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male&#44; 33 years old&#44; admitted in hospital due to adverse reaction to treatment for multibacillary leprosy &#40;dapsone&#41; after less than 1 month of use and presence of difficult-to-heal ulcers in lower limbs for 2 years&#44; even with previous antibiotic therapy&#46; Diagnosis of multibacillary leprosy through February&#47;2022 biopsy&#44; consistent with erythema nodosum leprosum with scar areas and negative AFB test&#46; Previous pathology reported treatment for tertiary syphilis 3 years ago&#44; without other comorbidities&#46; On admission&#44; evaluated by a dermatologist&#44; who questioned the initial diagnosis&#44; however&#44; he advised the use of empirical intravenous antibiotic therapy&#44; suspension of treatment for leprosy&#44; request markers for SLE and activity of rheumatologic disease&#44; in addition to the evaluation of rheumatology for a possible diagnosis of lupus&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">In the rheumatological evaluation&#44; he had the criteria of non-scarring alopecia&#44; discoid lupus&#44; photosensitivity&#44; hemolytic anemia&#44; leukopenia and pericardial effusion on echocardiography&#46; As for the results of the rheumatological markers&#44; they demonstrated&#44; through indirect immunofluorescence&#44; an ANA fine speckled nuclear pattern &#40;AC-4&#41; greater than 1&#47;640 and ANTI-dsDNA 1&#47;10&#59; through the enzyme-immunoassay method&#44; an Anti-SSA of 49&#46;7<span class="elsevierStyleHsp" style=""></span>U &#40;positive&#41;&#44; anticardiolipin IGG of 34&#46;3 GPL &#40;positive&#41; and anticardiolipin IGM of 145&#46;5 MPL &#40;positive&#41;&#59; the lupus anticoagulant&#44; through the coagulometric method&#44; was also positive with 1&#46;22&#59; and through turbidimetry&#44; a reduction in serum complement proteins C3 and C4 was also evidenced&#44; with 35<span class="elsevierStyleHsp" style=""></span>mg&#47;dL and &#60;8<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#44; 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vitamin and mineral supplementation and follow-up with rheumatology&#44; infectiology and ophthalmology&#46; After 1 month&#44; the patient returned for evaluation with a rheumatologist and presented with improvement of the vasculitis lesions&#44; although still without complete healing and maintained normal renal function values&#46; However&#44; he maintained the same values of proteinuria in the follow-up after one month&#58; proteinuria<span class="elsevierStyleHsp" style=""></span>&#62;<span class="elsevierStyleHsp" style=""></span>0&#46;5<span class="elsevierStyleHsp" style=""></span>g&#47;24<span class="elsevierStyleHsp" style=""></span>h&#46; After 1 month&#44; the patient was referred to another reference unit for his own interest&#44; as this other unit was closer to where he lived&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Discussion</span><p id="par0020" class="elsevierStylePara elsevierViewall">Some forms of leprosy&#44; such as lepromatous and borderline leprosy&#44; may present with serological alterations and clinical alterations that are also consistent with other rheumatic pathologies&#44; mainly rheumatoid arthritis and SLE&#46;<a class="elsevierStyleCrossRefs" href="#bib0120"><span class="elsevierStyleSup">8&#8211;10</span></a> Among the most common serological abnormalities we have rheumatoid factor &#40;which may even be present in population without disease&#41;&#44; ANA&#44; anti-DNA and anticardiolipin antibody&#46;<a class="elsevierStyleCrossRefs" href="#bib0110"><span class="elsevierStyleSup">6&#44;7</span></a> Clinical changes involve erythema nodosum and vasculitis&#44; skin changes that are very common in leprosy and which should be considered by health professionals&#44; especially in regions where this disease is endemic&#46; Other similar clinical manifestations between the two conditions can also occur such as livedo reticularis&#44; malar rash&#44; skin thickening&#44; Raynaud&#39;s phenomenon&#44; oral ulcers and even glomerulonephritis&#46;<a class="elsevierStyleCrossRefs" href="#bib0120"><span class="elsevierStyleSup">8&#8211;11</span></a> There are several goals when developing a treatment plan for the patient with SLE&#58; reducing disease activity &#40;induction of remission&#41;&#44; preventing exacerbations&#44; treating them when they occur&#44; and decreasing damage to organs and systems&#44; as well as complications of the disease&#46; disease and treatment&#46;<a class="elsevierStyleCrossRefs" href="#bib0095"><span class="elsevierStyleSup">3&#44;11</span></a> Among the drugs available today&#44; corticosteroids and immunosuppressants are generally used&#44; which