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1.
J Clin Aesthet Dermatol ; 15(8): E61-E66, 2022 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-36061478

RESUMO

Objective: We sought to evaluate the impact of the coronavirus-19 (COVID-19) pandemic on sun-seeking and sun-safe behaviors. Methods: We conducted an online, cross-sectional, population-based survey. Results: In total, 1,001 respondents participated in the survey and reported being exposed to 12 or more hours of sunlight (i.e., direct and indirect ultraviolet light, and blue light) each day. Participants self-reported a net increase in all types of light exposure since the onset of the COVID-19 pandemic, especially to blue light (+38%). Notably, while the effects of direct sunlight were well known among survey respondents, they were less aware of the potential damaging impact of indirect sunlight and blue light. Limitations: As the survey was only conducted among residents of the United States, results might not be generalizable to all geographical regions. Conclusion: Social outreach strategies are required to improve sun-safe behaviors. Future behavioral interventions should encourage the implementation of broad-spectrum sun protection.

2.
J Am Acad Dermatol ; 54(5 Suppl): S206-9, 2006 May.
Artigo em Inglês | MEDLINE | ID: mdl-16631941

RESUMO

Although the specific IgA autoantibody responsible for the pathogenesis of dermatitis herpetiformis (DH) is unknown, the presence of IgA is considered essential in the pathogenesis of DH. To date, no cases of IgA deficiency have been reported in DH. In contrast, IgA deficiency is found in 2% to 3% of patients with celiac disease, a rate 10 to 15 times higher than the normal population. We report 2 patients with DH who also have partial IgA deficiency. We evaluated the sera of these patients for the presence of IgA autoantibodies to endomysium, tissue transglutaminase, epidermal transglutaminase, and gliadin. Both patients were found to have IgA endomysial and tissue transglutaminase antibodies, and serologic markers for DH. Corresponding IgG autoantibodies were not useful serologic markers of DH in the setting of IgA deficiency, as they often are in celiac disease. We then screened 98 DH sera for total IgA levels and identified 1 additional case with IgA deficiency. In conclusion, DH may develop in patients with partial IgA deficiency, indicating that pathogenically directed IgA antibodies are likely sufficient for cutaneous IgA deposition in this disease.


Assuntos
Autoanticorpos/imunologia , Dermatite Herpetiforme/complicações , Dermatite Herpetiforme/imunologia , Deficiência de IgA/complicações , Deficiência de IgA/imunologia , Imunoglobulina A/imunologia , Adulto , Autoanticorpos/sangue , Dermatite Herpetiforme/metabolismo , Humanos , Imunoglobulina A/sangue , Imunoglobulina A/metabolismo , Masculino , Pessoa de Meia-Idade , Miofibrilas/imunologia , Pele/metabolismo , Transglutaminases/imunologia
6.
J Cutan Pathol ; 31(6): 453-7, 2004 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-15186434

RESUMO

BACKGROUND: Post-transplant lymphoproliferative disorder (PTLD) is a condition affecting immunosuppressed transplant patients and has a variety of clinical presentations. It is rarely found in the skin, and cases of PTLD in the skin are usually linked with lymph node or other organ involvement. METHODS: We report a case of plasmacytoid PTLD that is limited to the skin. A 63-year-old man with a history of cardiac transplant presented with exophytic tumors involving the lower extremity. The diagnosis and classification of the various forms of PTLD are discussed. RESULTS: Histology, immunohistochemical stains, and in situ hybridization revealed an aggressive plasmacytoid tumor that was Epstein-Barr virus positive. The patient's tumors resolved with decreased immunosuppression and localized radiation. CONCLUSION: This case is unusual for several reasons including involvement limited to the skin, presentation 15 years following transplant, and plasmacytoid phenotype of the tumor. This disorder will likely be seen by dermatologists and dermatopathologists with the increasing use of immunosuppressive medications in the dermatologist's patient population.


Assuntos
Transplante de Coração/efeitos adversos , Transtornos Linfoproliferativos/etiologia , Transtornos Linfoproliferativos/patologia , Neoplasias Cutâneas/etiologia , Neoplasias Cutâneas/patologia , Infecções por Vírus Epstein-Barr/imunologia , Herpesvirus Humano 4/isolamento & purificação , Humanos , Hospedeiro Imunocomprometido , Imuno-Histoquímica , Hibridização In Situ , Transtornos Linfoproliferativos/virologia , Masculino , Pessoa de Meia-Idade , Neoplasias Cutâneas/virologia
7.
Pediatr Dermatol ; 19(4): 326-9, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12220278

RESUMO

Aplasia cutis congenita (ACC) is the absence of localized or widespread areas of skin at birth. A frequently cited classification schema is based on location and the presence of associated anomalies. Histologically it is characterized by dermal fibrosis and absence of adenexal structures. We present a newborn female with extensive truncal ACC associated with fetus papyraceus.


Assuntos
Doenças em Gêmeos/diagnóstico , Displasia Ectodérmica/diagnóstico , Biópsia por Agulha , Displasia Ectodérmica/patologia , Epiderme/patologia , Feminino , Morte Fetal , Humanos , Recém-Nascido , Prognóstico , Medição de Risco
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