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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">A&#44; Red nodule with a smooth surface located in the upper third of the right nasogenian sulcus&#46; B&#44; Dermoscopy&#46; Reddish-white bed with irregular telangiectatic vessels and cotton-white areas&#46;</p>"
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Chondroid syringoma&#44; also known as a mixed skin tumor&#44; is an infrequent neoplasm that is derived from the sweat glands and forms part of the large group of cutaneous adnexal neoplasms&#46; Originally described by Billroth in 1859&#44; it was not until 1961 that Hirsch and Heldwig first used the term to describe this entity&#44; which is characterized by the presence of an epithelial component within a fibrochondroid stroma&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> This tumor accounts for less than 0&#46;1&#37; of all diagnosed skin tumors&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> Given its low incidence&#44; together with its silent and nonspecific clinical presentation&#44; clinicians often require histological data in order to establish diagnosis&#46; The differential diagnosis should include other adnexal tumors&#46; However&#44; to date there have been no published descriptions of a clinical presentation mimicking basal cell carcinoma&#44; as observed in the case reported here&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">A 48-year-old man with no medical history of interest consulted for an asymptomatic&#44; slow-growing nodular lesion &#40;1<span class="elsevierStyleHsp" style=""></span>cm in diameter&#41; with a smooth&#44; pearly surface&#44; located in the upper third of the right nasogenian sulcus &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>A&#41;&#46; Dermoscopy &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>B&#41; revealed irregular telangiectatic vessels associated with cotton-white structures on an erythematous-white bed&#46; The initial clinical suspicion was nodular basal cell carcinoma&#46; Histology&#44; performed after surgical removal of the tumor&#44; was compatible with chondroid syringoma &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Chondroid syringoma is a benign tumor of adnexal origin that is more frequent in young men&#44; and is typically located on the head and neck area&#44; in particular on the nose&#44; cheek&#44; and upper lip&#44; although involvement of other regions including the trunk&#44; genital area&#44; and extremities has also been described&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a> This tumor is usually solitary and rarely exceeds 2<span class="elsevierStyleHsp" style=""></span>cm in diameter&#46; Malignant transformation is very rare but should be suspected in cases of chondroid syringoma exceeding 3<span class="elsevierStyleHsp" style=""></span>cm and located on the trunk and extremities in young women&#46;<a class="elsevierStyleCrossRefs" href="#bib0070"><span class="elsevierStyleSup">4&#44;5</span></a> Up to 50&#37; of malignant chondroid syringomas metastasize to the lymph nodes&#44; lungs&#44; or bone&#46;<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">2&#44;6</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">Chondroid syringoma presents as a well-defined&#44; slow-growing&#44; firm&#44; mobile painless nodule&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a> There is no specific&#44; defined dermoscopic pattern that can provide diagnostically useful information&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">8</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">The nonspecific clinical and dermoscopic presentation of this neoplasm poses a real diagnostic challenge for dermatologists&#46; The differential diagnosis should include cylindroma&#44; hidradenoma&#44; eccrine poroma&#44; spiradenoma&#44; intradermal nevus&#44; papular mucinosis&#44; and epidermal cyst&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a> In our case&#44; the initial clinical suspicion was basal cell carcinoma owing to the atypical presentation of the tumor&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">Histology shows a well-defined tumor located in the dermis and&#47;or subcutaneous tissue with epithelial and stromal components&#46; The epithelial component includes glandular-like structures&#44; nests&#44; or cell strands that form ducts and tubules&#46; The stromal component is characterized by a prominent mucinous stroma that eventually becomes chondroid and may contain hyalinized areas and myoepithelial cells&#46;<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">9</span></a> Histological characteristics that are considered signs of malignant transformation include asymmetry&#44; cytological atypia&#44; infiltrative margins&#44; satellite tumor nodules&#44; necrosis&#44; and compromise of deep structures&#46;<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">2&#44;10</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">Complete surgical removal is the treatment of choice&#44; although other therapeutic alternatives such as electrocoagulation&#44; dermabrasion&#44; and vaporization with argon laser or CO<span class="elsevierStyleInf">2</span> laser have also been described&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> In cases involving malignant transformation&#44; removal with surgical margins of at least 1<span class="elsevierStyleHsp" style=""></span>cm is recommended&#44; and adjuvant radiotherapy may also be considered&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">5</span></a></p></span>"
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Case and Research Letters
Chondroid Syringoma Mimicking Basal Cell Carcinoma
Siringoma condroide simulando un carcinoma basocelular
L. Linares Gonzáleza,
Autor para correspondencia
laura.linares.gz@gmail.com

Corresponding author.
