溃疡被认为是对感觉异常的自我诱导。此病最常见于中年妇女,表现为鼻翼单侧月牙形溃疡,鼻尖不受影响。诊断是临床的,主要是基于排除其他可能的面部溃疡原因,重点是肿瘤、感染相关血管炎和人为疾病。没有特定的组织学或实验室征象。没有标准的治疗方案;然而,已经报道了许多不同的成功策略,包括药物和手术干预,经皮神经刺激和简单的闭塞敷料。由于这种疾病的自我造成的性质,管理的基石是患者教育与行为改变。在此,我们报告一例眼带状疱疹后的TTS,并回顾目前关于这一主题的文献。
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引用次数: 0
Primary biliary cholangitis-cause or association with psoriasis: a case report. 原发性胆道胆管炎与牛皮癣相关:1例报告。
IF 1.2 Q4 DERMATOLOGY Pub Date : 2023-03-01
Patricija Tomše, Valerija Balkovec

Primary biliary cholangitis is a chronic progressive cholestatic granulomatous and destructive inflammatory lesion of small intralobular and septal bile ducts that primarily affects women. The exact etiology of this disease has not yet been elucidated; however, it is believed to be the result of a combination of environmental triggers in genetically predisposed individuals. It can manifest itself simultaneously with, before, or after the onset of psoriasis and other skin autoimmune diseases. Standard treatment is ursodeoxycholic acid. A 65-year-old patient presenting with elevated hepatic laboratory findings that had persisted for several years and normal abdominal ultrasound was additionally diagnosed with primary biliary cholangitis after 2 years on a biological drug for psoriasis. She did not have other symptoms except elevated liver tests. The skin showed a strong response to biological therapy and treatment with ursodeoxycholic acid prompted lowering of liver enzymes. The skin was clear all throughout the treatment. This article emphasizes the importance of additional diagnostic workups in patients with psoriasis and elevated hepatic laboratory findings.

原发性胆管炎是一种慢性进行性胆汁淤积性肉芽肿和破坏性的小叶内和间隔胆管炎症性病变,主要影响女性。这种疾病的确切病因尚未阐明;然而,它被认为是遗传易感性个体的环境触发因素组合的结果。它可以与牛皮癣和其他皮肤自身免疫性疾病同时出现,在发病之前或之后。标准治疗是熊去氧胆酸。一名65岁的患者,肝脏实验室检查结果升高,持续数年,腹部超声正常,在服用牛皮癣生物药物2年后,又被诊断为原发性胆管炎。除了肝脏检查结果升高外,她没有其他症状。皮肤对生物疗法和熊去氧胆酸治疗表现出强烈的反应,导致肝酶降低。在整个治疗过程中,皮肤都很干净。这篇文章强调了银屑病患者和肝脏实验室检查结果升高的额外诊断检查的重要性。
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引用次数: 0
Trigeminal trophic syndrome, a rare and often overlooked cause of facial ulceration: a case report and literature review. 三叉神经营养综合征,一个罕见的和经常被忽视的原因面部溃疡:一个病例报告和文献复习。
IF 1.2 Q4 DERMATOLOGY Pub Date : 2023-03-01 DOI: 10.15570/actaapa.2023.7
Laura Đorđević Betetto, Vid Bajuk
Trigeminal trophic syndrome (TTS) is an uncommon and relatively unknown cause of facial ulceration that occurs after damage to the trigeminal nerve. It characteristically involves non-healing facial ulceration(s) with accompanying anesthesia, paresthesia, and dysesthesia along the distribution of a trigeminal dermatome. The ulcerations are believed to be self-induced in response to paresthesia. The disease is most common in middle-aged women, manifesting as a unilateral crescent-shaped ulceration on the ala nasi, with sparing of the nasal tip. The diagnosis is clinical and mostly based on exclusion of other possible causes of facial ulcerations, with emphasis on neoplasms, infection-associated vasculitis, and factitial disorders. There are no specific histological or laboratory signs. There is no standard treatment protocol; however, a number of different successful strategies have been reported, including pharmaceutical and surgical interventions, transcutaneous nerve stimulation, and simple occlusion dressings. Due to the self-inflicted nature of this disorder, the cornerstone of management is patient education with behavioral modification. Here, we report a case of TTS following herpes zoster ophthalmicus and review the current literature on this subject.
