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Dermoscopy revealed lobules and pink dots on a diffuse coppery-brown background&#44; and a fine brown network &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; With a diagnostic suspicion of a lichenoid rash&#44; lichen aureus &#40;LA&#41;&#44; or nevus flammeus&#8212;because of its congenital nature&#8212;one of the plaques was biopsied&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0010" class="elsevierStylePara elsevierViewall">Minimal hyperkeratosis&#44; mild acanthosis&#44; and mild epidermal spongiosis were observed on histology&#44; together with a dense&#44; band-like lichenoid inflammatory infiltrate in the papillary dermis&#44; with occasional apoptotic keratinocytes and extensive red cell extravasation &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; The patient was diagnosed with LA and treatment was started with 0&#46;1&#37; methylprednisolone aceponate for a month&#46; No improvement was observed at the follow-up visit at 4 months&#44; although his parents considered the lesion to be less infiltrated&#46; He was then prescribed a 1-month course of treatment with 0&#46;25&#37; prednicarbate cream&#46; Four months later the lesion remained unchanged&#46; Given the benign and asymptomatic nature of the lesion and the lack of improvement&#44; it was decided to abstain from further therapy and to keep the patient on follow-up&#46; At the time of writing&#44; the lesion continues unchanged&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">LA is a rare entity in children&#44; with a higher incidence in young adults&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> It was first described in 1959 by Martin&#44; though it was not until 1960 that Calman coined the current name based on its characteristic golden halo&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> It is included in the group of pigmented purpuric dermatoses&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">The etiology of LA is unknown&#44; although several etiological factors and triggers have been proposed&#44; such as infection&#44; trauma&#44; toxins&#44; venous insufficiency&#44; contact allergy&#44; and underlying autoimmune diseases&#46;<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">2&#44;3</span></a> LA usually presents as brownish&#44; violaceous&#44; or copper-colored macules and papules or plaques&#44; with a peripheral golden-yellow halo&#44; fine superficial desquamation&#44; and shiny surface&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#44;3&#44;4</span></a> Lesions are typically unilateral on the limbs or trunk&#44; although they can be bilateral in around 10&#37; of cases&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> Up to now&#44; LA has most often been described as a lesion affecting the lower limbs&#44; but a recent series of 25 patients found the same prevalence on arms and legs&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">Dermoscopy is a useful diagnostic tool in this entity&#46; The reported findings are summarized in 4 points&#58; a diffuse brownish or copper-red background&#44; red lobules or dots&#44; grayish dots&#44; and a pigmented network or pseudonetwork&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">5</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">Histologically&#44; there is a characteristic band-like lymphocytic infiltrate and red-cell extravasation with hemosiderin deposits&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">6</span></a> Hemosiderin may not be seen in the early stages on staining with hematoxylin and eosin&#59; Perls stain is useful in these cases&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#44;7</span></a> The presence of a periadnexal and perineural infiltrate is a histological finding disputed in the literature and is more characteristic of lichen striatus&#46; In their series of 25 patients&#44; Zeng YP et al&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> found a periadnexal infiltrate in 12 patients and a perineural infiltrate in 5&#44; more common than previously reported in LA&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">It should be noted that LA can occasionally be confused with mycosis fungoides &#40;MF&#41;&#44; and some authors even defend a relationship between the 2 diseases&#44; suggesting that LA may have the capacity to progress to MF&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">The diagnosis is clinical and pathological and the differential diagnosis should include other pigmented purpuric dermatoses&#44; mycosis fungoides&#44; lichen striatus&#44; blaschkitis&#44; traumatic contusions&#44; contact dermatitis&#44; and Langerhans histiocytosis&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#44;8</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">The prognosis of the disease is variable and unpredictable&#59; most commonly there is spontaneous resolution with subsequent recurrences&#46;<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">3&#44;4&#44;9</span></a> A number of therapeutic alternatives have been proposed&#44; including topical corticosteroids&#44; phototherapy&#44; and calcineurin inhibitors&#44; although there is still no truly effective option&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">4</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">We have presented a case of segmental LA in a patient with a high skin phototype&#44; a factor that altered the color of the lesion&#44; giving it a more pigmented appearance than usual and masking the characteristic golden-yellow halo&#46; Dermoscopy and histology enabled us to reach a correct diagnosis&#46; Neonatal LA has been reported in the literature&#44;<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">10</span></a> but we have found no other cases of congenital LA&#46; In our patient&#44; the lesion observed when he was 9 years old was at the same site as the lesion described in the first neonatal examination&#46; In addition&#44; the patient&#39;s parents described it as the same lesion&#46; This would all support its congenital nature&#44; though this cannot be confirmed&#44; as no dermatologic follow-up was performed on this patient after birth&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflicts of Interest</span><p id="par0055" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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Case and Research Letters
Lichen Aureus: A Congenital Case?
