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1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Histopathology</span><p id="par0015" class="elsevierStylePara elsevierViewall">Histology of the lesion showed epidermal atrophy and deposits of an amorphous eosinophilic material throughout the papillary and reticular dermis&#46; Next to this material was a mild plasma cell infiltrate &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Congo red staining showed bright apple-green birefringence under polarized light &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>A&#41;&#44; and the deposited material exhibited fluorescence with thioflavin T staining under fluorescence microscopy &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>B&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Additional Tests</span><p id="par0020" class="elsevierStylePara elsevierViewall">Gene rearrangement analysis of the skin biopsy specimen showed B-cell clonality&#46; Laboratory tests&#44; which included a complete blood count&#44; kidney and liver function tests&#44; a protein profile and immunoglobulin tests&#44; showed no abnormalities&#46;</p><p id="par0065" class="elsevierStylePara elsevierViewall">What Is Your Diagnosis&#63;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Diagnosis</span><p id="par0025" class="elsevierStylePara elsevierViewall">Primary nodular localized cutaneous amyloidosis &#40;PNLCA&#41;&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Course</span><p id="par0030" class="elsevierStylePara elsevierViewall">Twelve months later&#44; the lesions are still stable and the patient attends periodic follow-up visits&#46;</p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Comment</span><p id="par0035" class="elsevierStylePara elsevierViewall">Amyloidosis refers to a spectrum of disorders characterized by amyloid deposits in the tissues&#46; 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Gene rearrangement studies have demonstrated plasma-cell but not bone marrow&#8211;cell clonality&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">The clinical presentation consists of firm erythematous or yellowish nodules or plaques with a shiny surface&#46; The lesions are usually solitary&#44; but multiple&#44; disseminated lesions may occasionally be observed&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> PNLCA tends to affect acral sites and the most frequently involved locations are the lower limbs&#44; the nose&#44; and the periauricular areas&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> The condition has been associated with systemic diseases such as Sj&#246;gren syndrome&#44;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> diabetes mellitus&#44; and CREST syndrome &#40;Calcinosis&#44; Raynaud phenomenon&#44; Esophageal dysmotility&#44; Sclerodactyly&#44; and Telangiectasia&#41;&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Histology findings include epidermal atrophy and deposits of amorphous eosinophilic material occupying the dermis and the hypodermis&#46; A perivascular plasma cell infiltrate is also a characteristic feature</p><p id="par0050" class="elsevierStylePara elsevierViewall">PNLCA generally runs an indolent course&#44; but close follow-up is recommended as there have been reports of progression to systemic amyloidosis&#46;</p></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">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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Cases for Diagnosis
Plaque on the Nose
Placa en la nariz
B. de Unamuno-Bustos
Autor para correspondencia
blancaunamuno@yahoo.es

Corresponding Author.
, R. Ballester-Sánchez, V. Alegre de Miquel
Servicio de Dermatología, Consorcio Hospital General Universitario de Valencia, Valencia, Spain
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        "titulo" => "Placa en la nariz"
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Medical History</span><p id="par0005" class="elsevierStylePara elsevierViewall">A 45-year-old man with no relevant past history presented with a lesion of 2 years&#8217; duration on the left wing of the nose&#46; He reported no itching&#44; pain&#44; or any other symptoms&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Physical Examination</span><p id="par0010" class="elsevierStylePara elsevierViewall">Examination showed a poorly circumscribed&#44; firm erythematous plaque with a diameter of approximately 3<span class="elsevierStyleHsp" style=""></span>cm on the left wing of the nose and cheek&#46; There were also several nodules with a hard consistency and a slight yellowish color on the plaque &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Histopathology</span><p id="par0015" class="elsevierStylePara elsevierViewall">Histology of the lesion showed epidermal atrophy and deposits of an amorphous eosinophilic material throughout the papillary and reticular dermis&#46; Next to this material was a mild plasma cell infiltrate &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Congo red staining showed bright apple-green birefringence under polarized light &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>A&#41;&#44; and