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Dermal Irritation, Sensitization, and Safety of Fixed-Dose Triple-Combination Clindamycin Phosphate 1.2%/Benzoyl Peroxide 3.1%/Adapalene 0.15% Gel in Healthy Participants 固定剂量三联克林霉素磷酸1.2%/过氧化苯甲酰3.1%/阿达帕烯0.15%凝胶对健康受试者的皮肤刺激、致敏和安全性
Pub Date : 2023-07-17 DOI: 10.25251/skin.7.supp.227
Z. Draelos, E. Tanghetti, L. Stein Gold, L. Kircik, N. Bhatia, J. Zeichner, Jeffrey Sugarman
Introduction: IDP-126 polymeric mesh gel (clindamycin phosphate 1.2%/benzoyl peroxide [BPO] 3.1%/adapalene 0.15%) is the first triple-combination, fixed-dose topical acne product in development and it addresses major acne pathophysiological processes. IDP-126 demonstrated superior efficacy to vehicle and component dyads, with good safety/tolerability in a phase 2 study of participants with moderate-to-severe acne. The objectives of this study were to assess dermal irritation/sensitization and safety of IDP-126 gel in two phase 1 studies and to compare irritancy of IDP-126 gel and commercially available BPO 2.5%/adapalene 0.3% gel in one phase 1 study of healthy participants. Methods: Two phase 1, randomized, evaluator-blinded, within-participant, dermal safety studies enrolled healthy participants aged ≥18 years (N=234, repeat insult patch test [RIPT]; N=45, cumulative irritation patch test [CIPT]). Patches were applied to the upper back multiple times over 6-8 weeks (RIPT) or every 24 hours for 21 days (CIPT). Patches contained: IDP-126 gel, vehicle gel, saline 0.9% (RIPT/CIPT), sodium lauryl sulfate (SLS) 0.5% (CIPT), or branded BPO 2.5%/adapalene 0.3% gel (CIPT). Participants in each study received all treatments. Endpoints comprised sensitization potential (RIPT), mean cumulative/total irritation scores, and treatment-emergent adverse events (TEAEs). Results: Overall, irritation with IDP-126 was moderate and not clinically significant. CIPT: IDP-126 was “moderately irritating” (mean score: 1.29), which was significantly less irritating than BPO/adapalene (1.96; P<0.001), statistically similar to SLS (1.17), and more irritating than saline or vehicle (~0.30; P<0.001). RIPT: no participants had investigator-confirmed sensitization to any treatments. In both studies, no TEAEs were related to treatment. Conclusions: In two phase 1 studies, fixed-dose, triple-combination clindamycin phosphate 1.2%/ BPO 3.1%/adapalene 0.15% polymeric mesh gel had moderate irritancy and no confirmed sensitization in healthy participants. Additionally, IDP-126 demonstrated significantly less irritation versus commercially available, branded BPO 2.5%/adapalene 0.3% gel. IDP-126 demonstrated good safety/tolerability, mirroring the phase 2 study results.   Funding: Ortho Dermatologics