, P. Aguayo Carrerasa, B. Rueda Villafrancab, F.J. Navarro-Triviñoa
a Unidad de Dermatología Médico-Quirúrgica y Venereología, Hospital Universitario San Cecilio, Granada, Spain
b Unidad de Gestión Clínica de Anatomía Patológica, Hospital Universitario San Cecilio, Granada, Spain
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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">A&#44; Red nodule with a smooth surface located in the upper third of the right nasogenian sulcus&#46; B&#44; Dermoscopy&#46; Reddish-white bed with irregular telangiectatic vessels and cotton-white areas&#46;</p>"
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Chondroid syringoma&#44; also known as a mixed skin tumor&#44; is an infrequent neoplasm that is derived from the sweat glands and forms part of the large group of cutaneous adnexal neoplasms&#46; Originally described by Billroth in 1859&#44; it was not until 1961 that Hirsch and Heldwig first used the term to describe this entity&#44; which is characterized by the presence of an epithelial component within a fibrochondroid stroma&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> This tumor accounts for less than 0&#46;1&#37; of all diagnosed skin tumors&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> Given its low incidence&#44; together with its silent and nonspecific clinical presentation&#44; clinicians often require histological data in order to establish diagnosis&#46; The differential diagnosis should include other adnexal tumors&#46; However&#44; to date there have been no published descriptions of a clinical presentation mimicking basal cell carcinoma&#44; as observed in the case reported here&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">A 48-year-old man with no medical history of interest consulted for an asymptomatic&#44; slow-growing nodular lesion &#40;1<span class="elsevierStyleHsp" style=""></span>cm in diameter&#41; with a smooth&#44; pearly surface&#44; located in the upper third of the right nasogenian sulcus &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>A&#41;&#46; Dermoscopy &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>B&#41; revealed irregular telangiectatic vessels associated with cotton-white structures on an erythematous-white bed&#46; The initial clinical suspicion was nodular basal cell carcinoma&#46; Histology&#44; performed after surgical removal of the tumor&#44; was compatible with chondroid syringoma &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Chondroid syringoma is a benign tumor of adnexal origin that is more frequent in young men&#44; and is typically located on the head and neck area&#44; in particular on the nose&#44; cheek&#44; and upper lip&#44; although involvement of other regions including the trunk&#44; genital area&#44; and extremities has also been described&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a> This tumor is usually solitary and rarely exceeds 2<span class="elsevierStyleHsp" style=""></span>cm in diameter&#46; Malignant transformation is very rare but should be suspected in cases of chondroid syringoma exceeding 3<span class="elsevierStyleHsp" style=""></span>cm and located on the trunk and extremities in young women&#46;<a class="elsevierStyleCrossRefs" href="#bib0070"><span class="elsevierStyleSup">4&#44;5</span></a> Up to 50&#37; of malignant chondroid syringomas metastasize to the lymph nodes&#44; lungs&#44; or bone&#46;<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">2&#44;6</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">Chondroid syringoma presents as a well-defined&#44; slow-growing&#44; firm&#44; mobile painless nodule&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a> There is no specific&#44; defined dermoscopic pattern that can provide diagnostically useful information&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">8</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">The nonspecific clinical and dermoscopic presentation of this neoplasm poses a real diagnostic challenge for dermatologists&#46; The differential diagnosis should include cylindroma&#44; hidradenoma&#44; eccrine poroma&#44; spiradenoma&#44; intradermal nevus&#44; papular mucinosis&#44; and epidermal cyst&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a> In our case&#44; the initial clinical suspicion was basal cell carcinoma owing to the atypical presentation of the tumor&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">Histology shows a well-defined tumor located in the dermis and&#47;or subcutaneous tissue with epithelial and stromal components&#46; The epithelial component includes glandular-like structures&#44; nests&#44; or cell strands that form ducts and tubules&#46; The stromal component is characterized by a prominent mucinous stroma that eventually becomes chondroid and may contain hyalinized areas and myoepithelial cells&#46;<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">9</span></a> Histological characteristics that are considered signs of malignant transformation include asymmetry&#44; cytological atypia&#44; infiltrative margins&#44; satellite tumor nodules&#44; necrosis&#44; and compromise of deep structures&#46;<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">2&#44;10</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">Complete surgical removal is the treatment of choice&#44; although other therapeutic alternatives such as electrocoagulation&#44; dermabrasion&#44; and vaporization with argon laser or CO<span class="elsevierStyleInf">2</span> laser have also been described&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> In cases involving malignant transformation&#44; removal with surgical margins of at least 1<span class="elsevierStyleHsp" style=""></span>cm is recommended&#44; and adjuvant radiotherapy may also be considered&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">5</span></a></p></span>"
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          "en" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">A&#44; Panoramic image showing a dermal tumor with well-defined borders and mild peripheral retraction &#40;hematoxylin-eosin &#91;HE&#93;&#44; original magnification &#215;10&#41;&#46; B&#44; Higher magnification image showing cuboidal cells with eosinophilic cytoplasm and without cytological atypia&#44; arranged in strands forming tubular structures &#40;HE&#44; original magnification &#215;20&#41;&#46; C&#44; ocally&#44; the stroma has a chondroid and myxoid appearance &#40;HE&#44; original magnification &#215;40&#41;&#46;</p>"
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