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Painful nodule on the left fifth finger
Pub Date : 2024-11-28 DOI: 10.1002/jvc2.583
Chihiro Hishinuma, Yuko Watanabe, Hideyuki Ishikawa, Atsuhito Nakazawa, Yukie Yamaguchi
<p>A 75-year-old Japanese man had a history of Stage IVb squamous cell lung cancer (cT3N1M1c) with metastases to the right ribs and left adrenal gland. He had previously tested negative for key nonsmall cell lung cancer driver mutations, including epidermal growth factor receptor, anaplastic lymphoma kinase, C-ros oncogene 1, v-raf murine sarcoma viral oncogene homolog B1 and programmed cell death protein 1. He presented with a painful nodule on the distal phalanx of his left fifth finger. The nodule had gradually increased to 3 cm in diameter and had a red, vascular surface (Figure 1). Initially, the nodule was diagnosed as paronychia and treated with antibiotics, but the condition did not improve. Radiography revealed complete destruction of the distal phalanx (Figure 2), and positron emission tomography-computed tomography showed abnormal uptake in the lesion. A biopsy was performed from the lesion on the left fifth finger (Figure 3a,b).</p><p>The patient was treated with a combination of pembrolizumab and cytotoxic anticancer agents, including paclitaxel and carboplatin. After starting treatment, the acrometastasis shrank dramatically and almost disappeared within 3 months (Figure 4) and dropped off spontaneously 5 months after treatment initiation. However, the patient's condition deteriorated due to the progression of the primary lung cancer, leading to a transition to palliative care. He passed away 2 weeks later.</p><p>Acrometastases refer to secondary lesions located distal to the elbow and knee, accounting for 0.1% of all bone metastases.<span><sup>1</sup></span> They are often misdiagnosed due to their rarity, with 56.8% of hand or wrist lesions initially mistaken for infections such as abscess, felon, osteomyelitis, paronychia or tuberculosis.<span><sup>2</sup></span> Symptoms typically include redness, swelling, pain and limited movement. Because patients with cancer typically have the primary tumour identified first, acrometastases should be considered in the differential diagnosis of distal lesions in patients with cancer.<span><sup>3, 4</sup></span> Our patient had a bone metastasis of lung cancer in the distal phalynx, which is the most common site of phalyngeal metastases.<span><sup>5</sup></span> Acrometastases may occur on either the right or left hand, with bilateral metastases being relatively rare.<span><sup>2</sup></span> The primary site in our patient was situated in the middle lobe of the left lung, disseminating to the right ribs and left adrenal gland. Notably, phalangeal metastases exhibit a nonlateralized distribution pattern with no discernible association with the laterality of the primary neoplasm, regardless of whether it is in the lung, breast or kidney.</p><p>The pathophysiology of acrometastasis is not fully understood but is believed to involve the hematogenous spread of tumour emboli. Mulvey et al.<span><sup>6</sup></span> speculated that venous erosion by a pulmonary neoplasm allows tumour emboli to dissem
一名 75 岁的日本男子曾患 IVb 期鳞状细胞肺癌(cT3N1M1c),右肋和左肾上腺均有转移。他之前的主要非小细胞肺癌驱动基因突变检测呈阴性,包括表皮生长因子受体、无性淋巴瘤激酶、C-ros 致癌基因 1、v-raf 小鼠肉瘤病毒癌基因同源物 B1 和程序性细胞死亡蛋白 1。结节逐渐增大到直径 3 厘米,表面呈红色血管状(图 1)。起初,该结节被诊断为副软骨病,并接受了抗生素治疗,但病情并未好转。放射线检查显示远端指骨完全破坏(图 2),正电子发射计算机断层扫描显示病变部位有异常摄取。患者接受了 pembrolizumab 和细胞毒性抗癌药(包括紫杉醇和卡铂)的联合治疗。开始治疗后,尖锐湿疣在 3 个月内显著缩小并几乎消失(图 4),并在治疗开始 5 个月后自行消退。然而,由于原发性肺癌的进展,患者病情恶化,转入姑息治疗。骨转移瘤是指位于肘部和膝部远端的继发性病变,占所有骨转移瘤的 0.1%。1 由于其罕见性,经常被误诊,56.8% 的手部或腕部病变最初被误诊为感染,如脓肿、梅毒、骨髓炎、骨痒或结核。2 症状通常包括红肿、疼痛和活动受限。由于癌症患者通常首先发现原发肿瘤,因此在癌症患者远端病变的鉴别诊断中应考虑肢端转移瘤。2 我们患者的原发部位位于左肺中叶,并向右肋和左肾上腺扩散。值得注意的是,趾骨转移瘤呈现非侧性分布模式,与原发肿瘤的侧位无明显关联,无论原发肿瘤位于肺、乳腺还是肾脏。Mulvey 等人6 推测,肺部肿瘤对静脉的侵蚀使肿瘤栓子扩散到左心房和心室,随后进入全身动脉循环。这一机制解释了为什么肺癌是数字转移的主要来源。它为肿瘤细胞到达手指提供了独特的途径,不像其他内脏肿瘤栓子不能直接进入动脉而表现为肢端转移。7 Umana 等人4 报告称,在 247 例肢端转移病例中,91 例(36.8%)与本病例一样来自肺癌。相当一部分(58.7%)肺尖骨转移瘤是肺癌最初发现的标志,或与肺癌诊断同时发现,这说明数字转移瘤可能是肺癌诊断的重要线索。远端指骨是最常发生骨转移的部位,这可能是由于远端指骨血流丰富且更容易受到创伤的影响。外伤后释放的趋化因子被认为会促进癌细胞的迁移和粘附,从而促进转移。10 在 Cattelan 等人报告的 482 例手部尖锐湿疣病例中,10 有 141 例接受了截肢治疗,90 例接受了放射治疗,34 例接受了化学放疗。截肢虽然有时是必要的,但会大大降低患者的生活质量。新兴的治疗方法,尤其是包括免疫检查点抑制剂在内的联合化疗--已被确立为肺癌的标准治疗方案--在实现转移灶的实质性消退方面已显示出前景。据我们所知,这是第一例在肺癌联合化疗中加入免疫检查点抑制剂而导致肢端转移灶完全消退的病例。 这一发现表明,与免疫检查点抑制剂联合化疗可能是截肢手术的一种微创替代疗法,对患者生活质量的负面影响较小。值得注意的是,该疗法对肢端转移瘤有效,但对原发肿瘤无效,这可能是由于原发部位和转移部位的血流和基因突变存在差异。与免疫检查点抑制剂联合治疗可能是治疗尖锐湿疣截肢手术的有效替代方法:写作-原稿准备。Yuko Watanabe:构思;写作-审阅和编辑。Hideyuki Ishikawa:指导。Atsuhito Nakazawa:调查;监督。Yukie Yamaguchi:构思;监督:作者声明无利益冲突。患者家属已就发表患者去身份化、匿名的病例细节(包括照片)出具书面知情同意书。伦理批准:不适用。
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引用次数: 0
A reply to “Letter to the editor in response to the article ‘To assess the attitudes of Irish patients attending a pigmented lesion clinic and healthcare staff employed in an academic hospital to biobanking, a quantitative study’” 回复“致编辑的信,回应文章‘评估在色素病变诊所就诊的爱尔兰患者和在学术医院工作的医护人员对生物银行的态度,一项定量研究’ ”
Pub Date : 2024-11-27 DOI: 10.1002/jvc2.558
Stephanie Bowe, Claire Quigley, Liana Victory, Eoin Storan