Liquen aureus: ¿un caso congénito?
O. Corral-Magaña
Autor para correspondencia
oricmag@gmail.com

Corresponding author.
, J. Escalas Taberner, A. Bauzá Alonso, A. Martin-Santiago
Servicio de Dermatología, Hospital Universitario Son Espases, Palma de Mallorca, Baleares, España
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Dermoscopy revealed lobules and pink dots on a diffuse coppery-brown background&#44; and a fine brown network &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; With a diagnostic suspicion of a lichenoid rash&#44; lichen aureus &#40;LA&#41;&#44; or nevus flammeus&#8212;because of its congenital nature&#8212;one of the plaques was biopsied&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0010" class="elsevierStylePara elsevierViewall">Minimal hyperkeratosis&#44; mild acanthosis&#44; and mild epidermal spongiosis were observed on histology&#44; together with a dense&#44; band-like lichenoid inflammatory infiltrate in the papillary dermis&#44; with occasional apoptotic keratinocytes and extensive red cell extravasation &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; The patient was diagnosed with LA and treatment was started with 0&#46;1&#37; methylprednisolone aceponate for a month&#46; No improvement was observed at the follow-up visit at 4 months&#44; although his parents considered the lesion to be less infiltrated&#46; He was then prescribed a 1-month course of treatment with 0&#46;25&#37; prednicarbate cream&#46; Four months later the lesion remained unchanged&#46; Given the benign and asymptomatic nature of the lesion and the lack of improvement&#44; it was decided to abstain from further therapy and to keep the patient on follow-up&#46; At the time of writing&#44; the lesion continues unchanged&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">LA is a rare entity in children&#44; with a higher incidence in young adults&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> It was first described in 1959 by Martin&#44; though it was not until 1960 that Calman coined the current name based on its characteristic golden halo&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> It is included in the group of pigmented purpuric dermatoses&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">The etiology of LA is unknown&#44; although several etiological factors and triggers have been proposed&#44; such as infection&#44; trauma&#44; toxins&#44; venous insufficiency&#44; contact allergy&#44; and underlying autoimmune diseases&#46;<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">2&#44;3</span></a> LA usually presents as brownish&#44; violaceous&#44; or copper-colored macules and papules or plaques&#44; with a peripheral golden-yellow halo&#44; fine superficial desquamation&#44; and shiny surface&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#44;3&#44;4</span></a> Lesions are typically unilateral on the limbs or trunk&#44; although they can be bilateral in around 10&#37; of cases&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> Up to now&#44; LA has most often been described as a lesion affecting the lower limbs&#44; but a recent series of 25 patients found the same prevalence on arms and legs&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">Dermoscopy is a useful diagnostic tool in this entity&#46; The reported findings are summarized in 4 points&#58; a diffuse brownish or copper-red background&#44; red lobules or dots&#44; grayish dots&#44; and a pigmented network or pseudonetwork&#46;<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">5</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">Histologically&#44; there is a characteristic band-like lymphocytic infiltrate and red-cell extravasation with hemosiderin deposits&#46;<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">6</span></a> Hemosiderin may not be seen in the early stages on staining with hematoxylin and eosin&#59; Perls stain is useful in these cases&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#44;7</span></a> The presence of a periadnexal and perineural infiltrate is a histological finding disputed in the literature and is more characteristic of lichen striatus&#46; In their series of 25 patients&#44; Zeng YP et al&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> found a periadnexal infiltrate in 12 patients and a perineural infiltrate in 5&#44; more common than previously reported in LA&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">It should be noted that LA can occasionally be confused with mycosis fungoides &#40;MF&#41;&#44; and some authors even defend a relationship between the 2 diseases&#44; suggesting that LA may have the capacity to progress to MF&#46;<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">7</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">The diagnosis is clinical and pathological and the differential diagnosis should include other pigmented purpuric dermatoses&#44; mycosis fungoides&#44; lichen striatus&#44; blaschkitis&#44; traumatic contusions&#44; contact dermatitis&#44; and Langerhans histiocytosis&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#44;8</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">The prognosis of the disease is variable and unpredictable&#59; most commonly there is spontaneous resolution with subsequent recurrences&#46;<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">3&#44;4&#44;9</span></a> A number of therapeutic alternatives have been proposed&#44; including topical corticosteroids&#44; phototherapy&#44; and calcineurin inhibitors&#44; although there is still no truly effective option&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">4</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">We have presented a case of segmental LA in a patient with a high skin phototype&#44; a factor that altered the color of the lesion&#44; giving it a more pigmented appearance than usual and masking the characteristic golden-yellow halo&#46; Dermoscopy and histology enabled us to reach a correct diagnosis&#46; Neonatal LA has been reported in the literature&#44;<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">10</span></a> but we have found no other cases of congenital LA&#46; 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