protect the organs from the inflammatory aggression caused by disorders in the immune system and induce remission of the disease&#44; but do not prevent or reverse the initial failure of the system&#46;<a class="elsevierStyleCrossRefs" href="#bib0140"><span class="elsevierStyleSup">12&#8211;14</span></a> Just as the diagnostic criteria allowed greater sensitivity to detect those affected by SLE&#44; some criteria were also developed to identify disease activity&#44; such as the SLEDAI &#40;Systemic Lupus Erythematosus Disease Activity Index&#41;&#44; widely used and reproducible in Brazil&#46;<a class="elsevierStyleCrossRefs" href="#bib0155"><span class="elsevierStyleSup">15&#44;16</span></a></p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Conclusion</span><p id="par0025" class="elsevierStylePara elsevierViewall">Although less frequent in men&#44; the diagnostic hypothesis of SLE should always be considered in patients with a chronic history of conditions without clinical improvement even after undergoing various therapies&#46; The case presented reveals that&#44; even showing typical changes for the disease with photosensitivity&#44; non-scarring alopecia and discoid lupus for more than 2 years&#44; the diagnosis of the disease was initially wrong&#44; requiring even a biopsy&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Information</span><p id="par0030" class="elsevierStylePara elsevierViewall">Consent was obtained for experimentation with human subjects&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Conflict of interest</span><p id="par0035" class="elsevierStylePara elsevierViewall">The authors declare they have no conflict of interest&#46;</p></span></span>"
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        "resumen" => "<span id="abst0010" class="elsevierStyleSection elsevierViewall"><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Describimos el caso de un var&#243;n con lupus eritematoso sist&#233;mico y nefritis l&#250;pica&#46; Se trata de un paciente con diagn&#243;stico inicial de lepra multibacilar&#44; una enfermedad infecciosa con s&#237;ntomas cl&#237;nicos desde hac&#237;a 2 a&#241;os&#46; Sin embargo&#44; tras su hospitalizaci&#243;n e investigaci&#243;n&#44; se revoc&#243; dicho diagn&#243;stico&#44; sustituy&#233;ndose por lupus eritematoso sist&#233;mico&#46; El objetivo de este estudio es resaltar la importancia de conocer los cambios cl&#237;nicos m&#225;s importantes y significativos del lupus eritematoso sist&#233;mico&#44; permitiendo as&#237; su diagn&#243;stico preciso y previniendo la progresi&#243;n de la enfermedad con compromiso de &#243;rganos diana&#44; as&#237; como un mejor manejo cl&#237;nico&#46;</p></span>"
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          "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">&#40;A&#41; Histological section of the lateral foot &#40;scar area&#41; revealing small vessel vasculitis associated with areas of scarring fibrosis and dystrophic calcification&#46; There are no alcohol-acid-resistant bacilli&#46; Compatible with erythema nodosum leprosum with scar areas&#46; &#40;B&#41; Histological section of the scalp region revealing mild hyperkeratosis&#44; epidermal atrophy&#44; ballooning of basal keratinocytes and discrete perivascular lymphohistiocytic infiltrate&#46; Compatible with lupus erythematosus&#46;</p>"
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                            4 => "A&#46;L&#46; Carvalho J&#250;nior"
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                          "etal" => false
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                            0 => "J&#46;C&#46;D&#46; Repka"
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                      "titulo" => "Manifesta&#231;&#245;es reum&#225;ticas da hansen&#237;ase"
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                          "etal" => false
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                            0 => "H&#46;L&#46;A&#46; Pereira"
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                      "titulo" => "Hydroxychloroquine short ages among patients with systemic l&#250;pus erythematosus during the COVID-19 pandemic&#58; experience of the Systemic Lupus International Collaborating Clinics"
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                            2 => "A&#46; Askane"
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Case report
Systemic lupus erythematosus mimicking leprosy: A challenge to early diagnosis
Lupus eritematoso sistémico que remeda lepra: reto para el diagnóstico temprano
Patrick Nunes Britoa,
Corresponding author
patrick091979@hotmail.com

Corresponding author.