简介:IDP-126聚合物网状凝胶(克林霉素磷酸酯1.2%/过氧化苯甲酰[BPO]3.1%/阿达帕林0.15%)是开发中的第一种三重组合、固定剂量的局部痤疮产品,它解决了主要的痤疮病理生理过程。在一项针对中度至重度痤疮参与者的2期研究中,IDP-126显示出优于载体和组件二元组的疗效,具有良好的安全性/耐受性。本研究的目的是在两项第一阶段研究中评估IDP-126凝胶的皮肤刺激性/致敏性和安全性,并在一项针对健康参与者的第一阶段研究中将IDP-126凝胶和市售BPO 2.5%/阿达帕林0.3%凝胶的刺激性进行比较。方法:两项1期、随机、评估者盲法、参与者内的皮肤安全性研究招募了年龄≥18岁的健康参与者(N=234,重复刺激性贴剂试验[RIPT];N=45,累积刺激性贴片试验[CIPT])。在6-8周内(RIPT)或每24小时在21天内(CIPT)在上背部多次施用贴片。贴片包含:IDP-126凝胶、载体凝胶、0.9%生理盐水(RIPT/CIPT)、0.5%十二烷基硫酸钠(SLS)(CIPT)或品牌BPO 2.5%/阿达帕林0.3%凝胶(CIPT)。每项研究的参与者都接受了所有的治疗。终点包括致敏潜能(RIPT)、平均累积/总刺激评分和治疗突发不良事件(TEAE)。结果:总体而言,IDP-126的刺激性为中度,无临床意义。CIPT:IDP-126具有“中度刺激性”(平均得分:1.29),其刺激性明显低于BPO/阿达帕林(1.96;P<0.001),在统计学上与SLS(1.17)相似,并且比生理盐水或赋形剂更具刺激性(~0.30;P<0.001。在这两项研究中,没有TEAE与治疗有关。结论:在两项1期研究中,固定剂量、三重组合克林霉素磷酸酯1.2%/BPO 3.1%/阿达帕林0.15%聚合物网状凝胶对健康参与者具有中度刺激性,未证实致敏。此外,与市售的品牌BPO 2.5%/阿达帕林0.3%凝胶相比,IDP-126的刺激性显著降低。IDP-126表现出良好的安全性/耐受性,反映了2期研究结果。资助:Ortho Dermatologics
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引用次数: 0
A Case of a Large, Painful Dermatofibrosarcoma Protuberans Arising from a Traumatic Scar 外伤性疤痕引起的巨大、疼痛的隆突性皮肤纤维肉瘤1例
Pub Date : 2023-05-20 DOI: 10.25251/skin.7.3.16
D. Fischer, Graham H Litchman
Here we report a case of dermatofibrosarcoma protuberans (DFSP) that presented originally to the emergency department with chief complaint of ‘chest pain arising from a chest wall mass’. This case is unique for multiple reasons including the fact that the DFSP caused this patient severe pain that radiated from the site of the mass to the patient’s back. The lesion originated from a traumatic scar that the patient had obtained following a car accident two years prior to presentation. In addition, the DFSP was significantly larger in size than what has typically been reported in the literature. This case illustrates that DFSP has the potential to present with multiple atypical features.
在此,我们报告一例隆突性皮肤纤维肉瘤(DFSP),最初以“胸壁肿块引起的胸痛”为主诉来到急诊科。由于多种原因,该病例是独特的,包括DFSP导致该患者从肿块部位放射到患者背部的严重疼痛。病变源于创伤性疤痕,该疤痕是患者在出现症状前两年发生车祸后留下的。此外,DFSP的大小明显大于文献中通常报道的。本病例说明DFSP有可能呈现多种非典型特征。
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引用次数: 0
Acne symptoms and impact of acne on social functioning, emotional functioning, and activities of daily living (ADL) among patients with moderate to severe non-nodular Acne Vulgaris (AV) in community practices across the U.S 在美国各地的社区实践中,中度至重度非结节性寻常痤疮(AV)患者的痤疮症状和痤疮对社交功能、情绪功能和日常生活活动的影响
Pub Date : 2023-05-20 DOI: 10.25251/skin.7.supp.208
E. Graber, H. Baldwin, A. Alexis, J. D. Del Rosso, R. Fried, J. Harper, Adelaide Hebert, L. Kircik, E. Rieder, L. Stein Gold, Siva Narayanan, V. Koscielny, I. Kasujee
Objective: Evaluate patient self-perceived AV symptoms and impact of AV on emotional/social functioning and ADL, among AV patients in community practices across the U.S. Methods: Single-arm, prospective cohort study (PROSES: NCT04820673) was conducted with moderate-to-severe non-nodular AV patients >9yrs who were prescribed sarecycline in real-world U.S community practices. Validated ASIS questionnaire (with Signs and Impact (emotional & social) domains) and an Expert