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they are initially soft and erythematous or purpuric&#44; with occasional ulceration&#46; Over time&#44; lesions may develop with hypo- or hyperchromia in the event of regression&#46; The nodular form is rarer&#44; usually occurring in patients with HIV infection&#46; Pruritus and burning pain in the lesions may be observed&#44; as well as arthralgias and ocular alterations&#44; such as nodular scleritis&#44; panuveitis&#44; autoimmune keratolysis&#44; and peripheral keratitis&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">The authors describe the case of a patient infected with HIV and hepatitis B virus &#40;HBV&#41; presenting with leukocytoclastic vasculitis diagnosed by biopsy of skin lesions&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Case report</span><p id="par0020" class="elsevierStylePara elsevierViewall">This was a 43-year-old black male patient with a 16-year history of HIV infection who was using lamivudine<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>tenofovir<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>lopinavir&#47;ritonavir &#40;viral load 25&#44;000<span class="elsevierStyleHsp" style=""></span>copies&#47;mL and CD4 count of 39<span class="elsevierStyleHsp" style=""></span>cells&#47;mm<span class="elsevierStyleSup">3</span>&#41;&#46; Three years before&#44; a single and nodular lesion had appeared in the right calcaneus&#59; others lesions on the extensor face of the left lower limb and left elbow were observed in subsequent months&#46; All lesions were itchy and progressed in number and size over time&#46; Physical examination disclosed symmetrically distributed erythematous-xanthochromic nodules on the knees and elbows&#44; and linear plaques and erythematous-violaceous nodules on the ankles&#44; toes&#44; and plantar region &#40;<a class="elsevierStyleCrossRefs" href="#fig0005">Figs&#46; 1 and 2</a>&#41;&#46; The patient denied visual alterations and arthralgias&#46; In this hospitalization&#44; the patient was diagnosed with neurotoxoplasmosis&#44; pneumocystosis&#44; and hepatitis B &#40;HbsAg&#44; total anti HBC&#44; and HBEAg reagents with AST&#47;TGO<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>20<span class="elsevierStyleHsp" style=""></span>U&#47;L and ALT&#47;TGP<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>11<span class="elsevierStyleHsp" style=""></span>U&#47;L&#41;&#46; Due to suspicion of tuberous xanthoma&#44; a lipid profile was requested&#44; which was normal&#46; Kaposi&#39;s sarcoma was also suspected&#46; Biopsies of two of the lesions were performed&#46; The anatomopathological examination demonstrated neutrophilic dermatitis with marked leukocytoclasia and presence of fibrotic nodules surrounding the neutrophilic infiltrate &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46; Clinical and pathological correlation indicated EED&#46; Treatment with dapsone 100<span class="elsevierStyleHsp" style=""></span>mg&#47;day was initiated&#44; which resolved the lesions within seven months &#40;<a class="elsevierStyleCrossRef" href="#fig0020">Fig&#46; 4</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><elsevierMultimedia ident="fig0020"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Discussion</span><p id="par0025" class="elsevierStylePara elsevierViewall">The diagnosis of EED is clinical and histopathological&#59; in the early stages&#44; the latter presents leukocytoclastic vasculitis with polymorphonuclear cells&#44; macrophages&#44; and histiocytes in the dermis&#44; and in the late stage&#44; granulation tissue&#44; fibrosis&#44; vascular proliferation&#44; lymphohistiocytic inflammatory infiltrate&#44; and focal areas containing neutrophils with leukocytoclasia&#46; In the late stage&#44; intra- and extracellular lipids &#40;cholesterol deposits&#41;&#44; although rare&#44; may be observed&#46; The differential diagnosis in the early phase may be Sweet&#39;s syndrome&#44; pyoderma gangrenosum&#44; facial granuloma&#44; drug-induced rash&#44; erythema multiforme&#44; cutaneous porphyria&#44; and bullous pemphigoid&#46; In the late stage&#44; the differential diagnosis considers dermatofibroma&#44; fibromatosis&#44; necrobiotic xanthogranuloma&#44; and tuberous xanthoma&#46; In patients with HIV infection&#44; Kaposi&#39;s sarcoma and bacillary angiomatosis should also be considered&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">The first choice of treatment is dapsone&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a> Alternatives are colchicine&#44; tetracyclines&#44; niacinamide&#44; and systemic corticosteroids such as prednisolone&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">4</span></a> Topical betamethasone may also be used&#46; New therapies with 5&#37; topical dapsone and plasmapheresis have been described&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a> In the late stage of the disease&#44; there is little response