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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Extrafacial edema is a rare manifestation of dermatomyositis &#40;DM&#41;&#46; We report 2 cases&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">Case no&#46; 1&#46; The patient was an 86-year-old woman who was admitted with dysphagia&#44; dyspnea&#44; weakness in her 4 extremities &#40;2&#47;5&#41; and edemas&#46; Four years earlier&#44; she had been diagnosed with cryptogenic organizing pneumonia detected by means of pulmonary function tests&#44; imaging studies and histology&#46; It was observed that&#44; aside from periorbital edema&#44; she had edema with fovea in upper and lower limbs&#46; She had plaques with vesiculobullous eruption on her forearms and erythematous and edematous eruption on her thighs &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; Biopsy of the thigh revealed epidermal atrophy&#44; subepidermal bullous disease&#44; necrotic keratinocytes&#44; superficial perivascular infiltrate&#44; mucin and dermal edema&#46; Direct immunofluorescence was negative&#44; as were tests for anti-Jo-1&#44; anti-PL7&#44; anti-PL12&#44; anti-SRP-54&#44; anti-Mi2&#44; anti-Ku and anti-PM&#47;Scl antibodies&#46; Creatine kinase &#40;CK&#41; was 1267<span class="elsevierStyleHsp" style=""></span>U&#47;L&#46; Electromyogram demonstrated the myopathic changes and muscle biopsy revealed perifascicular atrophy and CD4<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>perimysium and perivascular inflammatory infiltrate&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">A cardiac origin of the edema was ruled out&#44; as were renal&#44; hepatic and thyroid origin&#46; Albumin&#44; after multiple hospital admissions for dyspnea&#44; weakness and edemas&#44; had decreased &#40;2&#46;5&#8211;3&#46;2<span class="elsevierStyleHsp" style=""></span>g&#47;dL&#41; and reached normality after treatment with corticosteroids&#46; Having reviewed her history&#44; we finally discovered the diagnosis of her lung disease&#58; an elevated CK level &#40;1370<span class="elsevierStyleHsp" style=""></span>U&#47;L&#41;&#46; Computed tomography revealed a breast lesion that was found to be an infiltrating ductal carcinoma&#46; She was treated with prednisone at a dose of 1<span class="elsevierStyleHsp" style=""></span>mg&#47;kg body weight &#40;bw&#41;&#47;day and 5 sessions of plasmapheresis&#46; After mastectomy&#44; dysphagia persisted and we detected a diffuse disseminated signet ring cell adenocarcinoma&#46; She died 4 months later due to respiratory failure&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">Case no&#46; 2&#46; The patient was a 71-year-old man who had been treated 7 months earlier for cancer of the cavum&#46; He presented with weakness of his upper &#40;2&#47;5&#41; and lower &#40;3&#47;5&#41; limbs&#44; skin lesions and migratory swelling&#58; it began in his neck and supraclavicular region&#44; followed by ankles&#44; abdomen and upper limbs&#46; Other causes of edema were ruled out&#46; His CK level was 728<span class="elsevierStyleHsp" style=""></span>U&#47;L and the same antibody panel was negative&#46; Electromyogram and muscle biopsy were similar to those of case no&#46; 1&#46; A week with prednisone at a dose of 1<span class="elsevierStyleHsp" style=""></span>mg&#47;kg bw&#47;day&#44; resolved the edema&#59; treatment was increased with methotrexate at 20<span class="elsevierStyleHsp" style=""></span>mg&#47;week&#44; but he died 7 months later due to muscular respiratory failure&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">Edematous DM<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#8211;5</span></a> could constitute up to 6&#37; of the cases of DM&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> It is characterized by extrafacial&#44; localized or generalized edema&#44; with or without fovea&#44; with no other cause of edema&#46; It is more prevalent in women &#40;2&#58;1&#41;&#44; of ages between 23 and 93 years&#46; The diagnostic delay is more than 2 months&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> It is speculated that it is originated by ischemia of the microvasculature&#46; To date&#44; the migratory localization so characteristic of our case had not been reported&#46; Vesiculobullous DM consists of subepidermal vesiculobullae with biopsy results typical of DM&#44; with no other bullous dermatosis&#46; Its cause has been proposed to be friction&#44; dermal edema and mucin&#46; The specimen for the biopsy in the first case was taken from the patient&#39;s thigh&#44; where no clinical detachment was observed&#46; We subsequently considered that