Panel Questionnaire (EPQ; emotional functioning (items 1-4), social functioning (items 5-7), and ADL (items 8-11)) were completed by patients (>12yrs) and caregivers (for patients 9-11yrs) at baseline and week-12. All items were scored on five-point adjectival response scale (score: 0 (never/not at all) – 4 (all the time/very much/extremely)); a higher ASIS domain score indicate severe symptoms or negative impact of AV. ASIS domain scores and proportion of patients reporting score=2/3/4 (moderate to high burden/impact or parent understanding (EPQ10)) for EPQ items at baseline were analyzed. Results: A total of 253 AV patients completed the study (pediatric: 39.92%; female: 66.40%; moderate AV: 86.56%; severe AV: 13.44%). At baseline, patients reported moderate AV burden in most domains, as depicted by the following domain score: signs: 1.96, impact: 2.06, emotional impact subdomain: 2.43; social impact subdomain: 0.98. From EPQ items, proportion of patients reporting score=2/3/4 (moderate to severe burden) at baseline were: patients’ mood/anger (EPQ1) – 56.13%; worries about AV worsening (EPQ2) – 79.45%; thinking about acne (EPQ3) – 84.19%; level of acne worries (EPQ4) – 72.73; patients’ social media/’selfie’ activity (EPQ5) – 51.38%; impact on real-life plans (EPQ6) – 44.66%; efforts to hide AV (EPQ7) – 72.73%; picked-on/judged due to AV (EPQ8) – 26.88%; ability to reach future goals (EPQ9) – 27.27%; sleep impact (EPQ11) – 27.67%; parent understanding of AV concerns (for patients<18yrs; EPQ10) – 84.16%. Conclusion: Moderate to severe AV burden/impact was observed in this prospective cohort of AV patients in the U.S. Emotional impact and social impact of AV were especially more pronounced among the AV population.
目的:在美国各地的社区实践中,评估患者自我感知的AV症状以及AV对情绪/社会功能和ADL的影响。方法:单臂前瞻性队列研究(PROSES:NCT04820673)对9岁以上的中重度非结节性AV患者进行,这些患者在真实的美国社区实践中服用了沙环素。经验证的ASIS问卷(包括症状和影响(情绪和社会)领域)和专家小组问卷(EPQ;情绪功能(项目1-4)、社会功能(项目5-7)和ADL(项目8-11))由患者(>12岁)和护理人员(9-11岁患者)在基线和第12周完成。所有项目都在五分形容词反应量表上得分(得分:0(从未/根本没有)-4(一直/非常/非常));较高的ASIS域得分指示AV的严重症状或负面影响。分析ASIS领域得分和报告基线时EPQ项目得分=2/3/4(中等至高负担/影响或父母理解(EPQ10))的患者比例。结果:共有253名AV患者完成了研究(儿科:39.92%;女性:66.40%;中度AV:86.56%;重度AV:13.44%)。基线时,患者在大多数领域报告了中度AV负担,如以下领域得分所示:体征:1.96,影响:2.06,情绪影响子域:2.43;社会影响子域:0.98。从EPQ项目来看,基线时报告得分=2/3/4(中度至重度负担)的患者比例为:患者的情绪/愤怒(EPQ1)–56.13%;对AV恶化的担忧(EPQ2)-79.45%;思考痤疮(EPQ3)–84.19%;痤疮担忧水平(EPQ4)–72.73;患者的社交媒体/“自拍”活动(EPQ5)——51.38%;对现实生活计划的影响(EPQ6)——44.66%;努力隐藏AV(EPQ7)–72.73%;因AV(EPQ8)而被选中/判定–26.88%;实现未来目标的能力(EPQ9)-27.27%;睡眠影响(EPQ11)-27.67%;父母对AV问题的理解(对于<18岁的患者;EPQ10)-84.16%。结论:在美国AV患者的前瞻性队列中观察到中度至重度AV负担/影响。AV的情绪影响和社会影响在AV人群中尤为明显。
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引用次数: 0
Subtype performance of the ancillary diagnostic 23- and 35-gene expression profile (GEP) tests for difficult-to-diagnose melanocytic lesions 辅助诊断23和35基因表达谱(GEP)测试对难以诊断的黑色素细胞病变的亚型表现
Pub Date : 2023-05-20 DOI: 10.25251/skin.7.supp.214
