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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Adult Still&#39;s disease &#40;ASD&#41; is a systemic inflammatory disease of unknown etiology&#46; Renal involvement in ASD is a rare and rarely reported manifestation in the literature&#46; This report presents an atypical case of ASD with acute renal failure&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">A 39-year-old male with arterial hypertension treated with Ramipril 10<span class="elsevierStyleHsp" style=""></span>mg was admitted to the Emergency Department &#40;ED&#41; with a fever of up to 39<span class="elsevierStyleHsp" style=""></span>&#176;C&#44; right laterocervical edema&#44; dysphagia&#44; and odynophagia the last four days&#46; He started treatment with Amoxicillin-Clavulanate before consultation in the ED&#46; The patient did not report country outings or recent trips&#46; He highlighted an infestation of rodents in his building&#46; The patient denied consuming alcohol&#44; tobacco and other drugs&#44; or mushrooms&#44; herbal products&#44; or other substances that could have caused liver damage&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">Physical examination revealed mild jaundice&#44; a temperature of 38<span class="elsevierStyleHsp" style=""></span>&#176;C&#44; non-adhered right laterocervical lymphadenopathy of 1&#8211;2<span class="elsevierStyleHsp" style=""></span>cm&#44; enlarged tonsils with discrete whitish plaques on their surface&#44; and a macular and itchy rash on the upper trunk and forearms&#46; Laboratory tests at ED showed&#58; procalcitonin 1&#46;10<span class="elsevierStyleHsp" style=""></span>ng&#47;ml&#44; urea 69<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#44; creatinine 2&#46;79<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#44; sodium 135<span class="elsevierStyleHsp" style=""></span>mmol&#47;L&#44; potassium 4&#46;5<span class="elsevierStyleHsp" style=""></span>mmol&#47;L&#44; chlorine 98<span class="elsevierStyleHsp" style=""></span>mmol&#47;L&#44; GPT 114<span class="elsevierStyleHsp" style=""></span>U&#47;L&#44; CK 233<span class="elsevierStyleHsp" style=""></span>U&#47;L&#44; Amylase 35<span class="elsevierStyleHsp" style=""></span>U&#47;L&#44; C reactive protein &#40;CRP&#41; 286&#46;9<span class="elsevierStyleHsp" style=""></span>mg&#47;L&#44; leukocytes 15&#44;430&#47;mcL &#40;neutrophils 13&#44;740&#47;mcL&#41;&#44; prothrombin activity 63&#37;&#46; Abdominal ultrasound and chest X-ray were normal&#46; The patient presented the day after admission&#58; total bilirubin 9<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#44; direct bilirubin 8&#46;4<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#44; GGT 143<span class="elsevierStyleHsp" style=""></span>IU&#47;L&#44; and Alkaline Phosphatase 267<span class="elsevierStyleHsp" style=""></span>IU&#47;L&#46; Leukocytosis reached 33&#44;000&#47;mcL with 92&#37; polymorphonuclear cells&#46; The rise in ferritin levels was remarkable with 4&#46;104 mcg&#47;mL&#46; During admission&#44; the patient presented a rapid onset acute renal failure with anuria&#46; The renal function worsened with a creatinine of 10&#46;36<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#46; This clinical course led to hemodialysis therapy from the second day of admission&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">Immunoglobulin A level was 479<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#46; C3&#44; C4&#44; Antistreptolysin O&#44; antinuclear antibodies&#44; nuclear extractible antigen antibodies&#44; anti-DNA antibodies&#44; neutrophil anti-cytoplasmic antibodies were normal or negative&#46; Interleukin-6 was 148<span class="elsevierStyleHsp" style=""></span>pg&#47;mL&#46; Plasma protein electrophoresis was compatible with an acute inflammatory process&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">Nasopharyngeal swab for Polymerase Chain Reaction for SARS-CoV2 and pharyngeal swab for <span class="elsevierStyleItalic">Streptococcus pyogenes</span> were both negative&#46; Urine and blood cultures were negative&#46; Serologic studies ruled out acute infection by Cytomegalovirus&#44; Epstein-Bar virus&#44; Measles&#44; Q fever&#44; Leptospira&#44; hepatitis A and B viruses&#44; Human Immunodeficiency Virus&#44; and parvovirus B19&#46; A computed tomography &#40;CT&#41; scan showed a slightly enlarged 15-cm spleen&#46; A Positron Emission Tomography-CT scan was normal&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">Finally&#44; a renal biopsy showed an acute tubulointerstitial inflammatory infiltrate with some ruptured tubule and isolated eosinophils associated with a dense lymphoplasmacytic infiltrate and a mesangial deposit anti-IgA &#40;&#43;&#43;&#41; and minimal anti-C3&#44; all of which was compatible with IgA mesangial nephropathy and acute tubulointerstitial nephritis &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; However&#44; there was an absence of intratubular erythrocyte casts or crescents in the biopsy&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0035" class="elsevierStylePara elsevierViewall">Our patient meets the criteria of both Yamaguchi and Fautrel for presumptive diagnosis of ASD &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>&#41;&#46; Corticosteroid treatment