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One type of MDS is refractory anemia with blast excess &#40;RABE&#41;&#44; with the number of blasts being greater than 5&#37; and less than 10&#37; in type 1&#44; and between 10&#37; and 20&#37; in type 2&#46; These diseases are refractory to chemotherapy and stem cell transplant offers a cure&#46; In RABE&#44; supportive treatment is performed with red blood cell transfusions&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Case Report</span><p id="par0020" class="elsevierStylePara elsevierViewall">The patient is a 70 years old male with no history of interest&#44; who had recurrent episodes of 2 weeks with high fever&#44; leukocytosis&#44; and erythematous papules and plaques on the extremities&#44; with dense neutrophilic infiltrates in the biopsy &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The patient had asymmetric oligoarthritis affecting the wrist and knees&#46; Analytically&#44; there was an elevated sedimentation rate &#40;ESR&#41;&#44; leukocytosis&#44; and anemia&#46; Episodes were treated with glucocorticoids at 0&#46;5<span class="elsevierStyleHsp" style=""></span>mg&#47;kg&#44; with little response&#46; The disease became chronic and recurrent&#46; Indomethacin was prescribed a dose of 150<span class="elsevierStyleHsp" style=""></span>mg&#47;day and potassium iodide was added&#44; without improvement&#46; In parallel&#44; the patient was diagnosed with a type 1 RABE after the study of persistent anemia&#46; We performed multiple red blood cells transfusions&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">Patient outcome was not favorable&#44; with persisting episodes of fever&#44; and arthritis&#46; His anemia worsened and underwent a bone marrow transplant&#46; While waiting for a compatible donor&#44; the patient died&#44; possibly due to a complication of the hematologic process&#44; worsening of cytopenias or transformation to leukemia&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Discussion</span><p id="par0030" class="elsevierStylePara elsevierViewall">SS can be classified into 3 groups&#58; idiopathic&#44; associated with malignant disease and drug-induced&#46; Up to 54&#37; of patients may have a tumor or hematologic disease&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> Joint involvement may occur &#40;33&#37;&#8211;62&#37;&#41;&#44; as well as lung&#44; eye&#44; kidney&#44; liver&#44; or central nervous system compromise&#46; Chronic recurrent disease occurs in around 15&#37;&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> The disease is more common in women in the fifth decade of life&#46; The ESR is elevated and anemia present&#46; It can last from 1 week to 4 years&#46; The differential diagnosis must be made with erythema nodosum&#44; cellulitis and erysipelas&#44; erythema elevatum diutinum&#44; erythema multiforme&#44; leukocytoclastic vasculitis&#44; or pyoderma gangrenosum&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">Systemic glucocorticoids are the treatment of choice&#46; Indomethacin<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> is effective&#46; Colchicine&#44; potassium iodide&#44; dapsone&#44; cyclosporine&#44; interferon alpha or etretinate<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> are therapeutic alternatives&#46; There have been reports of SS and MDS successfully treated with intravenous immunoglobulin&#44;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a> glucocorticoids&#44; and doxycycline or stem cell transplantation&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">8&#44;9</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">The patient described had a case that progressed despite treatment&#46; Pending the transplantation we were able to use some of the treatments described in the literature&#44; although possibly the transplant would had been the only effective treatment&#46;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Conclusion</span><p id="par0045" class="elsevierStylePara elsevierViewall">SS is a rare dermatological entity&#44; which when accompanied by an MDS may worsen the patient&#39;s prognosis&#46; The treatment of choice for SS is the use of glucocorticoids&#44; although in most cases this may be insufficient and require alternative therapies&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Ethical disclosures</span><p id="par0055" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">Protection of human and animal subjects</span>&#46; The authors declare that no experiments were performed on humans or animals for this investigation&#46;<span class="elsevierStyleVsp" style="height:0.5px"></span></p><p id="par0060" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">Confidentiality of Data</span>&#46; The authors declare that they have followed the protocols of their work centre on the publication of patient data and that all the patients included in the study have received sufficient information and have given their informed consent in writing to participate in that study&#46;<span class="elsevierStyleVsp" style="height:0.5px"></span></p><p id="par0065" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">Right to privacy and informed consent</span>&#46; The authors must have obtained the informed consent of the patients and &#47;or subjects mentioned in the article&#46; The author for correspondence must be in possession of this document&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Disclosure</span><p id="par0050" class="elsevierStylePara elsevierViewall">The authors have no disclosures to make&#46;</p></span></span>"