Stephanie Bowe conceived and designed the analysis, collected the data, contributed data or analysis tools, performed the analysis, wrote the paper. Claire Quigley collected data at pigmented lesion clinics via paper forms. Liana Victory collected data at pigmented lesion clinics via paper forms. Eoin Storan supervised the project and edited the final paper.

The authors declare no conflict of interest.

All subjects gave their informed consent for inclusion before they participated in the study. The study was conducted in accordance with the Declaration of Helsinki, and the protocol was approved by the MMUH and Mater Private Hospital Dublin Institutional Review Board at a meeting in October 2022, with the project reference number: 1/378/2322.

Stephanie Bowe构思并设计了分析,收集数据,提供数据或分析工具,进行分析,撰写论文。克莱尔·奎格利通过纸质表格在色素病变诊所收集数据。Liana Victory通过纸质表格收集色素病变诊所的数据。约恩·斯托兰监督了这个项目,并编辑了最后的论文。作者声明无利益冲突。所有受试者在参与研究前都给予了纳入研究的知情同意。该研究是根据赫尔辛基宣言进行的,该议定书在2022年10月的一次会议上得到了MMUH和Mater私立医院都柏林机构审查委员会的批准,项目参考编号:1/378/2322。
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引用次数: 0
Iododerma with cryptococcus-like changes
Pub Date : 2024-11-27 DOI: 10.1002/jvc2.588
S. Subhadarshani, L. E. Flowers, C. Logan, K. E. Spicknall, C. Shaughnessy

Iododerma is a rare halogenoderma resulting from exposure to iodinated compounds. We present a case involving a 51-year-old Caucasian female with advanced renal disease who developed a hemorrhagic and papulonodular eruption following oral contrast exposure. Cryptococcoid bodies were noted on histopathological evaluation and raised suspicion for the diagnosis of iododerma, which was ultimately confirmed through serum and urine iodine studies. This case highlights a severe presentation of iododerma with important dermatopathology findings.

碘皮疹是一种因接触含碘化合物而导致的罕见卤素皮疹。我们介绍了一个病例,患者是一名 51 岁的高加索女性,患有晚期肾病,在口服造影剂后出现出血性和丘疹状糜烂。在组织病理学评估中发现了隐球菌体,引起了对碘皮病诊断的怀疑,最终通过血清和尿碘研究证实了这一诊断。该病例突出显示了碘皮病的严重表现和重要的皮肤病理学发现。
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引用次数: 0
Vitamin D in patients with psoriasis compared with healthy individuals or with other diseases: A systematic review and meta-analysis
Pub Date : 2024-11-26 DOI: 10.1002/jvc2.550
Bruny Carolina Llamas Castellanos, Wanderley Augusto Arias Ortíz

Background

Psoriasis is a chronic skin disorder characterized by the accelerated proliferation of keratinocytes, which leads to the formation of scaly plaques and a chronic inflammatory response. Vitamin D is an inhibitor of dendritic cells acting as an immune modulator; therefore, vitamin D deficiency could explain the increased incidence of psoriasis for the reduction of anti-inflammatory activity.

Objectives

To compare serum 25-hydroxy vitamin D levels in patients with psoriasis and healthy individuals.

