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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">In a young woman&#44; the differential diagnosis of ulcerated skin lesions on the lower limbs that heal leaving atrophic scars should include vasculitis and occlusive vasculopathy&#46; Cutaneous polyarteritis nodosa &#40;CPN&#41; is characterized by the presence of painful nodules that typically develop on the lower limbs&#44; frequently ulcerate&#44; and usually heal without residual hyperpigmentation&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Its diagnosis requires demonstration of necrotizing arteritis affecting medium-sized arteries&#46; Livedoid vasculopathy &#40;LV&#41; is an occlusive vasculopathy with painful lesions in the form of punched-out ulcers that heal leaving white atrophic scars with peripheral telangiectasia&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> Light microscopy shows a mild superficial perivascular infiltrate and extravasation of red blood cells without vasculitis&#44; although some arteries may present hyalinization of the wall and intraluminal fibrin deposits&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">We present a case in which the lesions showed the clinical and histological features of both disorders&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">The patient was 29-year-old woman with no past medical history of interest&#44; who had been receiving aspirin 100&#160;mg&#47;24&#160;h and pentoxifylline 400&#160;mg&#47;12&#160;h for the last 8 years due to a skin disorder identified in another hospital as livedo reticularis&#46; She was seen in our department for a 4-year history of outbreaks on the lower limbs of painful isolated lesions&#44; sometimes ulcerated with serosanguineous crusts&#44; and that disappeared after several months&#44; occasionally leaving residual hyperpigmentation&#46; The outbreaks appeared at random intervals and with no seasonal relationship&#46; She had been treated with betamethasone plus gentamicin ointment&#44; which&#44; according to the patient&#44; accelerated remission&#46; She did not present Raynaud&#39;s phenomenon or other systemic symptoms&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">There were 3 relevant findings on physical examination&#58; <span class="elsevierStyleItalic">a&#41;</span> hypopigmented stellate macules on the ankle&#44; dorsal surface of the foot&#44; and left pretibial region &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>A&#41;&#59; <span class="elsevierStyleItalic">b&#41;</span> an indurated erythematous red-brown plaque on the medial aspect of the left ankle with several well-defined ulcerated lesions &#40;the largest being 0&#46;8&#160;cm in diameter&#41; within its borders &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>B&#41;&#59; and <span class="elsevierStyleItalic">c&#41;</span> very faint reticulated violaceous macules on the upper and lower limbs&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">Skin biopsy from the area of the right lateral malleolus showed a necrotizing vasculitis affecting medium-sized vessels&#44; with superficial changes consisting of vascular congestion with extravasation of red blood cells and&#44; in some vessels&#44; thrombosis and hyalinosis of the wall &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0030" class="elsevierStylePara elsevierViewall">Blood analysis showed that antinuclear antibodies were negative &#40;titer of 1&#58;40&#41; and cytoplasmic antineutrophil cytoplasmic antibodies &#40;cANCA&#41; were positive at a titer of 1&#58;20 &#40;antiproteinase 3 and antimyeloperoxidase were negative on enzyme-linked immunosorbent assay&#41;&#46; A complete coagulation study was conducted which included prothrombin activity&#44; cephalin and thrombin times&#44; functional fibrinogen&#44; protein C and protein S&#44; antithrombin III&#44; homocysteine&#44; anticardiolipin and anti-&#946;2-glycoprotein I antibodies&#44; lupus anticoagulant&#44; and cryoglobulins and cold agglutinins&#59; the results led to the conclusion that the patient was heterozygous for the prothrombin gene 20210&#46; The possibility of systemic involvement was excluded based on the results of blood and urine analysis&#44; electroneurogram&#44; chest x-ray&#44; and assessment by the nephrology and hematology departments&#46; No palpable skin nodules were detected during follow-up&#46; Treatment for CPN was started with oral prednisone &#40;tapering regimen&#44; commencing with 0&#46;7&#160;mg&#47;kg&#47;d&#41; with the subsequent addition of azathioprine 200&#160;mg&#47;d&#44; leading to partial control of the symptoms&#59; subsequent tests for cANCA were