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        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Sweet&#39;s syndrome or acute neutrophilic febrile dermatosis is a systemic disease of unknown etiology characterized by the appearance of skin lesions produced by a neutrophilic dermal infiltrate&#44; fever&#44; and peripheral leukocytosis&#46; It may be associated with hematologic diseases&#44; including leukemia&#44; with immune diseases as rheumatoid arthritis&#44; or can occur in isolation&#46; The myelodysplasias are hematological disorders characterized by one or more cytopenias secondary to bone marrow dysfunction&#46; We present the case of a patient with Sweet&#39;s syndrome associated with myelodysplastic syndrome and treated with glucocorticoids who did not present a good clinical outcome&#46; We discuss the different treatment of these diseases because in most cases glucocorticoids&#44; which are the treatment of choice in Sweet&#39;s syndrome&#44; may be insufficient&#46;</p>"
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        "resumen" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">El s&#237;ndrome de Sweet o dermatosis neutrof&#237;lica febril aguda es una enfermedad sist&#233;mica de etiolog&#237;a desconocida&#44; caracterizada por la aparici&#243;n de lesiones cut&#225;neas producidas por un infiltrado d&#233;rmico neutrof&#237;lico&#44; fiebre y leucocitosis perif&#233;rica&#46; Puede estar asociado a enfermedades hematol&#243;gicas&#44; incluida la leucemia&#44; inmunol&#243;gicas como la artritis reumatoide o presentarse de forma aislada&#46; Las mielodisplasias son trastornos hematol&#243;gicos caracterizados por una o m&#225;s citopenias secundarias a la disfunci&#243;n de la m&#233;dula &#243;sea&#46; Se presenta el caso de un paciente con s&#237;ndrome de Sweet asociado a un s&#237;ndrome mielodispl&#225;sico que ha seguido tratamiento con glucocorticoides y no ha presentado una buena evoluci&#243;n cl&#237;nica&#46; Se discuten los diferentes tratamientos de estas enfermedades porque en la mayor&#237;a de las ocasiones los glucocorticoides&#44; que son el tratamiento de elecci&#243;n en el s&#237;ndrome de Sweet&#44; pueden ser insuficientes&#46;</p>"
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Case report
Sweet Syndrome Associated With Myelodysplastic Syndrome: Report of a Case. Review of the Literature
Síndrome de Sweet asociado a síndrome mielodisplásico: a propósito de un caso. Revisión de la literatura
Delia Reinaa,
Corresponding author
deliareinasanz@gmail.com

Corresponding author.
, Dacia Cerdàa, Daniel Roiga, Ramon Fígulsa, M. Luz Villegasb, Hèctor Corominasa
a Unidad de Reumatología, Hospital Sant Joan Despí Moisès Broggi, Sant Joan Despí, Barcelona, Spain
b Servicio de Medicina Interna, Hospital General de l’Hospitalet, Barcelona, Spain
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One type of MDS is refractory anemia with blast excess &#40;RABE&#41;&#44; with the number of blasts being greater than 5&#37; and less than 10&#37; in type 1&#44; and between 10&#37; and 20&#37; in type 2&#46; These diseases are refractory to chemotherapy and stem cell transplant offers a cure&#46; In RABE&#44; supportive treatment is performed with red blood cell transfusions&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Case Report</span><p id="par0020" class="elsevierStylePara elsevierViewall">The patient is a 70 years old male with no history of interest&#44; who had recurrent episodes of 2 weeks with high fever&#44; leukocytosis&#44; and erythematous papules and plaques on the extremities&#44; with dense neutrophilic infiltrates in the biopsy &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The patient had asymmetric oligoarthritis affecting the wrist and knees&#46; Analytically&#44; there was an elevated sedimentation rate &#40;ESR&#41;&#44; leukocytosis&#44; and anemia&#46; Episodes were treated with glucocorticoids at 0&#46;5<span class="elsevierStyleHsp" style=""></span>mg&#47;kg&#44; with little response&#46; The disease became chronic and recurrent&#46; Indomethacin was prescribed a dose of 150<span class="elsevierStyleHsp" style=""></span>mg&#47;day and potassium iodide was added&#44; without improvement&#46; In parallel&#44; the patient was diagnosed with a type 1 RABE after the study of persistent anemia&#46; We performed multiple red blood cells transfusions&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">Patient outcome was not favorable&#44; with persisting episodes of fever&#44; and arthritis&#46; His anemia worsened and underwent a bone marrow transplant&#46; While waiting for a compatible donor&#44; the patient died&#44; possibly due to a complication of the hematologic process&#44; worsening of cytopenias or transformation to leukemia&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Discussion</span><p id="par0030" class="elsevierStylePara elsevierViewall">SS can be classified into 3 groups&#58; idiopathic&#44; associated with malignant disease and drug-induced&#46; Up to 54&#37; of patients may have a tumor or hematologic disease&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> Joint involvement may occur &#40;33&#37;&#8211;62&#37;&#41;&#44; as well as lung&#44; eye&#44; kidney&#44; liver&#44; or central nervous system compromise&#46; Chronic recurrent disease occurs in around 15&#37;&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> The disease is more common in women in the fifth decade of life&#46; The ESR is elevated and anemia present&#46; It can last from 1 week to 4 years&#46; The differential diagnosis must be made with erythema nodosum&#44; cellulitis and erysipelas&#44; erythema elevatum diutinum&#44; erythema multiforme&#44; leukocytoclastic vasculitis&#44; or pyoderma