the deposited material exhibited fluorescence with thioflavin T staining under fluorescence microscopy &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>B&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Additional Tests</span><p id="par0020" class="elsevierStylePara elsevierViewall">Gene rearrangement analysis of the skin biopsy specimen showed B-cell clonality&#46; Laboratory tests&#44; which included a complete blood count&#44; kidney and liver function tests&#44; a protein profile and immunoglobulin tests&#44; showed no abnormalities&#46;</p><p id="par0065" class="elsevierStylePara elsevierViewall">What Is Your Diagnosis&#63;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Diagnosis</span><p id="par0025" class="elsevierStylePara elsevierViewall">Primary nodular localized cutaneous amyloidosis &#40;PNLCA&#41;&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Course</span><p id="par0030" class="elsevierStylePara elsevierViewall">Twelve months later&#44; the lesions are still stable and the patient attends periodic follow-up visits&#46;</p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Comment</span><p id="par0035" class="elsevierStylePara elsevierViewall">Amyloidosis refers to a spectrum of disorders characterized by amyloid deposits in the tissues&#46; In primary cutaneous amyloidosis&#44; the deposited material is confined to the skin&#44; without involvement of any other organs&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> A distinction is made between macular amyloidosis&#44; lichen amyloidosis&#44; and the less common form&#44; nodular amyloidosis&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> In macular and lichenoid amyloidosis&#44; the amyloid deposits&#44; which are typically found in the papillary dermis&#44; are derived from the degeneration of keratin filaments&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> In PNLCA&#44; the deposited material is observed in both the papillary and the reticular dermis&#44; and may extend as far as the subcutaneous tissue&#46; Because the amyloid proteins deposited in PNLCA are produced by plasma cells&#44; some authors have suggested that the condition should be considered an extramedullary plasmacytoma with local amyloid deposition&#46; Gene rearrangement studies have demonstrated plasma-cell but not bone marrow&#8211;cell clonality&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">The clinical presentation consists of firm erythematous or yellowish nodules or plaques with a shiny surface&#46; The lesions are usually solitary&#44; but multiple&#44; disseminated lesions may occasionally be observed&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> PNLCA tends to affect acral sites and the most frequently involved locations are the lower limbs&#44; the nose&#44; and the periauricular areas&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> The condition has been associated with systemic diseases such as Sj&#246;gren syndrome&#44;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> diabetes mellitus&#44; and CREST syndrome &#40;Calcinosis&#44; Raynaud phenomenon&#44; Esophageal dysmotility&#44; Sclerodactyly&#44; and Telangiectasia&#41;&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Histology findings include epidermal atrophy and deposits of amorphous eosinophilic material occupying the dermis and the hypodermis&#46; A perivascular plasma cell infiltrate is also a characteristic feature</p><p id="par0050" class="elsevierStylePara elsevierViewall">PNLCA generally runs an indolent course&#44; but close follow-up is recommended as there have been reports of progression to systemic amyloidosis&#46;</p></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">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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Información del artículo
ISSN: 15782190
Idioma original: Inglés
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2019 Noviembre 0 1 1
2019 Septiembre 4 1 5
2019 Julio 0 7 7
2019 Junio 2 11 13
2019 Mayo 0 17 17
2019 Abril 0 2 2
2019 Marzo 2 5 7
2019 Enero 1 0 1
2018 Octubre 2 0 2
2018 Septiembre 4 0 4
2018 Febrero 29 2 31
2018 Enero 62 3 65
2017 Diciembre 50 8 58
2017 Noviembre 47 5 52
2017 Octubre 41 4 45
2017 Septiembre 50 3 53
2017 Agosto 56 4 60
2017 Julio 41 7 48
2017 Junio 65 9 74
2017 Mayo 62 2 64
2017 Abril 53 5 58
2017 Marzo 36 17 53
2017 Febrero 37 5 42
2017 Enero 24 9 33
2016 Diciembre 40 7 47
2016 Noviembre 47 6 53
2016 Octubre 32 7 39
2016 Septiembre 40 10 50
2016 Agosto 53 8 61
2016 Julio 42 6 48
2016 Junio 10 4 14
2016 Mayo 6 4 10
2016 Abril 4 4 8
2016 Marzo 4 4 8
2016 Febrero 8 8 16
2016 Enero 8 9 17
2015 Diciembre 5 7 12
2015 Noviembre 5 7 12
2015 Octubre 5 5 10
2015 Septiembre 2 0 2
2015 Agosto 9 3 12
2015 Julio 41 3 44
2015 Junio 34 4 38
2015 Mayo 44 7 51
2015 Abril 28 2 30
2015 Marzo 20 2 22
2015 Febrero 28 1 29
2015 Enero 42 5 47
2014 Diciembre 38 5 43
2014 Noviembre 26 8 34
2014 Octubre 28 8 36
2014 Septiembre 34 6 40
2014 Agosto 18 4 22
2014 Julio 15 8 23
2014 Junio 24 8 32
2014 Mayo 25 8 33
2014 Abril 35 7 42
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