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Novel therapeutic approach for loxoscelism: efficacy of cefixime and netilmicin sulfate combination therapy. 头孢克肟与硫酸奈替米星联合治疗斜交症的疗效观察。
IF 1.3 Q2 DERMATOLOGY Pub Date : 2025-08-22 Epub Date: 2025-02-28 DOI: 10.4081/dr.2025.10215
Caterina Mariarosaria Giorgio, Gaetano Licata, Vittorio Tancredi, Paolino Franzese, Nicola Maria Giorgio, Giuseppe Argenziano, Eugenia Veronica Di Brizzi

Dear Editor, Loxoscelism, resulting from bites by Loxosceles spiders - particularly Loxosceles reclusa - is characterized by necrotic skin lesions and, in severe cases, systemic symptoms such as hemolysis, acute renal failure, and disseminated intravascular coagulation (DIC). [...].

Loxoscelism是由Loxosceles蜘蛛(尤其是隐士Loxosceles)叮咬引起的,表现为皮肤坏死,严重的情况下,会出现全身症状,如溶血、急性肾功能衰竭和弥散性血管内凝血(DIC)。这种毒液的鞘磷脂酶D (SMD)酶会引起直接的组织损伤和炎症反应,导致细胞死亡、皮肤坏死和血管通透性增加,从而导致溶血和血栓形成。[…]。
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引用次数: 0
Teledermatology: Canadian dermatologists' practice patterns, perceived challenges, and future recommendations. 远程皮肤科:加拿大皮肤科医生的实践模式,感知的挑战和未来的建议。
IF 1.3 Q2 DERMATOLOGY Pub Date : 2025-08-22 Epub Date: 2025-02-06 DOI: 10.4081/dr.2025.10197
Sidra Sarfaraz, Tarek Turk, Samuel A J Lowe, Luvneet Verma, Marlene Dytoc

The use of teledermatology has increased significantly in recent years. The objective of this study was to determine Canadian dermatologists' and dermatology residents' perspectives on teledermatology. An online survey was created to determine participants' teledermatology practice patterns and their perception of the challenges, education, training, and research in teledermatology. The survey was distributed through the Canadian Dermatology Association and by administrative staff at Canadian Dermatology departments. A total of 33 respondents completed the survey: 66.7% of respondents started using teledermatology during the COVID-19 pandemic, and 93.8% reported that teledermatology accounted for 0-25% of their practice. Convenience, access, and safety were identified as the primary advantages of teledermatology. Teledermatology was mainly utilized for medication monitoring or refills and to assess, manage, or follow up on dermatitis, other chronic inflammatory conditions, and pre-diagnosed dermatologic conditions. Poor photo quality (32.3%) and the inability to conduct physical examinations or accurately diagnose conditions (74.2%) were reported as significant challenges. Respondents recommended education on the medicolegal considerations of teledermatology and research on how teledermatology compares to in-person consultations. Overall, teledermatology improves convenience, access to care, and safety for both patients and healthcare professionals. However, addressing challenges related to physical examinations, accurate diagnoses, and photo quality is essential for optimal care delivery.

近年来,远程皮肤科的使用显著增加。本研究的目的是确定加拿大皮肤科医生和皮肤科住院医师对远程皮肤科的看法。创建了一项在线调查,以确定参与者的远程皮肤病学实践模式以及他们对远程皮肤病学挑战、教育、培训和研究的看法。这项调查是通过加拿大皮肤病协会和加拿大皮肤病部门的行政人员分发的。共有33名受访者:66.7%的受访者在COVID-19大流行期间开始使用远程皮肤科,93.8%的受访者表示远程皮肤科占其实践的0-25%。方便、可及性和安全性被认为是远程皮肤科的主要优势。远程皮肤病学主要用于药物监测或补药,以及评估、管理或随访皮炎、其他慢性炎症和预先诊断的皮肤疾病。照片质量差(32.3%)和无法进行身体检查或准确诊断疾病(74.2%)被报告为重大挑战。受访者建议对远程皮肤科的医学法律考虑进行教育,并研究如何将远程皮肤科与面对面咨询进行比较。总的来说,远程皮肤科为患者和医疗保健专业人员提供了便利、访问和改进的安全性。然而,解决与身体检查,准确诊断和照片质量相关的挑战对于最佳护理服务至关重要。
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引用次数: 0
A rare vascular manifestation in chronic myeloid leukemia: a case report and literature review of Bier's spot development during nilotinib treatment. 慢性髓系白血病中一种罕见的血管表现:尼洛替尼治疗期间Bier斑的1例报告及文献复习。
IF 1.3 Q2 DERMATOLOGY Pub Date : 2025-08-22 Epub Date: 2025-01-31 DOI: 10.4081/dr.2025.10160
Ahmed Alsaati, Turki Hakami, Sultan Bajawi, Gamil Mohammed, Nouf Bajawi, Nadya Al-Faraidy