J. Plaza, Sarah I. Estrada, B. Russell, J. Siegel, Jason Rogers, J. Wilkinson, S. Kurley, M. Goldberg, K. Motaparthi
Background: Histopathological examination is adequate for most melanocytic neoplasms; however, there is a subset of lesions that are difficult to diagnose. The 23- and 35-gene expression profile (GEP) tests deliver results of suggestive of benign neoplasm, suggestive of malignant neoplasm, or intermediate (cannot exclude malignancy). They are intended to provide clinicians with objective results to be interpreted in the context of clinical, laboratory, and histopathological features to achieve a definitive diagnosis. Both GEPs are stand-alone tests that are independently validated and clinically available. Greater than 99% benign or malignant reporting is achieved clinically when the 23-GEP test is processed first, and if an intermediate result or test failure occurs, the 35-GEP is utilized. Methods: The performance of the 23- and 35-GEP tests using this methodology was tested on unequivocal cases from a variety of subtypes (101 benign, 249 malignant). Lesions were included if 2/3 dermatopathologist diagnoses were concordant. Subtype designation was determined by the dermatopathologist that submitted the lesion for the study. Results: The overall accuracy metrics in this cohort were 96.0% sensitivity and 87.8% specificity. The results demonstrated 100% sensitivity in several melanoma subtypes including acral lentiginous (n=15), desmoplastic (n=20), melanoma in situ (n=16), and nevoid (n=16). Other melanoma subtypes showed sensitivity metrics of: lentigo maligna, 96.7% (n=31); nodular, 95.1% (n=81); superficial spreading, 97.7% (n=42); and spitzoid, 85.0% (n=20). Subtypes of benign nevi showed a specificity of: blue, 96.7% (n=30); compound, 85.7% (n=42); junctional, 77.8% (n=18); and Spitz, 100% (n=7). Conclusions: Overall, we demonstrate that use of the 23- and 35-GEP diagnostic test workflow results in high accuracy across many subtypes of benign and malignant melanocytic neoplasms. Financial Disclosures: JAP has served as a consultant for Castle Biosciences, Inc. SIE is a consultant and shareholder of Castle Biosciences, Inc. BHR, JJS, JHR, JKW, SJK, and MSG are employee shareholders of Castle Biosciences, Inc. KM has served as a consultant and investigator for studies supported by Castle Biosciences, Inc. This study was supported by Castle Biosciences, Inc.
背景:组织病理学检查对大多数黑色素细胞肿瘤是足够的;然而,有一部分病变很难诊断。23和35基因表达谱(GEP)测试提供了提示良性肿瘤、提示恶性肿瘤或中间(不能排除恶性肿瘤)的结果。它们旨在为临床医生提供客观的结果,以便在临床、实验室和组织病理学特征的背景下进行解释,以实现最终诊断。两种GEP都是独立测试,经过独立验证并可在临床上使用。当首先处理23-GEP测试时,临床上达到99%以上的良性或恶性报告,如果出现中间结果或测试失败,则使用35-GEP。方法:使用该方法对各种亚型(101例良性,249例恶性)的明确病例进行23和35-GEP测试。如果2/3的皮肤病理学家诊断一致,则包括病变。亚型指定由提交病变进行研究的皮肤病理学家确定。结果:该队列的总体准确度指标为96.0%的敏感性和87.8%的特异性。结果表明,几种黑色素瘤亚型的敏感性为100%,包括肢端雀斑样(n=15)、促结缔组织增生性(n=20)、原位黑色素瘤(n=16)和痣样(n=16。其他黑色素瘤亚型的敏感性指标为:恶性扁豆,96.7%(n=31);结节性占95.1%(n=81);浅表铺展97.7%(n=42);斯皮唑类占85.0%(n=20)。良性痣的亚型特异性为:蓝色,96.7%(n=30);化合物85.7%(n=42);交界型占77.8%(n=18);Spitz为100%(n=7)。结论:总的来说,我们证明使用23和35-GEP诊断测试工作流程在许多良性和恶性黑色素细胞肿瘤亚型中具有较高的准确性。财务披露:JAP曾担任Castle Biosciences,股份有限公司的顾问。SIE是Castle Biosciences,股份有限公司的顾问和股东。BHR、JJS、JHR、JKW、SJK和MSG是Castle生物科学,股份有限公司的员工股东。
