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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Medical history</span><p id="par0005" class="elsevierStylePara elsevierViewall">A 87 year-old-man presented with a two-month history of pruritic lesions on the scrotal area&#46; He developed a similar episode one year earlier&#44; that lasted for a couple of weeks and improved spontaneously&#46; There were no associated cutaneous or extracutaneous symptoms&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">He was chronically under enalapril and allopurinol&#44; but denied the introduction of new systemic drugs or the application of skin products on that area&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Physical examination</span><p id="par0015" class="elsevierStylePara elsevierViewall">On physical examination we observed several tense bullae and vesicles located on the scrotal area&#44; filled with clear citric fluid&#44; grouped over erythematous patches &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; Some of the lesions had already ruptured&#44; leaving eroded and crusted areas&#46; He had no other cutaneous or mucosal lesions&#46; Nikolsky&#8217;s and Asboe-Hansen&#8217;s sings were negative&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Histopathologic evaluation</span><p id="par0020" class="elsevierStylePara elsevierViewall">A punch biopsy specimen was obtained for histopathologic evaluation&#44; revealing a subepidermal blister &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>A&#41; accompanied by a dermal inflammatory infiltrate composed of mononuclear cells and eosinophils &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>B&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Other Tests</span><p id="par0025" class="elsevierStylePara elsevierViewall">Direct immunofluorescence was temporarily unavailable&#44; however indirect immunofluorescence and ELISA revealed IgG autoantibodies directed against bullous pemphigoid &#40;BP&#41; antigen 230&#44; on a titer of 56&#46;9 U&#47;mL &#40;N&#8239;&#60;&#8239;20&#41;&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">What is the diagnosis&#63;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Diagnosis</span><p id="par0035" class="elsevierStylePara elsevierViewall">Genital bullous pemphigoid &#40;GBP&#41;&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Clinical Course and Treatment</span><p id="par0040" class="elsevierStylePara elsevierViewall">The patient then began treatment with ultrapotent topical corticosteroids &#40;0&#46;05&#37; clobetasol propionate ointment once a day&#41;&#44; leading to complete resolution of skin lesions over the course of 4 weeks&#46; No recurrence was observed during a 6-month follow-up&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Comment</span><p id="par0045" class="elsevierStylePara elsevierViewall">Bullous pemphigoid &#40;BP&#41; is a common autoimmune subepidermal blistering disease&#44; presenting typically in the elderly patients as a generalized pruritic bullous eruption&#46; This entity is an example of an immune-mediated disease that is associated with a humoral and cellular response directed against two self-antigens&#58; BP antigen 180 and BP antigen 230<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;2</span></a>&#46; The clinical presentation can be rather polymorphic&#44; particularly during the early stages of the disease or in atypical variants&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Localized BP is a clinical variant of bullous pemphigoid and its exact pathogenesis is yet to be elucidated&#44; although factors such as trauma&#44; ultraviolet light and hydrostatic pressure have been proposed<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a>&#46; Genital bullous pemphigoid &#40;GBP&#41; is a rarely reported localized subset<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#44;5</span></a> that affects mainly women and paediatric patients&#46; GBP in adult men is exceptionally rare&#44; and to our knowledge only three cases were previously reported<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a>&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">The clinical differential diagnosis of GBP includes several other conditions&#44; such as acute eczema&#44; herpetic and fungal infections&#44; epidermolysis bullosa and linear IgA disease&#46; Clinical-pathological correlation is of major importance&#44; and these entities can be differentiated on the basis of distinctive immunopathologic findings and clinical context&#46; Early diagnosis will help avoid unnecessary and costly treatment for unrelated conditions&#46;</p></span></span>"
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Case for Diagnosis
Isolated Bullae of the Scrotum in an 87 Year-Old-Man
Ampollas aisladas del escroto en un varón de 87 años
F. Alves
Corresponding author
francisca.alves37@gmail.com

Corresponding author.
, A. Pinho, J.C. Cardoso
Servicio de Dermatologia, Centro Hospitalario y Universitario de Coimbra, Coimbra, Portugal
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Medical history</span><p id="par0005" class="elsevierStylePara elsevierViewall">A 87 year-old-man presented with a two-month history of pruritic lesions on the scrotal area&#46; He developed a similar episode one year earlier&#44; that lasted for a couple of weeks and improved spontaneously&#46; There were no associated cutaneous or extracutaneous symptoms&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">He was chronically under enalapril and allopurinol&#44; but denied the introduction of new systemic drugs or the application of skin products on that area&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Physical examination</span><p id="par0015" class="elsevierStylePara elsevierViewall">On physical examination we observed several tense bullae and vesicles located on the scrotal area&#44; filled with clear citric fluid&#44; grouped over erythematous patches &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; Some of the lesions had already ruptured&#44; leaving eroded and crusted areas&#46; He had no other cutaneous or mucosal lesions&#46; Nikolsky&#8217;s and Asboe-Hansen&#8217;s sings were negative&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Histopathologic evaluation</span><p id="par0020" class="elsevierStylePara elsevierViewall">A punch biopsy specimen was obtained for histopathologic evaluation&#44; revealing a subepidermal blister &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>A&#41; accompanied by a dermal inflammatory infiltrate composed of mononuclear cells and eosinophils &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>B&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Other Tests</span><p id="par0025" class="elsevierStylePara elsevierViewall">Direct immunofluorescence was temporarily unavailable&#44; however indirect immunofluorescence and ELISA revealed IgG autoantibodies directed against bullous pemphigoid &#40;BP&#41; antigen 230&#44; on a titer of 56&#46;9 U&#47;mL &#40;N&#8239;&#60;&#8239;20&#41;&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">What is the diagnosis&#63;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Diagnosis</span><p id="par0035" class="elsevierStylePara elsevierViewall">Genital bullous pemphigoid &#40;GBP&#41;&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Clinical Course and Treatment</span><p id="par0040" class="elsevierStylePara elsevierViewall">The patient then began treatment with ultrapotent topical corticosteroids &#40;0&#46;05&#37; clobetasol propionate ointment once a day&#41;&#44; leading to complete resolution of skin lesions over the course of 4 weeks&#46; No recurrence was observed during a 6-month follow-up&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Comment</span><p id="par0045" class="elsevierStylePara elsevierViewall">Bullous pemphigoid &#40;BP&#41; is a common autoimmune subepidermal blistering disease&#44; presenting typically in the elderly patients as a generalized pruritic bullous eruption&#46; This entity is an example of an immune-mediated disease that is associated with a humoral and cellular response directed against two self-antigens&#58; BP antigen 180 and BP antigen 230<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;2</span></a>&#46; The clinical presentation can be rather polymorphic&#44; particularly during the early stages of the disease or in atypical variants&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Localized BP is a clinical variant of bullous pemphigoid and its exact pathogenesis is yet to be elucidated&#44; although factors such as trauma&#44; ultraviolet light and hydrostatic pressure have been proposed<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a>&#46; Genital bullous pemphigoid &#40;GBP&#41; is a rarely reported localized subset<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#44;5</span></a> that affects mainly women and paediatric patients&#46; GBP in adult men is exceptionally rare&#44; and to our knowledge only three cases were previously reported<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a>&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">The clinical differential diagnosis of GBP includes several other conditions&#44; such as acute eczema&#44; herpetic and fungal infections&#44; epidermolysis bullosa and linear IgA disease&#46; Clinical-pathological correlation is of major importance&#44; and these entities can be differentiated on the basis of distinctive immunopathologic findings and clinical context&#46; Early diagnosis will help avoid unnecessary and costly treatment for unrelated conditions&#46;</p></span></span>"
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ISSN: 15782190
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