negative&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">The recently established diagnostic criteria for CPN &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>&#41; allowed us to consider that this was the most likely diagnosis in our case&#46; However&#44; the patient also presented clinical and histological features characteristic of LV&#46; The coexistence of clinical and histological features of CPN and LV has rarely been described&#44; although this may be due to an underestimation of their incidence&#46; In a study of 29 patients with atrophie blanche lesions &#40;mean follow-up&#44; 18 years&#41;&#44; skin biopsy demonstrated the presence of arteritis affecting medium-sized arteries&#44; consistent with a diagnosis of CPN&#44; in 21&#37; of cases&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> Those authors suggested that occlusion of the dermal arteries by fibrin thrombi could be secondary to the partial obliteration of larger arteries affected by a primary necrotizing vasculitic process&#46; The phenomenon is considered to be a reactive angioendotheliomatosis&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> In the case described&#44; heterozygosity for prothrombin gene 20210&#44; present in 1&#37; to 5&#37; of the white population&#44; could be implicated in the occlusion of the dermal arteries that was observed concomitantly with the vasculitic changes&#46; In this regard&#44; there is a case report that describes a patient with LV who had the same genetic anomaly and a similar clinical presentation to that of our patient<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a>&#59; however&#44; vasculitis was absent&#46; It is well known that the pathogenesis of LV involves coagulation abnormalities such as decreased levels of activated protein C or increased levels of fibrinopeptide A&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> Its diagnosis must fulfill both clinical and histological criteria in the absence of signs or symptoms of systemic involvement&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0040" class="elsevierStylePara elsevierViewall">In the case described&#44; it appears improbable that the LV progressed to CPN&#44; given the pathogenic differences between the 2 disorders&#44;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a> although some authors have suggested that the initial thrombotic phenomenon of LV could trigger a necrotizing vasculitis in susceptible patients&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Finally&#44; a case of pANCA-positive CPN associated with minocycline therapy has been described&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> In our case&#44; we identified a low titer of cANCA which&#44; together with the negative results of further tests following treatment&#44; suggests that these antibodies were not relevant from a clinical point of view&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">In summary&#44; atrophie blanche may be a clinical manifestation of CPN and may coexist with other more typical manifestations&#46; Skin biopsies that include the deep subcutaneous tissue are required for diagnosis&#46;</p></span>"
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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">Compatible clinical 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">Nodules&#44; livedo&#44; purpura&#44; ulcers&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><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">Necrotizing vasculitis&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">Small and medium-sized vessels&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><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">The following should be excluded in patients without systemic involvement&#58;&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">Fever &#62;38<span class="elsevierStyleHsp" style=""></span>&#176;C for more than 15 dWeight loss &#62;6<span class="elsevierStyleHsp" style=""></span>kg in 6 moHypertensionRenal involvementIschemic or hemorrhagic strokeAcute myocardial infarction or pericarditisPleuritisIntestinal ischemia or hemorrhageNeuropathy in territories distant from the affected areaWidespread joint or muscle painCompatible changes on arteriography&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr></tbody></table>
                  """
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Case and Research Letters
Cutaneous Polyarteritis Nodosa With Manifestations of Livedoid Vasculopathy
Panarteritis nodosa cutánea con clínica de vasculopatía livedoide
M. Llamas-Velascoa,
Autor para correspondencia
mar.llamasvelasco@gmail.com

Corresponding author.
