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Ormond's disease: Experience with five cases
Enfermedad de Ormond: experiencia de cinco casos
Natalia Castro-Iglesiasa, Moncef Belhassen-Garcíaa,
Corresponding author
mbelhassen@hotmail.com

Corresponding author.
, Virginia Velasco-Tiradoa, Adela Carpio-Péreza, Sandra Inés-Revueltab, Sheila Martín-Barbaa, Javier Pardo-Lledíasc
a Servicio de Medicina Interna III, Hospital Clínico Universitario de Salamanca, Salamanca, Spain
b Servicio de Medicina Interna II, Hospital Clínico Universitario de Salamanca, Salamanca, Spain
c Servicio de Medicina Interna, Hospital General de Segovia, Segovia, Spain
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      "es" => array:1 [
        "titulo" => "Enfermedad de Ormond&#58; experiencia de cinco casos"
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    "fechaRecibido" => "2009-05-06"
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            0 => "Ormond&#39;s disease"
            1 => "Retroperitoneal fibrosis"
            2 => "Chronic periaortitis"
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            0 => "Enfermedad de Ormond"
            1 => "Fibrosis retroperitoneal"
            2 => "Periaortitis cr&#243;nica"
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      "en" => array:2 [
        "titulo" => "Abstract"
        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Ormond&#39;s disease &#40;OD&#41; is an uncommon process with an annual incidence nearing 1 per million inhabitants&#46; The etiology in most of the cases is unknown and several pathogenic mechanisms are implicated in secondary OD&#46; Ormond disease is characterized by a fibrotic and inflammatory mass with three different clinical features&#58; 1&#41; retroperitoneal fibrosis&#44; 2&#41; perianeurysmatic retroperitoneal fibrosis and 3&#41; inflammatory abdominal aortic aneurysms&#46; Classic management is based on surgical treatment associated or not with steroids&#46; Immunosuppressive agents have been used in the last years with unclear results&#46; We report five cases from the University Hospital of Salamanca occurring during 2000&#8211;2008&#46; We highlight the lack of trials designed to establish clinical guidelines for the treatment of the disease and improvement of outcome&#46;</p>"
      ]
      "es" => array:2 [
        "titulo" => "Resumen"
        "resumen" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">La enfermedad de Ormond &#40;EO&#41; es una enfermedad infrecuente con una incidencia aproximada de 1&#47;1&#46;000&#46;000 personas-a&#241;o&#46; La etiolog&#237;a en la mayor&#237;a de los casos es desconocida&#44; y en la EO secundaria se han implicado m&#250;ltiples procesos patog&#233;nicos&#46; La EO se caracteriza por la presencia de una masa fibroinflamatoria retroperitoneal con tres formas cl&#237;nicas diferentes&#58; <span class="elsevierStyleItalic">i</span>&#41; fibrosis retroperitoneal&#59; <span class="elsevierStyleItalic">ii</span>&#41; fibrosis perianeurism&#225;tica retroperitoneal&#44; y <span class="elsevierStyleItalic">iii</span>&#41; inflamaci&#243;n de los aneurismas de la aorta abdominal&#46; El manejo cl&#225;sico se basa en el tratamiento quir&#250;rgico y puede asociarse a esteroides&#46; En estos &#250;ltimos a&#241;os se han empleado otros inmunosupresores sin resultados bien establecidos&#46; Presentamos cinco casos acontecidos en el Hospital Cl&#237;nico Universitario de Salamanca durante el per&#237;odo 2000&#8211;2008&#46; Destacamos la falta de estudios para establecer gu&#237;as de pr&#225;ctica cl&#237;nica que faciliten el manejo y mejoren el pron&#243;stico&#46;</p>"
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Article information
ISSN: 21735743
Original language: English
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Idiomas
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