Bier's spots are rare angiospastic macules often associated with physiologic vasoconstriction. This case report describes a 35-year-old man with chronic myeloid leukemia (CML) treated with nilotinib who developed Bier's spots, a previously unreported adverse effect of the drug. The patient presented with asymptomatic hypopigmented macules on the hands and legs that appeared during venous stasis and resolved with elevation. This case emphasizes the need to recognize potential vascular side effects of tyrosine kinase inhibitors (TKIs) and highlights Bier's spots as a benign but remarkable manifestation in patients undergoing nilotinib therapy.

比尔氏斑是一种罕见的血管痉挛斑,通常与生理性血管收缩有关。本病例报告描述了一名35岁的慢性髓性白血病患者接受尼罗替尼治疗后出现了比尔氏斑,这是该药物以前未报道的不良反应。患者表现为手部和腿部无症状的低色素斑,在静脉淤积期间出现,并随着升高而消失。本病例强调需要认识到酪氨酸激酶抑制剂的潜在血管副作用,并强调Bier斑是接受尼罗替尼治疗的患者的一种良性但显著的表现。
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引用次数: 0
Adalimumab-induced facial erysipelas and its successful resolution with azithromycin in a 19-year-old female. 阿达木单抗致面部丹毒及阿奇霉素成功治疗一例19岁女性。
IF 1.3 Q2 DERMATOLOGY Pub Date : 2025-08-22 Epub Date: 2025-02-21 DOI: 10.4081/dr.2025.10278
Caterina Mariarosaria Giorgio, Anna Balato, Gaetano Licata, Giuseppe Argenziano, Vittorio Tancredi, Eugenia Veronica Di Brizzi

A 19-year-old female with severe hidradenitis suppurativa (HS), treated with adalimumab for 10 months, developed facial erysipelas following an episode of pharyngitis. The infection presented with fever, severe cough, and a rapidly progressing erythematous plaque with edema on the left cheek, forehead, and periocular region. Laboratory tests confirmed a streptococcal infection. Due to allergies and intolerance to first-line antibiotics, azithromycin was administered, leading to complete resolution. This case highlights the increased risk of severe infections in immunosuppressed patients and underscores the importance of careful antibiotic selection and close monitoring for infections in patients receiving TNF-α inhibitors.

一名患有严重化脓性汗腺炎(HS)的19岁女性,经阿达木单抗治疗10个月后,在咽炎发作后出现面部丹毒。感染表现为发热,严重咳嗽,左脸颊,前额和眼周区域出现迅速发展的红斑斑块伴水肿。实验室检查证实是链球菌感染。由于对一线抗生素过敏和不耐受,给予阿奇霉素,导致完全解决。该病例强调了免疫抑制患者严重感染的风险增加,并强调了谨慎选择抗生素和密切监测接受TNF-α抑制剂患者感染的重要性。
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引用次数: 0
Skin infection by larva migrans and scabies mites: case reports on unusual skin localizations. 由幼虫迁移和疥螨引起的皮肤感染:异常皮肤定位的病例报告。
IF 1.3 Q2 DERMATOLOGY Pub Date : 2025-08-22 Epub Date: 2025-02-19 DOI: 10.4081/dr.2025.10098
Alessandro Martella

Unusual skin infection localization represents a challenge to physicians regarding presentation and mode of acquisition, which may influence the diagnosis. At the same time, the administration of incorrect drugs due to a misdiagnosis might have a negative impact on the disease course. This article presents two cases detailing the unusual presentation of larva migrans and scabies mite infection in two Italian patients, highlighting the importance of clinical vigilance and comprehensive evaluation of patients. These cases suggest how an accurate diagnosis requires a high index of suspicion and appropriate diagnostic tools, such as dermoscopy, for the prompt recognition of skin infections and the consequent optimal patient outcome.

