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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">&#40;A&#8211;C&#41; Computed tomography image depicting diffuse ground-glass opacities in both lung fields&#46; &#40;D&#41; Bronchoalveolar lavage fluid with a markedly cloudy appearance&#46;</p>"
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Pulmonary alveolar proteinosis &#40;PAP&#41; is a rare respiratory disease and is pathogenetically classified into the following three types&#58; autoimmune PAP&#44; secondary PAP &#40;sPAP&#41;&#44; and congenital PAP&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> sPAP is not associated with anti-granulocyte macrophage colony-stimulating factor &#40;GM-CSF&#41; antibody and accounts for 5&#8211;10&#37; of PAP cases&#46; sPAP is primarily caused by hematological disorders&#59; sPAP caused by autoimmune diseases is extremely rare<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;3</span></a>&#59; therefore&#44; clinicians may not always consider the possibility of sPAP when abnormal findings on chest radiography and&#47;or computed tomography &#40;CT&#41; are seen in patients with autoimmune diseases&#46; We report here&#44; a case of sPAP in a patient with systemic lupus erythematosus &#40;SLE&#41;&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">A 70-year-old woman presented to our hospital with a 1-month history of exertional dyspnea&#46; She was a known case of SLE and had a 37-year-history of treatment with corticosteroids and immunosuppressive agents&#46; Her respiratory sounds were normal&#44; and she had no fever or cough&#59; her oxygen saturation was 94&#37; in room air&#46; Chest radiography and computed tomography revealed diffuse ground-glass opacities in the lung fields bilaterally &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>A&#8211;C&#41;&#46; Serum level of Krebs von den Lungen-6&#44; a marker of interstitial pneumonia&#44; was elevated &#40;6416&#8239;U&#47;mL&#41;&#59; &#946;-<span class="elsevierStyleSmallCaps">d</span>-glucan and cytomegalovirus antigenemia were absent&#46; Non-infectious acute interstitial pneumonia was suspected&#44; and a high-dose corticosteroid was administered&#59; however&#44; radiographic findings and symptoms did not improve&#46; Furthermore&#44; multiple nodules with cavitation appeared in the lower lobe of the left lung&#46; Bronchoscopy was performed&#59; the bronchoalveolar lavage fluid &#40;BALF&#41; was markedly cloudy &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>D&#41;&#44; and showed deposition of acidophilic granular material and foamy macrophages on microscopy&#46; Additionally&#44; <span class="elsevierStyleItalic">Nocardia</span> was detected in the nodules of the left lower lobe&#46; Serum anti-GM-CSF antibody was absent&#46; Finally&#44; she was diagnosed with sPAP associated with SLE&#44; and pulmonary nocardiosis&#46; Early treatment of nocardiosis was necessary&#59; therefore&#44; antibiotics were administered&#44; while the corticosteroid dose was tapered&#46; Unfortunately&#44; pulmonary nocardiosis was refractory to treatment&#59; furthermore&#44; complications set in due to the cytomegalovirus pneumonia and non-tuberculous mycobacteriosis&#46; Two months later&#44; the patient died of exacerbating infections&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">In this case report&#44; there were two important clinical observations&#46; First&#44; sPAP might develop in a patient with SLE&#46; To the best of our knowledge&#44; only one case of sPAP with SLE has been reported in the literature until date&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> According to previous reports&#44; autoimmune diseases account for approximately 7&#37; of the underlying causes of sPAP<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;3</span></a>&#59; however&#44; autoimmune diseases include Behcet&#8217;s disease&#44; Wegener&#8217;s granulomatosis&#44; microscopic polyangiitis&#44; Sjogren&#8217;s syndrome&#44; and dermatomyositis&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;3</span></a> There are few specific diseases&#59; therefore&#44; every autoimmune disease should be considered as a potential cause of sPAP&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">Second&#44; chest CT findings of sPAP might be confused with those of acute interstitial pneumonia and pulmonary alveolar hemorrhage&#46; In many cases of sPAP&#44; such as the present one&#44; chest CT shows ground-glass opacities in the lung fields bilaterally&#44;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> which are also seen in acute interstitial pneumonia and diffuse alveolar hemorrhage&#44; which are pulmonary disorders of SLE&#46;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#8211;8</span></a> The treatment of acute interstitial pneumonia and diffuse alveolar hemorrhage requires administration of high-dose corticosteroid and frequently an immunomodulatory agent as well&#46; The