se ha leído el artículo
array:24 [ "pii" => "S157821901400119X" "issn" => "15782190" "doi" => "10.1016/j.adengl.2014.04.013" "estado" => "S300" "fechaPublicacion" => "2014-06-01" "aid" => "885" "copyright" => "Elsevier España, S.L. and AEDV" "copyrightAnyo" => "2013" "documento" => "simple-article" "crossmark" => 0 "subdocumento" => "cor" "cita" => "Actas Dermosifiliogr. 2014;105:524-5" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 2107 "formatos" => array:3 [ "EPUB" => 43 "HTML" => 1534 "PDF" => 530 ] ] "Traduccion" => array:1 [ "es" => array:19 [ "pii" => "S0001731013002883" "issn" => "00017310" "doi" => "10.1016/j.ad.2013.08.005" "estado" => "S300" "fechaPublicacion" => "2014-06-01" "aid" => "885" "copyright" => "Elsevier España, S.L. y AEDV" "documento" => "simple-article" "crossmark" => 0 "subdocumento" => "cor" "cita" => "Actas Dermosifiliogr. 2014;105:524-5" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 2366 "formatos" => array:3 [ "EPUB" => 2 "HTML" => 1690 "PDF" => 674 ] ] "es" => array:11 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Carta científico-Clínica</span>" "titulo" => "Mosaicismo tipo 2 en glomangiomatosis familiar" "tienePdf" => "es" "tieneTextoCompleto" => "es" "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "524" "paginaFinal" => "525" ] ] "titulosAlternativos" => array:1 [ "en" => array:1 [ "titulo" => "Type 2 Mosaicism in Familial Glomangiomatosis" ] ] "contieneTextoCompleto" => array:1 [ "es" => true ] "contienePdf" => array:1 [ "es" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0015" "etiqueta" => "Figura 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 698 "Ancho" => 1000 "Tamanyo" => 268111 ] ] "descripcion" => array:1 [ "es" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Estudio histológico de una de las lesiones maternas con presencia de una neoformación vascular en la dermis profunda con grandes luces vasculares revestidas por células glómicas (hematoxilina-eosina ×<span class="elsevierStyleHsp" style=""></span>40).</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "S. de la Fuente, A. Hernández-Martín, R. Happle, A. Torrelo" "autores" => array:4 [ 0 => array:2 [ "nombre" => "S." "apellidos" => "de la Fuente" ] 1 => array:2 [ "nombre" => "A." "apellidos" => "Hernández-Martín" ] 2 => array:2 [ "nombre" => "R." "apellidos" => "Happle" ] 3 => array:2 [ "nombre" => "A." "apellidos" => "Torrelo" ] ] ] ] ] "idiomaDefecto" => "es" "Traduccion" => array:1 [ "en" => array:9 [ "pii" => "S157821901400119X" "doi" => "10.1016/j.adengl.2014.04.013" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S157821901400119X?idApp=UINPBA000044" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0001731013002883?idApp=UINPBA000044" "url" => "/00017310/0000010500000005/v1_201405270041/S0001731013002883/v1_201405270041/es/main.assets" ] ] "itemSiguiente" => array:19 [ "pii" => "S1578219014001152" "issn" => "15782190" "doi" => "10.1016/j.adengl.2014.04.009" "estado" => "S300" "fechaPublicacion" => "2014-06-01" "aid" => "890" "copyright" => "Elsevier España, S.L. and AEDV" "documento" => "simple-article" "crossmark" => 0 "subdocumento" => "cor" "cita" => "Actas Dermosifiliogr. 2014;105:526-8" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 2011 "formatos" => array:3 [ "EPUB" => 39 "HTML" => 1538 "PDF" => 434 ] ] "en" => array:11 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Case and Research Letter</span>" "titulo" => "Pemphigus Herpetiformis With Progression to Pemphigus Foliaceus: A Case Report" "tienePdf" => "en" "tieneTextoCompleto" => "en" "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "526" "paginaFinal" => "528" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Pénfigo herpetiforme con evolución a pénfigo foliáceo. Descripción de un caso" ] ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0015" "etiqueta" => "Figure 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 752 "Ancho" => 1293 "Tamanyo" => 188891 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">A, Erythematous scaling plaque in the retroauricular area. B, Acantholytic subcorneal vesicle (hematoxylin eosin, original magnification ×400).