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2.
JAMA Dermatol ; 157(5): 577-582, 2021 05 01.
Artículo en Inglés | MEDLINE | ID: mdl-33760001

RESUMEN

Importance: Cutaneous immune-related adverse events (cirAEs) are some of the earliest toxic reactions to emerge following immune-checkpoint inhibitor (ICI) initiation. As an early indicator of robust inflammatory response, cirAEs may be associated with patterns of immune-mediated toxic effects, but associations between these events and noncutaneous immune-related adverse events (irAEs) remain underexplored. Objectives: To characterize patterns of cirAEs and irAEs across care settings and examine associations between the features of first cirAE, overall irAE risk, and risk of specific irAE subtypes. Design, Setting, and Participants: A retrospective cohort study was conducted at a single academic medical center. The cohort included 358 patients with cancer who initiated anti-programmed death 1/ligand 1 and/or anticytotoxic-T-lymphocyte-4 ICI therapy between January 1, 2016, and March 8, 2019, and developed 1 or more cirAEs, identified using International Statistical Classification of Diseases and Related Health Problems, Tenth Revision codes and confirmed via manual medical record review. All relevant information documented before March 31, 2020, was included. Exposures: Anti-programmed death 1/ligand 1 and/or anticytotoxic-T-lymphocyte-4 therapy. Main Outcomes and Measures: Associations between specific cirAE morphologic classes and patterns of irAEs (occurrence, timeline, organ class, and specific toxic effects). Given the potential that shared underlying factors are associated with the risk of both noncutaneous and cutaneous toxic effects, the presence of observed positive associations between certain cirAE and irAE subtypes was hypothesized. Results: Of the 358 patients, 213 were men (59.5%); median age was 65 years (interquartile range, 55-73 years). Nearly half of the patients (177 [49.4%]) with cirAE also developed a noncutaneous irAE. Most patients (128 [72.3%]) experienced their first cirAE before developing any irAE. Several cirAE morphologic classes were found to be associated with overall, organ-based, and specific irAEs. More specifically, mucositis was found to be associated with overall irAE risk (odds ratio [OR], 5.28; 95% CI, 1.11-24.26; P = .04), gastrointestinal irAEs (OR, 5.70; 95% CI, 1.11-29.40; P = .04), and the specific diagnosis of gastroenterocolitis (OR, 6.80; 95% CI, 1.24-37.39; P = .03). In addition, psoriasis was associated with an increased risk of endocrine irAEs (OR, 4.54; 95% CI, 1.21-17.04; P = .03). Conclusions and Relevance: In this cohort study, these findings underscore the risk of multisystem toxic effects in patients experiencing cirAEs and highlight potential opportunities for dermatologists in the management of noncutaneous toxic effects.


Asunto(s)
Erupciones por Medicamentos/diagnóstico , Erupciones por Medicamentos/epidemiología , Inhibidores de Puntos de Control Inmunológico/efectos adversos , Neoplasias/tratamiento farmacológico , Anciano , Erupciones por Medicamentos/terapia , Femenino , Humanos , Masculino , Persona de Mediana Edad , Neoplasias/complicaciones , Neoplasias/patología , Estudios Retrospectivos , Medición de Riesgo
3.
Dermatitis ; 31(3): 185-190, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-32217881

RESUMEN

: Wine, beer, liquor, and spirits are widely consumed in many cultures across the globe, and for some individuals, ingestion, cutaneous contact, or other exposure can lead to dermatologic findings. However, there currently exist no comprehensive reviews on alcohol-related dermatitis. Herein, we will provide an overview of alcohol-related dermatitis and contact urticaria, including the epidemiology and clinical manifestations, potential allergens found in alcoholic beverages, testing approaches, and strategies for allergen avoidance.


Asunto(s)
Bebidas Alcohólicas/efectos adversos , Dermatitis Alérgica por Contacto/epidemiología , Urticaria/epidemiología , Bálsamos/efectos adversos , Cerveza/efectos adversos , Cromo/efectos adversos , Citrus/efectos adversos , Cobalto/efectos adversos , Dermatitis/epidemiología , Dermatitis/fisiopatología , Dermatitis/terapia , Dermatitis Alérgica por Contacto/etiología , Dermatitis Alérgica por Contacto/fisiopatología , Dermatitis Alérgica por Contacto/terapia , Conservantes de Alimentos/efectos adversos , Oro/efectos adversos , Humanos , Hipersensibilidad Tardía/epidemiología , Hipersensibilidad Tardía/etiología , Hipersensibilidad Tardía/fisiopatología , Hipersensibilidad Tardía/terapia , Hipersensibilidad Inmediata/epidemiología , Hipersensibilidad Inmediata/etiología , Hipersensibilidad Inmediata/fisiopatología , Hipersensibilidad Inmediata/terapia , Isotiocianatos/efectos adversos , Níquel/efectos adversos , Propilenglicol/efectos adversos , Sulfitos/efectos adversos , Urticaria/etiología , Urticaria/fisiopatología , Urticaria/terapia , Vino/efectos adversos
4.
Dermatol Clin ; 38(1): 165-175, 2020 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-31753189

RESUMEN

An interaction between light's radiation and certain exogenous and endogenous substances can lead to the development of photoallergic and/or phototoxic dermatoses. Clinically, reactions may range from acute and self-limited to chronic and recurrent. Delays in diagnosis are not uncommon due to complex clinical presentations, broad differentials, and limited number of specialists who perform phototesting. Therefore, a critical understanding of these dermatoses is essential for accurate diagnosis and appropriate management. The epidemiology, light sources, mechanisms, clinical presentations, evaluation protocols, common culprits, treatments, key challenges, and future directions related to photoallergy and phototoxicity are reviewed herein.


Asunto(s)
Dermatitis Fotoalérgica/diagnóstico , Dermatitis Fototóxica/diagnóstico , Manejo de la Enfermedad , Dermatitis Fotoalérgica/terapia , Dermatitis Fototóxica/terapia , Humanos , Pruebas Cutáneas/métodos
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