treatment of sPAP needs to be quite different &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>&#41; but as the mechanism underlying sPAP is still uncertain&#44; there are no specific treatment indications for sPAP This may lead to high-dose corticosteroid and&#47;or immunomodulatory agent being administered for pulmonary infections&#44; as in case here presented&#46; It is therefore important that in patients with SLE and diffuse pulmonary ground-glass opacities&#44; clinicians should consider sPAP in addition to acute interstitial pneumonia and diffuse alveolar hemorrhage in the differential diagnosis&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">sPAP has a poor prognosis compared to autoimmune PAP&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> Acute interstitial pneumonia and diffuse alveolar hemorrhage associated with SLE have sudden onset with severe symptoms&#44; while the progression of sPAP is relatively slow and symptoms are relatively mild&#46; Regular and close follow-up on chest radiography is necessary for early detection of sPAP in patients with SLE&#46; For early initiation of appropriate treatment&#44; awareness of the possibility of sPAP in patients with ground-glass opacities in both lung fields is important&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Author contributions</span><p id="par0030" class="elsevierStylePara elsevierViewall">Study conception and design&#58; Masahiro Yamasaki&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">Data acquisition&#58; Masahiro Yamasaki&#44; Kazuma Kawamoto&#44; Shota Nakano&#44; Masaya Taniwaki&#44; Naoko Matsumoto&#44; Shinji Nabeshima&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Data analysis and interpretation&#58; Masahiro Yamasaki&#44; Kazuma Kawamoto&#44; Shota Nakano&#44; Noboru Hattori&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Drafting of the manuscript&#58; Masahiro Yamasaki&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Critical revision of the manuscript for important intellectual content&#58; Noboru Hattori&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">All authors had access to the data and played a role in writing this manuscript&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Conflict of interest</span><p id="par0060" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span></span>"
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          "leyenda" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">SLE&#44; systemic lupus erythematosus&#59; sPAP&#44; secondary alveolar proteinosis&#59; AIP&#44; acute interstitial pneumonitis&#59; DAH&#44; diffuse alveolar hemorrhage&#59; HRCT&#44; high resolution computed tomography&#59; GGO&#44; ground-glass opacities&#59; BAL&#44; bronchoalveolar lavage&#46;</p>"
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                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Characteristics&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttop\n
                  \t\t\t\t">Diffuse GGO&#59; patchy geographic pattern&#59; crazy paving pattern&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Diffuse GGO and areas of consolidation&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Diffuse or patchy GGO and&#47;or consolidation&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">BAL findings&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Cloudy appearance&#59; acidophilic granular material deposition and foamy macrophages&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Incleased cellularity with activated polymorphonuclear leukocytes&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Bloody appearance&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Treatment&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Removing offending exposure or treating the underlying disorder&#59; whole lung lavage&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">High-dose corticosteroid and&#47;or immunomodulatory agent&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">High-dose corticosteroid and&#47;or immunomodulatory agent&#44; occasionally plasmapheresis&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Prognosis&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-entry\n
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                  \t\t\t\t">Poorer than autoimmune PAP&#59; median survival time &#60;20 months&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t">Short-time mortality of 50&#37;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Short-time mortality of 50&#37;&nbsp;\t\t\t\t\t\t\n
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Letter to the Editor
Secondary pulmonary alveolar proteinosis in a patient with systemic lupus erythematosus
M. Yamasakia,
Corresponding author
myamasanjp@yahoo.co.jp

Corresponding author at: Department of Respiratory Medicine, Hiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital, 1-9-6 Senda-machi, Naka-ku, Hiroshima 730-8619, Japan.
