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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">we read with interest a case series of acquired port wine stain &#40;PWS&#41; in 3 otherwise healthy children &#40;2 females and 1 male&#41; by Mill&#225;n-Cayetano et al&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">1</span></a> published in Actas Dermo-Sifiliogr&#225;ficas journal&#46; The authors stated &#8220;acquired capillary malformation may be considered simply to be a late-onset capillary malformation with a variable latency period&#8221;&#46; Actually&#44; acquired PWS is not as &#8220;simple&#8221; as considered by the authors&#46; The authors underestimated skin diseases masquerading as PWS&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">Linear morphea is a form of morphea that can affect an entire extremity and follow the lines of Blaschko&#46; Children are more likely than adults to have linear morphea on the face&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">2</span></a> In many cases&#44; the affected skin is initially erythematous and may resemble a PWS&#46; Vascular damage&#44; such as microvascular injury&#44; and T-cell activation&#44; with subsequent abnormal collagen production by fibroblasts&#44; is thought to be involved in its pathomechanism&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">3</span></a> Nihjawan et al&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">4</span></a> reported four cases that had presented with erythematous vascular-appearing patches resembling PWS&#46; Three lesions were located on the face and one was on the leg&#46; The initial biopsies of two patients revealed telangiectatic dermal vessels&#44; consistent with PWS&#46; However&#44; further biopsies revealed dermal fibrosis with patchy lymphocytic infiltrate&#44; consistent with morphea&#46; Diagnosis of morphea was made approximately 6 months to 3 years after the onset of the acquired PWS&#46; On the other hand&#44; perineural inflammation has rarely been reported to be an early histopathological feature of morphea&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">5</span></a> Singh et al&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">6</span></a> reported 2 cases of morphea with subtle sclerotic changes initially&#44; presented with perineural and intraneural lymphoplasmacytic infiltration&#46; According to Nihjawan et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">4</span></a> there was prominent perineural inflammation which prompted the diagnosis of early morphea&#46; In other words&#44; early inflammatory morphea can present initially with a vascular&#44; nonindurated patch&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">7</span></a> Biopsies of these lesions may not reveal the characteristic features of established morphea and the diagnosis has to be considered if perineural inflammation is seen&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">4</span></a> Nihjawan et al&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">4</span></a> recommended&#44; in patients with acquired PWS&#44; delaying PDL treatment until a diagnosis of early morphea can be excluded&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">4</span></a> However&#44; it is difficult to ascertain whether laser therapy to the initial lesions triggered the increase in fibrosis as some of the reported cases did not receive laser treatment&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">7</span></a> Treatment of PWS using the PDL may reduce the skin erythema&#44; but did not prevent subsequent sclerosis&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">To sum up&#44; acquired PWS is not a simple stain&#46; Inflammatory morphea should be considered in the differential diagnosis whenever an acquired PWS has been identified&#44; especially on the face&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">2</span></a> Early stages of morphea are sometimes difficult to recognize&#44; and histology may not helpful in early cases because there is overlap&#44; leading to misdiagnosis&#46; Clinicopathological correlation is of paramount importance in such cases&#46; Morphea should be considered if perineural inflammation is seen in histopathology&#46; Dermoscopy can assist in the early diagnosis of localized scleroderma &#40;LS&#41;&#44; with no need for invasive examinations&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">8</span></a> Noteworthy&#44; ultrasound used for LS has demonstrated clear differences from healthy skin and improvement after initiation of treatment&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">9</span></a></p></span>"
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Letter to the Editor
Acquired Port-Wine Stain: Not a simple stain!
Mancha de vino de Oporto adquirida: ¡no es una simple mancha!