三叉神经营养综合征(TTS)是一种罕见且相对未知的原因,发生在三叉神经损伤后的面部溃疡。它的特征包括伴有麻醉、感觉异常和沿三叉皮节分布的感觉不良的面部溃疡。溃疡被认为是对感觉异常的自我诱导。此病最常见于中年妇女,表现为鼻翼单侧月牙形溃疡,鼻尖不受影响。诊断是临床的,主要是基于排除其他可能的面部溃疡原因,重点是肿瘤、感染相关血管炎和人为疾病。没有特定的组织学或实验室征象。没有标准的治疗方案;然而,已经报道了许多不同的成功策略,包括药物和手术干预,经皮神经刺激和简单的闭塞敷料。由于这种疾病的自我造成的性质,管理的基石是患者教育与行为改变。在此,我们报告一例眼带状疱疹后的TTS,并回顾目前关于这一主题的文献。
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引用次数: 1
Linear IgA bullous dermatosis in an acute myeloid leukemia patient: a rare case report. 急性髓系白血病患者线状IgA大疱性皮肤病:罕见病例报告。
IF 1.2 Q4 DERMATOLOGY Pub Date : 2023-03-01 DOI: 10.15570/actaapa.2023.5
Deisy Vania Kianindra, A. Rosa, Dina Pebriany, W. Dewiyanti, A. Madjid
Linear IgA bullous dermatosis (LABD) is a rare autoimmune bullous disease characterized by linear IgA deposition along the skin basal membrane. In children, LABD classically presents with a "cluster of jewels" appearance, whereas in adults the classic presentation is itchy papules with tense vesicles and bullae on an erythematous base. We report the case of a 41-year-old woman with LABD that we suspect was induced by acute myeloid leukemia presenting with multiple vesicles and bullae that coalesced, forming the typical clinical manifestation of LABD and confirmed with histopathological and direct immunofluorescence. The patient was treated with a combination of oral and topical corticosteroids with excellent results.
线性IgA大疱性皮肤病(LABD)是一种罕见的自身免疫性大疱性疾病,其特征是IgA沿皮肤基膜呈线性沉积。在儿童中,LABD典型表现为“宝石簇”外观,而在成人中,典型表现为瘙痒丘疹,红斑基础上有紧张的囊泡和大泡。我们报告一例41岁女性LABD,我们怀疑是由急性髓性白血病引起的,表现为多个囊泡和大泡合并,形成LABD的典型临床表现,并经组织病理学和直接免疫荧光证实。患者接受口服和外用皮质类固醇联合治疗,效果良好。
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引用次数: 0
Pembrolizumab-induced lichen planus in patients with metastatic melanoma: a report of two cases and prognostic implications of cutaneous immune-related adverse events pembrolizumab诱导的转移性黑色素瘤患者扁平苔藓:两例皮肤免疫相关不良事件的报告及其预后意义
Q4 DERMATOLOGY Pub Date : 2023-01-01 DOI: 10.15570/actaapa.2023.22
Tanja Tirnanić, Danica Tiodorović, Nataša Vidović, Mirjana Balić, Nenad Petrov, Lidija Kandolf, Željko Mijušković
Patients receiving immune checkpoint inhibitors (ICIs) commonly experience cutaneous immune-related adverse events (irAEs). We present two cases, a 51-year-old female and a 70-year-old male, that were undergoing treatment with pembrolizumab for metastatic melanoma and developed scaly, erythematous papules on their skin. Following skin biopsies, histological analysis confirmed the diagnosis of lichen planus. In the first patient, acitretin at a dosage of 25 mg/day was administered for 6 months, resulting in complete resolution of lichen lesions. Imaging scans showed no signs of melanoma. The second patient was treated with topical betamethasone dipropionate ointment for several weeks, which led to a favorable therapeutic response. During follow-up, a thoracic CT scan showed several micronodular lesions in the right lung, whereas brain and abdomen CT scans showed no signs of the disease. Lichen planus is not a commonly reported irAE in patients treated with ICIs. This report underscores the importance of conducting skin biopsies in patients receiving ICI therapy and highlights the potential prognostic importance of skin irAEs in patients with melanoma receiving such treatment.
