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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">The patient was an 89-year-old woman who had been diagnosed 40 years earlier with multiple trichilemmal cysts&#44; and had no other medical history of interest&#46; She was referred to our clinic for an asymptomatic ulcerated lesion on the scalp that had appeared 2 months earlier&#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 solid-to-keratotic&#44; exophytic&#44; crateriform tumor of 4&#160;cm in diameter located in the occipital region and adhered to deep planes &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The lesion was surrounded by multiple previously diagnosed trichilemmal cysts&#46; No other lesions were detected&#44; and lymph node enlargement was absent&#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">The lesion was excised for pathological examination&#44; which revealed a well-delimited and unencapsulated epithelial proliferation located in the superficial reticular dermis with an endophytic and exophytic growth pattern&#46; This hyperplasia consisted of multiple partially cystic epithelial cords and lobules&#44; with peripheral palisading and central trichilemmal keratinization&#46; More detailed analysis revealed mild-to-moderate cellular atypia&#44; with no aberrant mitoses or areas of necrosis &#40;<a class="elsevierStyleCrossRefs" href="#fig0010">Figs&#46; 2 and 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">What Is Your Diagnosis&#63;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Diagnosis</span><p id="par0025" class="elsevierStylePara elsevierViewall">Proliferating pilar tumor &#40;PPT&#41;&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Course</span><p id="par0030" class="elsevierStylePara elsevierViewall">The patient showed no recurrence after 6 months of follow-up&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Comment</span><p id="par0035" class="elsevierStylePara elsevierViewall">PPT is an adnexal tumor derived from the external radicular membrane of the hair follicle&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">1</span></a> It usually presents as an exophytic scalp tumor&#44; in many cases with ulceration&#44; bleeding&#44; and&#47;or superinfection&#44; and typically affects women aged 40 years and older&#46; However&#44; cases involving tumors in atypical locations&#44; including the thorax&#44; back&#44; buttock&#44; nose&#44; and vulva&#44; have also been described&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">2</span></a> In most cases PPT arises from a pre-existing trichilemmal cyst&#44; although de novo forms&#44; which develop in the absence of pre-existing lesions&#44; are also described&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">3</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">Histologically&#44; PPT is characterized by hyperplasia consisting of solid or partially cystic epithelial cords or lobules&#44; with peripheral palisading and trichilemmal keratinization&#46;<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">1&#8211;3</span></a> Areas of necrosis&#44; anaplastic cells&#44; and aberrant mitoses are common&#46;<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">3&#44;4</span></a> PPT can be associated with foreign body reaction&#44; dystrophic calcification&#44; squamous eddies&#44; and areas of vacuolization or dyskeratosis&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">2&#44;4</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">When differentiating PPT from squamous cell carcinoma&#44; foci of trichilemmal keratinization&#44; sharp delimitation&#44; areas of calcification&#44; and the absence of premalignant epidermal lesions help orient the diagnosis towards PPT&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">5</span></a> The differential diagnosis should also include sebaceous carcinoma&#44; clear cell hidradenocarcinoma&#44; pilomatrixoma&#44; and trichoblastoma&#46;<a class="elsevierStyleCrossRefs" href="#bib0075"><span class="elsevierStyleSup">6&#44;7</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">PPT follows an unpredictable course and lies on a spectrum ranging from benign trichilemmal cysts with minimal epithelial proliferation to malignant PPT with local invasion&#44; 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Case for Diagnosis
Fast-Growing Occipital Tumor
Tumoración occipital de rápido crecimiento
E. Varas-Meis
Corresponding author
edu.varas.meis@gmail.com

Corresponding author.
