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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Papillary syringocystadenoma is a rare neoplasm of sweat glands&#44; which is present at birth in 50&#37; of cases&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> It has predominantly apocrine differentiation&#44; although an eccrine origin has been described in some reports&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">2&#44;3</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">It usually presents as papule or plaque with a crustal surface that occurs almost exclusively in the head and cervical region&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">This report details the clinical observations as well as the dermatoscopic and histopathological findings of a case in an unusual location&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">A 6-year-old male&#44; a native and resident of S&#227;o Jos&#233; dos Campos&#44; SP&#44; presented a lesion with progressive growth five years ago on the left flank&#46; At the dermatological examination&#44; a papule of pink-erythematous coloration was observed&#44; with a smooth surface and a fibroelastic consistency&#44; measuring 5<span class="elsevierStyleHsp" style=""></span>mm<span class="elsevierStyleHsp" style=""></span>&#215;<span class="elsevierStyleHsp" style=""></span>3<span class="elsevierStyleHsp" style=""></span>mm &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; Dermoscopic examination showed rounded structures of whitish-yellow color separated by whitish linear structures on an erythematous background &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; The patient was referred for excision&#46; Histopathological examination revealed the following&#58; cystic invaginations covered by cells&#44; sometimes squamous and sometimes columnar&#44; with papilliferous projections to the light&#59; tubular glands with large lights&#44; covered by apocrine cells &#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="par0025" class="elsevierStylePara elsevierViewall">Papillary syringocystadenoma &#40;SCAP&#41; is a rare adnexal tumor most often derived from apocrine cells&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">3&#44;4</span></a> It predominates in children and adolescents&#44; and is observed at birth in 50&#37; of cases&#44;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> which differs from the case reported above&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">In 75&#37; of cases&#44; it is located on the head or cervical region&#46; Some cases in other topographies have already been described &#40;scrotal region&#44; vulva&#44; back&#44; abdomen&#44; and axilla&#41;&#46; These locations&#44; as well as that of the case described&#44; are even rarer&#46; When located on the scalp&#44; it may be associated with the sebaceous nevus of Jadassohn&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">Despite variable clinical presentation&#44; a papule plaque is the most commonly found lesion type&#46; In the majority&#44; it is asymptomatic&#44; but it can present pruritus&#44; pain&#44; and&#47;or bleeding&#59; it usually presents progressive growth&#44; as in the case described&#46;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">1&#44;4</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">To date&#44; articles on the dermoscopic findings of SCAP are scarce&#46; There is a description of a horseshoe vascular pattern&#44; which was not observed in the present case&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">3&#44;5</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">SCAP can infect&#44; bleed&#44; ulcerate&#44; and&#44; in rare cases&#44; it can progress to basal cell carcinoma &#40;9&#37;&#41; or papillary syringo-cystadenocarcinoma&#46; For these reasons&#44; it was decided to perform the excision&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a></p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Financial support</span><p id="par0050" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Authors&#8217; contribution</span><p id="par0055" class="elsevierStylePara elsevierViewall">Giovanna de Araujo Horcel&#58; 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Case Letter
Papillary syringocystadenoma in an uncommon location
Giovanna de Araujo Horcel
Autor para correspondência
giohorcel@hotmail.com

Corresponding author.
, Juliana Milhomem, Samuel Henrique Mandelbaum, Rodrigo Ieiri
Dermatology Service, Santa Casa de São José dos Campos, São José dos Campos, São Paulo, SP, Brazil
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Papillary syringocystadenoma is a rare neoplasm of sweat glands&#44; which is present at birth in 50&#37; of cases&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> It has predominantly apocrine differentiation&#44; although an eccrine origin has been described in some reports&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">2&#44;3</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">It usually presents as papule or plaque with a crustal surface that occurs almost exclusively in the head and cervical region&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">This report details the clinical observations as well as the dermatoscopic and histopathological findings of a case in an unusual location&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">A 6-year-old male&#44; a native and resident of S&#227;o Jos&#233; dos Campos&#44; SP&#44; presented a lesion with progressive growth five years ago on the left flank&#46; At the dermatological examination&#44; a papule of pink-erythematous coloration was observed&#44; with a smooth surface and a fibroelastic consistency&#44; measuring 5<span class="elsevierStyleHsp" style=""></span>mm<span class="elsevierStyleHsp" style=""></span>&#215;<span class="elsevierStyleHsp" style=""></span>3<span class="elsevierStyleHsp" style=""></span>mm &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; Dermoscopic examination showed rounded structures of whitish-yellow color separated by whitish linear structures on an erythematous background &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; The patient was referred for excision&#46; Histopathological examination revealed the following&#58; cystic invaginations covered by cells&#44; sometimes squamous and sometimes columnar&#44; with papilliferous projections to the light&#59; tubular glands with large lights&#44; covered by apocrine cells &#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="par0025" class="elsevierStylePara elsevierViewall">Papillary syringocystadenoma &#40;SCAP&#41; is a rare adnexal tumor most often derived from apocrine cells&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">3&#44;4</span></a> It predominates in children and adolescents&#44; and is observed at birth in 50&#37; of cases&#44;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> which differs from the case reported above&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">In 75&#37; of cases&#44; it is located on the head or cervical region&#46; Some cases in other topographies have already been described &#40;scrotal region&#44; vulva&#44; back&#44; abdomen&#44; and axilla&#41;&#46; These locations&#44; as well as that of the case described&#44; are even rarer&#46; When located on the scalp&#44; it may be associated with the sebaceous nevus of Jadassohn&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">Despite variable clinical presentation&#44; a papule plaque is the most commonly found lesion type&#46; In the majority&#44; it is asymptomatic&#44; but it can present pruritus&#44; pain&#44; and&#47;or bleeding&#59; it usually presents progressive growth&#44; as in the case described&#46;<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">1&#44;4</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">To date&#44; articles on the dermoscopic findings of SCAP are scarce&#46; There is a description of a horseshoe vascular pattern&#44; which was not observed in the present case&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">3&#44;5</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">SCAP can infect&#44; bleed&#44; ulcerate&#44; and&#44; in rare cases&#44; it can progress to basal cell carcinoma &#40;9&#37;&#41; or papillary syringo-cystadenocarcinoma&#46; For these reasons&#44; it was decided to perform the excision&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a></p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Financial support</span><p id="par0050" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Authors&#8217; contribution</span><p id="par0055" class="elsevierStylePara elsevierViewall">Giovanna de Araujo Horcel&#58; Conception and planning of the study&#59; composition of the manuscript&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">Juliana Milhomem&#58; Conception and planning of the study&#46;</p><p id="par0065" class="elsevierStylePara elsevierViewall">Samuel Henrique Mandelbaum&#58; Critical review of the literature&#59; critical review of the manuscript&#46;</p><p id="par0070" class="elsevierStylePara elsevierViewall">Rodrigo Ieiri&#58; Participation in the design of the study&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Conflicts of interest</span><p id="par0075" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span></span>"
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