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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 49-year-old man with no medical or surgical history of interest consulted for a lesion on the skin of the right pectoral area that had appeared at least 2 years earlier&#46; The lesion was asymptomatic and had not increased in size or shown other changes&#44; although the patient reported discomfort caused by rubbing&#44; and for this reason requested excision of the lesion&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Physical Examination</span><p id="par0010" class="elsevierStylePara elsevierViewall">Physical examination revealed a solitary tumor of 15&#160;mm in diameter located on the chest&#46; The lesion was similar in color to the surrounding skin&#44; and had a firm consistency with a keratotic&#44; crateriform center &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Histopathology</span><p id="par0015" class="elsevierStylePara elsevierViewall">Histopathology showed a branched&#44; endophytic tumor of epithelial origin that had neat borders and a follicular appearance&#44; contained clear cells without atypia&#44; and did not reach the resection margin &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Additional Tests</span><p id="par0020" class="elsevierStylePara elsevierViewall">Dermoscopy revealed a tumor with a keratinized center and irregular yellowish areas&#46; Fine radial vessels and some poorly focused fine telangiectasias were visible in the periphery &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">What is Your Diagnosis&#63;</span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Diagnosis</span><p id="par0025" class="elsevierStylePara elsevierViewall">Inverted follicular keratosis&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Course</span><p id="par0030" class="elsevierStylePara elsevierViewall">Complete excision of the lesion was carried out&#44; without having confirmed recurrence during follow-up&#46;</p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Comment</span><p id="par0035" class="elsevierStylePara elsevierViewall">Inverted follicular keratosis is a rare benign tumor originating in the follicular infundibulum&#46; It typically presents as a single nodule or papule&#44; usually located on the face &#40;mainly the eyelid&#44; nose&#44; upper lip&#44; and cheek&#41; and is more common in elderly men&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;2</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">Histology reveals an endophytic tumor in the form of an inverted cone that originates from the infundibular portion of the hair follicle and forms a lobulated mass of follicular sheath epithelium that extends into the dermis&#46; The peripheral portion is composed of several rows of cells with a basaloid appearance&#46; The center contains smaller basaloid cells mixed with keratinizing cells and keratin pearls&#46; The lesion may be accompanied by fibrosis&#44; a chronic inflammatory infiltrate&#44; or increased vascularity&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Some authors consider it a variant of seborrheic keratosis or the common wart&#44; while others classify it as an independent entity owing to its follicular origin&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> It has been speculated that inverted follicular keratosis is a lesion caused by human papillomavirus &#40;HPV&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> The presence of this lesion could constitute a marker of Cowden syndrome&#44; especially in patients with multiple lesions&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">The differential diagnosis includes keratinizing tumors&#44; such as cutaneous squamous carcinoma and keratoacanthoma&#44; as well as other variants of pigmented keratosis pilaris&#44; including pigmented basal cell carcinoma&#44; seborrheic keratosis&#44; common warts&#44; and even melanoma&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> Diagnosis is usually established based on histology of the excised lesion&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">The most common dermoscopic finding in patients with inverted follicular keratosis is a keratoacanthoma-like pattern&#44; with a central keratinized area surrounded by radially arranged hairpin vessels&#46; The presence of a whitish-yellowish central area with radially arranged peripheral vessels and&#47;or whitish or red blood cells has also been described&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">The most common treatment is surgical excision&#44; although complete resolution has been reported after treatment with 5&#37; imiquimod&#46; Recurrence after complete excision is very rare&#46;</p></span></span></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Funding</span><p id="par0065" class="elsevierStylePara elsevierViewall">This work has not received any type of funding&#46;</p></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Conflicts of Interest</span><p id="par0070" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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Case for Diagnosis
Crateriform Tumor of 2 Years’ Duration
Tumor crateriforme de dos años de evolución
P.J. Gómez Arias
Autor para correspondencia
pjga10@hotmail.com

Corresponding author.
