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Suárez-Diaz y Caminal-Montero en referencia al artículo especial «Recomendaciones SER sobre prevención de infección en enfermedades reumáticas autoinmunes sistémicas»" ] ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Íñigo Rúa-Figueroa Fernández de Larrinoa, Patricia Carreira Delgado, Noé Brito García, Beatriz Tejera Segura, Julián de la Torre Cisneros" "autores" => array:5 [ 0 => array:2 [ "nombre" => "Íñigo" "apellidos" => "Rúa-Figueroa Fernández de Larrinoa" ] 1 => array:2 [ "nombre" => "Patricia" "apellidos" => "Carreira Delgado" ] 2 => array:2 [ "nombre" => "Noé" "apellidos" => "Brito García" ] 3 => array:2 [ "nombre" => "Beatriz" "apellidos" => "Tejera Segura" ] 4 => array:2 [ "nombre" => "Julián" "apellidos" => "de la Torre Cisneros" ] ] ] ] ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2173574323000205?idApp=UINPBA00004M" "url" => "/21735743/0000001900000003/v1_202303101257/S2173574323000205/v1_202303101257/en/main.assets" ] "itemAnterior" => array:18 [ "pii" => "S2173574323000187" "issn" => "21735743" "doi" => "10.1016/j.reumae.2021.10.003" "estado" => "S300" "fechaPublicacion" => "2023-03-01" "aid" => "1584" "copyright" => "Elsevier España, S.L.U. and Sociedad Española de Reumatología y Colegio Mexicano de Reumatología" "documento" => "simple-article" "crossmark" => 1 "subdocumento" => "crp" "cita" => "Reumatol Clin. 2023;19:168-70" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:1 [ "total" => 0 ] "en" => array:13 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Case report</span>" "titulo" => "CLIPPERS Syndrome After Vaccination. An Unusual ASIA Presentation" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => array:2 [ 0 => "en" 1 => "es" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "168" "paginaFinal" => "170" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Síndrome de CLIPPERS posterior a vacunación. Una presentación inusual de ASIA" ] ] "contieneResumen" => array:2 [ "en" => true "es" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0005" "etiqueta" => "Fig. 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1585 "Ancho" => 1675 "Tamanyo" => 258895 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">(A, B) MRI of the brain T2 Flair at presentation with hyperintense lesions (arrows). (C) MRI of the brain T1 post-gadolinium at presentation, showing foci of pontine “peppering” enhancement lesion highly suggestive of a perivascular distribution. (D) MRI of the brain T1 post-gadolinium at one-month follow-up showing full recovery after corticosteroids treatment.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Juan Saénz-Silva, Alberto Ordinola Navarro" "autores" => array:2 [ 0 => array:2 [ "nombre" => "Juan" "apellidos" => "Saénz-Silva" ] 1 => array:2 [ "nombre" => "Alberto" "apellidos" => "Ordinola Navarro" ] ] ] ] ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2173574323000187?idApp=UINPBA00004M" "url" => "/21735743/0000001900000003/v1_202303101257/S2173574323000187/v1_202303101257/en/main.assets" ] "en" => array:16 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Images in Clinical Rheumatology</span>" "titulo" => "The classic triad of Löfgren’s syndrome in images" "tieneTextoCompleto" => true "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "171" "paginaFinal" => "172" ] ] "autores" => array:1 [ 0 => array:4 [ "autoresLista" => "Rami Qanneta" "autores" => array:1 [ 0 => array:4 [ "nombre" => "Rami" "apellidos" => "Qanneta" "email" => array:1 [ 0 => "rqanneta.gipss@gencat.cat" ] "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">*</span>" "identificador" => "cor0005" ] ] ] ] "afiliaciones" => array:1 [ 0 => array:2 [ "entidad" => "Medicina Interna, Hospital Sociosanitari Francolí, Gestió i Prestació de Serveis de Salut (GiPSS), Tarragona, Spain" "identificador" => "aff0005" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "La tríada clásica del síndrome de Löfgren en imágenes" ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:8 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1219 "Ancho" => 1755 "Tamanyo" => 419129 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0005" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">(A and B) Skin lesions in the form of erythematous indurate papules at pretibial level on the right leg and left forearm, respectively, indicative of erythema nodosum. (C) Tumefaction of the right hand, indicative of periarthritis. (D, E and F) Simple x-ray of the thorax, CT image of the thorax and gallium-67 gammagraphy showing bilateral hilar lymphadenopathies. (G, H and I) Histopathology of a skin lesion showing predominantly septal histiocytic inflammatory infiltrate, without necrosis or vasculitis.</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Sarcoidosis is chronic non-caseifying granulomatous disease that is multisystemic and idiopathic.<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1,2</span></a> Löfgren’s syndrome (LS) is an acute grade I form of sarcoidosis which evolves benignly and without sequelae in 95% of cases.<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3,4</span></a> It gives rise to stereotyped clinical findings: erythema nodosum (EN), bilateral hilar lymphadenopathies, involvement of the joints and fever (the classic triad).<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3,4</span></a> We present the case of a patient who debuted with classic LS.