Methods

A systematic review of the literature and meta-analysis was performed by searching PubMed, Embase, Cochrane, Lilacs, Ovid and ProQuest databases to find the best available evidence from 2013 to 2024. We also conducted a snowballing literature search to expand the included studies. The methodological quality and risk of bias were assessed through the Newcastle–Ottawa scale. A random effect meta-analysis model was applied.

Results

A total of 27 articles were included in the systematic review of these three cross-sectional studies included in the first meta-analysis, the synthesized standardized mean difference (SMD) in serum vitamin D between psoriatic arthritis and psoriasis was −0.13 (95% CI [−0.46, 0.20], p = 0.45). The second meta-analysis included two case controls, the synthesized SMD in serum vitamin D between psoriasis and controls was −0.71 (95% CI [−0.85, −0.57], p = 0.00).

Conclusions

No difference in vitamin D levels between psoriasis and psoriatic arthritis was found. Psoriasis patients have lower vitamin D levels than the general population. However, further studies are essential to understand how vitamin D levels contribute to the pathogenesis of psoriasis or vice versa and its role in severity.

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引用次数: 0
Multiple keratotic papulonodular lesions in a human immunodeficiency virus-negative patient
Pub Date : 2024-11-26 DOI: 10.1002/jvc2.578
Rawan Almutairi, Khaled Alobaid, Humoud Al-Sabah, Ahmed Attia, Atlal Allafi
<p>A 52-year-old Bangladeshi female patient presented to the dermatology clinic, in Kuwait, with a painful ulcer and two skin abscesses on her neck accompanied by multiple keratotic papulonodular lesions located in the right mandibular area of her face. The lesions had appeared 3 weeks before, and had gradually increased in size. The patient also mentioned loss of weight, 4 kg in 2 months, with loss of appetite. She did not complain of night sweats, but had a chronic cough with clear sputum. Her medical history revealed that she was diagnosed with haemoglobin E trait since childhood. She had been infected with pulmonary tuberculosis in Bangladesh 25 years ago.</p><p>The patient's vital signs were normal except for elevated temperature (37.3°C). Skin examination revealed a unilateral right mandibular distribution of keratotic papulonodular skin lesions, some of which coalesced to form plaques. These lesions also involved the pre- and postauricular areas. One ulcer measuring 1.5 × 2 cm and two skin abscesses were present in the right lateral neck (Figure 1). No other skin lesions were seen in the other parts of the body. Multiple tender cervical lymph nodes were also observed. Abdominal examination revealed hepatomegaly. The rest of systemic examination was otherwise normal.</p><p>Laboratory investigations revealed mild anaemia (haemoglobin = 10.2), eosinophilia, and an elevated erythrocyte sedimentation rate. HbA1C level is 5.7%. Repeated HIV test was negative. Acid-fast bacillus staining and culture from sputum specimen were negative. The chest radiograph was unremarkable. A high-resolution CT chest showed atelectatic bands in the right upper lobe. Tissue culture for tuberculosis was negative. Extractable nuclear antigen panel was negative for autoantibodies. A skin biopsy was taken (Figure 2).</p><p>Histoplasmosis is an infection caused by the fungus <i>H. capsulatum</i>, which is present in contaminated soil and materials containing bat and bird waste. Histoplasmosis is rare in immunocompetent individuals, and is rarely reported in Kuwait.<span><sup>1</sup></span> Histoplasmosis is classified in four types according to its clinical manifestations: asymptomatic (95%), acute pulmonary, chronic pulmonary, and disseminated.<span><sup>2</sup></span> Disseminated histoplasmosis particularly affects the reticulohistiocytic system. The liver, spleen, pancreas, and intestines, are often affected. Hence, patients with disseminated histoplasmosis may exhibit a range of clinical manifestations, including fever, anorexia, weight loss, cough, vomiting, diarrhoea, abdominal pain, and hepatosplenomegaly.</p><p>Up to 17% of patients with disseminated histoplasmosis develop cutaneous lesions that are diverse and nonspecific and are caused either by the fungus, which causes papules, plaques, nodules, or ulceration, or by an immune response to the infection, such as erythema nodosum or erythema multiforme.<span><sup>3</sup></span> The face, trunk, and extremities