to dapsone&#44; given the predominant fibrosis&#46; In this case&#44; intralesional corticosteroids or lesion excision are the treatments of choice<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">5</span></a> The disease has a prolonged duration&#44; with reports of spontaneous resolution ranging from five to ten years&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a> Relapse may occur after dapsone discontinuation&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">In the literature&#44; approximately 25 cases of EED and HIV infection have been described&#44;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">6</span></a> one of which in Brazil&#44;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a> and three cases of HIV&#47;HBV&#47;EED co-occurrence&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">8</span></a> EED is most commonly seen in patients with a CD4 count<span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>200<span class="elsevierStyleHsp" style=""></span>cells&#47;mm<span class="elsevierStyleSup">3</span>&#44; and both immunosuppression and antigen-antibody reactions caused by HIV and HBV are believed to be the triggering factors of this disease&#46; Nonetheless&#44; in the study by Muratori et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">9</span></a> in four out of five patients with HIV infection&#44; the triggering factor was streptococcal infection&#46; In these patients&#44; the nodular form is the most prevalent&#44;<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">10</span></a> and the palmoplantar region may be involved&#44; as in the present case&#46; Differential diagnosis should include bacillary angiomatosis&#44; Kaposi&#39;s sarcoma&#44; and rheumatoid nodules&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">The present case is relevant&#44; due to the few reports of EED&#47;HIV&#47;HBV patients in the literature&#46; It is common to find skin lesions in immunosuppressed patients&#44; which may suggest diseases of various etiologies&#46; Thus&#44; histopathological confirmation is essential to establish the diagnosis&#44; the stage of the disease&#44; and guide treatment&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Financial support</span><p id="par0065" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Authors&#8217; contributions</span><p id="par0045" class="elsevierStylePara elsevierViewall">Sayuri Aparecida Hirayama&#58; Approval of the final version of the manuscript&#59; conception and planning of the study&#59; elaboration and writing of the manuscript&#59; obtaining&#44; analyzing&#44; and interpreting the data&#59; critical review of the literature&#59; critical review of the manuscript&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Cezar Arthur Tavares Pinheiro&#58; Preparation and writing of the manuscript&#59; effective participation in research orientation&#59; intellectual participation in propaedeutic and&#47;or therapeutic conduct of studied cases&#59; critical review of the manuscript&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">Isabelle Maffei Guarenti&#58; Approval of the final version of the manuscript&#59; effective participation in research orientation&#59; critical review of the manuscript&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">Danise Senna Oliveira&#58; Intellectual participation in propaedeutic and&#47;or therapeutic conduct of studied cases&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Conflicts of interest</span><p id="par0070" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span></span>"
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        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Erythema elevatum diutinum is a small vessel vasculitis which is benign&#44; rare&#44; and chronic&#46; It is clinically characterized by violaceous&#44; brown&#44; or yellowish plaques&#44; nodules&#44; and papules&#46; It has been associated with autoimmune&#44; infectious&#44; and neoplastic processes&#46; The following case describes a patient with hepatitis B virus and human immunodeficiency virus with CD4 count<span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>200<span class="elsevierStyleHsp" style=""></span>mm<span class="elsevierStyleSup">3</span>&#44; HIV-seropositive for 16 years&#44; and diagnosed with hepatitis B virus at the hospital&#46; The patient was treated with oral dapsone 100<span class="elsevierStyleHsp" style=""></span>mg&#47;day&#44; showing regression after seven months of treatment&#46; The authors found three cases in the literature of association of erythema elevatum diutinum&#44; human immunodeficiency virus&#44; and hepatitis B virus&#46;</p></span>"
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Case Report
Exuberant case of erythema elevatum diutinum in a patient infected with HIV and hepatitis B virus
Sayuri Aparecida Hirayamaa,
Corresponding author
sayuri.hirayama@hotmail.com

Corresponding author.
