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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">In 1984&#44; Andersen et al&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> reported three patients who developed erythematous lesions on the gluteal region&#44; inner thighs and armpits&#44; without accompanying overall symptoms and who were systemically exposed to allergens to which they had previous contact sensitization&#46; By analogy of the lesions to the gluteal morphological aspect of baboons &#40;<span class="elsevierStyleItalic">Papio papio</span>&#41;&#44; the name Baboon syndrome &#40;BS&#41; was suggested for these cases&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Hausermann et al&#46;&#44; in 2004&#44; proposed the designation symmetrical drug-related intertriginous and flexural exanthema &#40;SDRIFE&#41; for cases of systemic drug sensitization&#44; without topical exposure&#44; clinically identical to BS&#44; and highlighted the absence of accompanying systemic signs and symptoms&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">This is the report of a 56-year-old male patient complaining of lesions on the inguinal and axillary regions that were slightly pruritic and not associated with other systemic symptoms&#46; He reported a two-day use of paracetamol&#44; exclusively&#44; and a condition identical to the current one in previous exposures&#46; Upon physical examination&#44; well-delimited&#44; erythematous&#44; wine-colored lesions were observed&#44; without signs of excoriation&#44; with a bilateral and symmetrical distribution on the axillary&#44; inguinocrural&#44; gluteal regions&#44; and lateral aspect of the thighs&#44; including the popliteal region &#40;<a class="elsevierStyleCrossRefs" href="#fig0005">Figs&#46; 1 and 2</a>&#41;&#46; Histopathological examination of a biopsy in an axillary lesion showed epidermis with mild spongiosis&#44; moderate dermal&#44; lymphohistiocytic&#44; perivascular infiltrate&#44; and vasodilation&#46; The absence of necrotic keratinocytes and pigmentary incontinence was observed&#44; which ruled out fixed drug eruption &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Therefore&#44; the clinical&#44; dermatological&#44; and histopathological data allowed the diagnosis of paracetamol-induced SDRIFE&#46; The lesions disappeared within a few weeks after drug discontinuation and the use of topical corticosteroids&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">In 2011&#44; Miyahara et al&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> proposed the classification of Baboon syndrome into four subtypes&#58; 1&#41; classic BS&#44; resulting from sensitization by contact allergens and triggered by systemic exposure to them&#59; 2&#41; BS induced by contact with drugs&#44; triggered by absorption after skin re-exposure&#59; 3&#41; BS induced by systemic sensitization and a condition triggered by cutaneous exposure to the drug&#59; and 4&#41; SDRIFE&#44; which corresponds to systemic sensitization and manifestation when there is systemic re-exposure&#44; excluding contact allergens&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;3</span></a> Clinically&#44; SDRIFE is characterized by symmetrical exanthema in the gluteal&#44; intergluteal and inguinal area&#44; in addition to the involvement of at least one intertriginous and flexural area such as axillary&#44; cubital&#44; and popliteal areas&#46; It is considered a rare and benign manifestation of a hypersensitivity reaction with an absence of systemic symptoms&#46; The onset occurs in hours to two days after exposure to the causative agent&#46; The most often implicated medications are beta-lactams&#44; particularly amoxicillin&#44; sulfamides&#44; anti-inflammatory drugs&#44; barbiturates&#44; tetracyclines&#44; and carbamazepine&#46; In the literature&#44; there are only two reported cases of SDRIFE associated with the use of paracetamol&#46;<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#44;5</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">The pathogenesis is not completely understood&#44; but&#44; as in allergic contact dermatitis&#44; the picture suggests a delayed hypersensitivity reaction mediated by T cells&#46; A greater density of eccrine sweat glands in skinfold regions would explain their restricted or predominant manifestation in intertriginous locations&#44; where the excretion of the sensitizing drug would precipitate the dermatosis&#46; Treatment involves suspicion and interruption of the drugs being used&#46; Topical or systemic steroids can speed up resolution&#46; Case reports and identification of the triggering drug are useful from a instructive and epidemiological viewpoint&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Financial support</span><p id="par0030" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Authors&#8217; contributions</span><p id="par0035" class="elsevierStylePara elsevierViewall">Joana Alexandria Ferreira Dias&#58; Approval of the final version of the manuscript&#59; design and planning of the study&#59; critical review of the literature&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Luana Moraes Campos&#58; Approval of the final version of the manuscript&#59; critical review of the manuscript&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Juliano Vilaverde Schmitt&#58; Approval of the final version of the manuscript&#59; collection&#44; analysis and interpretation of data&#59; critical review of the manuscript&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Silvio Alencar Marques&#58; Approval of the final version of the manuscript&#59; drafting and editing of the manuscript&#59; critical review of the literature&#59; critical review of the manuscript&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Conflicts of interest</span><p id="par0055" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span></span>"
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Case Letter
Symmetrical intertriginous and flexural exanthema related to the use of paracetamol
Joana Alexandria Ferreira Dias, Luana Moraes Campos, Juliano Vilaverde Schmitt, Sílvio Alencar Marques
Corresponding author
silvio.marques@unesp.br

Corresponding author.