一名 52 岁的孟加拉籍女性患者因颈部疼痛性溃疡和两个皮肤脓肿,并伴有面部右下颌区域多处角化性丘疹性病变,来到科威特的皮肤科诊所就诊。皮损在 3 周前出现,并逐渐增大。患者还提到体重下降,2 个月内体重下降了 4 公斤,并伴有食欲不振。她没有抱怨盗汗,但长期咳嗽,痰液清澈。病史显示,她从小就被诊断出患有血红蛋白 E 特质。除了体温升高(37.3°C)外,患者的生命体征正常。皮肤检查显示,患者右下颌单侧分布有角化性丘疹状皮损,其中一些皮损凝聚成斑块。这些皮损还累及耳前和耳后区域。右侧颈部有一个 1.5 × 2 厘米的溃疡和两个皮肤脓肿(图 1)。身体其他部位未见其他皮肤病变。此外,还观察到多个触痛的颈部淋巴结。腹部检查发现肝脏肿大。实验室检查发现轻度贫血(血红蛋白=10.2)、嗜酸性粒细胞增多和红细胞沉降率升高。HbA1C 水平为 5.7%。反复进行的艾滋病毒检测呈阴性。痰标本的酸性无菌染色和培养均为阴性。胸片无异常。高分辨率胸部 CT 显示右上叶有无气泡带。结核组织培养呈阴性。可提取核抗原检测结果显示自身抗体阴性。组织胞浆菌病是由真菌 H. capsulatum 引起的感染,这种真菌存在于受污染的土壤以及含有蝙蝠和鸟类排泄物的材料中。1 组织胞浆菌病根据其临床表现可分为四种类型:无症状型(95%)、急性肺部型、慢性肺部型和播散型2 。肝脏、脾脏、胰腺和肠道经常受到影响。因此,播散性组织胞浆菌病患者可能表现出一系列临床表现,包括发热、厌食、体重减轻、咳嗽、呕吐、腹泻、腹痛和肝脾肿大。多达 17% 的播散性组织胞浆菌病患者会出现各种非特异性皮肤病变,这些病变或由真菌引起,导致丘疹、斑块、结节或溃疡,或由感染引起的免疫反应引起,如结节性红斑或多形性红斑。面部、躯干和四肢是最常受影响的解剖部位。4 我们的患者面部局部分布的皮损延伸至颈部外侧区域,累及耳前和耳后区域,但未引起听力问题。一份病例报告显示,局部溃疡性病变的分布与此类似,并影响到外耳道5。例如,组织胞浆菌病的皮肤表现在免疫力低下的人,尤其是艾滋病毒/艾滋病患者中更为常见和多态。丘疹和脓疱通常见于组织胞浆菌病的初期表现,而斑块和溃疡则见于病情较重的病例,尤其是播散性病例。由于真菌的血行播散,还可能出现植物性病变,导致大量病变。此外,在免疫力低下的患者中,病变可能表现为痤疮样丘疹、结节、牙龈肿块或溃疡,基底为肉芽肿。6, 7 相反,皮肤组织胞浆菌病在免疫功能正常的人中很少见,通常是真菌通过皮肤直接接种所致。8 组织病理学上,组织胞浆菌病的特征是存在 2-4 微米大小的酵母细胞,这些细胞在巨噬细胞和某些情况下在巨细胞的胞浆内出芽分化。荚膜组织胞浆菌孢子在苏木精和伊红染色以及周期性酸性希夫、吉尔萨和甲氰胺银染色等特殊染色的切片中可见。孢子呈圆形或椭圆形,周围有透明的空间,最初被解释为蒴果,因此被称为 "蒴果孢子"。肉芽肿性炎症,有时伴有酪质坏死。
{"title":"Multiple keratotic papulonodular lesions in a human immunodeficiency virus-negative patient","authors":"Rawan Almutairi,&nbsp;Khaled Alobaid,&nbsp;Humoud Al-Sabah,&nbsp;Ahmed Attia,&nbsp;Atlal Allafi","doi":"10.1002/jvc2.578","DOIUrl":"https://doi.org/10.1002/jvc2.578","url":null,"abstract":"&lt;p&gt;A 52-year-old Bangladeshi female patient presented to the dermatology clinic, in Kuwait, with a painful ulcer and two skin abscesses on her neck accompanied by multiple keratotic papulonodular lesions located in the right mandibular area of her face. The lesions had appeared 3 weeks before, and had gradually increased in size. The patient also mentioned loss of weight, 4 kg in 2 months, with loss of appetite. She did not complain of night sweats, but had a chronic cough with clear sputum. Her medical history revealed that she was diagnosed with haemoglobin E trait since childhood. She had been infected with pulmonary tuberculosis in Bangladesh 25 years ago.&lt;/p&gt;&lt;p&gt;The patient's vital signs were normal except for elevated temperature (37.3°C). Skin examination revealed a unilateral right mandibular distribution of keratotic papulonodular skin lesions, some of which coalesced to form plaques. These lesions also involved the pre- and postauricular areas. One ulcer measuring 1.5 × 2 cm and two skin abscesses were present in the right lateral neck (Figure 1). No other skin lesions were seen in the other parts of the body. Multiple tender cervical lymph nodes were also observed. Abdominal examination revealed hepatomegaly. The rest of systemic examination was otherwise normal.&lt;/p&gt;&lt;p&gt;Laboratory investigations revealed mild anaemia (haemoglobin = 10.2), eosinophilia, and an elevated erythrocyte sedimentation rate. HbA1C level is 5.7%. Repeated HIV test was negative. Acid-fast bacillus staining and culture from sputum specimen were negative. The chest radiograph was unremarkable. A high-resolution CT chest showed atelectatic bands in the right upper lobe. Tissue culture for tuberculosis was negative. Extractable nuclear antigen panel was negative for autoantibodies. A skin biopsy was taken (Figure 2).&lt;/p&gt;&lt;p&gt;Histoplasmosis is an infection caused by the fungus &lt;i&gt;H. capsulatum&lt;/i&gt;, which is present in contaminated soil and materials containing bat and bird waste. Histoplasmosis is rare in immunocompetent individuals, and is rarely reported in Kuwait.&lt;span&gt;&lt;sup&gt;1&lt;/sup&gt;&lt;/span&gt; Histoplasmosis is classified in four types according to its clinical manifestations: asymptomatic (95%), acute pulmonary, chronic pulmonary, and disseminated.&lt;span&gt;&lt;sup&gt;2&lt;/sup&gt;&lt;/span&gt; Disseminated histoplasmosis particularly affects the reticulohistiocytic system. The liver, spleen, pancreas, and intestines, are often affected. Hence, patients with disseminated histoplasmosis may exhibit a range of clinical manifestations, including fever, anorexia, weight loss, cough, vomiting, diarrhoea, abdominal pain, and hepatosplenomegaly.&lt;/p&gt;&lt;p&gt;Up to 17% of patients with disseminated histoplasmosis develop cutaneous lesions that are diverse and nonspecific and are caused either by the fungus, which causes papules, plaques, nodules, or ulceration, or by an immune response to the infection, such as erythema nodosum or erythema multiforme.&lt;span&gt;&lt;sup&gt;3&lt;/sup&gt;&lt;/span&gt; The face, trunk, and extremities ","PeriodicalId":94325,"journal":{"name":"JEADV clinical practice","volume":"4 1","pages":"359-363"},"PeriodicalIF":0.0,"publicationDate":"2024-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jvc2.578","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143530744","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
AI powered detection and assessment of onychomycosis: A spotlight on yellow and deep learning
Pub Date : 2024-11-25 DOI: 10.1002/jvc2.577
C. Agostini, R. Ranjan, M. Molnarova, A. Hadzic, O. Kubesch, V. Schnidar, H. Schnidar