接受免疫检查点抑制剂(ICIs)的患者通常会经历皮肤免疫相关不良事件(irAEs)。我们报告了两例病例,一名51岁的女性和一名70岁的男性,他们接受了派姆单抗治疗转移性黑色素瘤,并在皮肤上出现了鳞片状的红斑丘疹。皮肤活检后,组织学分析证实了扁平苔藓的诊断。在第一个患者中,阿维甲素的剂量为25mg /天,持续6个月,导致地衣病变完全消退。成像扫描显示没有黑色素瘤的迹象。第二例患者局部应用二丙酸倍他米松软膏治疗数周,治疗效果良好。在随访期间,胸部CT扫描显示右肺有几个小结节病变,而脑部和腹部CT扫描未显示该疾病的迹象。扁平苔藓在接受ICIs治疗的患者中并不是常见的irAE。本报告强调了在接受ICI治疗的患者中进行皮肤活检的重要性,并强调了在接受这种治疗的黑色素瘤患者中皮肤irae的潜在预后重要性。
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引用次数: 1
Prevalence of the HLA-Cw6 genotype and zinc deficiency in psoriasis vulgaris patients in Indonesia 印度尼西亚寻常型银屑病患者HLA-Cw6基因型和锌缺乏症的患病率
Q4 DERMATOLOGY Pub Date : 2023-01-01 DOI: 10.15570/actaapa.2023.19
Timothy Yusuf Sangian, Nurelly Noro Waspodo, Faridha Ilyas, Khairuddin Djawad, Arifin Seweng, Suryani Tawali
INTRODUCTION Psoriasis vulgaris is an immune-mediated inflammatory disease influenced by genetic and immunologic factors, including micronutrient deficiencies. The HLA-Cw6 gene and zinc level have been separately studied in psoriasis patients, yielding inconsistent findings. A descriptive study regarding HLA-Cw6 allele expression, zinc levels, and their direct correlation in Indonesia is lacking. METHODS This prospective case-control study involved 33 psoriasis patients and 33 age- and sex-matched control patients at the dermatology clinic affiliated with Hasanuddin University in South Sulawesi in 2021. Cases were classified into mild, moderate, and severe psoriasis according to Psoriasis Area and Severity Index (PASI) score. An EDTA tube was used to take a 5 ml blood sample, followed by analysis for PCR of the HLA-Cw6 allele and a colorimetric assay to measure zinc level. Statistical analysis was performed to determine the association between HLA-Cw6 and zinc level and psoriasis disease severity. RESULTS Among the 33 psoriatic patients enrolled in this study, three (9.1%) of the cases were classified as mild psoriasis, 10 (30.3%) were classified as moderate psoriasis, and 20 (60.6%) were classified as severe psoriasis. The HLA-Cw6 allele was detected in 93.9% of psoriasis cases and in 3% of control patients (p < 0.001). The HLA-Cw6 allele was detected consecutively in 66.7%, 90.0%, and 100% of mild, moderate, and severe psoriasis patients, respectively. Zinc levels were lower in psoriasis patients compared to controls (16.85 ± 3.55 vs. 13.74 ± 3.78 μmol/l). Severe psoriasis patients exhibited the lowest average zinc level (14.76 ± 1.40 μmol/l, 15.48 ± 4.20 μmol/l, and 12.72 ± 3.56 μmol/l in mild, moderate, and severe patients, respectively). The mean zinc level in HLA-Cw6-positive patients was 13.68 μmol/l, and 14.6 μmol/l in HLA-Cw6-negative patients (p = 0.495). CONCLUSIONS The study revealed the presence of HLA-Cw6 allele expression and decreased serum zinc levels in psoriasis patients compared to controls. Both factors demonstrated associations with psoriasis disease severity.
寻常型银屑病是一种受遗传和免疫因素影响的免疫介导的炎症性疾病,包括微量营养素缺乏。银屑病患者的HLA-Cw6基因和锌水平分别研究,结果不一致。在印度尼西亚缺乏关于HLA-Cw6等位基因表达、锌水平及其直接相关性的描述性研究。这项前瞻性病例对照研究于2021年在南苏拉威西Hasanuddin大学附属皮肤科诊所纳入了33名牛皮癣患者和33名年龄和性别匹配的对照患者。根据银屑病面积及严重程度指数(psoriasis Area and Severity Index, PASI)评分将患者分为轻度、中度和重度。用EDTA管取5 ml血样,随后进行HLA-Cw6等位基因PCR分析和比色法测定锌水平。统计分析HLA-Cw6和锌水平与银屑病严重程度之间的关系。本研究纳入的33例银屑病患者中,轻度银屑病3例(9.1%),中度银屑病10例(30.3%),重度银屑病20例(60.6%)。HLA-Cw6等位基因在93.9%的银屑病患者和3%的对照患者中检测到(p < 0.001)。HLA-Cw6等位基因在轻、中、重度牛皮癣患者中分别连续检测到66.7%、90.0%和100%。银屑病患者的锌水平低于对照组(16.85±3.55 μmol/l vs. 13.74±3.78 μmol/l)。重度银屑病患者的平均锌含量最低(轻、中、重度患者分别为14.76±1.40 μmol/l、15.48±4.20 μmol/l、12.72±3.56 μmol/l)。hla - cw6阳性患者的平均锌水平为13.68 μmol/l,阴性患者的平均锌水平为14.6 μmol/l (p = 0.495)。该研究显示,与对照组相比,银屑病患者存在HLA-Cw6等位基因表达和血清锌水平下降。这两个因素都与银屑病的严重程度有关。
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引用次数: 0
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Acta Dermatovenerologica Alpina Pannonica et Adriatica
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