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引用次数: 0
High-grade Undifferentiated Pleomorphic Sarcoma Presenting as Acquired Lymphangioma Circumscriptum 表现为获得性淋巴管瘤的高级别未分化多形性肉瘤
Pub Date : 2023-05-20 DOI: 10.25251/skin.7.3.20
P. Rambhia, S. D’Angelo, P. Shah
A previously healthy woman in her 40s presented to the dermatology clinic with a 1-year history of a tender, draining, enlarging mass on the left buttock. Physical examination revealed an extensively indurated hyperpigmented nodule with numerous overlying clustered exophytic verrucous papules on the L medial buttock (see figure 1). Initial skin biopsy of verrucous lesions was notable for lymphangioma with overlying condyloma, D2-40 positive. MRI abdomen and pelvis with contrast demonstrated a left gluteal enhancing subcutaneous soft tissue mass, 10.3 x 8.2 x 8.8 cm in size, overlying and involving the left gluteus maximus, along with satellite nodules present in the medial gluteus maximus and paraspinal muscles, with bilateral pelvic and inguinal adenopathy. Excisional deep tissue biopsy revealed a diagnosis of a high-grade, multifocal spindle and undifferentiated pleomorphic sarcoma. The patient subsequently underwent 4 cycles of neoadjuvant chemotherapy AIM (doxorubicin, iphosphamide, MESNA), followed by radical resection of the left gluteal region, with positive margins, followed by repeat surgical resection and reconstruction with left-sided latissimus dorsi myocutaneous free flap. The patient has now completed radiation therapy. Soft tissue sarcoma is a heterogeneous group of rare malignancies of mesenchymal origin, that represents 0.8% of all adult cancers. Prognostic factors associated with poor outcome include high histologic grade, large tumor size, presence of metastases, and unresectability1. Herein, we report a novel case of high-grade soft-tissue undifferentiated pleomorphic sarcoma, masquerading as acquired lymphangioma circumscriptum (ALC), as noted on initial skin biopsy of grouped flesh-colored verrucous papules overlying an indurated tender mass. ALC is a lymphatic malformation occurring as sequela to any process which interrupts previously normal lymphatic drainage. As such, subcutaneous lymphatic cisterns are unable to drain completely into the general lymphatic system, resulting in lymphatic dilation and subsequent development of vesicular and papular lesions on the trunk, extremities, and anogenital areas.2 ALC can mimic common infectious growths including molluscum contagiosum and condyloma accuminata, and accordingly be mismanaged. Etiologic causes of ALC including malignancy, and has previously been reported in the setting of cervical carcinoma, vulvar carcinoma, endometrial carcinoma, Hodgkin lymphoma, rhabdomyosarcoma, rectal carcinoma, melanoma, and high-grade penile dysplasia2,3,4. Other etiologic causes can include surgery, trauma, radiation therapy, chronic inflammatory conditions including hidradenitis suppurativa, and inflammatory bowel disease.  