Background

Despite significant advances in computer-aided diagnostics, onychomycosis, a widespread fungal nail infection, lacks an automated approach for objective analysis and classification.

Objectives

Our study aimed to develop and validate automated machine learning models to accurately detect and classify onychomycosis-affected areas in toenails.

Methods

The images in this study were captured using the Scarletred® Vision mobile App and SkinPatch, a CE certified medical device system working seamlessly together to deliver auto-color calibrated, high-resolution clinical images. Considering a total of 1687 images from 440 subjects, the research explores various degrees of onychomycosis and evaluates the infection extent in the toenails detected. We developed an advanced machine learning algorithm for precise segmentation and classification of onychomycosis-affected toenails, utilizing expert annotations and advanced post-processing techniques. Additionally, an analysis of nail growth was performed, and a comparison graph with the percentage of infection was estimated.

Results

Using advanced machine learning algorithms, we successfully detected toenails, enabling detailed analysis of intricate structures within the images. We achieved a final validation loss of 0.0236 and an F1 score of 0.8566 for accurate toenail detection, while the Random Forest algorithm demonstrated 81% accuracy in classifying and distinguishing between infected and healthy toenail areas. Our applied superpixel method furthermore improved the algorithm's precision in identifying the infected regions.

Conclusions

Our AI-powered image analysis method, initially focused on the big toe's toenail, shows great promise for broader validation on comprehensive datasets, enabling more detailed assessments of onychomycosis severity and disease dynamics. The potential impact of limited patient diversity, particularly with darker skin tones, needs further assessment. Proven to measure nail growth and assess treatment effectiveness over time, our developed AI is the first of its kind to demonstrate this capability, representing a significant advancement as a novel decision support tool for clinical research and routine medical practice.

