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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">We report the case of a 63-year-old woman who presented a 3-month history of hyperpigmented and pruritic skin lesions in the lumbar region&#46; Physical examination revealed violaceous-brown macules in a linear distribution with an italic S morphology &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The nails and mucosas were not affected&#46; The patient did not report using systemic or topical treatments&#44; exposure to the sun&#44; or trauma prior to the onset of the lesions&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0010" class="elsevierStylePara elsevierViewall">Dermoscopy revealed longitudinal pearly-white lines suggestive of Wickham striae &#40;WS&#41; and regressing brown macules in which there were grayish-brown dots and globules&#44; some in a linear distribution following the outline of the WS or clustered in the depressed center of the WS &#40;&#8220;ashy holes&#8221;&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Skin biopsy revealed interface dermatitis with a lymphohistiocytic infiltrate&#44; vacuolar degeneration of the basal layer&#44; and apoptotic keratinocytes &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Based on the clinical&#44; dermoscopic&#44; and histologic findings&#44; we made a diagnosis of pigmented linear lichen planus &#40;LLP&#41;&#46; A course of oral antihistamines and topical corticosteroids was prescribed&#44; daily for the first month followed by an alternating regimen for 3 months&#46; This produced a gradual resolution of the lesions&#44; which left a residual postinflammatory hyperpigmentation&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">LLP is a condition of unknown etiology&#46; It presents as hyperpigmented macules that usually arise in sun-exposed areas&#44; but that are sometimes widespread&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> LLP differs clinically from classic lichen planus &#40;LP&#41; not only by the pigmentation&#44; but also by its longer clinical course and the fact that the scalp&#44; nails&#44; and mucosas are not usually affected&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#8211;5</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">One of the peculiarities of this case is the Blaschkoid distribution in an italic S shape&#46; A review of the literature has revealed very few reports of LLP with isolated segmental manifestations&#44; whether in a zosteriform distribution<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> &#40;in which case a history of herpes zoster must be sought&#44; as this would suggest Wolf&#39;s isotopic phenomenon<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a>&#41; or following the Blaschko lines&#44;<a class="elsevierStyleCrossRefs" href="#bib0070"><span class="elsevierStyleSup">4&#44;5</span></a> or with overlapping segmental manifestations&#44;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a> in which linear lesions are associated with widespread nonsegmental lesions&#44; indicative of diseases with a polygenic inheritance&#44; including LP and other common dermatoses&#44; such as psoriasis&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">6</span></a> However&#44; with the exception of our patient&#44; all affected individuals have been of Middle Eastern or South American origin<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#8211;5</span></a>&#59; our patient is the first reported case of LLP in a Caucasian woman&#46; The differential diagnosis is broad and includes linear dermatoses such as lichen striatus&#44; inflammatory linear verrucous epidermal nevus&#44; linear and whorled nevoid hypermelanosis&#44; and the segmental manifestations of ashy dermatosis&#46;<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">3&#44;7</span></a> Differentiation from ashy dermatosis can be difficult and some authors even suggest that they are the same condition&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a> In our case&#44; the presence of pruritus&#44; the absence of an erythematous border&#44; and the histology and dermoscopy findings that included the presence of WS&#44; led us to make a diagnosis of LLP&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">We believe it is important to highlight the role of dermoscopy as a useful tool for diagnosis&#46; Whitish striae or WS are the most significant dermoscopic pattern and are considered to be pathognomic of LP&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">8</span></a> Striae of different morphologies&#8212;round&#44; arboriform&#44; reticular&#44; annular&#8212;have been described&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">8</span></a> The presence of pigmentation in the form of grayish-brown dots and globules has also been described&#59; this can coexist with WS&#44; outlining the lesions&#44; or grouped within the central area of those with a round morphology &#40;ashy holes&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">9</span></a> In more advanced stages&#44; the WS may disappear&#44; leaving only the pigmentation&#46;<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">9</span></a> V&#225;zquez et al&#46;<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">10</span></a>described 3 dermoscopic patterns in LLP&#58; dots&#44; diffuse&#44; and mixed&#59; those authors suggested that the more intense the granular deposits&#44; the slower and more persistent the course of the disease&#44; whereas a diffuse pattern of pigmentation with an absence of globules or dots was associated with earlier resolution&#46;<a class="elsevierStyleCrossRefs" href="#bib0095"><span class="elsevierStyleSup">9&#44;10</span></a> In our patient we observed a mottled pattern formed by clusters of numerous brown dots and globules and&#44; as predicted&#44; the course clinical was slow and the condition persisted for a year after diagnosis&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">In conclusion&#44; we have presented a rare case of LLP with a Blaschkoid distribution and we have described the most relevant dermoscopic features of this disease&#46; Ever more cases like this one demonstrate the usefulness of dermoscopy not only in the diagnosis of inflammatory diseases of the skin&#44; but also as a tool to predict the prognosis&#46;</p></span>"
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Case and Research Letter
Value of Dermoscopy in the Diagnosis and Prognostic Evaluation of Linear Pigmented Lichen Planus
Aportación de la dermatoscopia en el diagnóstico y pronóstico del liquen plano pigmentado lineal
E. Baquero Sánchez, A.I. Lorente-Lavirgen
Autor para correspondencia
ariselae84@gmail.com

Corresponding author.