To date, acquired lymphangioma circumscriptum has not been reported in the setting of underlying high-grade pleomorphic soft tissue sarcoma. As such, clinical presence of grouped frogspawn-like or verrucous papules, in an area of tender induration or lymphedema, should
一位40多岁的健康女性在皮肤科诊所就诊,她有一年的左臀压痛、引流、增大肿块的病史。体格检查显示,L内侧臀部有一个广泛硬结的色素沉着结节,上面有许多成簇的外生疣状丘疹(见图1)。疣状病变的初次皮肤活检以淋巴管瘤伴尖锐湿疣为显著,D2-40阳性。MRI腹部和骨盆对比显示,左侧臀大肌增强皮下软组织肿块,大小为10.3 x 8.2 x 8.8 cm,覆盖并累及左侧臀大肌肉,臀大肌内侧和棘旁肌存在卫星结节,伴有双侧骨盆和腹股沟腺病。切除深层组织活检显示诊断为高级别、多灶梭形和未分化多形性肉瘤。患者随后接受了4个周期的新辅助化疗AIM(阿霉素、异丙酰胺、MESNA),然后对左侧臀肌区域进行根治性切除,切缘为正,然后重复手术切除并用左侧背阔肌肌皮瓣重建。病人现在已经完成了放射治疗。软组织肉瘤是一组罕见的间充质恶性肿瘤,占所有成人癌症的0.8%。与不良预后相关的预后因素包括组织学分级高、肿瘤大小大、存在转移和不可切除1。在此,我们报告了一例新的高级软组织未分化多形性肉瘤,伪装为获得性局限性淋巴管瘤(ALC),如在硬结性压痛块上的肉色疣状丘疹的初次皮肤活检中所述。ALC是一种淋巴畸形,是任何中断先前正常淋巴引流的过程的后遗症。因此,皮下淋巴池无法完全排入一般淋巴系统,导致淋巴扩张,随后在躯干、四肢和肛门生殖器区域形成水泡和丘疹病变。2 ALC可以模仿常见的感染性生长,包括传染性软体动物和尖锐湿疣,因此管理不当。ALC的病因包括恶性肿瘤,以前曾报道过宫颈癌、外阴癌、子宫内膜癌、霍奇金淋巴瘤、横纹肌肉瘤、直肠癌、黑色素瘤和高级别阴茎发育不良2,3,4。其他病因可能包括手术、创伤、放射治疗、慢性炎症性疾病(包括化脓性汗炎)和炎症性肠病。到目前为止,获得性局限性淋巴管瘤在潜在的高度多形性软组织肉瘤中还没有报道。因此,在压痛硬结或淋巴水肿区域,临床上出现成群的蛙状或疣状丘疹,应促使进行检查,以排除潜在的恶性病因,因为新发的ALC可能掩盖了潜在的恶性。
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引用次数: 0
Treatment of Severe Recalcitrant Atopic Dermatitis with Dupilumab in a Kidney Transplant Patient 杜匹单抗治疗肾移植患者严重难治性特应性皮炎
Pub Date : 2023-05-20 DOI: 10.25251/skin.7.3.10
Vivian Li, Sophie Guenin, M. Lebwohl
This case report highlights the successful treatment of refractory atopic dermatitis (AD) in an immunosuppressed patient using dupilumab, a biologic agent that selectively targets cytokines crucial in the pathogenesis of AD. The patient had a history of failed treatment with numerous topical and systemic immunomodulating agents, including corticosteroids and immunosuppressive drugs for organ transplant. Dupilumab treatment resulted in significant improvement of symptoms, including reduced pruritus, and ultimately achieved disease control. Importantly, the patient experienced no adverse effects apart from one COVID-19 infection over three years of co-administration of dupilumab with immunosuppressive transplant rejection treatment. The safety of dupilumab in immunocompromised and transplant patients has been a concern, but studies have shown its safety and efficacy in these patient populations. This case highlights the potential for dupilumab as a safe and effective treatment option for patients with severe AD who are immunocompromised or have undergone solid organ transplantation.  