, D. de Argilaa, J. Fragab, A. García-Dieza
a Servicio de Dermatología, Hospital Universitario de La Princesa, Madrid, Spain
b Servicio de Anatomía Patológica, Hospital Universitario de La Princesa, Madrid, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">In a young woman&#44; the differential diagnosis of ulcerated skin lesions on the lower limbs that heal leaving atrophic scars should include vasculitis and occlusive vasculopathy&#46; Cutaneous polyarteritis nodosa &#40;CPN&#41; is characterized by the presence of painful nodules that typically develop on the lower limbs&#44; frequently ulcerate&#44; and usually heal without residual hyperpigmentation&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Its diagnosis requires demonstration of necrotizing arteritis affecting medium-sized arteries&#46; Livedoid vasculopathy &#40;LV&#41; is an occlusive vasculopathy with painful lesions in the form of punched-out ulcers that heal leaving white atrophic scars with peripheral telangiectasia&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> Light microscopy shows a mild superficial perivascular infiltrate and extravasation of red blood cells without vasculitis&#44; although some arteries may present hyalinization of the wall and intraluminal fibrin deposits&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">We present a case in which the lesions showed the clinical and histological features of both disorders&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">The patient was 29-year-old woman with no past medical history of interest&#44; who had been receiving aspirin 100&#160;mg&#47;24&#160;h and pentoxifylline 400&#160;mg&#47;12&#160;h for the last 8 years due to a skin disorder identified in another hospital as livedo reticularis&#46; She was seen in our department for a 4-year history of outbreaks on the lower limbs of painful isolated lesions&#44; sometimes ulcerated with serosanguineous crusts&#44; and that disappeared after several months&#44; occasionally leaving residual hyperpigmentation&#46; The outbreaks appeared at random intervals and with no seasonal relationship&#46; She had been treated with betamethasone plus gentamicin ointment&#44; which&#44; according to the patient&#44; accelerated remission&#46; She did not present Raynaud&#39;s phenomenon or other systemic symptoms&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">There were 3 relevant findings on physical examination&#58; <span class="elsevierStyleItalic">a&#41;</span> hypopigmented stellate macules on the ankle&#44; dorsal surface of the foot&#44; and left pretibial region &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>A&#41;&#59; <span class="elsevierStyleItalic">b&#41;</span> an indurated erythematous red-brown plaque on the medial aspect of the left ankle with several well-defined ulcerated lesions &#40;the largest being 0&#46;8&#160;cm in diameter&#41; within its borders &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>B&#41;&#59; and <span class="elsevierStyleItalic">c&#41;</span> very faint reticulated violaceous macules on the upper and lower limbs&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">Skin biopsy from the area of the right lateral malleolus showed a necrotizing vasculitis affecting medium-sized vessels&#44; with superficial changes consisting of vascular congestion with extravasation of red blood cells and&#44; in some vessels&#44; thrombosis and hyalinosis of the wall &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0030" class="elsevierStylePara elsevierViewall">Blood analysis showed that antinuclear antibodies were negative &#40;titer of 1&#58;40&#41; and cytoplasmic antineutrophil cytoplasmic antibodies &#40;cANCA&#41; were positive at a titer of 1&#58;20 &#40;antiproteinase 3 and antimyeloperoxidase were negative on enzyme-linked immunosorbent assay&#41;&#46; A complete coagulation study was conducted which included prothrombin activity&#44; cephalin and thrombin times&#44; functional fibrinogen&#44; protein C and protein S&#44; antithrombin III&#44; homocysteine&#44; anticardiolipin and anti-&#946;2-glycoprotein I antibodies&#44; lupus anticoagulant&#44; and cryoglobulins and cold agglutinins&#59; the results led to the conclusion that the patient was heterozygous for the prothrombin gene 20210&#46; The possibility of systemic involvement was excluded based on the results of blood and urine analysis&#44; electroneurogram&#44; chest x-ray&#44; and assessment by the nephrology and hematology departments&#46; No palpable skin nodules were detected during follow-up&#46; Treatment for CPN was started with oral prednisone &#40;tapering regimen&#44; commencing with 0&#46;7&#160;mg&#47;kg&#47;d&#41; with the subsequent addition of azathioprine 200&#160;mg&#47;d&#44; leading to partial control of the symptoms&#59; subsequent tests for cANCA were negative&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">The recently established diagnostic criteria for CPN &#40;<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>&#41; allowed us to consider that this was the most likely diagnosis in our case&#46; However&#44; the patient also presented clinical and histological features characteristic of LV&#46; The coexistence of clinical and histological features of CPN and LV has rarely been described&#44; although this may be due to an underestimation of their incidence&#46; In a study of 29 patients with atrophie blanche lesions &#40;mean follow-up&#44; 18 years&#41;&#44; skin biopsy demonstrated the presence of arteritis affecting medium-sized arteries&#44; consistent with a diagnosis of CPN&#44; in 21&#37; of cases&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> Those authors suggested that occlusion of the dermal arteries by fibrin thrombi could be secondary to the partial obliteration of larger arteries affected by a primary necrotizing vasculitic process&#46; The phenomenon is considered