</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "P. Fuentes-Finkelstein, M. Barnadas, C. Gelpi, L. Puig" "autores" => array:4 [ 0 => array:2 [ "nombre" => "P." "apellidos" => "Fuentes-Finkelstein" ] 1 => array:2 [ "nombre" => "M." "apellidos" => "Barnadas" ] 2 => array:2 [ "nombre" => "C." "apellidos" => "Gelpi" ] 3 => array:2 [ "nombre" => "L." "apellidos" => "Puig" ] ] ] ] ] "idiomaDefecto" => "en" "Traduccion" => array:1 [ "es" => array:9 [ "pii" => "S0001731013003189" "doi" => "10.1016/j.ad.2013.08.009" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "es" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0001731013003189?idApp=UINPBA000044" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1578219014001152?idApp=UINPBA000044" "url" => "/15782190/0000010500000005/v1_201405281018/S1578219014001152/v1_201405281018/en/main.assets" ] "itemAnterior" => array:19 [ "pii" => "S1578219014001206" "issn" => "15782190" "doi" => "10.1016/j.adengl.2014.04.014" "estado" => "S300" "fechaPublicacion" => "2014-06-01" "aid" => "886" "copyright" => "Elsevier España, S.L. and AEDV" "documento" => "simple-article" "crossmark" => 0 "subdocumento" => "cor" "cita" => "Actas Dermosifiliogr. 2014;105:522-4" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 1990 "formatos" => array:3 [ "EPUB" => 37 "HTML" => 1431 "PDF" => 522 ] ] "en" => array:11 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Case and Research Letters</span>" "titulo" => "Autochthonous Cutaneous Myiasis Due to <span class="elsevierStyleItalic">Chrysomya bezziana</span>" "tienePdf" => "en" "tieneTextoCompleto" => "en" "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "522" "paginaFinal" => "524" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Miasis cutánea no importada por <span class="elsevierStyleItalic">Chrysomya bezziana</span>" ] ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 667 "Ancho" => 1002 "Tamanyo" => 190006 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Ulcer on the left calf. Note the erythematous surface, which is papilliform in appearance, and abundant exudate. Several larvae can be seen on the surface of the lesion.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "M. Aguado Lobo, A. Hernández-Núñez, M. Isabel García-Arata, J. Borbujo" "autores" => array:4 [ 0 => array:2 [ "nombre" => "M." "apellidos" => "Aguado Lobo" ] 1 => array:2 [ "nombre" => "A." "apellidos" => "Hernández-Núñez" ] 2 => array:2 [ "nombre" => "M." "apellidos" => "Isabel García-Arata" ] 3 => array:2 [ "nombre" => "J." "apellidos" => "Borbujo" ] ] ] ] ] "idiomaDefecto" => "en" "Traduccion" => array:1 [ "es" => array:9 [ "pii" => "S0001731013002895" "doi" => "10.1016/j.ad.2013.07.005" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "es" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0001731013002895?idApp=UINPBA000044" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1578219014001206?idApp=UINPBA000044" "url" => "/15782190/0000010500000005/v1_201405281018/S1578219014001206/v1_201405281018/en/main.assets" ] "en" => array:14 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Case and Research Letter</span>" "titulo" => "Type 2 Mosaicism in Familial Glomangiomatosis" "tieneTextoCompleto" => true "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "524" "paginaFinal" => "525" ] ] "autores" => array:1 [ 0 => array:4 [ "autoresLista" => "S. de la Fuente, A. Hernández-Martín, R. Happle, A. Torrelo" "autores" => array:4 [ 0 => array:4 [ "nombre" => "S." "apellidos" => "de la Fuente" "email" => array:1 [ 0 => "delafuente.sonia@gmail.com" ] "referencia" => array:2 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">¿</span>" "identificador" => "cor0005" ] ] ] 1 => array:3 [ "nombre" => "A." "apellidos" => "Hernández-Martín" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] ] ] 2 => array:3 [ "nombre" => "R." "apellidos" => "Happle" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] ] ] 3 => array:3 [ "nombre" => "A." "apellidos" => "Torrelo" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] ] ] ] "afiliaciones" => array:2 [ 0 => array:3 [ "entidad" => "Servicio de Dermatología, Hospital del Niño Jesús, Madrid, Spain" "etiqueta" => "a" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "Servicio de Dermatología, Universidad de Friburgo, Friburgo, Germany" "etiqueta" => "b" "identificador" => "aff0010" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Mosaicismo tipo 2 en glomangiomatosis familiar" ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 661 "Ancho" => 997 "Tamanyo" => 102326 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Segmentally distributed bluish plaque extending from the right groin along the medial aspect of the right thigh and leg to the right foot.