A. Abdelmaksouda, M. Vestitab,
Autor para correspondencia
michelangelovestita@gmail.com

Corresponding author.
a Unidad de Dermatología, Venereología y Leprología, Hospital Universitario de Mansoura, Mansoura, Egipto
b Unidad de Cirugía Plástica y Reconstructiva, Departamento de Urgencias y Trasplantes, Universidad de Bari, Bari, Italia
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      "es" => array:1 [
        "titulo" => "Mancha de vino de Oporto adquirida&#58; &#161;no es una simple mancha&#33;"
      ]
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">we read with interest a case series of acquired port wine stain &#40;PWS&#41; in 3 otherwise healthy children &#40;2 females and 1 male&#41; by Mill&#225;n-Cayetano et al&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">1</span></a> published in Actas Dermo-Sifiliogr&#225;ficas journal&#46; The authors stated &#8220;acquired capillary malformation may be considered simply to be a late-onset capillary malformation with a variable latency period&#8221;&#46; Actually&#44; acquired PWS is not as &#8220;simple&#8221; as considered by the authors&#46; The authors underestimated skin diseases masquerading as PWS&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">Linear morphea is a form of morphea that can affect an entire extremity and follow the lines of Blaschko&#46; Children are more likely than adults to have linear morphea on the face&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">2</span></a> In many cases&#44; the affected skin is initially erythematous and may resemble a PWS&#46; Vascular damage&#44; such as microvascular injury&#44; and T-cell activation&#44; with subsequent abnormal collagen production by fibroblasts&#44; is thought to be involved in its pathomechanism&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">3</span></a> Nihjawan et al&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">4</span></a> reported four cases that had presented with erythematous vascular-appearing patches resembling PWS&#46; Three lesions were located on the face and one was on the leg&#46; The initial biopsies of two patients revealed telangiectatic dermal vessels&#44; consistent with PWS&#46; However&#44; further biopsies revealed dermal fibrosis with patchy lymphocytic infiltrate&#44; consistent with morphea&#46; Diagnosis of morphea was made approximately 6 months to 3 years after the onset of the acquired PWS&#46; On the other hand&#44; perineural inflammation has rarely been reported to be an early histopathological feature of morphea&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">5</span></a> Singh et al&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">6</span></a> reported 2 cases of morphea with subtle sclerotic changes initially&#44; presented with perineural and intraneural lymphoplasmacytic infiltration&#46; According to Nihjawan et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">4</span></a> there was prominent perineural inflammation which prompted the diagnosis of early morphea&#46; In other words&#44; early inflammatory morphea can present initially with a vascular&#44; nonindurated patch&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">7</span></a> Biopsies of these lesions may not reveal the characteristic features of established morphea and the diagnosis has to be considered if perineural inflammation is seen&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">4</span></a> Nihjawan et al&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">4</span></a> recommended&#44; in patients with acquired PWS&#44; delaying PDL treatment until a diagnosis of early morphea can be excluded&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">4</span></a> However&#44; it is difficult to ascertain whether laser therapy to the initial lesions triggered the increase in fibrosis as some of the reported cases did not receive laser treatment&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">7</span></a> Treatment of PWS using the PDL may reduce the skin erythema&#44; but did not prevent subsequent sclerosis&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">To sum up&#44; acquired PWS is not a simple stain&#46; Inflammatory morphea should be considered in the differential diagnosis whenever an acquired PWS has been identified&#44; especially on the face&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">2</span></a> Early stages of morphea are sometimes difficult to recognize&#44; and histology may not helpful in early cases because there is overlap&#44; leading to misdiagnosis&#46; Clinicopathological correlation is of paramount importance in such cases&#46; Morphea should be considered if perineural inflammation is seen in histopathology&#46; Dermoscopy can assist in the early diagnosis of localized scleroderma &#40;LS&#41;&#44; with no need for invasive examinations&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">8</span></a> Noteworthy&#44; ultrasound used for LS has demonstrated clear differences from healthy skin and improvement after initiation of treatment&#46;<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">9</span></a></p></span>"
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        "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as&#58; Abdelmaksoud A&#44; Vestita M&#46; Mancha de vino de Oporto adquirida&#58; &#161;no es una simple mancha&#33;&#46; Actas Dermosifiliogr&#46; 2018&#59;109&#58;462&#8211;463&#46;</p>"
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