was started initially with Prednisone 60<span class="elsevierStyleHsp" style=""></span>mg&#47;day&#44; and subsequently escalating to 500<span class="elsevierStyleHsp" style=""></span>mg of 6-Methylprednisolone daily associated with Anakinra at 100<span class="elsevierStyleHsp" style=""></span>mg&#47;week&#44; causing a rapid and progressive improvement in the general condition and rash&#44; a decrease in the acute phase reactants and leukocytosis&#44; and an improvement in his renal function&#46; The patient recovered normal diuresis and was discharged with a creatinine of 2&#46;04<span class="elsevierStyleHsp" style=""></span>mg&#47;dL with proteinuria of 25<span class="elsevierStyleHsp" style=""></span>mg&#47;dL in basic urine examination&#46; After discharge from the hospital&#44; the patient fully recovers renal function with a creatinine of 1<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0040" class="elsevierStylePara elsevierViewall">Since there are currently no specific diagnostic tests&#44; ASD diagnosis is usually based on the clinical recognition of the entity&#44; always ruling out other possible etiologies such as infections or neoplasms&#46; Among the criteria used for its diagnosis are the Yamaguchi criteria<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> and the Fautrel criteria<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>&#41;&#46; Elevated procalcitonin&#44; C-reactive protein&#44; and leukocytosis with neutrophilia could lead the clinician to suspect other etiologies&#44; especially infectious&#44; and diagnostic delay&#46; Serum ferritin or cytokines&#44; such as IL-6&#44; can help diagnosis&#46; The combination that has shown the greatest diagnostic accuracy was serum ferritin<span class="elsevierStyleHsp" style=""></span>&#62;<span class="elsevierStyleHsp" style=""></span>1000<span class="elsevierStyleHsp" style=""></span>mcg&#47;L or values five times above the upper limit of normal&#44; together with a fraction of glycated ferritin<span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>20&#37;&#46; Its sensitivity and specificity are 70&#46;5&#37; and 92&#46;9&#37;&#44; respectively&#46;<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">3&#44;4</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Still&#39;s disease can present more atypical manifestations&#44; such as acute renal failure of rapid onset&#46; Entities associated in previous literature were Amyloidosis&#44;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">5</span></a> Thrombotic Microangiopathy&#44;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">6</span></a> IgA Glomerulonephritis&#44;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a> and more recently&#44; cases of collapsing glomerulopathy&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">8</span></a> However&#44; despite being described in reviews on Still&#39;s disease&#44;<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">9</span></a> only one case of interstitial nephritis has been found reported in the consulted bibliography&#46;<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">10</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Therefore&#44; it is essential to include ASD in the differential diagnoses of acute renal failure accompanied by analytical markers such as elevated IL-6 or ferritin of up to five times its standard value&#46; Early treatment of this disease can lead to the complete recovery of the patient&#39;s previous renal function&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Informed consent</span><p id="par0055" class="elsevierStylePara elsevierViewall">The patient reported here has provided written informed consent for publication of this case report&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Funding</span><p id="par0060" class="elsevierStylePara elsevierViewall">This work has no funding&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Conflict of interest</span><p id="par0065" class="elsevierStylePara elsevierViewall">None&#46;</p></span></span>"
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                  \t\t\t\t"><span class="elsevierStyleItalic">Minor criteria</span>&#58;- Odynophagia- Lymphadenopathy- Splenomegaly- Alteration of liver function tests- Rheumatoid factor and ANA negatives&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Criteria of Fautrel et al&#46; &#91;5&#93;<a class="elsevierStyleCrossRef" href="#tblfn0010"><span class="elsevierStyleSup">b</span></a></th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="\n
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                  \t\t\t\t"><span class="elsevierStyleItalic">Minor criteria</span>&#58;- Maculopapular rash- Leukocytosis<span class="elsevierStyleHsp" style=""></span>&#62;<span class="elsevierStyleHsp" style=""></span>10&#44;000&#47;mm<span class="elsevierStyleSup">3</span>&nbsp;\t\t\t\t\t\t\n
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Letter to the Editor
Acute renal failure as a debut manifestation in Still's disease
Insuficiencia renal aguda como manifestación inicial en la enfermedad de Still
Samuel Blas Gómeza, Fernando Mateos Rodríguezb, María Luisa Illescas Fernández-Bermejoa, Syonghyun Nam Chac, Julián Solís García del Pozob,
Corresponding author
julianeloysolis@gmail.com

Corresponding author.
