Síndrome de Vogt-Koyanagi-Harada

0Citations
Citations of this article
23Readers
Mendeley users who have this article in their library.

Abstract

Vogt-Koyanagi-Harada disease is an infrequent, systemic syndrome that evolves in stages and compromises organs containing melanocytes. Typically, patients experience four different phases: meningoencephalitic, uveitic, convalescence with dermatologic involvement, and the chronic phase. Treatment of choice is high dose corticosteroids which may be combined with immunosuppressive agents. It should be initiated as early as possible to prevent eye damage. We present the case of a patient with the first two phases of the disease in addition to erythema multiform lesions. During convalescence phase, and in coincidence with the location of the latter, he developed vitiligo lesions that complete the syndrome.

Cite

CITATION STYLE

APA

Caviedes, M. P., Baztan Piñero, M. C., Guzzi Maqueda, M., Staiger, H., Torre, A. C., Volonteri, V. I., & Galimberti, R. L. (2012). Síndrome de Vogt-Koyanagi-Harada. Dermatologia Cosmetica, Medica y Quirurgica, 10(1), 33–36. https://doi.org/10.31053/1853.0605.v73.n2.13263

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free