背景 尽管计算机辅助诊断技术取得了重大进展,但作为一种广泛存在的真菌性指甲感染,甲癣仍缺乏一种可进行客观分析和分类的自动化方法。 目标 我们的研究旨在开发和验证自动机器学习模型,以准确检测和分类脚趾甲中受甲癣影响的区域。 方法 本研究中的图像是使用 Scarletred® Vision 移动应用程序和 SkinPatch 采集的,Scarletred® Vision 移动应用程序和 SkinPatch 是通过 CE 认证的医疗设备系统,可无缝协作提供自动校色的高分辨率临床图像。研究共使用了来自 440 名受试者的 1687 张图像,探讨了不同程度的甲癣,并对检测到的趾甲感染程度进行了评估。我们开发了一种先进的机器学习算法,利用专家注释和先进的后处理技术,对受甲癣影响的脚趾甲进行精确分割和分类。此外,还对指甲生长情况进行了分析,并估算了感染比例对比图。 结果 利用先进的机器学习算法,我们成功地检测出了脚趾甲,并对图像中的复杂结构进行了详细分析。在准确检测脚趾甲方面,我们取得了 0.0236 的最终验证损失和 0.8566 的 F1 分数,而随机森林算法在分类和区分感染和健康脚趾甲区域方面的准确率达到了 81%。我们应用的超像素方法进一步提高了算法识别感染区域的精确度。 结论 我们的人工智能图像分析方法最初主要针对大脚趾的趾甲,但在综合数据集上进行更广泛的验证,从而对癣菌病的严重程度和疾病动态进行更详细的评估方面显示出巨大的前景。患者多样性有限,尤其是肤色较深的患者,其潜在影响需要进一步评估。我们开发的人工智能已证明可以测量指甲生长情况并评估一段时间内的治疗效果,是同类产品中首款具备这种能力的产品,作为临床研究和常规医疗实践的新型决策支持工具,这是一项重大进步。
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引用次数: 0
Immunocryosurgery for facial, non-superficial basal cell carcinoma triggers consistent but transient cell counts alterations in the circulating innate immune cell lines
Pub Date : 2024-11-24 DOI: 10.1002/jvc2.573
G. Gaitanis, A. Ganiatsa, G. Vartholomatos, K. Seretis, I. D. Bassukas
<p>Immunocryosurgery, a fixed-time combination of imiquimod and cryosurgery,<span><sup>1</sup></span> is a highly effective modality for basal cell carcinomas (BCCs),<span><sup>2</sup></span> including non-superficial tumors amenable to excision.<span><sup>3</sup></span> Previous studies, both in tissue and peripheral blood, have focused on the role of T-regulatory lymphocytes as antitumor effectors during immunocryosurgery for BCC.<span><sup>4, 5</sup></span> In the present study we addressed the influence of an immunocryosurgery treatment cycle for BCC on the peripheral blood cell counts.</p><p>Institutional Review Committee approval was granted (Θ59 45/17-11-2022). Immunocryosurgery entails the application of 5% imiquimod cream once daily for 5 weeks and a single cryosurgery session on Day 14 of the treatment cycle (liquid N<sub>2</sub>, open spray, two freeze-thaw cycles of 20 s freezing time each).<span><sup>1</sup></span> As previously,<span><sup>5</sup></span> peripheral blood cell counts were determined at four time points: within 4 days before the initiation of treatment (“Week 0,” ‘baseline’), on the day of cryosurgery (“Week 2”), on the last day (plus a maximum of 2 days) of treatment (“Week 5”), and at 4 weeks follow up (±2 days: “Week 9”). The distributions of continuous variables are represented as medians and means±standard deviations (SD). Friedman tests (four measurements/patient) with <i>post-hoc</i> Dunn's tests were calculated using SPSS, with <i>p</i> < 0.05 indicating statistical significance.</p><p>Thirteen immunocompetent patients were included (age: 67–81 years; 11 men), each with a facial, biopsy confirmed non-superficial BCC (median BCC diameter: 15 mm, range: 7–19 mm). All tumors responded with vivid local inflammatory alterations, cleared completely after one treatment cycle and remained recurrence-free for at least 12 months. A discrete pattern of temporal variation was encountered in the counts of all leukocyte cell lines, except for monocytes, during imiquimod treatment (Table 1). The whole leukocytes and the three granulocyte subpopulations (neutrophils, eosinophils, and basophils) cell counts reduced significantly compared to baseline during imiquimod application (<i>p</i> < 0.0001, Friedman test) and recovered within 1 month thereafter. Also, for lymphocytes, nadir counts were observed at the end of imiquimod treatment; however, the perturbations of the lymphocyte numbers did not present a similar deviation degree as the cell lines of the innate immunity (<i>p</i> = 0.0153, Friedman test). Nonetheless, in no case did the cell numbers at nadir drop below the corresponding normal cell counts limits (Figure 1) or did we observe any clinical signs of immunosuppression.</p><p>Our results document a systemic, to date underrecognized immunocryosurgery effect on the peripheral blood cell counts. Thereby the role of imiquimod is central as the counts drop was evident before cryosurgery. Our findings add to the spar
{"title":"Immunocryosurgery for facial, non-superficial basal cell carcinoma triggers consistent but transient cell counts alterations in the circulating innate immune cell lines","authors":"G. Gaitanis,&nbsp;A. Ganiatsa,&nbsp;G. Vartholomatos,&nbsp;K. Seretis,&nbsp;I. D. Bassukas","doi":"10.1002/jvc2.573","DOIUrl":"https://doi.org/10.1002/jvc2.573","url":null,"abstract":"&lt;p&gt;Immunocryosurgery, a fixed-time combination of imiquimod and cryosurgery,&lt;span&gt;&lt;sup&gt;1&lt;/sup&gt;&lt;/span&gt; is a highly effective modality for basal cell carcinomas (BCCs),&lt;span&gt;&lt;sup&gt;2&lt;/sup&gt;&lt;/span&gt; including non-superficial tumors amenable to excision.&lt;span&gt;&lt;sup&gt;3&lt;/sup&gt;&lt;/span&gt; Previous studies, both in tissue and peripheral blood, have focused on the role of T-regulatory lymphocytes as antitumor effectors during immunocryosurgery for BCC.&lt;span&gt;&lt;sup&gt;4, 5&lt;/sup&gt;&lt;/span&gt; In the present study we addressed the influence of an immunocryosurgery treatment cycle for BCC on the peripheral blood cell counts.&lt;/p&gt;&lt;p&gt;Institutional Review Committee approval was granted (Θ59 45/17-11-2022). Immunocryosurgery entails the application of 5% imiquimod cream once daily for 5 weeks and a single cryosurgery session on Day 14 of the treatment cycle (liquid N&lt;sub&gt;2&lt;/sub&gt;, open spray, two freeze-thaw cycles of 20 s freezing time each).&lt;span&gt;&lt;sup&gt;1&lt;/sup&gt;&lt;/span&gt; As previously,&lt;span&gt;&lt;sup&gt;5&lt;/sup&gt;&lt;/span&gt; peripheral blood cell counts were determined at four time points: within 4 days before the initiation of treatment (“Week 0,” ‘baseline’), on the day of cryosurgery (“Week 2”), on the last day (plus a maximum of 2 days) of treatment (“Week 5”), and at 4 weeks follow up (±2 days: “Week 9”). The distributions of continuous variables are represented as medians and means±standard deviations (SD). Friedman tests (four measurements/patient) with &lt;i&gt;post-hoc&lt;/i&gt; Dunn's tests were calculated using SPSS, with &lt;i&gt;p&lt;/i&gt; &lt; 0.05 indicating statistical significance.&lt;/p&gt;&lt;p&gt;Thirteen immunocompetent patients were included (age: 67–81 years; 11 men), each with a facial, biopsy confirmed non-superficial BCC (median BCC diameter: 15 mm, range: 7–19 mm). All tumors responded with vivid local inflammatory alterations, cleared completely after one treatment cycle and remained recurrence-free for at least 12 months. A discrete pattern of temporal variation was encountered in the counts of all leukocyte cell lines, except for monocytes, during imiquimod treatment (Table 1). The whole leukocytes and the three granulocyte subpopulations (neutrophils, eosinophils, and basophils) cell counts reduced significantly compared to baseline during imiquimod application (&lt;i&gt;p&lt;/i&gt; &lt; 0.0001, Friedman test) and recovered within 1 month thereafter. Also, for lymphocytes, nadir counts were observed at the end of imiquimod treatment; however, the perturbations of the lymphocyte numbers did not present a similar deviation degree as the cell lines of the innate immunity (&lt;i&gt;p&lt;/i&gt; = 0.0153, Friedman test). Nonetheless, in no case did the cell numbers at nadir drop below the corresponding normal cell counts limits (Figure 1) or did we observe any clinical signs of immunosuppression.&lt;/p&gt;&lt;p&gt;Our results document a systemic, to date underrecognized immunocryosurgery effect on the peripheral blood cell counts. Thereby the role of imiquimod is central as the counts drop was evident before cryosurgery. Our findings add to the spar","PeriodicalId":94325,"journal":{"name":"JEADV clinical practice","volume":"4 1","pages":"316-319"},"PeriodicalIF":0.0,"publicationDate":"2024-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jvc2.573","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143530612","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
Efficacy of brodalumab in psoriasis patients with a body weight >100 kg: Real-world evidence (RWE) from the LIBERO study
Pub Date : 2024-11-21 DOI: 10.1002/jvc2.556
Ralph von Kiedrowski, Khusru Asadullah, Bernhard Korge, Konstantina Tsarovina, Matthias Augustin