gangrenosum&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">Systemic glucocorticoids are the treatment of choice&#46; Indomethacin<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> is effective&#46; Colchicine&#44; potassium iodide&#44; dapsone&#44; cyclosporine&#44; interferon alpha or etretinate<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> are therapeutic alternatives&#46; There have been reports of SS and MDS successfully treated with intravenous immunoglobulin&#44;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a> glucocorticoids&#44; and doxycycline or stem cell transplantation&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">8&#44;9</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">The patient described had a case that progressed despite treatment&#46; Pending the transplantation we were able to use some of the treatments described in the literature&#44; although possibly the transplant would had been the only effective treatment&#46;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Conclusion</span><p id="par0045" class="elsevierStylePara elsevierViewall">SS is a rare dermatological entity&#44; which when accompanied by an MDS may worsen the patient&#39;s prognosis&#46; The treatment of choice for SS is the use of glucocorticoids&#44; although in most cases this may be insufficient and require alternative therapies&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Ethical disclosures</span><p id="par0055" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">Protection of human and animal subjects</span>&#46; The authors declare that no experiments were performed on humans or animals for this investigation&#46;<span class="elsevierStyleVsp" style="height:0.5px"></span></p><p id="par0060" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">Confidentiality of Data</span>&#46; The authors declare that they have followed the protocols of their work centre on the publication of patient data and that all the patients included in the study have received sufficient information and have given their informed consent in writing to participate in that study&#46;<span class="elsevierStyleVsp" style="height:0.5px"></span></p><p id="par0065" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">Right to privacy and informed consent</span>&#46; The authors must have obtained the informed consent of the patients and &#47;or subjects mentioned in the article&#46; The author for correspondence must be in possession of this document&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Disclosure</span><p id="par0050" class="elsevierStylePara elsevierViewall">The authors have no disclosures to make&#46;</p></span></span>"
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            0 => "Sweet syndrome"
            1 => "Myelodysplastic syndrome"
            2 => "Arthritis"
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            0 => "S&#237;ndrome de Sweet"
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        "titulo" => "Abstract"
        "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Sweet&#39;s syndrome or acute neutrophilic febrile dermatosis is a systemic disease of unknown etiology characterized by the appearance of skin lesions produced by a neutrophilic dermal infiltrate&#44; fever&#44; and peripheral leukocytosis&#46; It may be associated with hematologic diseases&#44; including leukemia&#44; with immune diseases as rheumatoid arthritis&#44; or can occur in isolation&#46; The myelodysplasias are hematological disorders characterized by one or more cytopenias secondary to bone marrow dysfunction&#46; We present the case of a patient with Sweet&#39;s syndrome associated with myelodysplastic syndrome and treated with glucocorticoids who did not present a good clinical outcome&#46; We discuss the different treatment of these diseases because in most cases glucocorticoids&#44; which are the treatment of choice in Sweet&#39;s syndrome&#44; may be insufficient&#46;</p>"
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      "es" => array:2 [
        "titulo" => "Resumen"
        "resumen" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">El s&#237;ndrome de Sweet o dermatosis neutrof&#237;lica febril aguda es una enfermedad sist&#233;mica de etiolog&#237;a desconocida&#44; caracterizada por la aparici&#243;n de lesiones cut&#225;neas producidas por un infiltrado d&#233;rmico neutrof&#237;lico&#44; fiebre y leucocitosis perif&#233;rica&#46; Puede estar asociado a enfermedades hematol&#243;gicas&#44; incluida la leucemia&#44; inmunol&#243;gicas como la artritis reumatoide o presentarse de forma aislada&#46; Las mielodisplasias son trastornos hematol&#243;gicos caracterizados por una o m&#225;s citopenias secundarias a la disfunci&#243;n de la m&#233;dula &#243;sea&#46; Se presenta el caso de un paciente con s&#237;ndrome de Sweet asociado a un s&#237;ndrome mielodispl&#225;sico que ha seguido tratamiento con glucocorticoides y no ha presentado una buena evoluci&#243;n cl&#237;nica&#46; Se discuten los diferentes tratamientos de estas enfermedades porque en la mayor&#237;a de las ocasiones los glucocorticoides&#44; que son el tratamiento de elecci&#243;n en el s&#237;ndrome de Sweet&#44; pueden ser insuficientes&#46;</p>"
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        "etiqueta" => "&#9734;"
        "nota" => "<p class="elsevierStyleNotepara">Please cite this article as&#58; Reina D&#44; et al&#46; S&#237;ndrome de Sweet asociado a s&#237;ndrome mielodispl&#225;sico&#58; a prop&#243;sito de un caso&#46; Revisi&#243;n de la literatura&#46; Reumatol Clin&#46; 2013&#59;9&#58;246&#8211;7&#46;</p>"
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