</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Autosomal dominant skin diseases can sometimes present as linear mosaicism or as segmental mosaicism that follows the Blaschko lines. Type 1 mosaicism is characterized by the presence of a body segment affected by the disease in a healthy individual as a consequence of a postzygotic germline mutation in the segment. Type 2 mosaicism is characterized by the diffuse presentation of the disease in association with superimposition of a more involved body segment and is caused by the loss of heterozygosity in this segment during embryonic development in an individual who is heterozygous for the disease.<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">A 6-year-old girl with no personal history of interest presented with an asymptomatic segmentally distributed congenital bluish lesion that extended from the right groin along the medial aspect of the right thigh and leg to the right foot. The lesion had grown in proportion to the patient's own physical development. She also presented solitary nodular lesions that had begun to appear when she was 3 years old. These were painful to pressure and to changes in temperature and were scattered on all 4 limbs. Physical examination revealed a bluish plaque with palpable elastic nodules on the medial and posterior aspects of the right thigh and medial aspect of the right foot following a segmental course (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>). In addition, papules and nodules that were painful to pressure were observed on the contralateral foot and at distal sites on the other extremities. The patient's family history was remarkable in that her mother had scattered bluish nodular lesions (approximately 1<span class="elsevierStyleHsp" style=""></span>cm in diameter) on the limbs and trunk that first began to appear during adolescence and were similar to those of the patient (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>). These lesions had not been examined previously. Biopsy specimens of the mother's lesions were taken, and histopathology revealed a new vascular formation in the deep dermis with wide vascular lumens filled with red cells and lined by glomus cells. The picture was consistent with glomuvenous malformations (<a class="elsevierStyleCrossRef" href="#fig0015">Fig. 3</a>). The congenital bluish plaque, the subsequent appearance of scattered lesions, and the mother's history of findings that were consistent with glomangiomatosis led us to make a diagnosis of type 2 mosaicism in familial glomangiomatosis. Given that the patient's quality of life is not affected, a wait-and-see approach with regular follow-up was adopted.</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Glomangioma, or glomuvenous malformation, is a hamartoma of the dermal glomus bodies, which are responsible for temperature regulation. The 2 clinical forms described are solitary glomus tumor and glomuvenous malformations, or multiple glomangiomas. The first presentation is the more common and manifests typically in adults as painful isolated bluish nodules at acral sites. Glomuvenous malformations, or multiple glomangiomas, are characterized by the progressive early onset (infancy or adolescence) of scattered solitary bluish nodules or papules all over the body. Since the condition is autosomal dominant with incomplete penetrance or variable expressivity, a family history is only found in 60% of cases. This presentation has been shown to occur as a consequence of a mutation in the glomulin gene, which is present on chromosome 1p21-22.<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> Congenital glomuvenous malformations are rare, and most cases of this manifestation reported to date are type 2 mosaicism, with an initial segmentally distributed lesion and subsequent appearance of distant scattered lesions, as in the present case. Familiar glomangiomatosis presenting as type 2 mosaicism was first reported by Happle and König.