</p><p id="par0010" class="elsevierStylePara elsevierViewall">A woman in the third decade of life, Caucasian, an active smoker with a BMI of 34 and subclinical hypothyroidism, without other noteworthy medical factors. She was admitted due to symptoms that had evolved over 4 weeks, of asthenia, 38 °C fever and cutaneous bilateral pretibial and forearm lesions (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>Aand B) that are clinically indicative of EN: erythematous papules, indurate, painful and not pruriginous, as well as pain and tumefaction in both ankles, knees and hands, indicative of periarthritis (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>C). The rest of the physical examination was normal. In blood analysis the erythrocyte sedimentation rate in the first hour of 78 mm stood out, with 13,000/mm<span class="elsevierStyleSup">3</span> leucocytosis. Viral and bacterial serology was performed, together with ACE, autoantibodies, calciuria, blood and Mantoux cultures, all of which were negative. Thoracic x-ray (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>D) showed bilateral hilar lymphadenopathies, corroborated by high resolution thoracic CT imaging (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>E) and gammagraphy using gallium-67 (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>F), with a normal pulmonary parenchyma. Biopsy of a skin lesion showed predominantly septal histiocytic inflammatory infiltrate, without necrosis or vasculitis, with negative Ziehl-Neelsen staining, compatible with EN (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>G, H and I). Bronchoscopy, respiratory function tests, eye fundus and the bone x-ray series were normal. The Ziehl-Neelsen staining and Löwenstein–Jensen bronchoaspirate culture from the bronchoscopy were negative. LS was diagnosed by exclusion and clinical-radiological means. Treatment with 40 mg oral prednisone commenced (in decreasing doses), with a favourable evolution after 12 and 24 weeks of clinical, radiological and respiratory function follow-up.</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Transbronchial biopsy is indicated in all probable cases of sarcoidosis, except for those with classic LS (only in the case of unilateral hilar or isolated right paratracheal lymphadenopathies).<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1–4</span></a> Nevertheless, several entities should be considered in the differential diagnosis with LS or stage I sarcoidosis (Hodgkin’s lymphoma, tuberculous lymphadenitis, Whipple’s disease, yersiniosis, brucelosis, syphilis and the initial phase of HIV), which were all reasonably excluded in our case. On the other hand, the diagnosis of EN is clinical, and skin biopsy is indicated in certain cases (persistent symptoms, atypical location, ulceration, the suspicion of infection by <span class="elsevierStyleItalic">Mycobacterium</span> or leukocytoclastic vasculitis).<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1–4</span></a> In our case this was not indispensable. Although up to two thirds of cases may remit spontaneously, steroid therapy for LS is the first line of treatment.<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1,2</span></a> It should be underlined that a response to treatment does not necessarily confirm the diagnosis of sarcoidosis; an exhaustive follow-up is therefore essential, re-evaluating the case and ruling out other diseases in the case of resistance or relapse. It is also necessary to take into account non-adherence, inappropriate doses or progression of the disease. Likewise, measurement of ACE levels in serum is not very sensitive, and nor is it specific as a diagnostic test or a therapeutic guide.<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1,2</span></a></p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflict of interests</span><p id="par0020" class="elsevierStylePara elsevierViewall">The authors have no conflict of interests to declare.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:2 [ 0 => array:2 [ "identificador" => "sec0005" "titulo" => "Conflict of interests" ] 1 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2022-08-03" "fechaAceptado" => "2022-09-03" "multimedia" => array:1 [ 0 => array:8 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1219 "Ancho" => 1755 "Tamanyo" => 419129 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0005" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">(A and B) Skin lesions in the form of erythematous indurate papules at pretibial level on the right leg and left forearm, respectively, indicative of erythema nodosum. (C) Tumefaction of the right hand, indicative of periarthritis. (D, E and F) Simple x-ray of the thorax, CT image of the thorax and gallium-67 gammagraphy showing bilateral hilar lymphadenopathies. (G, H and I) Histopathology of a skin lesion showing predominantly septal histiocytic inflammatory infiltrate, without necrosis or vasculitis.</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:4 [ 0 => array:3 [ "identificador" => "bib0005" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Sarcoidosis" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:3 [ 0 => "P. Brito-Zerón" 1 => "R. Pérez-Alvárez" 2 => "M. Ramos-Casals" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1016/j.medcli.2022.03.009" "Revista" => array:7 [ "tituloSerie" => "Med Clin (Barc)." "fecha" => "2022" "volumen" => "159" "numero" => "4" "paginaInicial" => "195" "paginaFinal" => "204" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/35680449" "web" => "Medline" ] ] ] ] ] ] ] ] 1 => array:3 [ "identificador" => "bib0010" "etiqueta" => "2" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Sarcoidosis" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:3 [ 0 => "M.C. Iannuzzi" 1 => "B.A. Rybicki" 2 => "A.S. Teirstein" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1056/NEJMra071714" "Revista" => array:7 [ "tituloSerie" => "N Engl J Med." 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"fecha" => "2021" "volumen" => "14" "numero" => "6" ] ] ] ] ] ] ] ] ] ] ] "idiomaDefecto" => "en" "url" => "/21735743/0000001900000003/v1_202303101257/S2173574323000199/v1_202303101257/en/main.assets" "Apartado" => array:4 [ "identificador" => "5795" "tipo" => "SECCION" "en" => array:2 [ "titulo" => "Images in Clinical Rheumatology" "idiomaDefecto" => true ] "idiomaDefecto" => "en" ] "PDF" => "https://static.elsevier.es/multimedia/21735743/0000001900000003/v1_202303101257/S2173574323000199/v1_202303101257/en/main.pdf?idApp=UINPBA00004M&text.app=https://reumatologiaclinica.org/" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2173574323000199?idApp=UINPBA00004M" ]
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