a Nephrology, Albacete University Hospital Complex, Albacete, Spain
b Infectious Diseases, Albacete University Hospital Complex, Albacete, Spain
c Pathology, Albacete University Hospital Complex, Albacete, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Adult Still&#39;s disease &#40;ASD&#41; is a systemic inflammatory disease of unknown etiology&#46; Renal involvement in ASD is a rare and rarely reported manifestation in the literature&#46; This report presents an atypical case of ASD with acute renal failure&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">A 39-year-old male with arterial hypertension treated with Ramipril 10<span class="elsevierStyleHsp" style=""></span>mg was admitted to the Emergency Department &#40;ED&#41; with a fever of up to 39<span class="elsevierStyleHsp" style=""></span>&#176;C&#44; right laterocervical edema&#44; dysphagia&#44; and odynophagia the last four days&#46; He started treatment with Amoxicillin-Clavulanate before consultation in the ED&#46; The patient did not report country outings or recent trips&#46; He highlighted an infestation of rodents in his building&#46; The patient denied consuming alcohol&#44; tobacco and other drugs&#44; or mushrooms&#44; herbal products&#44; or other substances that could have caused liver damage&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">Physical examination revealed mild jaundice&#44; a temperature of 38<span class="elsevierStyleHsp" style=""></span>&#176;C&#44; non-adhered right laterocervical lymphadenopathy of 1&#8211;2<span class="elsevierStyleHsp" style=""></span>cm&#44; enlarged tonsils with discrete whitish plaques on their surface&#44; and a macular and itchy rash on the upper trunk and forearms&#46; Laboratory tests at ED showed&#58; procalcitonin 1&#46;10<span class="elsevierStyleHsp" style=""></span>ng&#47;ml&#44; urea 69<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#44; creatinine 2&#46;79<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#44; sodium 135<span class="elsevierStyleHsp" style=""></span>mmol&#47;L&#44; potassium 4&#46;5<span class="elsevierStyleHsp" style=""></span>mmol&#47;L&#44; chlorine 98<span class="elsevierStyleHsp" style=""></span>mmol&#47;L&#44; GPT 114<span class="elsevierStyleHsp" style=""></span>U&#47;L&#44; CK 233<span class="elsevierStyleHsp" style=""></span>U&#47;L&#44; Amylase 35<span class="elsevierStyleHsp" style=""></span>U&#47;L&#44; C reactive protein &#40;CRP&#41; 286&#46;9<span class="elsevierStyleHsp" style=""></span>mg&#47;L&#44; leukocytes 15&#44;430&#47;mcL &#40;neutrophils 13&#44;740&#47;mcL&#41;&#44; prothrombin activity 63&#37;&#46; Abdominal ultrasound and chest X-ray were normal&#46; The patient presented the day after admission&#58; total bilirubin 9<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#44; direct bilirubin 8&#46;4<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#44; GGT 143<span class="elsevierStyleHsp" style=""></span>IU&#47;L&#44; and Alkaline Phosphatase 267<span class="elsevierStyleHsp" style=""></span>IU&#47;L&#46; Leukocytosis reached 33&#44;000&#47;mcL with 92&#37; polymorphonuclear cells&#46; The rise in ferritin levels was remarkable with 4&#46;104 mcg&#47;mL&#46; During admission&#44; the patient presented a rapid onset acute renal failure with anuria&#46; The renal function worsened with a creatinine of 10&#46;36<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#46; This clinical course led to hemodialysis therapy from the second day of admission&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">Immunoglobulin A level was 479<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#46; C3&#44; C4&#44; Antistreptolysin O&#44; antinuclear antibodies&#44; nuclear extractible antigen antibodies&#44; anti-DNA antibodies&#44; neutrophil anti-cytoplasmic antibodies were normal or negative&#46; Interleukin-6 was 148<span class="elsevierStyleHsp" style=""></span>pg&#47;mL&#46; Plasma protein electrophoresis was compatible with an acute inflammatory process&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">Nasopharyngeal swab for Polymerase Chain Reaction for SARS-CoV2 and pharyngeal swab for <span class="elsevierStyleItalic">Streptococcus pyogenes</span> were both negative&#46; Urine and blood cultures were negative&#46; Serologic studies ruled out acute infection by Cytomegalovirus&#44; Epstein-Bar virus&#44; Measles&#44; Q fever&#44; Leptospira&#44; hepatitis A and B viruses&#44; Human Immunodeficiency Virus&#44; and parvovirus B19&#46; A computed tomography &#40;CT&#41; scan showed a slightly enlarged 15-cm spleen&#46; A Positron Emission Tomography-CT scan was normal&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">Finally&#44; a renal biopsy showed an acute tubulointerstitial inflammatory infiltrate with some ruptured tubule and isolated eosinophils associated with a dense