, K. Kawamotoa, S. Nakanob, M. Taniwakia, N. Matsumotoa, N. Hattoric
a Department of Respiratory Medicine, Hiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital, Naka-ku, Hiroshima, Japan
b Department of Rheumatology, Hiroshima Red Cross Hospital & Atomic-bomb Survivors Hospital, Naka-ku, Hiroshima, Japan
c Department of Molecular and Internal Medicine, Institute of Biomedical & Health Sciences, Hiroshima University, Minami-ku, Hiroshima, Japan
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        "autoresLista" => "M&#46; Yamasaki, K&#46; Kawamoto, S&#46; Nakano, M&#46; Taniwaki, N&#46; Matsumoto, N&#46; Hattori"
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            "nombre" => "M&#46;"
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            "entidad" => "Department of Respiratory Medicine&#44; Hiroshima Red Cross Hospital &#38; Atomic-bomb Survivors Hospital&#44; Naka-ku&#44; Hiroshima&#44; Japan"
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            "entidad" => "Department of Rheumatology&#44; Hiroshima Red Cross Hospital &#38; Atomic-bomb Survivors Hospital&#44; Naka-ku&#44; Hiroshima&#44; Japan"
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            "entidad" => "Department of Molecular and Internal Medicine&#44; Institute of Biomedical &#38; Health Sciences&#44; Hiroshima University&#44; Minami-ku&#44; Hiroshima&#44; Japan"
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            "correspondencia" => "Corresponding author at&#58; Department of Respiratory Medicine&#44; Hiroshima Red Cross Hospital &#38; Atomic-bomb Survivors Hospital&#44; 1-9-6 Senda-machi&#44; Naka-ku&#44; Hiroshima 730-8619&#44; Japan&#46;"
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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">&#40;A&#8211;C&#41; Computed tomography image depicting diffuse ground-glass opacities in both lung fields&#46; &#40;D&#41; Bronchoalveolar lavage fluid with a markedly cloudy appearance&#46;</p>"
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Pulmonary alveolar proteinosis &#40;PAP&#41; is a rare respiratory disease and is pathogenetically classified into the following three types&#58; autoimmune PAP&#44; secondary PAP &#40;sPAP&#41;&#44; and congenital PAP&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> sPAP is not associated with anti-granulocyte macrophage colony-stimulating factor &#40;GM-CSF&#41; antibody and accounts for 5&#8211;10&#37; of PAP cases&#46; sPAP is primarily caused by hematological disorders&#59; sPAP caused by autoimmune diseases is extremely rare<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;3</span></a>&#59; therefore&#44; clinicians may not always consider the possibility of sPAP when abnormal findings on chest radiography and&#47;or computed tomography &#40;CT&#41; are seen in patients with autoimmune diseases&#46; We report here&#44; a case of sPAP in a patient with systemic lupus erythematosus &#40;SLE&#41;&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">A 70-year-old woman presented to our hospital with a 1-month history of exertional dyspnea&#46; She was a known case of SLE and had a 37-year-history of treatment with corticosteroids and immunosuppressive agents&#46; Her respiratory sounds were normal&#44; and she had no fever or cough&#59; her oxygen saturation was 94&#37; in room air&#46; Chest radiography and computed tomography revealed diffuse ground-glass opacities in the lung fields bilaterally &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>A&#8211;C&#41;&#46; Serum level of Krebs von den Lungen-6&#44; a marker of interstitial pneumonia&#44; was elevated &#40;6416&#8239;U&#47;mL&#41;&#59; &#946;-<span class="elsevierStyleSmallCaps">d</span>-glucan and cytomegalovirus antigenemia were absent&#46; Non-infectious acute interstitial pneumonia was suspected&#44; and a high-dose corticosteroid was administered&#59; however&#44; radiographic findings and symptoms did not improve&#46; Furthermore&#44; multiple nodules with cavitation appeared in the lower lobe of the left lung&#46; Bronchoscopy was performed&#59; the bronchoalveolar lavage fluid &#40;BALF&#41; was markedly cloudy &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>D&#41;&#44; and showed deposition of acidophilic granular material and foamy macrophages on microscopy&#46; Additionally&#44; <span class="elsevierStyleItalic">Nocardia</span> was detected in the nodules of the left lower lobe&#46; Serum anti-GM-CSF antibody was absent&#46; Finally&#44; she was diagnosed with sPAP associated with SLE&#44; and pulmonary nocardiosis&#46; Early treatment of nocardiosis was necessary&#59; therefore&#44; antibiotics were administered&#44; while the corticosteroid dose was tapered&#46; Unfortunately&#44; pulmonary nocardiosis was refractory to treatment&#59; furthermore&#44; complications set in due to the cytomegalovirus pneumonia and non-tuberculous mycobacteriosis&#46; Two months later&#44; the patient died of exacerbating infections&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">In this case report&#44; there were two important clinical observations&#46; First&#44; sPAP might develop in a patient with SLE&#46; To the best of our knowledge&#44; only one case of sPAP with SLE has been reported in the literature until date&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> According to previous reports&#44; autoimmune diseases account for approximately 7&#37; of the underlying causes of sPAP<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;3</span></a>&#59; however&#44; autoimmune diseases include Behcet&#8217;s disease&#44; Wegener&#8217;s granulomatosis&#44; microscopic polyangiitis&#44; Sjogren&#8217;s syndrome&#44; and dermatomyositis&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;3</span></a> There are few specific diseases&#59; therefore&#44; every autoimmune disease should be considered as a potential cause of sPAP&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">Second&#44; chest CT findings of sPAP might be confused with those of acute interstitial pneumonia and pulmonary alveolar hemorrhage&#46; In many cases of sPAP&#44; such as the present one&#44; chest CT shows ground-glass opacities in the lung fields bilaterally&#44;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> which are also seen in acute interstitial pneumonia and diffuse alveolar hemorrhage&#44; which are pulmonary disorders of SLE&#46;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#8211;8</span></a> The treatment of acute interstitial pneumonia and diffuse alveolar hemorrhage requires administration of high-dose corticosteroid and frequently an immunomodulatory agent as well&#46; The treatment of sPAP needs to be quite different &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>&#41; but as the mechanism underlying sPAP is still uncertain&#44; there are no specific treatment indications for sPAP This may lead to high-dose corticosteroid and&#47;or immunomodulatory agent being administered for pulmonary infections&#44; as in case here presented&#46; It is therefore important that in patients with SLE and diffuse pulmonary ground-glass opacities&#44; clinicians should consider sPAP in addition to acute interstitial pneumonia and diffuse alveolar hemorrhage in the differential diagnosis&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">sPAP has a poor prognosis compared to autoimmune PAP&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> Acute interstitial pneumonia and diffuse alveolar hemorrhage associated with SLE have sudden onset with severe symptoms&#44; while the progression of sPAP is relatively slow and symptoms are relatively mild&#46; Regular and close follow-up on chest radiography is necessary for early detection of sPAP in patients with SLE&#46; For early initiation of appropriate treatment&#44; awareness of the possibility of sPAP in patients with ground-glass opacities in both lung fields is important&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Author contributions</span><p id="par0030" class="elsevierStylePara elsevierViewall">Study conception and design&#58; Masahiro Yamasaki&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">Data acquisition&#58; Masahiro Yamasaki&#44; Kazuma Kawamoto&#44; Shota Nakano&#44; Masaya Taniwaki&#44; Naoko Matsumoto&#44; Shinji Nabeshima&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Data analysis and interpretation&#58; Masahiro Yamasaki&#44; Kazuma Kawamoto&#44; Shota Nakano&#44; Noboru Hattori&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Drafting of the manuscript&#58; Masahiro Yamasaki&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Critical revision of the manuscript for important intellectual content&#58; Noboru Hattori&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">All authors had access to the data and played a role in writing this manuscript&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Conflict of interest</span><p id="par0060" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span></span>"
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          "titulo" => "Conflict of interest"
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        2 => array:2 [
          "identificador" => "xack503232"
          "titulo" => "Acknowledgments"
        ]
        3 => array:1 [
          "titulo" => "References"
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      ]
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    "fechaRecibido" => "2020-06-16"
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          "leyenda" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">SLE&#44; systemic lupus erythematosus&#59; sPAP&#44; secondary alveolar proteinosis&#59; AIP&#44; acute interstitial pneumonitis&#59; DAH&#44; diffuse alveolar hemorrhage&#59; HRCT&#44; high resolution computed tomography&#59; GGO&#44; ground-glass opacities&#59; BAL&#44; bronchoalveolar lavage&#46;</p>"
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                0 => """
                  <table border="0" frame="\n
                  \t\t\t\t\tvoid\n
                  \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">Characteristics&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">sPAP&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">AIP in SLE&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th><th class="td" title="\n
                  \t\t\t\t\ttable-head\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t" scope="col" style="border-bottom: 2px solid black">DAH in SLE&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Progression rate&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t">Relatively slowly progression&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Sudden onset&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Sudden onset&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Symptoms&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t">Dyspnea&#59; cough&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t">Dyspnea&#59; cough&#59; fever&#59; sometimes hemoptysis&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t">Dyspnea&#59; cough&#59; hemoptysis&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n
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                  \t\t\t\t">HRCT findings&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t">Diffuse GGO&#59; patchy geographic pattern&#59; crazy paving pattern&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t">Diffuse GGO and areas of consolidation&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t">Diffuse or patchy GGO and&#47;or consolidation&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
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                  \t\t\t\t">BAL findings&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
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                  \t\t\t\t">Cloudy appearance&#59; acidophilic granular material deposition and foamy macrophages&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t">Incleased cellularity with activated polymorphonuclear leukocytes&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t">Bloody appearance&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
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                  \t\t\t\t">Treatment&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t">Removing offending exposure or treating the underlying disorder&#59; whole lung lavage&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t">High-dose corticosteroid and&#47;or immunomodulatory agent&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t">High-dose corticosteroid and&#47;or immunomodulatory agent&#44; occasionally plasmapheresis&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n
                  \t\t\t\t\ttable-entry\n
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                  \t\t\t\t">Prognosis&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t">Poorer than autoimmune PAP&#59; median survival time &#60;20 months&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t">Short-time mortality of 50&#37;&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t\ttable-entry\n
                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Short-time mortality of 50&#37;&nbsp;\t\t\t\t\t\t\n
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Article information
ISSN: 25310437
Original language: English
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