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3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Additional Tests</span><p id="par0020" class="elsevierStylePara elsevierViewall">The results of additional tests &#40;complete blood count&#44; routine biochemistry&#44; thyroid function tests&#44; autoimmune studies&#44; serology for syphilis&#44; chest x-ray&#44; Mantoux test&#41; were within the normal range&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">What Is Your Diagnosis&#63;</span></p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Diagnosis</span><p id="par0030" class="elsevierStylePara elsevierViewall">Extrafacial granuloma faciale&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Clinical Course and Treatment</span><p id="par0035" class="elsevierStylePara elsevierViewall">Treatment with twice daily applications of tacrolimus ointment 0&#46;1&#37; 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However&#44; UV radiation appears to be involved&#44; as most cases are found in the facial region in middle-aged to elderly patients with high cumulative sun exposure or even chronic sun-induced damage&#46; Other authors propose an immunologic etiology for this disorder&#44; postulating a delayed hypersensitivity reaction or vasculitis mediated by immune complexes&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">The histopathologic characteristics of extrafacial granuloma faciale have been widely described and include a normal or moderately atrophied epidermis&#46; Almost all cases are characterized by a well-demarcated Grenz zone and a polymorphous inflammatory infiltrate rich in eosinophils and arranged in a distinctive periadnexal and vascular pattern&#46; Extrafacial granuloma faciale shares common features with erythema elevatum diutinum&#46; Both conditions involve what Carlson and LeBoit called chronic fibrosing vasculitis&#44; although the presence of this histologic feature will depend on the stage of evolution of the lesion because the initial stages point to classic leukocytoclastic vasculitis&#46;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;4</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">Caldarola et al<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> have recently contributed to furthering our knowledge of extrafacial granuloma faciale by defining its dermoscopic pattern&#46; A uniform grayish-white background with whitish streaks reveals elongated vascular loops&#44; whose morphology varies significantly after treatment with tacrolimus&#46; The pattern is not specific to this condition and is found in others such as sarcoidosis and lupus&#46;</p><p id="par0065" class="elsevierStylePara elsevierViewall">Treatment of extrafacial granuloma faciale is complicated and often ineffective and there is no first-line therapy or well-defined therapeutic pathways&#46; 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Case for Diagnosis
Atrophic Plaque of 8 Years’ Duration on the Scalp
Placa atrófica en cuero cabelludo de 8 años de evolución
M. Galán-Gutiérreza, R. Ruiz-Villaverdea,
Corresponding author
ismenios@hotmail.com

Corresponding author.
, A. Sanz-Trellesb
a Servicio de Dermatología, Unidad de gestión clínica de cirugía mayor ambulatoria, Complejo Hospitalario de Jaen, Jaen, Spain
b Servicio de Anatomía Patológica, Hospital Carlos Haya, Málaga, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Medical History</span><p id="par0005" class="elsevierStylePara elsevierViewall">A 51-year-old man with no relevant personal or family history presented to our dermatology department with a lesion on the scalp that had appeared 8 years earlier and had been biopsied at another center 4 years previously&#46; The histologic diagnosis was compatible with granulomatous dermatitis with eosinophilia&#44; resulting from arthropod bites&#46; However&#44; at the original consultation and again when he consulted our department&#44; the patient denied any prior history of trauma or insect bite&#46; In recent months the lesion had increased in size and occasionally gave rise to itching&#44; despite no change in the original morphologic features&#46; There were no associated systemic symptoms&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Physical Examination</span><p id="par0010" class="elsevierStylePara elsevierViewall">The patient presented a well-defined&#44; slightly raised annular lesion&#44; measuring 3<span class="elsevierStyleHsp" style=""></span>x<span class="elsevierStyleHsp" style=""></span>3&#46;5<span class="elsevierStyleHsp" style=""></span>cm&#44; with an atrophic appearance and superficial telangiectases &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; There were no palpable locoregional lymph nodes&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Histology</span><p id="par0015" class="elsevierStylePara elsevierViewall">Histopathology showed a moderately atrophic epidermis&#44; with an abundant inflammatory infiltrate characterized by polymorphism in the mid to deep dermis &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; It contained neutrophils&#44; eosinophils&#44; and lymphocytes and was particularly intense in periadnexal regions &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Additional Tests</span><p id="par0020" class="elsevierStylePara elsevierViewall">The results of additional tests &#40;complete blood count&#44; routine biochemistry&#44; thyroid function tests&#44; autoimmune studies&#44; serology for syphilis&#44; chest x-ray&#44; Mantoux test&#41; were within the normal range&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">What Is Your Diagnosis&#63;</span></p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Diagnosis</span><p id="par0030" class="elsevierStylePara elsevierViewall">Extrafacial granuloma faciale&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Clinical Course and Treatment</span><p id="par0035" class="elsevierStylePara elsevierViewall">Treatment with twice daily applications of tacrolimus ointment 0&#46;1&#37; achieved a moderate response at 3 months after diagnosis&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Comment</span><p id="par0040" class="elsevierStylePara elsevierViewall">Extrafacial granuloma faciale is a dermatosis of unknown origin that can present as a single or multiple lesion&#59; the clinical course is slow and progressive&#46; An extrafacial site is extremely rare and fewer than 30 cases have been reported in the literature&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">When the lesion is extrafacial&#44; the most common sites are the trunk&#44; upper and lower limbs&#44; and the scalp&#46; In fact&#44; it is not uncommon for facial lesions to precede the development of others at extrafacial sites&#46; Clinically&#44; lesions are usually well-demarcated papules&#44; plaques&#44; or nodules&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">There is no generally accepted pathophysiological hypothesis&#46; However&#44; UV radiation appears to be involved&#44; as most cases are found in the facial region in middle-aged to elderly patients with high cumulative sun exposure or even chronic sun-induced damage&#46; Other authors propose an immunologic etiology for this disorder&#44; postulating a delayed hypersensitivity reaction or vasculitis mediated by immune complexes&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">The histopathologic characteristics of extrafacial granuloma faciale have been widely described and include a normal or moderately atrophied epidermis&#46; Almost all cases are characterized by a well-demarcated Grenz zone and a polymorphous inflammatory infiltrate rich in eosinophils and arranged in a distinctive periadnexal and vascular pattern&#46; Extrafacial granuloma faciale shares common features with erythema elevatum diutinum&#46; Both conditions involve what Carlson and LeBoit called chronic fibrosing vasculitis&#44; although the presence of this histologic feature will depend on the stage of evolution of the lesion because the initial stages point to classic leukocytoclastic vasculitis&#46;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;4</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">Caldarola et al<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> have recently contributed to furthering our knowledge of extrafacial granuloma faciale by defining its dermoscopic pattern&#46; A uniform grayish-white background with whitish streaks reveals elongated vascular loops&#44; whose morphology varies significantly after treatment with tacrolimus&#46; The pattern is not specific to this condition and is found in others such as sarcoidosis and lupus&#46;</p><p id="par0065" class="elsevierStylePara elsevierViewall">Treatment of extrafacial granuloma faciale is complicated and often ineffective and there is no first-line therapy or well-defined therapeutic pathways&#46; Some authors have reported a good response to topical tacrolimus&#44;<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5&#44;6</span></a> which is emerging as the treatment of choice because of its good risk-benefit profile&#46; Other interesting options include intralesional corticosteroids&#44; dapsone&#44; cryosurgery&#44; and pulsed dye laser&#44; although recurrence is common after discontinuation of treatment&#46;</p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">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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Article information
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Original language: English
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Idiomas
Actas Dermo-Sifiliográficas
es en

¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

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