, Cezar Arthur Tavares Pinheirob, Isabelle Maffei Guarentic, Danise Senna Oliveiraa
a Department of General Medicine, Teaching Hospital, Universidade Federal de Pelotas, Pelotas, RS, Brazil
b HIV/AIDS Specialized Care Service, Universidade Federal de Pelotas, Pelotas, RS, Brazil
c Empresa Brasileira de Serviços Hospitalares, Teaching Hospital, Universidade Federal de Pelotas, Pelotas, RS, Brazil
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Erythema elevatum diutinum &#40;EED&#41; is a distinct form of cutaneous leukocytoclastic vasculitis&#44; first recorded in 1878 by Hutchinson and later in 1879 by Bury&#46; It was officially named by Radcliff-Crocker and Williams in 1892<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> &#40;apud Jose SK&#44; 2016&#44; p&#46; 81&#41;&#46; It occurs predominantly in adults from 40 to 60 years&#44; being slightly more prevalent in men&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> Although its pathogenesis is still unknown&#44; it is believed that immune complexes are deposited on the wall of venules and other vessels by continuous antigen stimulation or other infections&#46; Therefore&#44; EED is associated with hematological&#44; autoimmune&#44; neoplastic&#44; and infectious diseases&#44; such as human immunodeficiency virus &#40;HIV&#41; infection and hepatitis&#46; This deposition of immune complexes leads to activation of the complement cascade <span class="elsevierStyleItalic">via</span> IL-8&#44; with neutrophil chemotaxis&#44; releasing lysozymes&#44; collagenases&#44; myeloperoxidases&#44; and hydrolases that induce fibrin deposition and cholesterol crystals in the capillaries and venules&#44; leading to damage&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#44;2</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">This condition is characterized by papules&#44; plaques&#44; and nodules on the extensor surfaces of extremities&#44; with a predilection for hands&#44; feet&#44; elbows&#44; knees&#44; and Achilles tendons&#44; while sometimes being observed on the face and ears&#46; These lesions occur symmetrically and bilaterally&#59; they are initially soft and erythematous or purpuric&#44; with occasional ulceration&#46; Over time&#44; lesions may develop with hypo- or hyperchromia in the event of regression&#46; The nodular form is rarer&#44; usually occurring in patients with HIV infection&#46; Pruritus and burning pain in the lesions may be observed&#44; as well as arthralgias and ocular alterations&#44; such as nodular scleritis&#44; panuveitis&#44; autoimmune keratolysis&#44; and peripheral keratitis&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">The authors describe the case of a patient infected with HIV and hepatitis B virus &#40;HBV&#41; presenting with leukocytoclastic vasculitis diagnosed by biopsy of skin lesions&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Case report</span><p id="par0020" class="elsevierStylePara elsevierViewall">This was a 43-year-old black male patient with a 16-year history of HIV infection who was using lamivudine<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>tenofovir<span class="elsevierStyleHsp" style=""></span>&#43;<span class="elsevierStyleHsp" style=""></span>lopinavir&#47;ritonavir &#40;viral load 25&#44;000<span class="elsevierStyleHsp" style=""></span>copies&#47;mL and CD4 count of 39<span class="elsevierStyleHsp" style=""></span>cells&#47;mm<span class="elsevierStyleSup">3</span>&#41;&#46; Three years before&#44; a single and nodular lesion had appeared in the right calcaneus&#59; others lesions on the extensor face of the left lower limb and left elbow were observed in subsequent months&#46; All lesions were itchy and progressed in number and size over time&#46; Physical examination disclosed symmetrically distributed erythematous-xanthochromic nodules on the knees and elbows&#44; and linear plaques and erythematous-violaceous nodules on the ankles&#44; toes&#44; and plantar region &#40;<a class="elsevierStyleCrossRefs" href="#fig0005">Figs&#46; 1 and 2</a>&#41;&#46; The patient denied visual alterations and arthralgias&#46; In this hospitalization&#44; the patient was diagnosed with neurotoxoplasmosis&#44; pneumocystosis&#44; and hepatitis B &#40;HbsAg&#44; total anti HBC&#44; and HBEAg reagents with AST&#47;TGO<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>20<span class="elsevierStyleHsp" style=""></span>U&#47;L and ALT&#47;TGP<span class="elsevierStyleHsp" style=""></span>&#61;<span class="elsevierStyleHsp" style=""></span>11<span class="elsevierStyleHsp" style=""></span>U&#47;L&#41;&#46; Due to suspicion of tuberous xanthoma&#44; a lipid profile was requested&#44; which was normal&#46; Kaposi&#39;s sarcoma was also suspected&#46; Biopsies of two of the lesions were performed&#46; The anatomopathological examination demonstrated neutrophilic dermatitis with marked leukocytoclasia and presence of fibrotic nodules surrounding the neutrophilic infiltrate &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46; Clinical and pathological correlation indicated EED&#46; Treatment with dapsone 100<span class="elsevierStyleHsp" style=""></span>mg&#47;day was initiated&#44; which resolved the lesions within seven months &#40;<a class="elsevierStyleCrossRef" href="#fig0020">Fig&#46; 4</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><elsevierMultimedia ident="fig0020"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Discussion</span><p id="par0025" class="elsevierStylePara elsevierViewall">The diagnosis of EED is clinical and histopathological&#59; in the early stages&#44; the latter presents leukocytoclastic vasculitis with polymorphonuclear cells&#44; macrophages&#44; and histiocytes in the dermis&#44; and in the late stage&#44; granulation tissue&#44; fibrosis&#44; vascular proliferation&#44; lymphohistiocytic inflammatory infiltrate&#44; and focal areas containing neutrophils with leukocytoclasia&#46; In the late stage&#44; intra- and extracellular lipids &#40;cholesterol deposits&#41;&#44; although