lymphoplasmacytic infiltrate and a mesangial deposit anti-IgA &#40;&#43;&#43;&#41; and minimal anti-C3&#44; all of which was compatible with IgA mesangial nephropathy and acute tubulointerstitial nephritis &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; However&#44; there was an absence of intratubular erythrocyte casts or crescents in the biopsy&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0035" class="elsevierStylePara elsevierViewall">Our patient meets the criteria of both Yamaguchi and Fautrel for presumptive diagnosis of ASD &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>&#41;&#46; Corticosteroid treatment was started initially with Prednisone 60<span class="elsevierStyleHsp" style=""></span>mg&#47;day&#44; and subsequently escalating to 500<span class="elsevierStyleHsp" style=""></span>mg of 6-Methylprednisolone daily associated with Anakinra at 100<span class="elsevierStyleHsp" style=""></span>mg&#47;week&#44; causing a rapid and progressive improvement in the general condition and rash&#44; a decrease in the acute phase reactants and leukocytosis&#44; and an improvement in his renal function&#46; The patient recovered normal diuresis and was discharged with a creatinine of 2&#46;04<span class="elsevierStyleHsp" style=""></span>mg&#47;dL with proteinuria of 25<span class="elsevierStyleHsp" style=""></span>mg&#47;dL in basic urine examination&#46; After discharge from the hospital&#44; the patient fully recovers renal function with a creatinine of 1<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0040" class="elsevierStylePara elsevierViewall">Since there are currently no specific diagnostic tests&#44; ASD diagnosis is usually based on the clinical recognition of the entity&#44; always ruling out other possible etiologies such as infections or neoplasms&#46; Among the criteria used for its diagnosis are the Yamaguchi criteria<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> and the Fautrel criteria<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>&#41;&#46; Elevated procalcitonin&#44; C-reactive protein&#44; and leukocytosis with neutrophilia could lead the clinician to suspect other etiologies&#44; especially infectious&#44; and diagnostic delay&#46; Serum ferritin or cytokines&#44; such as IL-6&#44; can help diagnosis&#46; The combination that has shown the greatest diagnostic accuracy was serum ferritin<span class="elsevierStyleHsp" style=""></span>&#62;<span class="elsevierStyleHsp" style=""></span>1000<span class="elsevierStyleHsp" style=""></span>mcg&#47;L or values five times above the upper limit of normal&#44; together with a fraction of glycated ferritin<span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>20&#37;&#46; Its sensitivity and specificity are 70&#46;5&#37; and 92&#46;9&#37;&#44; respectively&#46;<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">3&#44;4</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Still&#39;s disease can present more atypical manifestations&#44; such as acute renal failure of rapid onset&#46; Entities associated in previous literature were Amyloidosis&#44;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">5</span></a> Thrombotic Microangiopathy&#44;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">6</span></a> IgA Glomerulonephritis&#44;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a> and more recently&#44; cases of collapsing glomerulopathy&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">8</span></a> However&#44; despite being described in reviews on Still&#39;s disease&#44;<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">9</span></a> only one case of interstitial nephritis has been found reported in the consulted bibliography&#46;<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">10</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Therefore&#44; it is essential to include ASD in the differential diagnoses of acute renal failure accompanied by analytical markers such as elevated IL-6 or ferritin of up to five times its standard value&#46; Early treatment of this disease can lead to the complete recovery of the patient&#39;s previous renal function&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Informed consent</span><p id="par0055" class="elsevierStylePara elsevierViewall">The patient reported here has provided written informed consent for publication of this case report&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Funding</span><p id="par0060" class="elsevierStylePara elsevierViewall">This work has no funding&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Conflict of interest</span><p id="par0065" class="elsevierStylePara elsevierViewall">None&#46;</p></span></span>"
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Article information
ISSN: 20132514
Original language: English
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