, R. Salido Vallejo
UGC de Dermatología Médico-Quirúrgica y Venereología, Hospital Universitario Reina Sofía, Córdoba, Spain
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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 49-year-old man with no medical or surgical history of interest consulted for a lesion on the skin of the right pectoral area that had appeared at least 2 years earlier&#46; The lesion was asymptomatic and had not increased in size or shown other changes&#44; although the patient reported discomfort caused by rubbing&#44; and for this reason requested excision of the lesion&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Physical Examination</span><p id="par0010" class="elsevierStylePara elsevierViewall">Physical examination revealed a solitary tumor of 15&#160;mm in diameter located on the chest&#46; The lesion was similar in color to the surrounding skin&#44; and had a firm consistency with a keratotic&#44; crateriform center &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Histopathology</span><p id="par0015" class="elsevierStylePara elsevierViewall">Histopathology showed a branched&#44; endophytic tumor of epithelial origin that had neat borders and a follicular appearance&#44; contained clear cells without atypia&#44; and did not reach the resection margin &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Additional Tests</span><p id="par0020" class="elsevierStylePara elsevierViewall">Dermoscopy revealed a tumor with a keratinized center and irregular yellowish areas&#46; Fine radial vessels and some poorly focused fine telangiectasias were visible in the periphery &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">What is Your Diagnosis&#63;</span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Diagnosis</span><p id="par0025" class="elsevierStylePara elsevierViewall">Inverted follicular keratosis&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Course</span><p id="par0030" class="elsevierStylePara elsevierViewall">Complete excision of the lesion was carried out&#44; without having confirmed recurrence during follow-up&#46;</p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Comment</span><p id="par0035" class="elsevierStylePara elsevierViewall">Inverted follicular keratosis is a rare benign tumor originating in the follicular infundibulum&#46; It typically presents as a single nodule or papule&#44; usually located on the face &#40;mainly the eyelid&#44; nose&#44; upper lip&#44; and cheek&#41; and is more common in elderly men&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;2</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">Histology reveals an endophytic tumor in the form of an inverted cone that originates from the infundibular portion of the hair follicle and forms a lobulated mass of follicular sheath epithelium that extends into the dermis&#46; The peripheral portion is composed of several rows of cells with a basaloid appearance&#46; The center contains smaller basaloid cells mixed with keratinizing cells and keratin pearls&#46; The lesion may be accompanied by fibrosis&#44; a chronic inflammatory infiltrate&#44; or increased vascularity&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Some authors consider it a variant of seborrheic keratosis or the common wart&#44; while others classify it as an independent entity owing to its follicular origin&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> It has been speculated that inverted follicular keratosis is a lesion caused by human papillomavirus &#40;HPV&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> The presence of this lesion could constitute a marker of Cowden syndrome&#44; especially in patients with multiple lesions&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">The differential diagnosis includes keratinizing tumors&#44; such as cutaneous squamous carcinoma and keratoacanthoma&#44; as well as other variants of pigmented keratosis pilaris&#44; including pigmented basal cell carcinoma&#44; seborrheic keratosis&#44; common warts&#44; and even melanoma&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> Diagnosis is usually established based on histology of the excised lesion&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">The most common dermoscopic finding in patients with inverted follicular keratosis is a keratoacanthoma-like pattern&#44; with a central keratinized area surrounded by radially arranged hairpin vessels&#46; The presence of a whitish-yellowish central area with radially arranged peripheral vessels and&#47;or whitish or red blood cells has also been described&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">The most common treatment is surgical excision&#44; although complete resolution has been reported after treatment with 5&#37; imiquimod&#46; Recurrence after complete excision is very rare&#46;</p></span></span></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Funding</span><p id="par0065" class="elsevierStylePara elsevierViewall">This work has not received any type of funding&#46;</p></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Conflicts of Interest</span><p id="par0070" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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                          "etal" => false
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        "texto" => "<p id="par0075" class="elsevierStylePara elsevierViewall">The authors thank Dr&#46; Jos&#233; Luis Rodr&#237;guez Peralto for his essential assistance with the histopathological diagnosis and description of the case&#46;</p>"
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