<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> Our review of the literature revealed 9 subsequent cases with this clinical presentation<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2–9</span></a>; therefore, 14 cases with this presentation have been reported to date, although none have been confirmed using molecular techniques. Besides being described in glomangiomatosis, type 2 mosaicism has been reported in several autosomal dominant diseases,<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> although mosaicism has only been confirmed by genetic testing in a few of these cases.</p><p id="par0020" class="elsevierStylePara elsevierViewall">In the case we present, it is clear that both the mother and the daughter present familial glomangiomatosis, even without confirmation by a genetic study. Given the clinical presentation as a superimposed congenital lesion in the daughter and the subsequent appearance of scattered lesions, we think that the present case can be considered a new example of type 2 mosaicism in glomangiomatosis.</p></span>" "pdfFichero" => "main.pdf" "tienePdf" => true "NotaPie" => array:1 [ 0 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as: de la Fuente S, Hernández-Martín A, Happle R, Torrelo A. Mosaicismo tipo 2 en glomangiomatosis familiar. Actas Dermosifiliogr. 2014;105:531–532.</p>" ] ] "multimedia" => array:3 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 661 "Ancho" => 997 "Tamanyo" => 102326 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Segmentally distributed bluish plaque extending from the right groin along the medial aspect of the right thigh and leg to the right foot.</p>" ] ] 1 => array:7 [ "identificador" => "fig0010" "etiqueta" => "Figure 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 654 "Ancho" => 1000 "Tamanyo" => 110610 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Bluish nodule on the mother's right forearm.</p>" ] ] 2 => array:7 [ "identificador" => "fig0015" "etiqueta" => "Figure 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 699 "Ancho" => 1000 "Tamanyo" => 265071 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Histopathology of the mother's lesions showing presence of a new vascular formation in the deep dermis with large vascular lumens covered by glomus cells (hematoxylin-eosin, original magnification ×<span class="elsevierStyleHsp" style=""></span>40).</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:10 [ 0 => array:3 [ "identificador" => "bib0005" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "A rule concerning the segmental manifestation of autosomal dominant skin disorders: Review of clinical examples providing evidence for dichotomous types of severity" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:1 [ 0 => "R. Happle" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ "tituloSerie" => "Arch Dermatol" "fecha" => "1997" "volumen" => "133" "paginaInicial" => "1505" "paginaFinal" => "1509" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/9420534" "web" => "Medline" ] ] ] ] ] ] ] ] 1 => array:3 [ "identificador" => "bib0010" "etiqueta" => "2" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Congenital glomangioma of the breast: Type 2 segmental manifestation" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:5 [ 0 => "C. Munoz" 1 => "F. Bobadilla" 2 => "H. Fuenzalida" 3 => "R. Glodner" 4 => "B. Sina" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1111/j.1365-4632.2010.04565.x" "Revista" => array:6 [ "tituloSerie" => "Int J Dermatol" "fecha" => "2011" "volumen" => "50" "paginaInicial" => "346" "paginaFinal" => "349" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/21342169" "web" => "Medline" ] ] ] ] ] ] ] ] 2 => array:3 [ "identificador" => "bib0015" "etiqueta" => "3" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Type 2 segmental manifestation of multiple glomus tumors: A review and reclassification of 5 case reports" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:2 [ 0 => "R. Happle" 1 => "A. König" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "18128" "Revista" => array:6 [ "tituloSerie" => "Dermatology" "fecha" => "1999" "volumen" => "198" "paginaInicial" => "270" "paginaFinal" => "272" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/10393451" "web" => "Medline" ] ] ] ] ] ] ] ] 