本病例报告强调了使用dupilumab成功治疗免疫抑制患者的难治性特应性皮炎(AD), dupilumab是一种选择性靶向在AD发病机制中至关重要的细胞因子的生物制剂。患者有大量局部和全身免疫调节剂治疗失败的历史,包括用于器官移植的皮质类固醇和免疫抑制药物。Dupilumab治疗导致症状显著改善,包括瘙痒减轻,并最终实现疾病控制。重要的是,在dupilumab与免疫抑制移植排斥治疗联合使用的三年中,除了一次COVID-19感染外,患者没有出现任何不良反应。dupilumab在免疫功能低下和移植患者中的安全性一直是一个问题,但研究表明其在这些患者群体中的安全性和有效性。该病例强调了dupilumab作为免疫功能低下或接受实体器官移植的严重AD患者安全有效的治疗选择的潜力。
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引用次数: 0
Disseminated Varicella-zoster Virus Infection in an Immunocompetent Host 免疫宿主中的播散性水痘-带状疱疹病毒感染
Pub Date : 2023-05-20 DOI: 10.25251/skin.7.3.19
Alan G. Mulholland, Brandon Tang, S. Shumak, Linda Zhou
Disseminated varicella-zoster virus (VZV) infection has devastating impacts on patients’ quality of life, with increasing morbidity and mortality. Thus, it is imperative that a diagnosis be made early. This case description illustrates a unique and dramatic presentation of disseminated VZV infection with important clinical implications.
播散性水痘-带状疱疹病毒(VZV)感染对患者的生活质量具有破坏性影响,发病率和死亡率不断上升。因此,及早诊断是十分必要的。本病例描述说明了播散性VZV感染的独特和戏剧性表现,具有重要的临床意义。
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引用次数: 0
Efficacy and Safety of Calcipotriene/Betamethasone Dipropionate Cream for the Treatment of Plaque Psoriasis Evaluated from Pooled Phase 3 Data 从合并的3期数据评估钙三烯/二丙酸倍他米松乳膏治疗斑块型银屑病的有效性和安全性
Pub Date : 2023-05-20 DOI: 10.25251/skin.7.supp.204
L. Stein Gold, A. Pinter, M. Augustin
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引用次数: 0
The Importance of Medication Adherence in the Treatment of Actinic Keratosis: An Expert Consensus Panel 药物依从性在光化性角化病治疗中的重要性:专家共识小组
Pub Date : 2023-05-20 DOI: 10.25251/skin.7.3.1
D. Zakria, A. Armstrong, B. Berman, J. D. Del Rosso, M. Lebwohl, T. Schlesinger, D. Rigel
Background: Actinic keratosis (AK) is one of the most common dermatologic diagnoses. While there are several treatment options, many topical therapies have poor adherence due to duration of treatment and local skin reactions (LSRs). Objective: To review the available literature on the most commonly used patient-administered field-directed therapies for AK and create consensus statements on the role of medication adherence in improving AK outcomes. Methods: A literature search of PubMed was completed for English-language original research articles reporting efficacy, safety, and tolerability data for 5-FU, diclofenac gel, imiquimod cream, and tirbanibulin. Once the articles were selected, they were distributed to a panel consisting of seven dermatologists with extensive expertise in managing AKs. Each panelist reviewed the articles and assigned them a level of evidence based on Strength of Recommendation Taxonomy (SORT) criteria. The panelists then met to review and discuss the studies and created consensus statements on the management of AKs and the importance of medication compliance. A modified Delphi process was used to approve the adoption of each statement. Results: The literature search produced 1,326 articles that met search criteria. After screening these articles for relevance and applying the inclusion criteria, 17 articles were chosen to be reviewed by the panel and assigned a level of evidence based on SORT criteria. The panel then created six consensus statements that received a unanimous vote for adoption. Conclusion: While there are several options for the treatment of AK, there is little consensus on a standard of care. Clearance rates for the most common topical field therapies vary significantly but are also difficult to directly compare due to differences in methodology for measuring and assessing outcomes. Overall, it is clear that an efficacious, tolerable, and convenient treatment for AKs is critical to optimal adherence and management and, given the results of recent studies, tirbanibulin may be the best topical option for meeting these criteria.
