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1.
Asia Pacific Allergy ; (4): 8-2020.
Artículo en Inglés | WPRIM | ID: wpr-785457

RESUMEN

There are geographical, regional, and ethnic differences in the phenotypes and endotypes of patients with drug hypersensitivity reactions (DHRs) in different parts of the world. In Asia, aspects of drug hypersensitivity of regional importance include IgE-mediated allergies and T-cell-mediated reactions, including severe cutaneous adverse reactions (SCARs), to beta-lactam antibiotics, antituberculous drugs, nonsteroidal anti-inflammatory drugs (NSAIDs) and radiocontrast agents. Delabeling of low-risk penicillin allergy using direct oral provocation tests without skin tests have been found to be useful where the drug plausibility of the index reaction is low. Genetic risk associations of relevance to Asia include human leucocyte antigen (HLA)-B*1502 with carbamazepine SCAR, and HLA-B*5801 with allopurinol SCAR in some Asian ethnic groups. There remains a lack of safe and accurate diagnostic tests for antituberculous drug allergy, other than relatively high-risk desensitization regimes to first-line antituberculous therapy. NSAID hypersensitivity is common among both adults and children in Asia, with regional differences in phenotype especially among adults. Low dose aspirin desensitization is an important therapeutic modality in individuals with cross-reactive NSAID hypersensitivity and coronary artery disease following percutaneous coronary intervention. Skin testing allows patients with radiocontrast media hypersensitivity to confirm the suspected agent and test for alternatives, especially when contrasted scans are needed for future monitoring of disease relapse or progression, especially cancers.


Asunto(s)
Adulto , Niño , Humanos , Alopurinol , Anafilaxia , Antibacterianos , Asia , Pueblo Asiatico , Aspirina , Asma , Carbamazepina , Cicatriz , Medios de Contraste , Enfermedad de la Arteria Coronaria , Pruebas Diagnósticas de Rutina , Hipersensibilidad a las Drogas , Etnicidad , Hipersensibilidad , Penicilinas , Intervención Coronaria Percutánea , Fenotipo , Recurrencia , Pruebas Cutáneas
2.
Annals of Dermatology ; : 597-601, 2018.
Artículo en Inglés | WPRIM | ID: wpr-717761

RESUMEN

We studied a family with Gorlin-Goltz syndrome. The novel mutations of our cases were located on the 21st exon of the PTCH1 gene (c.3450C>G). The father, who received a strategic 56-day vismodegib treatment for disease control, was the first patient with Gorlin syndrome treated with the hedgehog inhibitor in Taiwan. The lesions regressed gradually, with scar formation, and were subsequently removed via a wide excision. Further details are provided below.


Asunto(s)
Humanos , Síndrome del Nevo Basocelular , Cicatriz , Exones , Padre , Erizos , Taiwán
3.
Asia Pacific Allergy ; (4): 59-67, 2015.
Artículo en Inglés | WPRIM | ID: wpr-750025

RESUMEN

Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and drug reaction with eosinophilia and systemic symptoms (DRESS) are severe cutaneous adverse reactions (SCAR) which are majorly caused by drugs. Though the incidence rate is low, SCAR sometimes can be life-threatening and leads to lifelong sequelae. Many pharmacogenomic associations in immune and nonimmune related genes with the development of SCAR have been discovered recently and the pharmacogenetic tests have been applied to prevent specific drug-induced SCAR. In this review, we discuss the recent advances of pharmacogenomics in SCAR.


Asunto(s)
Cicatriz , Síndrome de Hipersensibilidad a Medicamentos , Incidencia , Farmacogenética , Síndrome de Stevens-Johnson
4.
Indian J Dermatol Venereol Leprol ; 2011 Jul-Aug; 77(4): 537
Artículo en Inglés | IMSEAR | ID: sea-140912
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