不寻常的皮肤感染定位对医生的表现和获得方式提出了挑战,所有这些都可能影响诊断。同时,由于误诊而使用不正确的药物可能对病程产生负面影响。本文介绍了两个病例报告,详细介绍了两名意大利患者的幼虫迁移和疥螨感染的不寻常表现,强调了临床警惕和患者综合评估的重要性。这些病例表明,准确的诊断需要高度的怀疑指数和适当的诊断工具,如皮肤镜检查,以便及时识别皮肤感染并由此获得最佳的患者结果。
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引用次数: 0
Growth hormone deficiency and secondary adrenal insufficiency in petrified ear syndrome: a case report and literature review. 生长激素缺乏和继发性肾上腺功能不全伴石化耳综合征1例报告并文献复习。
IF 1.3 Q2 DERMATOLOGY Pub Date : 2025-08-22 Epub Date: 2025-01-31 DOI: 10.4081/dr.2025.10263
Sebastiano Recalcati, Alberto Vassallo, Marta Villanova, Roberto Lanzi, Marco Losa, Maria Grazia Patricelli, Paola Carrera, Fabrizio Fantini

Petrified ear is a rare clinical entity characterized by the progressive hardening of normal, flexible auricular cartilage, leading to partial or complete auricular stiffness. In many cases, it provides a valuable clinical clue that allows the clinician to detect endocrinopathies (particularly Addison's disease) in a patient who has not received a diagnosis. We present the first documented case of petrified ears, which resulted in the diagnosis of both secondary hypoadrenalism and growth hormone deficiency (GHD). Additionally, we review the relevant literature. Petrified ear syndrome is probably an underreported clinical manifestation of other systemic disorders. It may, at times, serve as a valuable and simple clinical clue to suspect underlying endocrinopathies even in the absence of typical features.

石化耳是一种罕见的临床实体,其特征是正常的柔性耳廓软骨进行性硬化,导致部分或完全耳廓僵硬。在许多情况下,它提供了有价值的临床线索,使临床医生能够在未得到诊断的患者中发现内分泌病变(特别是Addison病)。我们提出了第一个记录的石化耳病例,导致继发性肾上腺素减退和生长激素缺乏症(GHD)的诊断。此外,我们回顾了相关文献。石化耳综合征可能是其他全身性疾病的一种被低估的临床表现。有时,即使在没有典型特征的情况下,它也可以作为怀疑潜在内分泌疾病的有用而简单的临床线索。
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引用次数: 0
Yellow urticaria as a rare dermatological manifestation of biliary obstruction: a case report. 胆道梗阻的罕见皮肤病表现:黄色荨麻疹1例。
IF 1.3 Q2 DERMATOLOGY Pub Date : 2025-08-22 Epub Date: 2025-02-28 DOI: 10.4081/dr.2025.10248
Mohammad Almutairi, Khalid Nabil Nagshabandi, Reem Alsergani, Sultan Alsalem

Urticaria is a prevalent inflammatory dermatological condition with a global estimated lifetime prevalence of up to 20%. Yellow urticaria is not a distinct medical condition; rather, it refers to the manifestation of yellow-colored wheals that appear in certain individuals with elevated serum bilirubin levels. This excess bilirubin accumulates in various tissues, including the conjunctiva and skin. The occurrence of yellow urticaria is notably rare and uncommon. In this report, we present a case of yellow-colored urticaria in a patient diagnosed with obstructive biliary stones, complemented by a concise review of previously documented cases in the literature.