背景:光化性角化病(AK)是最常见的皮肤科诊断之一。虽然有几种治疗选择,但由于治疗持续时间和局部皮肤反应(LSR),许多局部疗法的依从性较差。目的:回顾最常用的AK患者现场指导治疗的现有文献,并就药物依从性在改善AK结果中的作用达成共识。方法:在PubMed上检索英文原创研究文章,报告5-FU、双氯芬酸凝胶、咪喹莫特乳膏和替巴尼布林的疗效、安全性和耐受性数据。一旦这些文章被选中,它们就被分发给一个由七名皮肤科医生组成的小组,他们在管理AK方面具有广泛的专业知识。每个小组成员都审查了这些文章,并根据推荐分类的强度(SORT)标准为它们分配了一定程度的证据。小组成员随后开会审查和讨论研究,并就AKs的管理和药物依从性的重要性达成共识。采用了修改后的德尔菲程序来批准采用每一项声明。结果:文献检索共产生1326篇符合检索标准的文章。在筛选这些文章的相关性并应用纳入标准后,小组选择了17篇文章进行审查,并根据SORT标准分配了一定程度的证据。该小组随后制定了六项共识声明,并获得一致投票通过。结论:虽然AK的治疗有几种选择,但在护理标准上几乎没有达成共识。最常见的局部现场治疗的清除率差异很大,但由于测量和评估结果的方法不同,也很难直接比较。总的来说,很明显,有效、可耐受和方便的AKs治疗对于最佳的依从性和管理至关重要,鉴于最近的研究结果,替巴尼布林可能是满足这些标准的最佳局部选择。
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引用次数: 0
Leukemia Cutis as the Presenting Sign of Acute Myeloid Leukemia in an HIV+ patient 皮肤白血病是HIV阳性患者急性髓性白血病的表现
Pub Date : 2023-05-20 DOI: 10.25251/skin.7.3.11
Natalie Garcia, Charlotte Mcrae, Abigail O. Smith, L. Graham
Leukemia Cutis (LC) is a rare extramedullary cutaneous manifestation of leukemia that varies in terms of clinical presentation, leukemia type, and timing of presentation in relation to systemic leukemia. LC typically presents following diagnosis of systemic leukemia and during an active flare or relapse. An estimated 3.7% of patients with Acute Myeloid Leukemia (AML) develop LC. A 61-year-old male with poorly controlled HIV presented with a rash that began one month prior on his cheek as a red papule, which he believed was an ingrown hair. On exam, pink and yellow firm papules and nodules covered his entire body surface except the groin and axilla. One nodule held a peau d’orange appearance. The rash was overall asymptomatic, and he reported only increased fatigue. His CD4 count and viral load were 136 and 330,000 respectively. One punch biopsy revealed negative cultures for fungus, bacteria, and acid-fast bacilli. Two biopsies sent for pathologic evaluation revealed AML of the skin. Bone marrow biopsy confirmed AML. Clinically the presentation of LC is nonspecific, and systemic symptoms rarely appear in conjunction with LC. High clinical suspicion and histopathologic examination are necessary for diagnosis of LC.
皮肤白血病(LC)是一种罕见的白血病髓外皮肤表现,其临床表现、白血病类型和表现时间与系统性白血病有关。LC通常在系统性白血病诊断后以及活动性发作或复发期间出现。据估计,3.7%的急性髓细胞白血病(AML)患者发展为LC。一名61岁的男性,HIV控制不佳,一个月前在脸颊上出现皮疹,表现为红色丘疹,他认为这是向内生长的头发。在检查中,除了腹股沟和腋下,粉红色和黄色的丘疹和结节覆盖了他的整个身体表面。其中一个结节呈桔黄色。皮疹总体上没有症状,他只报告说疲劳加剧。他的CD4计数和病毒载量分别为136和33万。一次穿刺活检显示真菌、细菌和抗酸杆菌培养呈阴性。两次活检进行病理评估,发现皮肤AML。骨髓活检证实AML。LC的临床表现是非特异性的,系统症状很少与LC同时出现。高度的临床怀疑和组织病理学检查是诊断LC的必要条件。
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引用次数: 0
期刊
Skin (Milwood, N.Y.)
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