3 => array:3 [ "identificador" => "bib0020" "etiqueta" => "4" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Three cases of type 2 segmental manifestation of multiple glomus tumors: Association with linear multiple trichilemmal cyst in a patient" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:6 [ 0 => "A. Flórez" 1 => "C. Peteiro" 2 => "D. Sánchez-Aguilar" 3 => "V. Fernández-Redondo" 4 => "M. Pereiro Ferreirós" 5 => "J. Toribio" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "18324" "Revista" => array:6 [ "tituloSerie" => "Dermatology" "fecha" => "2000" "volumen" => "200" "paginaInicial" => "75" "paginaFinal" => "77" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/10681623" "web" => "Medline" ] ] ] ] ] ] ] ] 4 => array:3 [ "identificador" => "bib0025" "etiqueta" => "5" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Two cases of segmental multiple glomangiomas in a family: Type 1 or type 2 segemental manifestation?" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "C. Peña-Penabad" 1 => "J. García-Silva" 2 => "J. del Pozo" 3 => "M.T. Yebra-Pimentel" 4 => "E. Fonseca" 5 => "J. Cuevas" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "18435" "Revista" => array:6 [ "tituloSerie" => "Dermatology" "fecha" => "2000" "volumen" => "201" "paginaInicial" => "65" "paginaFinal" => "67" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/10971066" "web" => "Medline" ] ] ] ] ] ] ] ] 5 => array:3 [ "identificador" => "bib0030" "etiqueta" => "6" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Type 2 segmental manifestation of congenital miltiple glomangiomas" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:6 [ 0 => "C.J. Allombert-Blaise" 1 => "M.L. Batard" 2 => "M. Ségard" 3 => "E. Martin de Lasalle" 4 => "G.M. Brevière" 5 => "F. Piette" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "69944" "Revista" => array:6 [ "tituloSerie" => "Dermatology" "fecha" => "2003" "volumen" => "206" "paginaInicial" => "321" "paginaFinal" => "325" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/12771473" "web" => "Medline" ] ] ] ] ] ] ] ] 6 => array:3 [ "identificador" => "bib0035" "etiqueta" => "7" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Type 2 segmental glomangiomas" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:3 [ 0 => "R. Hoekzema" 1 => "I.M. Zonneveld" 2 => "A.C. Van der Wall" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:5 [ "tituloSerie" => "Dermatol Online J" "fecha" => "2010" "volumen" => "16" "paginaInicial" => "8" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/21199634" "web" => "Medline" ] ] ] ] ] ] ] ] 7 => array:3 [ "identificador" => "bib0040" "etiqueta" => "8" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Congenital glomangioma: Case report and review of the world literature" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:3 [ 0 => "S. Glick" 1 => "E.A. Markstein" 2 => "P. Herreid" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:5 [ "tituloSerie" => "Pediatric Dermatol" "fecha" => "1995" "volumen" => "12" "paginaInicial" => "242" "paginaFinal" => "244" ] ] ] ] ] ] 8 => array:3 [ "identificador" => "bib0045" "etiqueta" => "9" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Multiple congenital plaquelike glomuvenous malformations with type 2 segmental involvement" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:4 [ 0 => "M.A. Hazey" 1 => "A.J. Van Norman" 2 => "R.L. Powers" 3 => "D.L. Armistead" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ "tituloSerie" => "Cutis" "fecha" => "2009" "volumen" => "84" "paginaInicial" => "16" "paginaFinal" => "18" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/19743719" "web" => "Medline" ] ] ] ] ] ] ] ] 9 => array:3 [ "identificador" => "bib0050" "etiqueta" => "10" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Superimposed segmental manifestation of both rare and common cutaneous disorders: A new paradigm" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:1 [ 0 => "R. Happle" ] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:7 [ "tituloSerie" => "Actas Dermosifiliogr" "fecha" => "2009" "volumen" => "100" "numero" => "Suppl 