荨麻疹是一种常见的炎症性皮肤病,全球估计终生患病率高达20%。黄色荨麻疹不是一种特殊的医学疾病;相反,它是指在某些血清胆红素水平升高的个体中出现的黄色车轮的表现。这些多余的胆红素积聚在各种组织中,包括结膜和皮肤。黄色荨麻疹的发生非常罕见和不常见。在本报告中,我们提出了一个黄色荨麻疹的患者诊断为梗阻性胆结石,辅以简要回顾以前的文献记录的病例。
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引用次数: 0
Dermatological insight as the key to diagnosing intestinal Behçet's disease misdiagnosed as Crohn's: a case report. 诊断误诊为克罗恩病的关键在于皮肤病学洞察1例。
IF 1.3 Q2 DERMATOLOGY Pub Date : 2025-08-22 Epub Date: 2025-02-04 DOI: 10.4081/dr.2025.10232
Caterina Mariarosaria Giorgio, Eugenia Veronica Di Brizzi, Gaetano Licata, Carmine Fiorentino, Giuseppe Argenziano, Luca Damiani

This report presents the case of a 22-year-old male with recurrent genital ulcers, oral aphthae, and gastrointestinal ulcerations initially diagnosed as Crohn's disease by gastroenterologists. Despite overlapping clinical and histological features between Crohn's disease and intestinal Behçet's disease, a dermatological consultation raised suspicion for Behçet's, leading to a revised diagnosis. This case highlights the crucial role of dermatologists in preventing misdiagnosis and ensuring effective treatments for complex inflammatory conditions.

本报告报告一例22岁男性复发性生殖器溃疡,口腔溃疡和胃肠道溃疡最初被胃肠病学家诊断为克罗恩病。尽管克罗恩病和肠behaperet病之间的临床和组织学特征重叠,但一次皮肤科会诊引起了对behaperet病的怀疑,从而修改了诊断。本病例强调了皮肤科医生在避免误诊和确保适当治疗复杂炎症条件方面的有益作用。
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引用次数: 0
Refractory pityriasis rubra pilaris treated with abrocitinib. 阿布替尼治疗难治性毛疹红斑。
IF 1.3 Q2 DERMATOLOGY Pub Date : 2025-08-22 Epub Date: 2025-01-09 DOI: 10.4081/dr.2025.10105
Filip Rob

Pityriasis rubra pilaris is a rare idiopathic papulosquamous disorder that significantly impacts quality of life and is often refractory to conventional therapies. This study presents a case of successful treatment with an abrocitinib JAK1 inhibitor after several conventional and biologic therapies failed.

摘要毛疹糠疹是一种罕见的特发性丘疹鳞状疾病,严重影响患者的生活质量,通常难以接受常规治疗。本研究提出了一个案例,成功的治疗与阿布替尼JAK1抑制剂后,几个传统和生物治疗失败。
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引用次数: 0
Autochthonous Emergomyces pasteurianus subcutaneous infection in an Italian immunocompromised patient: case report and review. 一名意大利免疫力低下患者的巴氏自粘酵母菌皮下感染:病例报告与综述。
IF 1.3 Q2 DERMATOLOGY Pub Date : 2025-08-22 Epub Date: 2025-02-05 DOI: 10.4081/dr.2025.10251
Claudio Farina, Marco Cavallini, Daniele Gambini, Michele Parietti, Alessandra Tebaldi, Davide Guarneri, Paolo Sena

We describe the second case of infection by Emergomyces pasteurianus in Italy. The patient presented ulcerated nodular lesions primarily in the forehead, beneath the orbital and nasal areas, but also in the neck and fingers in the early stages. Treatment involved amphotericin B, followed by long-term itraconazole, which resulted in complete clinical resolution. A review of the literature is also included.

我们描述了发生在意大利的第二例巴氏冒出菌感染。患者表现为溃疡性结节性病变,主要在前额,眶下和鼻区,但在早期也在颈部和手指。治疗包括两性霉素B,随后长期伊曲康唑,导致完全的临床解决。文献综述也包括在内。
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引用次数: 0
期刊
Dermatology Reports
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