, C. Prada-García, P. Fernández-Canga, M.Á. Rodriguez-Prieto
Servicio de Dermatología, Complejo Asistencial Universitario de León, León, España
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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">The patient was an 89-year-old woman who had been diagnosed 40 years earlier with multiple trichilemmal cysts&#44; and had no other medical history of interest&#46; She was referred to our clinic for an asymptomatic ulcerated lesion on the scalp that had appeared 2 months earlier&#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 solid-to-keratotic&#44; exophytic&#44; crateriform tumor of 4&#160;cm in diameter located in the occipital region and adhered to deep planes &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The lesion was surrounded by multiple previously diagnosed trichilemmal cysts&#46; No other lesions were detected&#44; and lymph node enlargement was absent&#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">The lesion was excised for pathological examination&#44; which revealed a well-delimited and unencapsulated epithelial proliferation located in the superficial reticular dermis with an endophytic and exophytic growth pattern&#46; This hyperplasia consisted of multiple partially cystic epithelial cords and lobules&#44; with peripheral palisading and central trichilemmal keratinization&#46; More detailed analysis revealed mild-to-moderate cellular atypia&#44; with no aberrant mitoses or areas of necrosis &#40;<a class="elsevierStyleCrossRefs" href="#fig0010">Figs&#46; 2 and 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">What Is Your Diagnosis&#63;</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Diagnosis</span><p id="par0025" class="elsevierStylePara elsevierViewall">Proliferating pilar tumor &#40;PPT&#41;&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Course</span><p id="par0030" class="elsevierStylePara elsevierViewall">The patient showed no recurrence after 6 months of follow-up&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Comment</span><p id="par0035" class="elsevierStylePara elsevierViewall">PPT is an adnexal tumor derived from the external radicular membrane of the hair follicle&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">1</span></a> It usually presents as an exophytic scalp tumor&#44; in many cases with ulceration&#44; bleeding&#44; and&#47;or superinfection&#44; and typically affects women aged 40 years and older&#46; However&#44; cases involving tumors in atypical locations&#44; including the thorax&#44; back&#44; buttock&#44; nose&#44; and vulva&#44; have also been described&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">2</span></a> In most cases PPT arises from a pre-existing trichilemmal cyst&#44; although de novo forms&#44; which develop in the absence of pre-existing lesions&#44; are also described&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">3</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">Histologically&#44; PPT is characterized by hyperplasia consisting of solid or partially cystic epithelial cords or lobules&#44; with peripheral palisading and trichilemmal keratinization&#46;<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">1&#8211;3</span></a> Areas of necrosis&#44; anaplastic cells&#44; and aberrant mitoses are common&#46;<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">3&#44;4</span></a> PPT can be associated with foreign body reaction&#44; dystrophic calcification&#44; squamous eddies&#44; and areas of vacuolization or dyskeratosis&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">2&#44;4</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">When differentiating PPT from squamous cell carcinoma&#44; foci of trichilemmal keratinization&#44; sharp delimitation&#44; areas of calcification&#44; and the absence of premalignant epidermal lesions help orient the diagnosis towards PPT&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">5</span></a> The differential diagnosis should also include sebaceous carcinoma&#44; clear cell hidradenocarcinoma&#44; pilomatrixoma&#44; and trichoblastoma&#46;<a class="elsevierStyleCrossRefs" href="#bib0075"><span class="elsevierStyleSup">6&#44;7</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">PPT follows an unpredictable course and lies on a spectrum ranging from benign trichilemmal cysts with minimal epithelial proliferation to malignant PPT with local invasion&#44; a tendency to recur&#44; and occasional distant metastases&#46;<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">3&#44;5&#44;8</span></a> An infiltrative pattern with cellular anaplasia&#44; atypical mitoses&#44; and&#47;or areas of necrosis are considered histological markers of poor prognosis&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">2</span></a> The treatment of choice is exeresis with wide margins &#40;1&#8211;2&#160;cm&#41; or Mohs micrographic surgery&#44; although a good therapeutic response has also been reported in patients treated with radiotherapy&#46;<a class="elsevierStyleCrossRefs" href="#bib0085"><span class="elsevierStyleSup">8&#44;9</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">In conclusion&#44; we describe a representative case of a little-known adnexal lesion&#44; knowledge of which is necessary in order to select the appropriate therapeutic measures&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Conflicts of Interest</span><p id="par0060" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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        "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as&#58; Varas-Meis E&#44; Prada-Garc&#237;a C&#44; Fern&#225;ndez-Canga P&#44; Rodriguez-Prieto M&#193;&#46; Tumoraci&#243;n occipital de r&#225;pido crecimiento&#46; Actas Dermosifiliogr&#46; 2019&#59;110&#58;497&#8211;498&#46;</p>"
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ISSN: 15782190
Original language: English
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Idiomas
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¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?