rare&#44; may be observed&#46; The differential diagnosis in the early phase may be Sweet&#39;s syndrome&#44; pyoderma gangrenosum&#44; facial granuloma&#44; drug-induced rash&#44; erythema multiforme&#44; cutaneous porphyria&#44; and bullous pemphigoid&#46; In the late stage&#44; the differential diagnosis considers dermatofibroma&#44; fibromatosis&#44; necrobiotic xanthogranuloma&#44; and tuberous xanthoma&#46; In patients with HIV infection&#44; Kaposi&#39;s sarcoma and bacillary angiomatosis should also be considered&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">The first choice of treatment is dapsone&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a> Alternatives are colchicine&#44; tetracyclines&#44; niacinamide&#44; and systemic corticosteroids such as prednisolone&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">4</span></a> Topical betamethasone may also be used&#46; New therapies with 5&#37; topical dapsone and plasmapheresis have been described&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a> In the late stage of the disease&#44; there is little response to dapsone&#44; given the predominant fibrosis&#46; In this case&#44; intralesional corticosteroids or lesion excision are the treatments of choice<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">5</span></a> The disease has a prolonged duration&#44; with reports of spontaneous resolution ranging from five to ten years&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a> Relapse may occur after dapsone discontinuation&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">In the literature&#44; approximately 25 cases of EED and HIV infection have been described&#44;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">6</span></a> one of which in Brazil&#44;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a> and three cases of HIV&#47;HBV&#47;EED co-occurrence&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">8</span></a> EED is most commonly seen in patients with a CD4 count<span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>200<span class="elsevierStyleHsp" style=""></span>cells&#47;mm<span class="elsevierStyleSup">3</span>&#44; and both immunosuppression and antigen-antibody reactions caused by HIV and HBV are believed to be the triggering factors of this disease&#46; Nonetheless&#44; in the study by Muratori et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">9</span></a> in four out of five patients with HIV infection&#44; the triggering factor was streptococcal infection&#46; In these patients&#44; the nodular form is the most prevalent&#44;<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">10</span></a> and the palmoplantar region may be involved&#44; as in the present case&#46; Differential diagnosis should include bacillary angiomatosis&#44; Kaposi&#39;s sarcoma&#44; and rheumatoid nodules&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">The present case is relevant&#44; due to the few reports of EED&#47;HIV&#47;HBV patients in the literature&#46; It is common to find skin lesions in immunosuppressed patients&#44; which may suggest diseases of various etiologies&#46; Thus&#44; histopathological confirmation is essential to establish the diagnosis&#44; the stage of the disease&#44; and guide treatment&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Financial support</span><p id="par0065" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Authors&#8217; contributions</span><p id="par0045" class="elsevierStylePara elsevierViewall">Sayuri Aparecida Hirayama&#58; Approval of the final version of the manuscript&#59; conception and planning of the study&#59; elaboration and writing of the manuscript&#59; obtaining&#44; analyzing&#44; and interpreting the data&#59; critical review of the literature&#59; critical review of the manuscript&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Cezar Arthur Tavares Pinheiro&#58; Preparation and writing of the manuscript&#59; effective participation in research orientation&#59; intellectual participation in propaedeutic and&#47;or therapeutic conduct of studied cases&#59; critical review of the manuscript&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">Isabelle Maffei Guarenti&#58; Approval of the final version of the manuscript&#59; effective participation in research orientation&#59; critical review of the manuscript&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">Danise Senna Oliveira&#58; Intellectual participation in propaedeutic and&#47;or therapeutic conduct of studied cases&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Conflicts of interest</span><p id="par0070" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span></span>"
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        "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Erythema elevatum diutinum is a small vessel vasculitis which is benign&#44; rare&#44; and chronic&#46; It is clinically characterized by violaceous&#44; brown&#44; or yellowish plaques&#44; nodules&#44; and papules&#46; It has been associated with autoimmune&#44; infectious&#44; and neoplastic processes&#46; The following case describes a patient with hepatitis B virus and human immunodeficiency virus with CD4 count<span class="elsevierStyleHsp" style=""></span>&#60;<span class="elsevierStyleHsp" style=""></span>200<span class="elsevierStyleHsp" style=""></span>mm<span class="elsevierStyleSup">3</span>&#44; HIV-seropositive for 16 years&#44; and diagnosed with hepatitis B virus at the hospital&#46; The patient was treated with oral dapsone 100<span class="elsevierStyleHsp" style=""></span>mg&#47;day&#44; showing regression after seven months of treatment&#46; The authors found three cases in the literature of association of erythema elevatum diutinum&#44; human immunodeficiency virus&#44; and hepatitis B virus&#46;</p></span>"
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Article information
ISSN: 03650596
Original language: English
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