Faculty of Medicine, Universidade Estadual Paulista, Botucatu, SP, Brazil
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">In 1984&#44; Andersen et al&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> reported three patients who developed erythematous lesions on the gluteal region&#44; inner thighs and armpits&#44; without accompanying overall symptoms and who were systemically exposed to allergens to which they had previous contact sensitization&#46; By analogy of the lesions to the gluteal morphological aspect of baboons &#40;<span class="elsevierStyleItalic">Papio papio</span>&#41;&#44; the name Baboon syndrome &#40;BS&#41; was suggested for these cases&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Hausermann et al&#46;&#44; in 2004&#44; proposed the designation symmetrical drug-related intertriginous and flexural exanthema &#40;SDRIFE&#41; for cases of systemic drug sensitization&#44; without topical exposure&#44; clinically identical to BS&#44; and highlighted the absence of accompanying systemic signs and symptoms&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">This is the report of a 56-year-old male patient complaining of lesions on the inguinal and axillary regions that were slightly pruritic and not associated with other systemic symptoms&#46; He reported a two-day use of paracetamol&#44; exclusively&#44; and a condition identical to the current one in previous exposures&#46; Upon physical examination&#44; well-delimited&#44; erythematous&#44; wine-colored lesions were observed&#44; without signs of excoriation&#44; with a bilateral and symmetrical distribution on the axillary&#44; inguinocrural&#44; gluteal regions&#44; and lateral aspect of the thighs&#44; including the popliteal region &#40;<a class="elsevierStyleCrossRefs" href="#fig0005">Figs&#46; 1 and 2</a>&#41;&#46; Histopathological examination of a biopsy in an axillary lesion showed epidermis with mild spongiosis&#44; moderate dermal&#44; lymphohistiocytic&#44; perivascular infiltrate&#44; and vasodilation&#46; The absence of necrotic keratinocytes and pigmentary incontinence was observed&#44; which ruled out fixed drug eruption &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Therefore&#44; the clinical&#44; dermatological&#44; and histopathological data allowed the diagnosis of paracetamol-induced SDRIFE&#46; The lesions disappeared within a few weeks after drug discontinuation and the use of topical corticosteroids&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">In 2011&#44; Miyahara et al&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> proposed the classification of Baboon syndrome into four subtypes&#58; 1&#41; classic BS&#44; resulting from sensitization by contact allergens and triggered by systemic exposure to them&#59; 2&#41; BS induced by contact with drugs&#44; triggered by absorption after skin re-exposure&#59; 3&#41; BS induced by systemic sensitization and a condition triggered by cutaneous exposure to the drug&#59; and 4&#41; SDRIFE&#44; which corresponds to systemic sensitization and manifestation when there is systemic re-exposure&#44; excluding contact allergens&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;3</span></a> Clinically&#44; SDRIFE is characterized by symmetrical exanthema in the gluteal&#44; intergluteal and inguinal area&#44; in addition to the involvement of at least one intertriginous and flexural area such as axillary&#44; cubital&#44; and popliteal areas&#46; It is considered a rare and benign manifestation of a hypersensitivity reaction with an absence of systemic symptoms&#46; The onset occurs in hours to two days after exposure to the causative agent&#46; The most often implicated medications are beta-lactams&#44; particularly amoxicillin&#44; sulfamides&#44; anti-inflammatory drugs&#44; barbiturates&#44; tetracyclines&#44; and carbamazepine&#46; In the literature&#44; there are only two reported cases of SDRIFE associated with the use of paracetamol&#46;<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#44;5</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">The pathogenesis is not completely understood&#44; but&#44; as in allergic contact dermatitis&#44; the picture suggests a delayed hypersensitivity reaction mediated by T cells&#46; A greater density of eccrine sweat glands in skinfold regions would explain their restricted or predominant manifestation in intertriginous locations&#44; where the excretion of the sensitizing drug would precipitate the dermatosis&#46; Treatment involves suspicion and interruption of the drugs being used&#46; Topical or systemic steroids can speed up resolution&#46; Case reports and identification of the triggering drug are useful from a instructive and epidemiological viewpoint&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Financial support</span><p id="par0030" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Authors&#8217; contributions</span><p id="par0035" class="elsevierStylePara elsevierViewall">Joana Alexandria Ferreira Dias&#58; Approval of the final version of the manuscript&#59; design and planning of the study&#59; critical review of the literature&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Luana Moraes Campos&#58; Approval of the final version of the manuscript&#59; critical review of the manuscript&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Juliano Vilaverde Schmitt&#58; Approval of the final version of the manuscript&#59; collection&#44; analysis and interpretation of data&#59; critical review of the manuscript&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Silvio Alencar Marques&#58; Approval of the final version of the manuscript&#59; drafting and editing of the manuscript&#59; critical review of the literature&#59; critical review of the manuscript&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Conflicts of interest</span><p id="par0055" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span></span>"
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