Scientific letter
Mantle cell lymphoma: A rare cause of colon polyposis
Linfoma de células del manto: una causa rara de poliposis colónica
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Immunohistochemistry showing positive stain for cyclin D1.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Emanuel Dias, Margarida Marques, Daniel Melo, Guilherme Macedo" "autores" => array:4 [ 0 => array:2 [ "nombre" => "Emanuel" "apellidos" => "Dias" ] 1 => array:2 [ "nombre" => "Margarida" "apellidos" => "Marques" ] 2 => array:2 [ "nombre" => "Daniel" "apellidos" => "Melo" ] 3 => array:2 [ "nombre" => "Guilherme" "apellidos" => "Macedo" ] ] ] ] ] "idiomaDefecto" => "en" "Traduccion" => array:1 [ "en" => array:9 [ "pii" => "S0210570520303307" "doi" => "10.1016/j.gastrohep.2020.06.036" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0210570520303307?idApp=UINPBA00004N" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2444382421001139?idApp=UINPBA00004N" "url" => "/24443824/0000004400000005/v1_202105140801/S2444382421001139/v1_202105140801/en/main.assets" ] ] "itemSiguiente" => array:19 [ "pii" => "S0210570520302739" "issn" => "02105705" "doi" => "10.1016/j.gastrohep.2020.06.012" "estado" => "S300" "fechaPublicacion" => "2021-05-01" "aid" => "1608" "copyright" => "Elsevier España, S.L.U." "documento" => "article" "crossmark" => 1 "subdocumento" => "sco" "cita" => "Gastroenterol Hepatol. 2021;44:380-1" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:1 [ "total" => 0 ] "es" => array:11 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Imagen del mes</span>" "titulo" => "Úlcera colónica como hallazgo infrecuente de mastocitosis" "tienePdf" => "es" "tieneTextoCompleto" => "es" "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "380" "paginaFinal" => "381" ] ] "titulosAlternativos" => array:1 [ "en" => array:1 [ "titulo" => "Colonic ulcer as an uncommon finding of mastocytosis" ] ] "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" => 886 "Ancho" => 1500 "Tamanyo" => 565050 ] ] "descripcion" => array:1 [ "es" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Anatomía patológica: A y B) Hematoxilina-eosina ×10 y ×40: mucosa con ensanchamiento de la lámina propia, celularidad de amplio núcleo redondeado y basófilo. C) C-kit (CD117) ×20: tinción inmunohistoquímica citoplasmática con práctica totalidad de la celularidad inflamatoria (mastocitos).</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Carmen Pradera Cibreiro, Marta Ramos Alonso, Jose Ángel Vázquez Bueno, Gema Molina Arriero" "autores" => array:4 [ 0 => array:2 [ "nombre" => "Carmen" "apellidos" => "Pradera Cibreiro" ] 1 => array:2 [ "nombre" => "Marta" "apellidos" => "Ramos Alonso" ] 2 => array:2 [ "nombre" => "Jose Ángel" "apellidos" => "Vázquez Bueno" ] 3 => array:2 [ "nombre" => "Gema" "apellidos" => "Molina Arriero" ] ] ] ] ] "idiomaDefecto" => "es" "Traduccion" => array:1 [ "en" => array:9 [ "pii" => "S2444382421000985" "doi" => "10.1016/j.gastre.2020.06.026" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2444382421000985?idApp=UINPBA00004N" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0210570520302739?idApp=UINPBA00004N" "url" => "/02105705/0000004400000005/v1_202104280833/S0210570520302739/v1_202104280833/es/main.assets" ] "itemAnterior" => array:19 [ "pii" => "S0210570520303575" "issn" => "02105705" "doi" => "10.1016/j.gastrohep.2020.07.014" "estado" => "S300" "fechaPublicacion" => "2021-05-01" "aid" => "1652" "copyright" => "Elsevier España, S.L.U." 