Background

Patients with psoriasis often suffer from obesity. However, only limited data are available on the efficacy of brodalumab 210 mg, a fully human monoclonal immunoglobulin IgG2 antibody binding to the human interleukin 17 receptor subunit A, in obese patients in daily practice, to date.

Objectives

A subgroup analysis from the LIBERO study was conducted to compare the effectiveness of brodalumab in patients weighing ≤100 and >100 kg after ~12 weeks (W) and ~52 W.

Methods

LIBERO is a large prospective, multicenter, non-interventional, real-world-evidence study including adult patients with plaque psoriasis treated with brodalumab 210 mg.

Results

Four hundred and sixty-one patients with a body weight up to 100 kg (nonobese) and 161 patients with >100 kg body weight (obese) were included in this subgroup analysis. At baseline, the majority of patients in both groups had very severe (12.6%; 15.7%) or severe (49.4%; 55.0%) psoriasis, as assessed by Physician Global Assessment (PGA). As of W2, a significant reduction of the mean PASI could be achieved in both groups. In patients weighing ≤100 kg mean PASI decreased from 16.9 to 9.0 and further improved to 2.6 at ~W12 (p < 0.001). In the patient group >100 kg, the PASI decreased from 17.9 to 10.2 at ~W2 (p < 0.001) and improved further to 3.9 at ~W12 (p < 0.001). However, at ~W12 absolute PASI0-3 rates were lower in patients >100 kg than in patients ≤100 kg (68.4% vs. 80.5%, p = 0.006); there was no statistically significant difference between the groups at ~W52/last visit any more in any of the effectiveness parameters with, for example, a PGA0/1 response of 82.3% versus 86.5% (p = 0.6089), respectively.

Conclusions

This subgroup analysis of LIBERO confirmed, that in daily practice brodalumab can be equally beneficial patients with >100 and ≤100 kg in the long-term management of psoriasis.

背景 银屑病患者通常患有肥胖症。然而,迄今为止,关于布达鲁单抗 210 毫克(一种与人类白细胞介素 17 受体亚基 A 结合的全人源单克隆免疫球蛋白 IgG2 抗体)在肥胖患者日常治疗中的疗效,只有有限的数据。 目的 对 LIBERO 研究进行亚组分析,比较体重≤100 和 >100 公斤的患者在约 12 周(W)和约 52 周(W)后使用布达鲁单抗的疗效。 方法 LIBERO 是一项大型前瞻性、多中心、非干预性、真实世界证据研究,研究对象包括接受布达鲁单抗 210 毫克治疗的斑块状银屑病成年患者。 结果 461 名体重不超过 100 千克的患者(非肥胖)和 161 名体重达 100 千克的患者(肥胖)被纳入该亚组分析。在基线期,两组患者中的大多数人都患有非常严重(12.6%;15.7%)或严重(49.4%;55.0%)的银屑病,这是由医生全球评估(PGA)来评估的。截至第二周,两组患者的平均 PASI 均有明显下降。体重≤100 千克的患者的平均 PASI 从 16.9 降至 9.0,到第 12 个月时进一步降至 2.6(p <0.001)。在体重为 100 千克的患者组中,PASI 在 ~W2 时从 17.9 降至 10.2(p < 0.001),在 ~W12 时进一步降至 3.9(p < 0.001)。然而,在~W12时,体重为100 kg的患者的PASI0-3绝对值低于体重≤100 kg的患者(68.4% vs. 80.5%,p = 0.006);在~W52/最后一次就诊时,两组患者在任何疗效参数上都没有统计学意义上的显著差异,例如,PGA0/1反应率分别为82.3% vs. 86.5%(p = 0.6089)。 结论 LIBERO 的这项亚组分析证实,在日常治疗中,体重为 100 kg 和小于 100 kg 的患者在银屑病的长期治疗中同样受益。
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引用次数: 0
The role of wearable technology in real-time skin health monitoring
Pub Date : 2024-11-20 DOI: 10.1002/jvc2.587
Kelly Frasier, Vivian Li, Michelle Sobotka, Julia Vinagolu-Baur, Grace Herrick

