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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">The patient&#44; a 14-year-old boy with no relevant personal or family history&#44; presented with asymptomatic lesions on both hands that had first appeared approximately 1 year earlier&#46; He had received treatment with topical corticosteroids on several occasions&#46; The lesions had improved somewhat during each round of treatment&#44; only to worsen again after the medication was withdrawn&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Physical Examination</span><p id="par0010" class="elsevierStylePara elsevierViewall">Physical examination revealed yellowish-white keratotic plaques with well-defined borders on the dorsum of the right hand and on the lateral sides of the proximal phalanges of both hands &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#44; A and B&#41;&#46; A larger plaque with similar characteristics was located on the right thenar eminence&#44; stretching around to the lateral edge of the hand &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; The patient had no other lesions&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Histopathology</span><p id="par0015" class="elsevierStylePara elsevierViewall">Histopathology revealed marked orthokeratotic hyperkeratosis and mild epidermal acanthosis &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>A&#41;&#46; Orcein staining revealed a reduction &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>B&#41; and fragmentation &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>C&#41; of the elastic fibers in the dermis&#46;</p><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">Diagnosis</span><p id="par0025" class="elsevierStylePara elsevierViewall">Acrokeratoelastoidosis of Costa&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Clinical Course and Treatment</span><p id="par0030" class="elsevierStylePara elsevierViewall">Due to the benign nature of the condition and the absence of symptoms&#44; the patient was given no treatment&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Comment</span><p id="par0035" class="elsevierStylePara elsevierViewall">First described by Costa<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> in 1953&#44; acrokeratoelastoidosis &#40;AKE&#41; is a rare entity that can be either sporadic or familial&#46; Autosomal dominant and autosomal recessive inheritance patterns have been described&#44; as well as a possible linkage to chromosome 2&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> In most cases&#44; onset occurs before the age of 20 years&#44;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> and the disease exhibits no clear predilection for race or sex&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">The lesions are small&#44; translucent&#44; yellowish-white papules measuring 2 to 4<span class="elsevierStyleHsp" style=""></span>mm&#46; They can be round or polygonal&#44; have a flat or umbilicated surface&#44; and are often keratotic&#46; The most characteristic locations are the thenar and hypothenar eminences and the dorsal and lateral aspects of the fingers and toes&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2-5</span></a> The lesions typically occur across the areas where the dorsal and plantar or the dorsal and palmar surfaces meet&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> On the dorsa of the feet&#44; the papules tend to merge into plaques<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> that can extend as far as the anterior aspect of the legs&#59; lesions rarely occur on the soles of the feet&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> The lesions are usually asymptomatic&#44; although pruritus<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> and pain caused by fissuring have been reported&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> Hyperhidrosis is a common but variable finding&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;4</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Histology reveals epidermal acanthosis with orthokeratotic hyperkeratosis&#46; In the dermis&#44; a reduction and fragmentation of elastic fibers &#40;elastorrhexis&#41; is observed&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2-4</span></a> In some cases&#44; these changes in the skin can only be observed by electron microscopy&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">The cause of AKE is unknown&#44;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;4</span></a> but electron microscopic studies of patients with AKE have revealed fibroblasts containing dense cytoplasmic granules and an absence of extracellular fibers&#46; 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Cases for Diagnosis
Keratotic Plaques on the Hands
Placas queratósicas en manos
J. Alonso-González
Autor para correspondencia
julio.alonso.gonzalez@gmail.com

Corresponding author.