, Danielle Pereira Barrosa, Brenda Nunes Britob, Rayza Brito Silvac, Marcus Emilio Costa Maciela, Monica Camilo Nunes de Sousaa
a HDT-UFT – Hospital de Doenças Tropicais, Brazil
b Centro Universitário do Maranhão Imperatriz, Brazil
c Universidade Federal do Tocantins – UFNT, Brazil
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          "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">&#40;A&#41; Histological section of the lateral foot &#40;scar area&#41; revealing small vessel vasculitis associated with areas of scarring fibrosis and dystrophic calcification&#46; There are no alcohol-acid-resistant bacilli&#46; Compatible with erythema nodosum leprosum with scar areas&#46; &#40;B&#41; Histological section of the scalp region revealing mild hyperkeratosis&#44; epidermal atrophy&#44; ballooning of basal keratinocytes and discrete perivascular lymphohistiocytic infiltrate&#46; Compatible with lupus erythematosus&#46;</p>"
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Systemic lupus erythematosus &#40;SLE&#41; is a rare&#44; chronic inflammatory disease of connective tissue&#44; of an autoimmune nature and whose pathogenesis is heterogeneous&#44; generally characterized by the deposition of immune complexes and production of autoantibodies&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">1</span></a> The clinical presentation of SLE is variable and can affect any organ&#44; singly or cumulatively&#44; at any age&#46; As its clinical status is variable and sometimes nonspecific&#44; the diagnosis can be delayed and patients are often treated for conditions other than SLE&#46;<a class="elsevierStyleCrossRefs" href="#bib0090"><span class="elsevierStyleSup">2&#44;3</span></a> In the literature there are already descriptions of several cases of SLE that mimic leprosy and vice versa&#44;<a class="elsevierStyleCrossRefs" href="#bib0100"><span class="elsevierStyleSup">4&#8211;10</span></a> although it is still difficult to establish the prevalence of these conditions given that patients can spend a lot of time treating diseases with incorrect diagnosis&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Clinical observation</span><p id="par0010" class="elsevierStylePara elsevierViewall">Patient&#44; male&#44; 33 years old&#44; admitted in hospital due to adverse reaction to treatment for multibacillary leprosy &#40;dapsone&#41; after less than 1 month of use and presence of difficult-to-heal ulcers in lower limbs for 2 years&#44; even with previous antibiotic therapy&#46; Diagnosis of multibacillary leprosy through February&#47;2022 biopsy&#44; consistent with erythema nodosum leprosum with scar areas and negative AFB test&#46; Previous pathology reported treatment for tertiary syphilis 3 years ago&#44; without other comorbidities&#46; On admission&#44; evaluated by a dermatologist&#44; who questioned the initial diagnosis&#44; however&#44; he advised the use of empirical intravenous antibiotic therapy&#44; suspension of treatment for leprosy&#44; request markers for SLE and activity of rheumatologic disease&#44; in addition to the evaluation of rheumatology for a possible diagnosis of lupus&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">In the rheumatological evaluation&#44; he had the criteria of non-scarring alopecia&#44; discoid lupus&#44; photosensitivity&#44; hemolytic anemia&#44; leukopenia and pericardial effusion on echocardiography&#46; As for the results of the rheumatological markers&#44; they demonstrated&#44; through indirect immunofluorescence&#44; an ANA fine speckled nuclear pattern &#40;AC-4&#41; greater than 1&#47;640 and ANTI-dsDNA 1&#47;10&#59; through the enzyme-immunoassay method&#44; an Anti-SSA of 49&#46;7<span class="elsevierStyleHsp" style=""></span>U &#40;positive&#41;&#44; anticardiolipin IGG of 34&#46;3 GPL &#40;positive&#41; and anticardiolipin IGM of 145&#46;5 MPL &#40;positive&#41;&#59; the lupus anticoagulant&#44; through the coagulometric method&#44; was also positive with 1&#46;22&#59; and through turbidimetry&#44; a reduction in serum complement proteins C3 and C4 was also evidenced&#44; with 35<span class="elsevierStyleHsp" style=""></span>mg&#47;dL and &#60;8<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#44; respectively&#46; Thus scoring 28 points by the EULAR&#47;ACR-2019 criteria&#46; Clinical and laboratory diagnosis established for lupus&#44; as well as the result of a new biopsy &#40;scalp&#41; compatible with lupus erythematosus &#40;comparative between first and second biopsy in <a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The SELENA-SLEDAI criteria were used to initiate immunosuppressive therapy&#44; which considered vasculitis in the lower limbs &#40;ulcers without healing for 2 years&#41;&#44; 24-h proteinuria greater than 0&#46;5<span class="elsevierStyleHsp" style=""></span>g&#44; alopecia&#44; hypocomplementemia&#44; leukopenia&#44; fever&#44; scoring 19 and characterizing severe disease activity&#46; Opted for pulse therapy 3&#58;1 for 6 months&#44; with 3 days of methylprednisolone followed by 1 day of cyclophosphamide&#46; Patient was later discharged with prescription of hydroxychloroquine&#44; prednisone&#44; folic acid&#44; acetylsalicylic acid&#44; vitamin and mineral supplementation and follow-up with rheumatology&#44; infectiology and ophthalmology&#46; After 1 month&#44; the patient returned