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1.
J Drugs Dermatol ; 23(5): e132-e133, 2024 05 01.
Article in English | MEDLINE | ID: mdl-38709690

ABSTRACT

Skin self-examinations play a vital role in skin cancer detection and are often aided by online resources. Available reference photos must display the full spectrum of skin tones so patients may visualize how skin lesions can appear. This study investigated the portrayal of skin tones in skin cancer-related Google Images, discovering a significant underrepresentation of darker skin tones. J Drugs Dermatol. 2024;23(5):e132-e133.     doi:10.36849/JDD.7886e.


Subject(s)
Skin Neoplasms , Skin Pigmentation , Humans , Skin Neoplasms/diagnosis , Skin Neoplasms/pathology , Photography , Self-Examination/methods , Skin/pathology , Internet , Search Engine
2.
J Drugs Dermatol ; 23(5): e137-e138, 2024 05 01.
Article in English | MEDLINE | ID: mdl-38709691

ABSTRACT

When patients self-detect suspicious skin lesions, they often reference online photos prior to seeking medical evaluation. Online images must be available in the full spectrum of skin tones to provide accurate visualizations of disease, especially given the increased morbidity and mortality from skin cancer in patients with darker skin tones. The purpose of this study was to evaluate the representation of skin tones in photos of skin cancer on patient-facing websites. Six federally-based and organization websites were evaluated, and of the 372 total representations identified only 49 depicted darker skin tones (13.2%). This highlights the need to improve skin tone representation on patient-facing online resources. J Drugs Dermatol. 2024;23(5):e137-e138.     doi:10.36849/JDD.7905e.


Subject(s)
Internet , Patient Education as Topic , Skin Neoplasms , Skin Pigmentation , Humans , Skin Neoplasms/diagnosis , Patient Education as Topic/methods , Photography , Skin
3.
J Drugs Dermatol ; 23(2): 85-89, 2024 Feb 01.
Article in English | MEDLINE | ID: mdl-38306146

ABSTRACT

Sensitive skin (SS) is a common patient complaint presenting to the dermatology office, but there exists a lack of consensus on defining criteria and evidence-based management approaches. Furthermore, incorporation of SS training into the dermatology residency curriculum is unknown, and therefore the authors herein sought to determine dermatology resident physicians' exposure to education about SS, perspectives on SS, and management approaches. Ninety-nine percent of residents believe that SS should be included in some capacity in their dermatology residency training. However, less than half of responding residents received education specifically about SS during their training and less than one-fourth of residents reported feeling very knowledgeable about SS diagnosis, clinical evaluation, or management. Residents who had received specific education about SS were significantly more likely to self-describe as "very knowledgeable" about all queried topics. Residents reported challenges with all aspects of SS patient care, and cited heterogenous approaches to SS patients. These data highlight a gap in residency education, as indicated by limited consensus over diagnostic and management approaches to SS.J Drugs Dermatol. 2024;23(2):85-89.   doi:10.36849/JDD.7830.


Subject(s)
Dermatology , Internship and Residency , Skin Diseases , Humans , Dermatology/education , Surveys and Questionnaires , Curriculum
5.
J Drugs Dermatol ; 22(9): 950-952, 2023 09 01.
Article in English | MEDLINE | ID: mdl-37683063

ABSTRACT

Sensitive skin (SS) is a common patient complaint; however, there are no consistent guidelines to guide dermatologists' approaches to diagnosis and management of SS. Attendees of an international dermatology conference were surveyed to gauge dermatology providers' experiences and perspectives on SS. Survey results suggest that although the definition and diagnosis of SS are ambiguous, SS is increasingly being considered as a unique condition. Patients are commonly seeking dermatologic care for SS; however, dermatologists identified challenges with diagnosis, counseling patients, selecting products or medications, and assessing clinical improvement. These data highlight both a significant demand and a current need for improved provider resources for SS. Citation: McCormick ET, Desai S, Friedman A. Insight into dermatology providers’ perspectives on/and approaches to sensitive skin: a pilot survey. J Drugs Dermatol. 2023;22(9):950-951. doi:10.36849/JDD.7450.


Subject(s)
Dermatitis, Contact , Dermatology , Humans , Dermatitis, Contact/diagnosis , Dermatitis, Contact/therapy
6.
J Drugs Dermatol ; 22(9): 953-954, 2023 09 01.
Article in English | MEDLINE | ID: mdl-37683071

ABSTRACT

CITATION: McCormick ET, Desai S, Nelson K, et al. Fractional laser for prevention of non-melanoma skin cancer. J Drugs Dermatol. 2023;22(9):953-954. doi:10.36849/JDD.NVRN0923.


Subject(s)
Skin Neoplasms , Humans , Skin Neoplasms/etiology , Skin Neoplasms/prevention & control , Lasers
7.
Exp Dermatol ; 32(12): 2072-2083, 2023 12.
Article in English | MEDLINE | ID: mdl-37726950

ABSTRACT

Cutaneous lupus erythematosus (CLE) is a heterogeneous autoimmune skin disease which occurs independently and in conjunction with systemic lupus erythematosus. Drug development for CLE is severely lacking. Anandamide (AEA) is a primary endocannabinoid which exhibits immunomodulatory effects through mixed cannabinoid receptor agonism. We evaluated AEA as topical treatment for CLE and assessed benefits of nanoparticle encapsulation (AEA-NP) on cutaneous drug penetration, delivery and biological activity. Compared to untreated controls, AEA-NP decreased IL-6 and MCP-1 in UVB-stimulated keratinocytes (p < 0.05) in vitro. In BALB/c mice, AEA-NP displayed improved cutaneous penetration, extended release and persistence of AEA in the follicular unit extending to the base after 24 h. Utilizing the MRL-lpr lupus murine model, twice weekly treatment of lesions with topical AEA-NP for 10 weeks led to decreased clinical and histologic lesion scores compared to unencapsulated AEA and untreated controls (p < 0.05). Prophylactic application of AEA-NP to commonly involved areas on MRL-lpr mice similarly resulted in decreased clinical and histologic scores when compared to controls (p < 0.05), and reduced C3 and IBA-1 in lesional tissue (p < 0.05). The demonstrated clinical and immunomodulatory effects of treatment with AEA support its potential as therapy for CLE. This work also suggests that encapsulation of AEA improves penetration and treatment efficacy. Future studies will be conducted to assess full therapeutic potential.


Subject(s)
Lupus Erythematosus, Cutaneous , Lupus Erythematosus, Systemic , Mice , Animals , Cytokines , Endocannabinoids/pharmacology , Endocannabinoids/therapeutic use , Disease Models, Animal , Mice, Inbred MRL lpr , Lupus Erythematosus, Cutaneous/drug therapy
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