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"tienePdf" => "es" "tieneTextoCompleto" => "es" "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "376" "paginaFinal" => "377" ] ] "titulosAlternativos" => array:1 [ "en" => array:1 [ "titulo" => "Lynch-like syndrome: Lynch syndrome without known mutation?" ] ] "contieneTextoCompleto" => array:1 [ "es" => true ] "contienePdf" => array:1 [ "es" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figura 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1899 "Ancho" => 2500 "Tamanyo" => 955472 ] ] "descripcion" => array:1 [ "es" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Imagen histológica a 10 aumentos que en la tinción inmunohistoquímica muestra pérdida de expresión nuclear en MLH1 y PMS2 (fotos superiores) con expresión nuclear intacta para MSH2 y MSH6 (fotos inferiores).</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Luisa Adán-Merino, Fátima Valentín-Gómez, Seidi Tirado-Zambrana, Celia Zaera-de la Fuente, Olivia Crivillén-Anguita, Mercedes Aldeguer-Martínez" "autores" => array:6 [ 0 => array:2 [ "nombre" => "Luisa" "apellidos" => "Adán-Merino" ] 1 => array:2 [ "nombre" => "Fátima" "apellidos" => "Valentín-Gómez" ] 2 => array:2 [ "nombre" => "Seidi" "apellidos" => "Tirado-Zambrana" ] 3 => array:2 [ "nombre" => "Celia" "apellidos" => "Zaera-de la Fuente" ] 4 => array:2 [ "nombre" => "Olivia" "apellidos" => "Crivillén-Anguita" ] 5 => array:2 [ "nombre" => "Mercedes" "apellidos" => "Aldeguer-Martínez" ] ] ] ] ] "idiomaDefecto" => "es" "Traduccion" => array:1 [ "en" => array:9 [ "pii" => "S2444382421001000" "doi" => "10.1016/j.gastre.2020.07.009" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2444382421001000?idApp=UINPBA00004N" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0210570520303575?idApp=UINPBA00004N" "url" => "/02105705/0000004400000005/v1_202104280833/S0210570520303575/v1_202104280833/es/main.assets" ] "en" => array:14 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Scientific letter</span>" "titulo" => "Mantle cell lymphoma: A rare cause of colon polyposis" "tieneTextoCompleto" => true "saludo" => "Dear Editor:" "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "377" "paginaFinal" => "379" ] ] "autores" => array:1 [ 0 => array:4 [ "autoresLista" => "Emanuel Dias, Margarida Marques, Daniel Melo, Guilherme Macedo" "autores" => array:4 [ 0 => array:4 [ "nombre" => "Emanuel" "apellidos" => "Dias" "email" => array:1 [ 0 => "ea.dias91@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" => "Margarida" "apellidos" => "Marques" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] ] ] 2 => array:3 [ "nombre" => "Daniel" "apellidos" => "Melo" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] ] ] 3 => array:3 [ "nombre" => "Guilherme" "apellidos" => "Macedo" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] ] ] ] "afiliaciones" => array:2 [ 0 => array:3 [ "entidad" => "Gastroenterology Department, Centro Hospitalar de São João, Porto, Portugal" "etiqueta" => "a" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "Pathology Department, Centro Hospitalar de São João, Porto, Portugal" "etiqueta" => "b" "identificador" => "aff0010" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Linfoma de células del manto: una causa rara de poliposis colónica" ] ] "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" => 1197 "Ancho" => 1500 "Tamanyo" => 315438 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">A Multiple small yellowish polyps covered by normal mucosa were found along all colonic segments, from cecal region to rectum. B. A large polypoid lesion with approximately 25<span class="elsevierStyleHsp" style=""></span>mm was identified at the cecum and removed by endoscopic mucosal resection. C. A monomorphic infiltration of mucosa and submucosa by small-sized atypical lymphoid cells may be seen. These cells are characterized by irregular nuclei and scant cytoplasm and demonstrate a nodular infiltrative growth pattern (HE, 200×). D. