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Acta Dermatovenerologica Croatica最新文献

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Histological Skin Remodeling Following Autologous Fibroblast Application. 自体成纤维细胞应用后的组织学皮肤重塑。
IF 0.6 4区 医学 Q3 Medicine Pub Date : 2022-07-01
Sonja Grilc, Marko Kreft, Boštjan Luzar, Mateja Gabrijel, Mark S Bartenjev, Robert Zorec, Igor Bartenjev

The aim of this study was to quantify the effectiveness of intradermal application of autologous fibroblasts on lean tissue structures. The histological sections of the skin were analysed and evaluated for the expansion potential of autologous fibroblasts in the control skin patch area and the nearby pre-treated skin patch into which we had injected expanded autologous fibroblasts nine month earlier. The results show that the pre-injection of fibroblasts into the dermis leads to a long-term rejuvenation of the skin, as evaluated from the histological appearance and from the significantly increased density of fibroblasts in the pre-injected skin vs. controls, from around 60% to over 80%, determined as the percent of lean tissue by a novel image analysis approach. Interestingly, the rate of the in vitro fibroblast expansion from the pre-injected area of the skin was reduced in comparison with the controls, consistent with the view that fibroblasts exhibit a limited cell-division potential and that fibroblasts from the pre-injected skin already experienced expansion nine month earlier prior to the injection into the skin. We conclude that autologous fibroblast application results in a significant long-term augmentation of the lean tissue elements of the skin.

本研究的目的是量化皮内应用自体成纤维细胞对瘦组织结构的有效性。对皮肤的组织学切片进行分析和评估,以确定9个月前注射扩增的自体成纤维细胞的对照皮肤贴片区域和附近的预处理皮肤贴片中的自体成纤维细胞的扩张潜力。结果表明,从组织学外观和预注射皮肤中成纤维细胞密度显著增加(由一种新的图像分析方法确定的瘦组织百分比)来看,预注射成纤维细胞到真皮层导致皮肤长期恢复活力。有趣的是,与对照组相比,来自预注射皮肤区域的体外成纤维细胞扩增率降低,这与成纤维细胞表现出有限的细胞分裂潜力以及来自预注射皮肤的成纤维细胞在注射前9个月就已经经历了扩增的观点一致。我们的结论是,自体成纤维细胞的应用结果在一个显著的长期增加皮肤的瘦组织元素。
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引用次数: 0
The Relationship Between Disease Activity and Platelet Indices in Pemphigus: An Observational Preliminary Study. 天疱疮患者疾病活动性与血小板指数的关系:一项观察性初步研究。
IF 0.6 4区 医学 Q3 Medicine Pub Date : 2022-07-01
Metin Özaslan, Bilgen Erdoğan, Ayşe Gül Erdoğan, Ayşe Kavak

Tests which have proven their efficacy and reliability in the follow-up of pemphigus patients are used only on a limited scale or take time to complete due to a lack of technical facilities in several centers. Therefore, more accessible methods are being considered for monitoring disease activity. We aimed to investigate the relationship between platelet function and disease activity based on the change in proinflammatory cytokine profile in pemphigus pathogenesis. The size of platelets correlates positively with their activity. Platelet sizes can be evaluated by the platelet volume index consisting of mean platelet volume (MPV), platelet-crit (PCT), and platelet distribution width (PDW). These indicators can be easily measured in complete blood count (CBC) with automatic blood counting devices, which do not require additional costs and are readily available. Patients diagnosed with pemphigus between April 2010 and February 2016 (n=18) in our center were retrospectively included in the study. Demographic data, follow-up period, clinical variants of the patients, platelet parameters (MPV, PDW, PCT), and platelet count (PLT) in CBC analysis with concurrent clinical activity, as well as indirect immunofluorescence (IIF) findings (positive highest titer) at the 6th and 12th month were recorded for each patient. MPV changes were consistent with the course of the disease. A statistically significant decrease in PCT levels was observed at the 12th month compared with the baseline levels (P<0.05). According to the baseline measurement, a statistically significant positive correlation (58.9%) was found between the 12-month difference measurements of IIF and PCT. Our data demonstrated that PCT decrease is correlated with IIF values. The significant correlation between PCT and IIF values in our study is important in showing the possible role of platelet index in the measurement of disease activity.

在天疱疮患者的随访中已经证明其有效性和可靠性的测试仅在有限的规模上使用,或者由于几个中心缺乏技术设施而需要时间来完成。因此,正在考虑采用更容易获得的方法来监测疾病活动。我们的目的是基于天疱疮发病过程中促炎细胞因子谱的变化来研究血小板功能与疾病活动度的关系。血小板的大小与其活性呈正相关。血小板大小可以通过血小板体积指数来评估,该指数由平均血小板体积(MPV)、血小板临界值(PCT)和血小板分布宽度(PDW)组成。这些指标可以很容易地用全自动血液计数装置在全血细胞计数(CBC)中测量,不需要额外的费用,而且很容易获得。本研究回顾性纳入2010年4月至2016年2月在本中心诊断为天疱疮的患者(n=18)。记录每位患者的人口统计学数据、随访期、临床变异、血小板参数(MPV、PDW、PCT)和血小板计数(PLT)在CBC分析中的同步临床活性,以及第6个月和第12个月的间接免疫荧光(IIF)结果(阳性滴度最高)。MPV变化与病程一致。与基线水平相比,在第12个月观察到PCT水平有统计学意义的下降(P
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引用次数: 0
Psoriasis and 5HT-R2C Gene Polymorphism: Association between Clinical, Demographic and Therapeutic Parameters in the Turkish Population. 牛皮癣和5HT-R2C基因多态性:土耳其人群临床、人口统计学和治疗参数之间的关系
IF 0.6 4区 医学 Q3 Medicine Pub Date : 2021-12-01
Sehime G Temel, Serkan Yazici, İzel Yilmaz, Özgür Tosun, Mahmut Cerkez Ergoren, Emel Bulbul Baskan, Barbaros Oral, Kenan Aydogan

We aimed to investigate the relationship between single nucleotide polymorphism (SNP) in the promoter region of the 5-HT-R2C gene and stress-related disease psoriasis in the Turkish population. The putative association between the 5-HTR2C variant (rs6318 Cys23Ser allele) and patients with psoriasis was investigated. 100 patients with psoriasis and 100 age-sex matched, unrelated healthy subjects representing the control group were included in the study. The PCR-RFLP method was used for genotyping the 5-HTR2C variation. There was no statistically difference in terms of genotype distributions and allele frequencies between the control subjects and patients with psoriasis (P=0.360 and P=0.439, respectively). The comparison between the presence and absence of the 5-HTR2C gene rs6318 G allele within the determined clinical subsets resulted in a significant difference with regard to treatment methodology only when conventional therapy and one or more medical therapy was compared (P=0.021). This study is the first clinical study to investigate the association between 5-HTR2C polymorphism and psoriasis. The role of the 5-HTR2C gene should be examined with more parameters in a larger case series.

我们旨在研究土耳其人群中5-HT-R2C基因启动子区域的单核苷酸多态性(SNP)与应激相关疾病牛皮癣之间的关系。研究了5-HTR2C变异(rs6318 Cys23Ser等位基因)与牛皮癣患者之间的推定关联。研究包括100名牛皮癣患者和100名年龄性别匹配、不相关的健康受试者作为对照组。采用PCR-RFLP方法对5-HTR2C变异进行基因分型。对照组与银屑病患者的基因型分布、等位基因频率差异无统计学意义(P=0.360、P=0.439)。在确定的临床亚群中比较5-HTR2C基因rs6318 G等位基因的存在与缺失,只有在比较常规治疗和一种或多种药物治疗时,才会在治疗方法上产生显著差异(P=0.021)。本研究是首个探讨5-HTR2C多态性与银屑病之间关系的临床研究。5-HTR2C基因的作用应该在更大的病例序列中用更多的参数来检验。
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引用次数: 0
Modified Mohs Micrographic Surgery in Lentigo Maligna Treatment: A Series of Six Cases. 改良Mohs显微手术治疗恶性Lentigo 6例
IF 0.6 4区 医学 Q3 Medicine Pub Date : 2021-12-01
Alexandra Zota, Anca Stanciu, Cecilia Enescu, Tiberiu Tebeica, Mihaela Leventer

The surgical approach to lentigo maligna is a challenge to dermatologists, given its clinical and histopathological particularities. Staged excision with paraffin-embedded, permanent sections for histopathological evaluation of surgical margins is an effective treatment of lentigo maligna because it enables complete excision of the tumor, at the same time preserving maximum amount of healthy tissue. We report a case series of 6 patients diagnosed with lentigo maligna who underwent this procedure in our Institution and we describe the procedure we used. Complete excision of the tumors was achieved with one to three levels, with margins of excision ranging from 2 to 8 mm. There were no local recurrences at the median follow-up of 16 months, obtaining 100% cure rate with this technique. These are comparable with the margins and number of levels of excision described in previous case series reported in the literature. The technique described herein for the treatment of lentigo maligna provides excellent cure rates for this type of cutaneous malignancy notorious for its challenging management.

鉴于其临床和组织病理学的特殊性,手术方法对皮肤科医生来说是一个挑战。分期切除,石蜡包埋,永久切片手术边缘的组织病理学评估是一种有效的治疗恶性lentigo的方法,因为它可以完全切除肿瘤,同时保留最大数量的健康组织。我们报告了一个病例系列,6例诊断为恶性青光体的患者在我们的机构接受了这种手术,我们描述了我们使用的手术。完全切除肿瘤达到一至三个水平,切除边缘从2到8毫米。中位随访16个月无局部复发,治愈率100%。这些与文献中先前报道的病例系列中描述的边缘和切除水平相当。本文所描述的治疗恶性小晶状体的技术为这种因其挑战性管理而臭名昭著的皮肤恶性肿瘤提供了极好的治愈率。
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引用次数: 0
A Case of Nevoid Acanthosis Nigricans Successfully Treated with Topical Ketoconazole Plus Urea. 外用酮康唑加尿素治疗黑棘皮瘤1例。
IF 0.6 4区 医学 Q3 Medicine Pub Date : 2021-12-01
Ayaki Matsumoto, Kozo Nakai, Daisuke Tsuruta, Koji Sugawara

Dear Editor, Nevoid acanthosis nigricans (AN) is a rare form of benign AN that can be mostly found as a solitary lesion distributed along Blaschko's lines (1). It is not associated with any known syndrome, endocrinopathy, drugs, or internal malignancy. Treatments include retinoid, calcipotriol, and laser treatments (2). Herein we report a case of nevoid AN successfully treated with topical ketoconazole plus urea. A 15-year-old woman presented with a 3-year history of asymptomatic plaques on her abdomen that were increasing in size. She had no medical history and no family history and was not obese. Physical examination revealed dark-brownish pigmented plaques on the midline and right side of her abdomen (Figure 1, a). Potassium hydroxide test was negative. Thyroid function test, antinuclear antibody test, and liver and renal function tests were within normal limits. Histological examination of skin biopsy showed hyperkeratosis and papillomatosis with minimal acanthosis and a mild perivascular lymphocytic infiltration in the superficial dermis (Figure 1, b). Some melanophages were observed in the superficial dermis. Based on the clinical features and these histological findings, a diagnosis of nevoid AN was established. Additionally, there were numerous hyphae and spores in the stratum corneum that were confirmed by Grocott staining (Figure 1, c) and periodic acid-Schiff staining (Figure 1, d). Fungal infection was suggested, and the result of a potassium hydroxide test was considered to be pseudo-negative. Topical ketoconazole cream was initially administrated for one month, and the rough surface was markedly improved (Figure 1, e). Subsequently, topical 20 % urea cream was used and the area of skin lesion decreased in size after 6 months (Figure 1, f). We discontinued ketoconazole cream after 2 months. To the best of our knowledge, this is the first case of nevoid AN successfully treated with topical ketoconazole plus urea. Some cases of AN appear to have an associated endocrinopathy (1). However, genetic factors may also play a role in the pathogenesis of AN. It has been reported that mosaic mutation in fibroblast growth factor 3 (FGFR3) is associated with nevoid AN (3). All known mutations in FGFR3 are gain-of-function mutations, and the activity of the FGFR3 signal correlates with the severity of AN. Involvement of fungal infection has not been reported in the pathogenesis of nevoid AN. We did not identify the fungal species in our patient, but Malassezia infection was suggested. In general, potassium hydroxide test can reveal only yeast forms of Malassezia, and pseudo-negative results may often occur. The abundant hyphae and spores in the stratum corneum are a characteristic pathological feature of Malassezia infection, and the obvious effects of ketoconazole may support the Malassezia infection. Since Malassezia is known to promote cytokine production in human keratinocytes (4), an autocrine FGFR3 signal might accelerate the prolifera

Nevoid acanthosis nigricans (AN)是一种罕见的良性AN,主要是沿Blaschko线分布的孤立病变(1)。它与任何已知综合征、内分泌病变、药物或内部恶性肿瘤无关。治疗方法包括类维甲酸、钙化三醇和激光治疗(2)。在此,我们报告一例用局部酮康唑加尿素成功治疗血管性AN的病例。一名15岁女性,腹部无症状斑块3年病史,体积不断增大。患者无病史,无家族史,无肥胖。体格检查显示患者腹部中线及右侧有深棕色色斑(图1,a)。氢氧化钾试验阴性。甲状腺功能、抗核抗体、肝肾功能检查均正常。皮肤活检组织学检查显示角化过度和乳头状瘤病伴少量棘层增生,真皮浅层有轻度血管周围淋巴细胞浸润(图1,b)。真皮浅层可见一些噬黑细胞。根据临床特征和这些组织学结果,诊断为结节性AN。此外,角质层中有大量菌丝和孢子,经Grocott染色(图1,c)和周期性酸-希夫染色(图1,d)证实,可能是真菌感染,氢氧化钾试验结果为假阴性。最初局部使用酮康唑乳膏1个月,粗糙表面明显改善(图1,e)。随后,局部使用20%尿素乳膏,6个月后皮肤病变面积减小(图1,f)。2个月后停用酮康唑乳膏。据我们所知,这是第一例用局部酮康唑加尿素成功治疗的nevoid AN。一些AN病例似乎伴有内分泌病变(1)。然而,遗传因素也可能在AN的发病机制中发挥作用。据报道,成纤维细胞生长因子3 (FGFR3)的镶嵌突变与nevoid AN相关(3)。所有已知的FGFR3突变都是功能获得突变,FGFR3信号的活性与AN的严重程度相关。真菌感染的参与尚未报道在nevoid AN的发病机制。我们没有确定患者的真菌种类,但马拉色菌感染被认为是。一般情况下,氢氧化钾试验只能显示酵母形式的马拉色菌,并可能经常出现假阴性结果。角质层中菌丝和孢子丰富是马拉色菌感染的典型病理特征,酮康唑的明显作用可能支持马拉色菌感染。由于已知马拉色菌可促进人角化细胞中细胞因子的产生(4),自分泌的FGFR3信号可能会加速骨髓瘤细胞等角化细胞的增殖(5)。尿素是最广泛使用的保湿剂和角化剂,已被用于治疗各种角化过度的皮肤病。采用酮康唑和尿素联合用药治疗新发性鼻炎成功。这种联合治疗可能比以前报道的治疗有更少的副作用,可以考虑作为一种可选的治疗。致谢:本文中的患者已书面知情同意其病例详细信息的发表。
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引用次数: 0
Angiokeratoma Circumscriptum Naeviforme Presenting as a Dark Warty Plaque on the Leg. 新生状血管角化瘤表现为腿部的黑色疣状斑块。
IF 0.6 4区 医学 Q3 Medicine Pub Date : 2021-12-01
Diego Abbenante, Beatrice Raone, Carlotta Baraldi, Miriam Anna Carpanese, Annalisa Patrizi

Dear Editor, A 45-year-old man presented with a large, dark, keratotic, warty, and friable plaque on the distal posterior aspect of the left leg (Figure 1, a). The patient reported that the lesion was not present at birth but had appeared approximately at the age of three as an erythematous patch that progressively grew over the time. During adolescence, the surface of the lesion became rough and warty and was easily traumatized due to its location, resulting in recurrent bleeding episodes over a period of years. For this reason, the patient requested lesion removal. The patient did not report any other significant comorbidity, and physical examination revealed no other abnormalities. A shaving biopsy of the lesion was performed, and histopathology highlighted ectatic vascular spaces with some luminal red blood cell beneath a papillomatous and hyperkeratotic epidermis (Figure 1, b). Based on clinical and histopathological features, a diagnosis of angiokeratoma circumscriptum naeviforme (ACN) was established. ACN is one of the five disorders belonging to the group of angiokeratomas (AKs) that also include AK of Mibelli, AK of Fordyce, solitary or multiple AK, and AK corporis diffusum. Among these variants, ACN is the rarest and is seldom studied (1). AKs are benign vascular anomalies of the superficial vascular plexus that appear as dark red papules and plaques arranged either discretely or in clusters. ACN lesions are typically situated unilaterally on the lower limbs, especially on the legs and feet, but can occasionally occur elsewhere. Lesions are generally noted in early childhood. The early lesions are flat and reddish in color, while older lesions become increasingly studded and acquire a verrucous or warty surface. There is no tendency of spontaneous improvement, and minor traumas can easily cause beading and infection (2). While the plaques were linear in disposition in most of the cases reported in the literature, a peculiar feature of our case was the isolated, round, and giant appearance of the plaque. Even though ACN is not typically associated with other abnormalities, coexistence with other vascular malformations has been reported in some cases, including AK of Fordyce, Cobb syndrome, Klippel-Trenaunay syndrome, nevus flammeus, infantile hemangioma, and traumatic arteriovenous fistula (3). From a histological point of view, ACN appears as dilated dermal papillary capillaries drained by dilated venules. The overlying epidermis shows a variable degree of acanthosis, papillomatosis, and compact hyperkeratosis. Typically, the deep dermis and hypodermis are not involved, helping distinguish them from verrucous hemangioma (4). Lichen simplex chronicus, verrucous carcinoma, and verrucous melanoma must also be considered in the differential diagnosis (5). Recurrent bleeding or cosmetic reasons are common indications for treatment. Surgical excision represents the most effective option. Other possibilities include diathermy, electrocau

尊敬的编辑:一名45岁男性患者在左腿远端后侧出现了一个大的、深色的、角化的、疣状的、易碎的斑块(图1,A)。患者报告说,该病变在出生时不存在,但大约在三岁时出现了一个红斑斑块,随着时间的推移逐渐生长。在青少年时期,由于其位置,病变表面变得粗糙和疣状,容易受到创伤,导致多年来反复出血。因此,患者要求切除病变。患者未报告任何其他显著的合并症,体格检查未发现其他异常。对病变进行刮除活检,组织病理学显示在乳头状瘤和角化过度的表皮下有扩张的血管间隙和一些腔内红细胞(图1,b)。基于临床和组织病理学特征,建立了新状周缘血管角化瘤(ACN)的诊断。ACN是血管角化瘤(AKs)组的五种疾病之一,其他疾病还包括Mibelli型AK、Fordyce型AK、单发或多发AK和公司弥漫性AK。在这些变异中,ACN是最罕见的,很少被研究(1)。AKs是浅表血管丛的良性血管异常,表现为暗红色丘疹和斑块,可离散或成簇排列。ACN病变通常位于单侧下肢,尤其是腿和脚,但偶尔也会发生在其他地方。病变通常在儿童早期被发现。早期病变呈扁平和淡红色,而较老的病变越来越多,形成疣状或疣状表面。没有自发改善的趋势,轻微的创伤很容易引起出血和感染(2)。虽然在文献报道的大多数病例中,斑块呈线性分布,但我们病例的一个特殊特征是斑块孤立、圆形和巨大的外观。尽管ACN通常不与其他异常相关,但在某些情况下,已报道与其他血管畸形共存,包括Fordyce AK、Cobb综合征、Klippel-Trenaunay综合征、火焰痣、婴儿血管瘤和外伤性动静脉瘘(3)。从组织学角度来看,ACN表现为扩张的小静脉引流的真皮乳头状毛细血管扩张。上覆表皮可见不同程度的棘层增生、乳头状瘤病和紧密性角化过度。通常情况下,真皮深层和皮下不受影响,这有助于将它们与疣状血管瘤区分(4)。慢性单纯性苔藓、疣状癌和疣状黑色素瘤在鉴别诊断时也必须考虑(5)。复发性出血或美容原因是治疗的常见指征。手术切除是最有效的选择。其他可能包括透热、电灼、冷冻手术或激光(6)。在我们的病例中,剃须活检后没有肉眼残留的疾病。应用胶原蛋白敷料,伤口在三周内进行了第二次愈合。18个月后无局部复发迹象。参考文献:Das A, Mondal AK, Saha A, Chowdhury SN, Gharami RC。内形成性血管角化瘤:一种少见的实体。中华皮肤科杂志,2014;5:472- 464。米塔尔R, Aggarwal A, Srivastava G.血管角化瘤边缘:一个病例报告和文献复习。中华皮肤科杂志,2005;44(4):391 - 391。王志强,王志强,王志强,等。软组织肥大伴深静脉畸形的新生状缘血管角化瘤:Klippel-Trenaunay综合征的一种变异?中国皮肤科杂志,2014;5(增刊2):S109-S112。李建军,李建军,李建军。疣状血管瘤与边缘性血管瘤的组织病理学鉴别诊断。中国生物医学工程学报,2018;33(3):745 - 745。高曼L, Gibson SH, Richfield DF。血栓性血管角化瘤外围物模拟黑色素瘤。皮肤科杂志。1981;117:138-9。冯塞卡。血管角化瘤:二氧化碳激光汽化的成功治疗。皮肤外科杂志2005;31:232-6。
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引用次数: 0
Should Paraben Mix Be Removed from The European Baseline Series. 是否应该将对羟基苯甲酸酯混合物从欧洲基线系列中移除?
IF 0.6 4区 医学 Q3 Medicine Pub Date : 2021-12-01
Inês Gonçalves Nunes, Maria Relvas, Margarida Gonçalo

Dear Editor: The European Baseline Series (EBS) of contact allergens is used throughout Europe as a screening test to diagnose contact allergy as a proxy for allergy contact dermatitis and other hypersensitivity skin diseases (1). Parabens are alkyl esters of p-hydroxybenzoic acid with antimicrobial effects used as preservatives in cosmetics, foods, and drugs that have been included in the so called "baseline series" (2) for more than 40 years. Parabens, which are considered allergologically safe biocides and are classified as safe by the US Food and Drug Administration (FDA) and the Scientific Committee on Consumer Safety (SCCS) in Europe (2-4), are frequently present in cosmetics (5). Despite extensive and progressively expanding use worldwide, studies confirm that parabens are seldom responsible for allergic contact dermatitis to cosmetics, and the frequency of sensitivity to parabens has been low and stable for many decades (2). The frequency of positive reactions to paraben mix is less than 0.5% in most clinical series, although it seems that when it occurs it is often of high clinical relevance (6). Nevertheless, several authors have stated that these patients rarely or never have to avoid foods or cosmetics that contain parabens to control their dermatitis (2). Paraben allergy most frequently occurs in patients with long-lasting stasis dermatitis or disruption of skin integrity, with high use of topical drugs, and in those who do not get better under normal treatment and/or skin care (5). The EBS has been periodically adapted by the European Environmental and Contact Dermatitis Research Group (EECDRG) and the European Society of Contact Dermatitis (ESCD), according to frequency studies, but ensuring that tested haptens remain relevant (1). Bruze et al. recommend that haptens should be considered for inclusion in a baseline series when the contact allergy prevalence is 0.5-1.0% or above (7). So, why not exclude paraben mix from the EBS? We analysed all the EBS tests performed at our institution in the last 21 years (2000-2020) to evaluate the frequency of positive reactions to paraben mix 16% pet (Chemotechnique diagnostics, Vellinge Sweden). In total, 5885 patients were patch tested (MOAHLFA index - Table 1), of whom 29 (10 men and 19 women) patients presented with a positive reaction (1+ or more according to ESCD guidelines) to paraben mix (0.49%), with positivity rates varying between 1.79% and 0.0% and progressively falling for the past 20 years (Figure 1). Present or past clinical relevance was found in 19/29 (65.5%) patients (6 men and 13 women), and was related to the use of topical drugs in 16 patients (55.2%) and cosmetics in three patients (10.3%). Paraben reactions occurred mostly in patients with history of leg ulcer, leg dermatitis, and/or chronic venous insufficiency, which is in agreement with the overrepresentation of the group of patients with leg dermatitis compared with the whole population tested (Table 1). The pro

尊敬的编辑:欧洲接触性过敏原基线系列(EBS)在整个欧洲被用作诊断接触性过敏的筛选试验,作为过敏接触性皮炎和其他超敏性皮肤病的代表(1)。对羟基苯甲酸酯是具有抗菌作用的对羟基苯甲酸烷基酯,用作化妆品、食品和药物的防腐剂,已被列入所谓的“基线系列”(2)超过40年。对羟基苯甲酸酯被认为是过敏性安全的杀菌剂,被美国食品和药物管理局(FDA)和欧洲消费者安全科学委员会(SCCS)列为安全类(2-4),经常出现在化妆品中(5)。尽管在全球范围内广泛且逐步扩大使用,但研究证实,对羟基苯甲酸酯很少引起化妆品的过敏性接触性皮炎。几十年来,对羟基苯甲酸酯敏感的频率一直很低且稳定(2)。在大多数临床系列中,对羟基苯甲酸酯混合物的阳性反应的频率低于0.5%,尽管当它发生时,似乎往往具有很高的临床相关性(6)。一些作者指出,这些患者很少或从不需要避免含有对羟基苯甲酸酯的食物或化妆品来控制他们的皮炎(2)。对羟基苯甲酸酯过敏最常发生在长期停滞性皮炎或皮肤完整性破坏的患者中,外用药物的使用较多。以及那些在正常治疗和/或皮肤护理下没有好转的人(5)。根据频率研究,欧洲环境和接触性皮炎研究小组(EECDRG)和欧洲接触性皮炎学会(ESCD)定期对EBS进行调整,但要确保测试的半抗原保持相关性(1)。Bruze等人建议,当接触性过敏患病率为0.5-1.0%或更高时,应考虑将半抗原纳入基线系列(7)。为什么不从EBS中排除对羟基苯甲酸酯混合物?我们分析了过去21年(2000-2020年)在我们机构进行的所有EBS测试,以评估对羟基苯甲酸酯混合物16% pet的阳性反应频率(Chemotechnique diagnostics, Vellinge Sweden)。总共有5885名患者进行了斑贴试验(MOAHLFA指数-表1),其中29名(10名男性和19名女性)患者对对羟基苯甲酸酯混合物呈阳性反应(根据ESCD指南为1+或更多)(0.49%),阳性率在1.79%至0.0%之间变化,并在过去20年中逐渐下降(图1)。在19/29(65.5%)患者(6名男性和13名女性)中发现了目前或过去的临床相关性。与外用药物16例(55.2%)、化妆品3例(10.3%)有关。对羟基苯甲酸酯反应主要发生在有腿部溃疡、腿部皮炎和/或慢性静脉功能不全病史的患者中,这与与整个测试人群相比,腿部皮炎患者组的过度代表一致(表1)。与没有腿部皮炎的患者相比,腿部皮炎患者对对羟基苯甲酸酯混合物阳性反应的患者比例显着更高(P40 (P
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引用次数: 0
A Misdiagnosed Desmoplastic Neurotropic Melanoma of the Scalp: A Challenging Case for the Pathologist and Surgeon. 一个被误诊的头皮促纤维性嗜神经黑色素瘤:病理学家和外科医生的挑战案例。
IF 0.6 4区 医学 Q3 Medicine Pub Date : 2021-12-01
Tito Brambullo, Paolo Toninello, Regina Sonda, Roberto Salmaso, Diana Sacchi, Stefano Piaserico, Franco Bassetto

Desmoplastic neurotropic melanoma (DNM) is a rare melanoma subtype that shows tropism for the nerves, perineural invasion correlates to higher rate of local recurrence, poorer prognosis and worse morbidity. Given the paucity of typical melanoma features, both clinical and pathological, this confusing skin cancer may act as a pretender, thus leading clinician to misdiagnosis and subsequent inappropriate conservative treatment. Sarcomatoid-like cells rearrangement and absence of pigmentation can lead towards sarcoma diagnosis, so specific skills are required to pathologist to properly recognize this melanoma subtype. In this case report, we present an example of how challenging can be the diagnosis, and how it can affect clinical outcome.

促纤维增生性嗜神经性黑色素瘤(DNM)是一种罕见的黑色素瘤亚型,以神经为向性,侵袭神经周围,局部复发率高,预后差,发病率高。鉴于缺乏典型的黑色素瘤特征,无论是临床还是病理,这种令人困惑的皮肤癌可能充当伪君子,从而导致临床医生误诊和随后不适当的保守治疗。肉瘤样细胞重排和色素沉着的缺失可能导致肉瘤的诊断,因此病理学家需要特定的技能才能正确识别这种黑色素瘤亚型。在这个病例报告中,我们提出了一个如何具有挑战性的诊断,以及它如何影响临床结果的例子。
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引用次数: 0
Coxsackie B3 Virus-induced Acute Hemorrhagic Edema of Infancy. 柯萨奇B3病毒引起的婴儿急性出血性水肿。
IF 0.6 4区 医学 Q3 Medicine Pub Date : 2021-12-01
Ana Soler-Cardona, Adrian Tanew, Sonja Radakovic

Acute hemorrhagic edema of infancy (AHEI) is a cutaneous leukocytoclastic small vessel vasculitis of unknown incidence. It affects mostly infants aged 4 to 24 months. The distinctive features of AHEI include a generally healthy-appearing child with low-grade or absent fever and rarely painful targetoid purpuric edematous lesions. The disease usually resolves spontaneously within 3 weeks without late sequelae. The main differential diagnosis of AHEI is Henoch-Schönlein purpura (HSP). Initially, purpura fulminans should also be ruled out. We report the case of a 5-year-old girl with low fever and rapidly progressive skin lesions who had been admitted to the pediatric clinic. The child presented with palpable annular targetoid and purpuric plaques of different size predominantly affecting the face and extremities. In addition, there was a painful, hemorrhagic edema on the dorsum of her hands and feet. Based on the course of the disease and the typical clinical presentation, i.e., extensive characteristic skin lesions in a young child in a good general health condition, a diagnosis of AHEI was established. A virus serology test showed increased titers of enterovirus and coxsackievirus. Isolation of virus from feces confirmed an infection with coxsackie B3 virus. To our knowledge, this is the first report linking coxsackie B3 virus infection to AHEI.

婴儿急性出血性水肿(AHEI)是一种发病率未知的皮肤白细胞破坏性小血管炎。它主要影响4至24个月大的婴儿。AHEI的显著特征包括一个总体上看起来健康的孩子,有低度或无发烧,很少有疼痛的靶性紫癜性水肿病变。该病通常在3周内自行消退,无晚期后遗症。AHEI的主要鉴别诊断为Henoch-Schönlein紫癜(HSP)。最初,也应排除暴发性紫癜。我们报告的情况下,一个5岁的女孩与低烧和迅速进展的皮肤病变谁已被接纳到儿科诊所。患儿表现为可触及的不同大小的环形靶样斑和紫癜斑,主要影响面部和四肢。此外,她的手背和脚背有疼痛的出血性水肿。根据病程和典型的临床表现,即在一般健康状况良好的幼儿中出现广泛的特征性皮肤病变,确定了AHEI的诊断。病毒血清学检测显示肠病毒和柯萨奇病毒滴度升高。从粪便中分离病毒证实感染柯萨奇B3病毒。据我们所知,这是首例将柯萨奇B3病毒感染与急性脑损伤联系起来的报告。
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引用次数: 0
Potential Dermatological Conditions Resulting from a Prolonged Stay at Home during the COVID-19 Pandemic: A Review. COVID-19大流行期间长时间呆在家里可能导致的皮肤病:综述
IF 0.6 4区 医学 Q3 Medicine Pub Date : 2021-12-01
Diana Isabel Conde Hurtado, Jessica Inés Vergara Rueda, Jorge Luis Bermudez Florez, Silvia Carolina Cadena Infante, Alfonso Javier Rodriguez Morales

A new coronavirus emerged in 2019 in Wuhan, China named Severe Acute Respiratory Syndrome type 2 coronavirus (SARS-CoV-2). Later, this virus spread worldwide, causing a disease called coronavirus disease (COVID-19). To control the outbreak, many countries announced mandatory quarantine; thus, people changed their lifestyles and started engaging in most activities from home. This review explains how some dermatological pathologies may be precipitated by prolonged stays at home, considering that quarantine was a widely used public health measure during 2020. Most of these dermatoses had to be seen, diagnosed, and treated through tele-dermatology, a remote health care system that took force during the COVID-19 pandemic because of its ease and efficiency in connecting health care professionals and their patients; therefore, reducing the risk of contagion and costs associated to medical care. This review of the principal dermatologic conditions during confinement could allow for a better preparation of health professionals.

2019年,中国武汉出现了一种新的冠状病毒,名为“严重急性呼吸综合征2型冠状病毒”(SARS-CoV-2)。后来,这种病毒在全球传播,导致了一种名为冠状病毒病(COVID-19)的疾病。为控制疫情,许多国家宣布实施强制隔离;因此,人们改变了他们的生活方式,开始在家从事大部分活动。考虑到隔离是2020年广泛使用的公共卫生措施,本综述解释了长时间呆在家里可能导致一些皮肤疾病的原因。这些皮肤病中的大多数必须通过远程皮肤病学进行观察、诊断和治疗,这是一种远程医疗保健系统,在COVID-19大流行期间生效,因为它可以轻松高效地将医疗保健专业人员与患者联系起来;因此,减少传染的风险和与医疗保健有关的费用。对坐月子期间主要皮肤病的回顾可以为卫生专业人员提供更好的准备。
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引用次数: 0
期刊
Acta Dermatovenerologica Croatica
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