Chronic cutaneous lupus: a 10-year retrospective study in the Posadas Hospital
Keywords:
Lupus, cutaneous lupus, discoid lupusAbstract
Introduction: Lupus eritematosus (LE) is a multifactorial inflammatory autoimmune chronic disease that may involve many differents organs and can be triggered by multiple factors in genetically predisposed individuals.
Objectives: Analyse in the different clinical forms of Chronic Cutaneous Lupus (CCL) distribution by sex, age, time of evolution since the diagnosis, location of the lesions, presence of antibodies and systemic involvement, and compare the results with the literature.
Design: Retrospective and descriptive study.
Methods: We reviewed clinical histories of patients with both clinical and histophatological diagnosis of CCL who consulted the Dermatology Service between January 2, 2007 and July 31, 2017.
Results: We evaluated 48 patients, 43 women and 5 men, female predominance was 8,6:1. Discoid Lupus (DL) was the most frequent clinical form 87,5%, the mayority was the localized variety and only 2 cases with generalized DL. Secondly, 3 patients were diagnosed with lupus panniculitis (6,25%). The types tumid, chilblain and lupus lichen corresponded only to 1 patient for each clinical form. The age of presentation varied between 11 and 81 years, with an average of 37,81. 12 patients were positive for antinuclear antibodies (ANA) and 10 had systemic involvement.
Conclusions: Our findings were similar to those previously published, except the female predominance 8,6:1, four times higher in our patients.
References
I. Sontheimer RD, Maddison PJ, Reichlin M, Jordon RE, et ál. Serologic and HLA associations in subacute cutaneous lupus erythematosus, a clinical subset of lupus erythematosus. Ann Intern Med 1982;97:664-671.
II. Stringa O, Troielli P. Consenso sobre Lupus Eritematoso Cutáneo. Actualización 2016. Sociedad Argentina de Dermatología, Buenos Aires. http://sad.org.ar/wp-content/uploads/2016/04/LUPUS-FINAL-07122016.pdf
III. Ortega SM, Barbarulo A, Spelta MG, Gavazza S, et ál. Lupus eritematoso cutáneo: revisión de nuestra casuística en los últimos 15 años. Dermatol Argent 2011;17:116-122.
IV. Hassan ML. Lupus eritematoso. En: Hassan ML. Colagenopatías en dermatología. Con enfoque multidisciplinario. Akadia, Buenos Aires, 2017:103-178.
V. Salomón M, Samalvides F. Manifestaciones histopatológicas del lupus eritematoso cutáneo en pacientes del Servicio de Dermatología del Hospital Nacional Cayetano Heredia, 2003-2008. Folia Dermatol Perú 2009;20:64-70.
VI. Villaran P, Castro M, Mayeshiro E. Lupus eritematoso discoide en varón con implante de silicona. Folia Dermatol Perú2002;13:53-56.
VII. Hymes SR, Jordon RE. Chronic cutaneous lupus erythematosus. Med Clin North Am 1989;73:1055-1071.
VIII. Ziemer M, Milkova L, Kunz M. Lupus erythematosus. Part II: Clinical picture, diagnosis and treatment. J Dtsch Dermatol Ges 2014;12:285-301.
IX. Peters MS, Su WP. Lupus erythematosus paniculitis. Med Clin North Am 1989;73:1113-1126.10. Achenbach RE, Casas JG. Paniculitis lúpica (lupus profundo). Dermatol Argent 2009;90:134-139.
XI. Kaminsky A, Díaz M, Prada M, Dancziger E, et ál. Lupus eritematoso. Dermatol Argent 2003;4:78-97.
XII. Passardi S, Rey Campero M, Bourren P, Massone C, et ál. Lupus eritematoso túmido. Dermatol Argent 2012;18:65-67.
XIII. Okon LG, Werth VP. Cutaneous lupus erythematosus: Diagnosis and treatment. Best Pract Res Clin Rheumatol 2013;27:391-404.
XIV. Bansal S, Goel A. Chilblain lupus erythematosus in an adolescent girl. Indian Dermatol Online J 2014;5:30-32.
XV. Demirci GT, Altunay IK, Sarikaya S, Sakiz D. Lupus erythematosus and lichen planus overlap syndrome: a case report with a rapid response to topical corticosteroid therapy. Dermatol Rep2011;3:e48.
Downloads
Published
Issue
Section
License
Copyright (c) 2018 Argentine Society of Dermatology
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
El/los autor/es tranfieren todos los derechos de autor del manuscrito arriba mencionado a Dermatología Argentina en el caso de que el trabajo sea publicado. El/los autor/es declaran que el artículo es original, que no infringe ningún derecho de propiedad intelectual u otros derechos de terceros, que no se encuentra bajo consideración de otra revista y que no ha sido previamente publicado.
Le solicitamos haga click aquí para imprimir, firmar y enviar por correo postal la transferencia de los derechos de autor