The integration of wearable technology in real-time skin health monitoring represents a significant advancement in personalised healthcare. This review synthesises existing research on wearable devices tailored for skin condition monitoring, encompassing aspects such as ultraviolet exposure tracking, hydration level assessment, and early detection of potential dermatological diseases. Current literature underscores the efficacy of wearable sensors in providing timely insights into skin health parameters, enabling proactive skin care interventions and disease management. Moreover, the seamless integration of sensor data with smartphone applications facilitates user-friendly monitoring and personalised alerts, enhancing user engagement and adherence to skincare regimens. Moving forward, future research should prioritise the refinement of sensor accuracy and reliability, the development of standardised metrics for skin health assessment, and the exploration of novel applications such as artificial intelligence-driven predictive analytics for early disease detection. Additionally, interdisciplinary collaborations between engineers, dermatologists, and data scientists hold promise for unlocking the full potential of wearable technology in revolutionising skin health management. Incorporating wearable technology in real-time skin health monitoring not only revolutionises preventive skincare practices but also holds immense potential for transforming the management of chronic skin conditions, paving the way for personalised, proactive, and patient-centric dermatological care.

将可穿戴技术整合到实时皮肤健康监测中,是个性化医疗保健领域的一大进步。这篇综述综述了现有针对皮肤状况监测的可穿戴设备的研究,包括紫外线照射跟踪、水合水平评估和潜在皮肤病的早期检测等方面。目前的文献强调了可穿戴传感器在及时了解皮肤健康参数方面的功效,从而实现积极的皮肤护理干预和疾病管理。此外,传感器数据与智能手机应用程序的无缝整合还有利于进行用户友好型监测和个性化提醒,从而提高用户的参与度和对护肤方案的依从性。展望未来,未来的研究应优先考虑提高传感器的准确性和可靠性,开发用于皮肤健康评估的标准化指标,以及探索新型应用,如用于早期疾病检测的人工智能驱动的预测分析。此外,工程师、皮肤科医生和数据科学家之间的跨学科合作有望充分释放可穿戴技术的潜力,彻底改变皮肤健康管理模式。将可穿戴技术纳入实时皮肤健康监测不仅能彻底改变预防性护肤方法,还能为改变慢性皮肤病的管理带来巨大潜力,为个性化、前瞻性和以患者为中心的皮肤病护理铺平道路。
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引用次数: 0
Mechanobullous form of epidermolysis bullosa acquisita: Insights into disease mechanisms as inferred by response to rituximab, but not to JAK inhibitors
Pub Date : 2024-11-20 DOI: 10.1002/jvc2.568
L. Gueissaz, A. Junge, R. Wolf, C. Schlapbach, L. Feldmeyer, L. Borradori

Epidermolysis bullosa acquisita (EBA) is a rare autoimmune blistering disease associated with IgG autoantibodies directed against type VII collagen. Different clinical forms have been described, including the classical mechanobullous variant resembling epidermolysis bullosa dystrophica, which is typically treatment-resistant. We here describe a 67-year-old patient with a mechanobullous EBA characterized by trauma-induced blisters on her hands and feet for 9 months. Despite treatments with oral prednisolone, topical steroids or calcineurin inhibitors, doxycycline, ciclosporin, and baracitinib, no improvement was observed. The patient went into complete remission only after administration of rituximab with no lesions off therapy at the 10-month follow up. Our observation suggests that inflammatory cytokines are not primarily responsible for skin blistering and fragility in mechanobullous EBA. The effectiveness of rituximab provides some insights into the major direct role of autoantibodies in mediating dermo-epidermal separation in this variant of EBA.

获得性大疱性表皮松解症(EBA)是一种罕见的自身免疫性水疱病,与针对Ⅶ型胶原的IgG自身抗体有关。该病有不同的临床表现形式,包括典型的机械性大疱变异型,类似于表皮溶解性大疱性萎缩症,通常具有抗药性。我们在此描述了一名 67 岁的机械性大疱性表皮松解症患者,她的手脚因外伤引起的水疱长达 9 个月之久。尽管使用了口服泼尼松龙、外用类固醇或钙调磷酸酶抑制剂、强力霉素、环孢素和巴拉替尼等治疗方法,但病情未见好转。只有在使用利妥昔单抗后,患者的病情才完全缓解,并且在 10 个月的随访中没有发现病变。我们的观察结果表明,炎症细胞因子并不是导致机械性大疱性皮肤炎皮肤起泡和脆弱的主要原因。利妥昔单抗的疗效使我们对自身抗体在这种变异型 EBA 中介导真皮-表皮分离的主要直接作用有了一些了解。
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引用次数: 0
期刊
JEADV clinical practice
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