to be a reactive angioendotheliomatosis&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> In the case described&#44; heterozygosity for prothrombin gene 20210&#44; present in 1&#37; to 5&#37; of the white population&#44; could be implicated in the occlusion of the dermal arteries that was observed concomitantly with the vasculitic changes&#46; In this regard&#44; there is a case report that describes a patient with LV who had the same genetic anomaly and a similar clinical presentation to that of our patient<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a>&#59; however&#44; vasculitis was absent&#46; It is well known that the pathogenesis of LV involves coagulation abnormalities such as decreased levels of activated protein C or increased levels of fibrinopeptide A&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> Its diagnosis must fulfill both clinical and histological criteria in the absence of signs or symptoms of systemic involvement&#46;</p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0040" class="elsevierStylePara elsevierViewall">In the case described&#44; it appears improbable that the LV progressed to CPN&#44; given the pathogenic differences between the 2 disorders&#44;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a> although some authors have suggested that the initial thrombotic phenomenon of LV could trigger a necrotizing vasculitis in susceptible patients&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Finally&#44; a case of pANCA-positive CPN associated with minocycline therapy has been described&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> In our case&#44; we identified a low titer of cANCA which&#44; together with the negative results of further tests following treatment&#44; suggests that these antibodies were not relevant from a clinical point of view&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">In summary&#44; atrophie blanche may be a clinical manifestation of CPN and may coexist with other more typical manifestations&#46; Skin biopsies that include the deep subcutaneous tissue are required for diagnosis&#46;</p></span>"
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        "nota" => "<p class="elsevierStyleNotepara">Please cite this article as&#58; Llamas-Velasco M&#44; et al&#46; Panarteritis nodosa cut&#225;nea con cl&#237;nica de vasculopat&#237;a livedoide Actas Dermosifiliogr&#46; 2011&#59;102&#58;477-479&#46;</p>"
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          "leyenda" => "<p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Source&#58; Adapted from Nakamura et al&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a></p>"
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                  <table border="0" frame="\n
                  \t\t\t\t\tvoid\n
                  \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><td class="td" title="\n
                  \t\t\t\t\ttable-head\n
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                  \t\t\t\t\ttop\n
                  \t\t\t\t" style="border-bottom: 2px solid black">Findings&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t" style="border-bottom: 2px solid black">Description&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t</td><td class="td" title="\n
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                  \t\t\t\t  " align="left" valign="\n
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                  \t\t\t\t">Nodules&#44; livedo&#44; purpura&#44; ulcers&nbsp;\t\t\t\t\t\t\n
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                  \t\t\t\t  " align="left" valign="\n
                  \t\t\t\t\ttop\n
                  \t\t\t\t">Necrotizing vasculitis&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">Small and medium-sized vessels&nbsp;\t\t\t\t\t\t\n
                  \t\t\t\t</td></tr><tr title="table-row"><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">The following should be excluded in patients without systemic involvement&#58;&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">Fever &#62;38<span class="elsevierStyleHsp" style=""></span>&#176;C for more than 15 dWeight loss &#62;6<span class="elsevierStyleHsp" style=""></span>kg in 6 moHypertensionRenal involvementIschemic or hemorrhagic strokeAcute myocardial infarction or pericarditisPleuritisIntestinal ischemia or hemorrhageNeuropathy in territories distant from the affected areaWidespread joint or muscle painCompatible changes on arteriography&nbsp;\t\t\t\t\t\t\n
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                          "etal" => false
                          "autores" => array:4 [
                            0 => "J&#46;L&#46; D&#237;az-P&#233;rez"
                            1 => "Z&#46;M&#46; De Lagran"
                            2 => "J&#46;L&#46; D&#237;az-Ramon"
                            3 => "R&#46;K&#46; Winkelmann"
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                      "doi" => "10.1016/j.sder.2007.02.003"
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                        "tituloSerie" => "Semin Cutan Med Surg"
                        "fecha" => "2007"
                        "volumen" => "26"
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                          "autores" => array:2 [
                            0 => "J&#46;A&#46; Carlson"
                            1 => "K&#46;R&#46; Chen"
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                      "doi" => "10.1097/01.dad.0000245195.35106.3c"
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                        "tituloSerie" => "Am J Dermatopathol"
                        "fecha" => "2007"
                        "volumen" => "29"
                        "paginaInicial" => "44"
                        "paginaFinal" => "55"
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