, M. Ginarte, J. Toribio
Departamento de Dermatología, Complejo Hospitalario Universitario, Facultad de Medicina, Santiago de Compostela, Spain
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    "titulo" => "Keratotic Plaques on the Hands"
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        "titulo" => "Placas querat&#243;sicas en manos"
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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">A&#44; Hematoxylin-eosin&#44; original magnification &#215;100&#46; B&#44; Orcein&#44; original magnification &#215;250&#46; C&#44; Orcein&#44; original magnification &#215;400&#46;</p>"
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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">The patient&#44; a 14-year-old boy with no relevant personal or family history&#44; presented with asymptomatic lesions on both hands that had first appeared approximately 1 year earlier&#46; He had received treatment with topical corticosteroids on several occasions&#46; The lesions had improved somewhat during each round of treatment&#44; only to worsen again after the medication was withdrawn&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Physical Examination</span><p id="par0010" class="elsevierStylePara elsevierViewall">Physical examination revealed yellowish-white keratotic plaques with well-defined borders on the dorsum of the right hand and on the lateral sides of the proximal phalanges of both hands &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#44; A and B&#41;&#46; A larger plaque with similar characteristics was located on the right thenar eminence&#44; stretching around to the lateral edge of the hand &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; The patient had no other lesions&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Histopathology</span><p id="par0015" class="elsevierStylePara elsevierViewall">Histopathology revealed marked orthokeratotic hyperkeratosis and mild epidermal acanthosis &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>A&#41;&#46; Orcein staining revealed a reduction &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>B&#41; and fragmentation &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>C&#41; of the elastic fibers in the dermis&#46;</p><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">Diagnosis</span><p id="par0025" class="elsevierStylePara elsevierViewall">Acrokeratoelastoidosis of Costa&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Clinical Course and Treatment</span><p id="par0030" class="elsevierStylePara elsevierViewall">Due to the benign nature of the condition and the absence of symptoms&#44; the patient was given no treatment&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Comment</span><p id="par0035" class="elsevierStylePara elsevierViewall">First described by Costa<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> in 1953&#44; acrokeratoelastoidosis &#40;AKE&#41; is a rare entity that can be either sporadic or familial&#46; Autosomal dominant and autosomal recessive inheritance patterns have been described&#44; as well as a possible linkage to chromosome 2&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> In most cases&#44; onset occurs before the age of 20 years&#44;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> and the disease exhibits no clear predilection for race or sex&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">The lesions are small&#44; translucent&#44; yellowish-white papules measuring 2 to 4<span class="elsevierStyleHsp" style=""></span>mm&#46; They can be round or polygonal&#44; have a flat or umbilicated surface&#44; and are often keratotic&#46; The most characteristic locations are the thenar and hypothenar eminences and the dorsal and lateral aspects of the fingers and toes&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2-5</span></a> The lesions typically occur across the areas where the dorsal and plantar or the dorsal and palmar surfaces meet&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> On the dorsa of the feet&#44; the papules tend to merge into plaques<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> that can extend as far as the anterior aspect of the legs&#59; lesions rarely occur on the soles of the feet&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> The lesions are usually asymptomatic&#44; although pruritus<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> and pain caused by fissuring have been reported&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> Hyperhidrosis is a common but variable finding&#46;<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#44;4</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Histology reveals epidermal acanthosis with orthokeratotic hyperkeratosis&#46; In the dermis&#44; a reduction and fragmentation of elastic fibers &#40;elastorrhexis&#41; is observed&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2-4</span></a> In some cases&#44; these changes in the skin can only be observed by electron microscopy&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">The cause of AKE is unknown&#44;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;4</span></a> but electron microscopic studies of patients with AKE have revealed fibroblasts containing dense cytoplasmic granules and an absence of extracellular fibers&#46; These findings support the hypothesis that the underlying disease process is the inhibition of elastic fiber synthesis by fibroblasts&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">Key conditions that should be considered in the differential diagnosis include other marginal acrokeratodermas such as focal acral hyperkeratosis&#44; degenerative collagenous plaques of the hands&#44; keratoelastoidosis marginalis of the hands&#44; and lenticular acral keratosis in laundry workers&#46; Diagnosis is established on the basis of clinical findings and histologic examination of the lesions&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;4</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">Treatment is generally unnecessary&#44; as the lesions are usually asymptomatic&#46; Of the treatments used to date&#8212;dapsone&#44; methotrexate&#44; topical salicylic acid&#44; topical capsaicin&#44;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> liquid nitrogen&#44; oral and topical corticosteroids&#44; and erbium&#58;YAG laser treatment&#8212;oral retinoid treatment is the only one likely to lead to any improvement&#59; it should be noted&#44; however&#44; that the lesions recur after discontinuation of the treatment&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;4</span></a></p></span></span>"
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2013 Abril 21 6 27
2013 Marzo 22 11 33
2013 Febrero 29 4 33
2013 Enero 37 6 43
2012 Diciembre 18 4 22
2012 Agosto 0 1 1
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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?