for evaluation with a rheumatologist and presented with improvement of the vasculitis lesions&#44; although still without complete healing and maintained normal renal function values&#46; However&#44; he maintained the same values of proteinuria in the follow-up after one month&#58; proteinuria<span class="elsevierStyleHsp" style=""></span>&#62;<span class="elsevierStyleHsp" style=""></span>0&#46;5<span class="elsevierStyleHsp" style=""></span>g&#47;24<span class="elsevierStyleHsp" style=""></span>h&#46; After 1 month&#44; the patient was referred to another reference unit for his own interest&#44; as this other unit was closer to where he lived&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Discussion</span><p id="par0020" class="elsevierStylePara elsevierViewall">Some forms of leprosy&#44; such as lepromatous and borderline leprosy&#44; may present with serological alterations and clinical alterations that are also consistent with other rheumatic pathologies&#44; mainly rheumatoid arthritis and SLE&#46;<a class="elsevierStyleCrossRefs" href="#bib0120"><span class="elsevierStyleSup">8&#8211;10</span></a> Among the most common serological abnormalities we have rheumatoid factor &#40;which may even be present in population without disease&#41;&#44; ANA&#44; anti-DNA and anticardiolipin antibody&#46;<a class="elsevierStyleCrossRefs" href="#bib0110"><span class="elsevierStyleSup">6&#44;7</span></a> Clinical changes involve erythema nodosum and vasculitis&#44; skin changes that are very common in leprosy and which should be considered by health professionals&#44; especially in regions where this disease is endemic&#46; Other similar clinical manifestations between the two conditions can also occur such as livedo reticularis&#44; malar rash&#44; skin thickening&#44; Raynaud&#39;s phenomenon&#44; oral ulcers and even glomerulonephritis&#46;<a class="elsevierStyleCrossRefs" href="#bib0120"><span class="elsevierStyleSup">8&#8211;11</span></a> There are several goals when developing a treatment plan for the patient with SLE&#58; reducing disease activity &#40;induction of remission&#41;&#44; preventing exacerbations&#44; treating them when they occur&#44; and decreasing damage to organs and systems&#44; as well as complications of the disease&#46; disease and treatment&#46;<a class="elsevierStyleCrossRefs" href="#bib0095"><span class="elsevierStyleSup">3&#44;11</span></a> Among the drugs available today&#44; corticosteroids and immunosuppressants are generally used&#44; which protect the organs from the inflammatory aggression caused by disorders in the immune system and induce remission of the disease&#44; but do not prevent or reverse the initial failure of the system&#46;<a class="elsevierStyleCrossRefs" href="#bib0140"><span class="elsevierStyleSup">12&#8211;14</span></a> Just as the diagnostic criteria allowed greater sensitivity to detect those affected by SLE&#44; some criteria were also developed to identify disease activity&#44; such as the SLEDAI &#40;Systemic Lupus Erythematosus Disease Activity Index&#41;&#44; widely used and reproducible in Brazil&#46;<a class="elsevierStyleCrossRefs" href="#bib0155"><span class="elsevierStyleSup">15&#44;16</span></a></p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Conclusion</span><p id="par0025" class="elsevierStylePara elsevierViewall">Although less frequent in men&#44; the diagnostic hypothesis of SLE should always be considered in patients with a chronic history of conditions without clinical improvement even after undergoing various therapies&#46; The case presented reveals that&#44; even showing typical changes for the disease with photosensitivity&#44; non-scarring alopecia and discoid lupus for more than 2 years&#44; the diagnosis of the disease was initially wrong&#44; requiring even a biopsy&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Information</span><p id="par0030" class="elsevierStylePara elsevierViewall">Consent was obtained for experimentation with human subjects&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Conflict of interest</span><p id="par0035" class="elsevierStylePara elsevierViewall">The authors declare they have no conflict of interest&#46;</p></span></span>"
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        "titulo" => "Abstract"
        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">We describe a case of a male patient with systemic lupus erythematosus &#40;SLE&#41; and lupus nephritis&#46; A patient who was initially diagnosed with multibacillary leprosy&#44; an infectious disease&#44; with clinical symptoms for two years&#46; However&#44; after hospitalization and investigation&#44; his diagnosis was revoked and replaced with SLE&#46; The aim of this study is to emphasize the importance of knowing the most important and significant clinical changes in SLE and thus allowing an accurate diagnosis&#44; preventing disease progression with target organ involvement&#44; and allowing better clinical management&#46;</p></span>"
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        "titulo" => "Resumen"