1" "paginaInicial" => "77" "paginaFinal" => "85" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/20096200" "web" => "Medline" ] ] ] ] ] ] ] ] ] ] ] ] ] "idiomaDefecto" => "en" "url" => "/15782190/0000010500000005/v1_201405281018/S157821901400119X/v1_201405281018/en/main.assets" "Apartado" => array:4 [ "identificador" => "6157" "tipo" => "SECCION" "en" => array:2 [ "titulo" => "Case and Research Letters" "idiomaDefecto" => true ] "idiomaDefecto" => "en" ] "PDF" => "https://static.elsevier.es/multimedia/15782190/0000010500000005/v1_201405281018/S157821901400119X/v1_201405281018/en/main.pdf?idApp=UINPBA000044&text.app=https://www.actasdermo.org/" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S157821901400119X?idApp=UINPBA000044" ]
año/Mes | Html | Total | |
---|---|---|---|
2024 Noviembre | 18 | 18 | 36 |
2024 Octubre | 94 | 34 | 128 |
2024 Septiembre | 88 | 30 | 118 |
2024 Agosto | 141 | 53 | 194 |
2024 Julio | 107 | 38 | 145 |
2024 Junio | 109 | 26 | 135 |
2024 Mayo | 85 | 27 | 112 |
2024 Abril | 86 | 21 | 107 |
2024 Marzo | 74 | 24 | 98 |
2024 Febrero | 93 | 25 | 118 |
2024 Enero | 61 | 30 | 91 |
2023 Diciembre | 67 | 26 | 93 |
2023 Noviembre | 81 | 43 | 124 |
2023 Octubre | 100 | 35 | 135 |
2023 Septiembre | 88 | 32 | 120 |
2023 Agosto | 59 | 18 | 77 |
2023 Julio | 83 | 34 | 117 |
2023 Junio | 87 | 24 | 111 |
2023 Mayo | 83 | 26 | 109 |
2023 Abril | 72 | 31 | 103 |
2023 Marzo | 49 | 21 | 70 |
2023 Febrero | 62 | 24 | 86 |
2023 Enero | 49 | 40 | 89 |
2022 Diciembre | 74 | 43 | 117 |
2022 Noviembre | 39 | 29 | 68 |
2022 Octubre | 28 | 30 | 58 |
2022 Septiembre | 40 | 49 | 89 |
2022 Agosto | 35 | 35 | 70 |
2022 Julio | 33 | 37 | 70 |
2022 Junio | 35 | 33 | 68 |
2022 Mayo | 73 | 37 | 110 |
2022 Abril | 77 | 45 | 122 |
2022 Marzo | 94 | 55 | 149 |
2022 Febrero | 62 | 39 | 101 |
2022 Enero | 71 | 47 | 118 |
2021 Diciembre | 65 | 46 | 111 |
2021 Noviembre | 59 | 52 | 111 |
2021 Octubre | 51 | 50 | 101 |
2021 Septiembre | 43 | 32 | 75 |
2021 Agosto | 47 | 51 | 98 |
2021 Julio | 36 | 31 | 67 |
2021 Junio | 32 | 21 | 53 |
2021 Mayo | 32 | 18 | 50 |
2021 Abril | 69 | 65 | 134 |
2021 Marzo | 84 | 26 | 110 |
2021 Febrero | 68 | 29 | 97 |
2021 Enero | 42 | 22 | 64 |
2020 Diciembre | 40 | 19 | 59 |
2020 Noviembre | 30 | 16 | 46 |
2020 Octubre | 43 | 7 | 50 |
2020 Septiembre | 35 | 12 | 47 |
2020 Agosto | 21 | 18 | 39 |
2020 Julio | 18 | 23 | 41 |
2020 Junio | 42 | 27 | 69 |
2020 Mayo | 23 | 19 | 42 |
2020 Abril | 38 | 17 | 55 |
2020 Marzo | 34 | 15 | 49 |
2020 Febrero | 4 | 0 | 4 |
2020 Enero | 4 | 1 | 5 |
2019 Diciembre | 8 | 2 | 10 |
2019 Noviembre | 4 | 1 | 5 |
2019 Septiembre | 14 | 1 | 15 |
2019 Agosto | 4 | 1 | 5 |
2019 Julio | 2 | 5 | 7 |
2019 Junio | 6 | 15 | 21 |
2019 Mayo | 1 | 25 | 26 |
2019 Abril | 1 | 1 | 2 |
2019 Marzo | 2 | 4 | 6 |
2019 Enero | 1 | 1 | 2 |
2018 Diciembre | 2 | 5 | 7 |
2018 Noviembre | 9 | 0 | 9 |
2018 Octubre | 22 | 0 | 22 |
2018 Septiembre | 6 | 0 | 6 |
2018 Agosto | 0 | 3 | 3 |
2018 Julio | 0 | 1 | 1 |
2018 Junio | 0 | 3 | 3 |
2018 Mayo | 0 | 3 | 3 |
2018 Marzo | 0 | 4 | 4 |
2018 Febrero | 31 | 9 | 40 |
2018 Enero | 36 | 5 | 41 |
2017 Diciembre | 51 | 7 | 58 |
2017 Noviembre | 37 | 14 | 51 |
2017 Octubre | 34 | 7 | 41 |
2017 Septiembre | 38 | 11 | 49 |
2017 Agosto | 47 | 15 | 62 |
2017 Julio | 62 | 18 | 80 |
2017 Junio | 63 | 24 | 87 |
2017 Mayo | 48 | 12 | 60 |
2017 Abril | 46 | 20 | 66 |
2017 Marzo | 36 | 20 | 56 |
2017 Febrero | 32 | 14 | 46 |
2017 Enero | 26 | 18 | 44 |
2016 Diciembre | 39 | 12 | 51 |
2016 Noviembre | 58 | 17 | 75 |
2016 Octubre | 59 | 23 | 82 |
2016 Septiembre | 84 | 12 | 96 |
2016 Agosto | 76 | 11 | 87 |
2016 Julio | 36 | 10 | 46 |
2016 Junio | 13 | 8 | 21 |
2016 Mayo | 11 | 12 | 23 |
2016 Abril | 7 | 1 | 8 |
2016 Marzo | 4 | 10 | 14 |
2016 Febrero | 11 | 13 | 24 |
2016 Enero | 8 | 10 | 18 |
2015 Diciembre | 6 | 12 | 18 |
2015 Noviembre | 7 | 11 | 18 |
2015 Octubre | 11 | 1 | 12 |
2015 Septiembre | 6 | 4 | 10 |
2015 Agosto | 11 | 5 | 16 |
2015 Julio | 57 | 7 | 64 |
2015 Junio | 47 | 13 | 60 |
2015 Mayo | 37 | 15 | 52 |
2015 Abril | 25 | 8 | 33 |
2015 Marzo | 19 | 2 | 21 |
2015 Febrero | 28 | 4 | 32 |
2015 Enero | 23 | 4 | 27 |
2014 Diciembre | 29 | 7 | 36 |
2014 Noviembre | 22 | 5 | 27 |
2014 Octubre | 38 | 4 | 42 |
2014 Septiembre | 23 | 2 | 25 |
2014 Agosto | 22 | 4 | 26 |
2014 Julio | 22 | 6 | 28 |
2014 Junio | 20 | 6 | 26 |
2014 Mayo | 2 | 1 | 3 |