, J. Domínguez Cruz, J. Conejo-Mir
Servicio de Dermatología y Venereología, Hospital Universitario Virgen del Rocío, Sevilla, Spain
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          "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">A dense band-like inflammatory infiltrate can be seen at the interface&#44; with vacuolar degeneration of the basal layer and scattered apoptotic keratinocytes &#40;hematoxylin and eosin&#44; original magnification &#215;<span class="elsevierStyleHsp" style=""></span>10&#41;&#46;</p>"
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">We report the case of a 63-year-old woman who presented a 3-month history of hyperpigmented and pruritic skin lesions in the lumbar region&#46; Physical examination revealed violaceous-brown macules in a linear distribution with an italic S morphology &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The nails and mucosas were not affected&#46; The patient did not report using systemic or topical treatments&#44; exposure to the sun&#44; or trauma prior to the onset of the lesions&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0010" class="elsevierStylePara elsevierViewall">Dermoscopy revealed longitudinal pearly-white lines suggestive of Wickham striae &#40;WS&#41; and regressing brown macules in which there were grayish-brown dots and globules&#44; some in a linear distribution following the outline of the WS or clustered in the depressed center of the WS &#40;&#8220;ashy holes&#8221;&#41; &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Skin biopsy revealed interface dermatitis with a lymphohistiocytic infiltrate&#44; vacuolar degeneration of the basal layer&#44; and apoptotic keratinocytes &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Based on the clinical&#44; dermoscopic&#44; and histologic findings&#44; we made a diagnosis of pigmented linear lichen planus &#40;LLP&#41;&#46; A course of oral antihistamines and topical corticosteroids was prescribed&#44; daily for the first month followed by an alternating regimen for 3 months&#46; This produced a gradual resolution of the lesions&#44; which left a residual postinflammatory hyperpigmentation&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">LLP is a condition of unknown etiology&#46; It presents as hyperpigmented macules that usually arise in sun-exposed areas&#44; but that are sometimes widespread&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> LLP differs clinically from classic lichen planus &#40;LP&#41; not only by the pigmentation&#44; but also by its longer clinical course and the fact that the scalp&#44; nails&#44; and mucosas are not usually affected&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#8211;5</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">One of the peculiarities of this case is the Blaschkoid distribution in an italic S shape&#46; A review of the literature has revealed very few reports of LLP with isolated segmental manifestations&#44; whether in a zosteriform distribution<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> &#40;in which case a history of herpes zoster must be sought&#44; as this would suggest Wolf&#39;s isotopic phenomenon<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a>&#41; or following the Blaschko lines&#44;<a class="elsevierStyleCrossRefs" href="#bib0070"><span class="elsevierStyleSup">4&#44;5</span></a> or with overlapping segmental manifestations&#44;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a> in which linear lesions are associated with widespread nonsegmental lesions&#44; indicative of diseases with a polygenic inheritance&#44; including LP and other common dermatoses&#44; such as psoriasis&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">6</span></a> However&#44; with the exception of our patient&#44; all affected individuals have been of Middle Eastern or South American origin<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#8211;5</span></a>&#59; our patient is the first reported case of LLP in a Caucasian woman&#46; The differential diagnosis is broad and includes linear dermatoses such as lichen striatus&#44; inflammatory linear verrucous epidermal nevus&#44; linear and whorled nevoid hypermelanosis&#44; and the segmental manifestations of ashy dermatosis&#46;<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">3&#44;7</span></a> Differentiation from ashy dermatosis can be difficult and some authors even suggest that they are the same condition&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a> In our case&#44; the presence of pruritus&#44; the absence of an erythematous border&#44; and the histology and dermoscopy findings that included the presence of WS&#44; led us to make a diagnosis of LLP&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">We believe it is important to highlight the role of dermoscopy as a useful tool for diagnosis&#46; Whitish striae or WS are the most significant dermoscopic pattern and are considered to be pathognomic of LP&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">8</span></a> Striae of different morphologies&#8212;round&#44; arboriform&#44; reticular&#44; annular&#8212;have been described&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">8</span></a> The presence of pigmentation in the form of grayish-brown dots and globules has also been described&#59; this can coexist with WS&#44; outlining the lesions&#44; or grouped within the central area of those with a round morphology &#40;ashy holes&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">9</span></a> In more advanced stages&#44; the WS may disappear&#44; leaving only the pigmentation&#46;<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">9</span></a> V&#225;zquez et al&#46;<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">10</span></a>described 3 dermoscopic patterns in LLP&#58; dots&#44; diffuse&#44; and mixed&#59; those authors suggested that the more intense the granular deposits&#44; the slower and more persistent the course of the disease&#44; whereas a diffuse pattern of pigmentation with an absence of globules or dots was associated with earlier resolution&#46;<a class="elsevierStyleCrossRefs" href="#bib0095"><span class="elsevierStyleSup">9&#44;10</span></a> In our patient we observed a mottled pattern formed by clusters of numerous brown dots and globules and&#44; as predicted&#44; the course clinical was slow and the condition persisted for a year after diagnosis&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">In conclusion&#44; we have presented a rare case of LLP with a Blaschkoid distribution and we have described the most relevant dermoscopic features of this disease&#46; Ever more cases like this one demonstrate the usefulness of dermoscopy not only in the diagnosis of inflammatory diseases of the skin&#44; but also as a tool to predict the prognosis&#46;</p></span>"
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ISSN: 15782190
Idioma original: Inglés
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