        "resumen" => "<span id="abst0010" class="elsevierStyleSection elsevierViewall"><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Describimos el caso de un var&#243;n con lupus eritematoso sist&#233;mico y nefritis l&#250;pica&#46; Se trata de un paciente con diagn&#243;stico inicial de lepra multibacilar&#44; una enfermedad infecciosa con s&#237;ntomas cl&#237;nicos desde hac&#237;a 2 a&#241;os&#46; Sin embargo&#44; tras su hospitalizaci&#243;n e investigaci&#243;n&#44; se revoc&#243; dicho diagn&#243;stico&#44; sustituy&#233;ndose por lupus eritematoso sist&#233;mico&#46; El objetivo de este estudio es resaltar la importancia de conocer los cambios cl&#237;nicos m&#225;s importantes y significativos del lupus eritematoso sist&#233;mico&#44; permitiendo as&#237; su diagn&#243;stico preciso y previniendo la progresi&#243;n de la enfermedad con compromiso de &#243;rganos diana&#44; as&#237; como un mejor manejo cl&#237;nico&#46;</p></span>"
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          "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">&#40;A&#41; Histological section of the lateral foot &#40;scar area&#41; revealing small vessel vasculitis associated with areas of scarring fibrosis and dystrophic calcification&#46; There are no alcohol-acid-resistant bacilli&#46; Compatible with erythema nodosum leprosum with scar areas&#46; &#40;B&#41; Histological section of the scalp region revealing mild hyperkeratosis&#44; epidermal atrophy&#44; ballooning of basal keratinocytes and discrete perivascular lymphohistiocytic infiltrate&#46; Compatible with lupus erythematosus&#46;</p>"
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                      "titulo" => "Avalia&#231;&#227;o dos sintomas&#44; complica&#231;&#245;es&#44; tratamento e efeitos colaterais medicamentosos sobre a qualidade de vida de portadores de L&#250;pus Eritematoso Sist&#234;mico &#40;LES&#41;&#58; revis&#227;o de literatura"
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                            0 => "H&#46;C&#46; Sampaio J&#250;nior"
                            1 => "H&#46;C&#46; Lopes"
                            2 => "L&#46;S&#46;V&#46; Rocha"
                            3 => "M&#46;O&#46;B&#46; Cavalcante"
                            4 => "A&#46;L&#46; Carvalho J&#250;nior"
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                      "titulo" => "Epidemiology of systemic l&#250;pus erythematosus&#58; a comparation of world wide disease burden"
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                          "autores" => array:3 [
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                            0 => "D&#46;I&#46; Posner"
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                            2 => "L&#46;T&#46;L&#46; Costallat"
                            3 => "A&#46;M&#46; Samara"
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                      "titulo" => "Anticorpos anticardiolipina em pacientes com mal de hansen"
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                        0 => array:2 [
                          "etal" => false
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                            0 => "J&#46;C&#46;D&#46; Repka"
                            1 => "T&#46;L&#46; Skare"
                            2 => "G&#46; Salles J&#250;nior"
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                    0 => array:2 [
                      "titulo" => "Vasculite na hansen&#237;ase mimetizando doen&#231;as reum&#225;ticas"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:4 [
                            0 => "S&#46;L&#46;E&#46; Ribeiro"
                            1 => "E&#46;L&#46; Guedes"
                            2 => "H&#46;L&#46;A&#46; Pereira"
                            3 => "L&#46;S&#46; Souza"
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                        ]
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                      "titulo" => "Manifesta&#231;&#245;es reum&#225;ticas da hansen&#237;ase"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:3 [
                            0 => "H&#46;L&#46;A&#46; Pereira"
                            1 => "S&#46;L&#46;E&#46; Ribeiro"
                            2 => "E&#46;I&#46; Sato"
                          ]
                        ]
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                        "fecha" => "2008"
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                0 => array:2 [
                  "contribucion" => array:1 [
                    0 => array:2 [
                      "titulo" => "Lepromatous leprosy presenting with polyarthritis&#44; myositis and immune complexes glomerunonephritis"
                      "autores" => array:1 [
                        0 => array:2 [
                          "etal" => false
                          "autores" => array:4 [
                            0 => "J&#46;M&#46;I&#46; Iveson"
                            1 => "A&#46;C&#46; McDougall"
                            2 => "A&#46;J&#46; Leathem"
                            3 => "H&#46;J&#46; Harris"
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                        ]
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                    ]
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                    0 => array:2 [
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            9 => array:3 [
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ISSN: 21735743
Original language: English
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