the detachment was secondary to the edema and that the two clinical forms&#44; edematous and vesiculobullous&#44; could be the same manifestation or overlap&#46; The distribution does not indicate a mechanical cause and there are similar cases of severe edema in which detachment appeared&#46;<a class="elsevierStyleCrossRefs" href="#bib0075"><span class="elsevierStyleSup">5&#8211;7</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">The cause of hypoalbuminemia of the first case was due to the proinflammatory status of the interstitial lung disease and the DM that still had not been diagnosed&#46;<a class="elsevierStyleCrossRefs" href="#bib0090"><span class="elsevierStyleSup">8&#44;9</span></a> This hypoalbuminemia could be the cause of generalized edema&#44; but not of the erythematous and edematous and vesiculobullous plaques&#46; The literature demonstrates that edematous DM could be associated with a more severe myopathy and dysphagia&#44; a finding that was not observed in our patients&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#8211;3</span></a> Likewise&#44; vesiculobullous DM would be closely associated with neoplasms and a worse prognosis&#46;<a class="elsevierStyleCrossRefs" href="#bib0080"><span class="elsevierStyleSup">6&#44;10</span></a> Extrafacial edema in DM&#44; in any of its variants should alert physicians to a greater severity and lead to an active search for a neoplasm&#46;</p></span>"
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                      "titulo" => "Dermatomyositis presenting with severe subcutaneous edema&#58; five additional cases and review of the literature"
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                            0 => "J&#46;C&#46; Milisenda"
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Letter to the Editor
Edema and Dermatomyositis. Migratory Edema and Edematous and Vesiculobullous Dermatomyositis Overlap
Edema y dermatomiositis. Edema migratorio y solapamiento de dermatomiositis edematosa y vesiculoampollosa
Belén Lozano-Masdemonta,
Corresponding author
belenmasdemont@gmail.com

Corresponding author.
, Ana Pulido-Péreza, Verónica Parra-Blancob, José Antonio Avilés-Izquierdoa
a Servicio de Dermatología, Hospital General Universitario Gregorio Marañón, Madrid, Spain
b Servicio de Anatomía Patológica, Hospital General Universitario Gregorio Marañón, Madrid, Spain
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        "titulo" => "Edema y dermatomiositis&#46; Edema migratorio y solapamiento de dermatomiositis edematosa y vesiculoampollosa"
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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">&#40;a&#41; Erythematous and edematous plaque with superficial vasiculobullae in right upper limb&#46; &#40;b&#41; Edema and erythematous and edematous plaques on thighs&#46;</p>"
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Extrafacial edema is a rare manifestation of dermatomyositis &#40;DM&#41;&#46; We report 2 cases&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">Case no&#46; 1&#46; The patient was an 86-year-old woman who was admitted with dysphagia&#44; dyspnea&#44; weakness in her 4 extremities &#40;2&#47;5&#41; and edemas&#46; Four years earlier&#44; she had been diagnosed with cryptogenic organizing pneumonia detected by means of pulmonary function tests&#44; imaging studies and histology&#46; It was observed that&#44; aside from periorbital edema&#44; she had edema with fovea in upper and lower limbs&#46; She had plaques with vesiculobullous eruption on her forearms and erythematous and edematous eruption on her thighs &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; Biopsy of the thigh revealed epidermal atrophy&#44; subepidermal bullous disease&#44; necrotic keratinocytes&#44; superficial perivascular infiltrate&#44; mucin and dermal edema&#46; Direct immunofluorescence was negative&#44; as were tests for anti-Jo-1&#44; anti-PL7&#44; anti-PL12&#44; anti-SRP-54&#44; anti-Mi2&#44; anti-Ku and anti-PM&#47;Scl antibodies&#46; Creatine kinase &#40;CK&#41; was 1267<span class="elsevierStyleHsp" style=""></span>U&#47;L&#46; Electromyogram demonstrated the myopathic changes and muscle biopsy revealed perifascicular atrophy and CD4<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>perimysium and perivascular inflammatory infiltrate&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">A cardiac origin of the edema was ruled out&#44; as were renal&#44; hepatic and thyroid origin&#46; Albumin&#44; after multiple hospital admissions for dyspnea&#44; weakness and edemas&#44; had decreased &#40;2&#46;5&#8211;3&#46;2<span class="elsevierStyleHsp" style=""></span>g&#47;dL&#41; and reached normality after treatment with corticosteroids&#46; Having reviewed her history&#44; we finally discovered the diagnosis of her lung disease&#58; an elevated CK level &#40;1370<span class="elsevierStyleHsp" style=""></span>U&#47;L&#41;&#46; Computed tomography revealed a breast lesion that was found to be an infiltrating ductal carcinoma&#46; She was treated with prednisone at a dose of 1<span class="elsevierStyleHsp" style=""></span>mg&#47;kg body weight &#40;bw&#41;&#47;day and 5 sessions of plasmapheresis&#46; After mastectomy&#44; dysphagia persisted and we detected a diffuse disseminated signet ring cell adenocarcinoma&#46; She died 4 months later due to respiratory failure&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">Case no&#46; 2&#46; The patient was a 71-year-old man who had been treated 7 months earlier for cancer of the cavum&#46; He presented with weakness of his upper &#40;2&#47;5&#41; and lower &#40;3&#47;5&#41; limbs&#44; skin lesions and migratory swelling&#58; it began in his neck and supraclavicular region&#44; followed by ankles&#44; abdomen and upper limbs&#46; Other causes of edema were ruled out&#46; His CK level was 728<span class="elsevierStyleHsp" style=""></span>U&#47;L and the same antibody panel was negative&#46; Electromyogram and muscle biopsy were similar to those of case no&#46; 1&#46; A week with prednisone at a dose of 1<span class="elsevierStyleHsp" style=""></span>mg&#47;kg bw&#47;day&#44; resolved the edema&#59; treatment was increased with methotrexate at 20<span class="elsevierStyleHsp" style=""></span>mg&#47;week&#44; but he died 7 months later due to muscular respiratory failure&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">Edematous DM<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#8211;5</span></a> could constitute up to 6&#37; of the cases of DM&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> It is characterized by extrafacial&#44; localized or generalized edema&#44; with or without fovea&#44; with no other cause of edema&#46; It is more prevalent in women &#40;2&#58;1&#41;&#44; of ages between 23 and 93 years&#46; The diagnostic delay is more than 2 months&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> It is speculated that it is originated by ischemia of the microvasculature&#46; To date&#44; the migratory localization so characteristic of our case had not been reported&#46; Vesiculobullous DM consists of subepidermal vesiculobullae with biopsy results typical of DM&#44; with no other bullous dermatosis&#46; Its cause has been proposed to be friction&#44; dermal edema and mucin&#46; The specimen for the biopsy in the first case was taken from the patient&#39;s thigh&#44; where no clinical detachment was observed&#46; We subsequently considered that the detachment was secondary to the edema and that the two clinical forms&#44; edematous and vesiculobullous&#44; could be the same manifestation or overlap&#46; The distribution does not indicate a mechanical cause and there are similar cases of severe edema in which detachment appeared&#46;<a class="elsevierStyleCrossRefs" href="#bib0075"><span class="elsevierStyleSup">5&#8211;7</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">The cause of hypoalbuminemia of the first case was due to the proinflammatory status of the interstitial lung disease and the DM that still had not been diagnosed&#46;<a class="elsevierStyleCrossRefs" href="#bib0090"><span class="elsevierStyleSup">8&#44;9</span></a> This hypoalbuminemia could be the cause of generalized edema&#44; but not of the erythematous and edematous and vesiculobullous plaques&#46; The literature demonstrates that edematous DM could be associated with a more severe myopathy and dysphagia&#44; a finding that was not observed in our patients&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#8211;3</span></a> Likewise&#44; vesiculobullous DM would be closely associated with neoplasms and a worse prognosis&#46;<a class="elsevierStyleCrossRefs" href="#bib0080"><span class="elsevierStyleSup">6&#44;10</span></a> Extrafacial edema in DM&#44; in any of its variants should alert physicians to a greater severity and lead to an active search for a neoplasm&#46;</p></span>"
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        "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as&#58; Lozano-Masdemont B&#44; Pulido-P&#233;rez A&#44; Parra-Blanco V&#44; Avil&#233;s-Izquierdo JA&#46; Edema y dermatomiositis&#46; Edema migratorio y solapamiento de dermatomiositis edematosa y vesiculoampollosa&#46; Reumatol Clin&#46; 2018&#59;14&#58;313&#8211;314&#46;</p>"
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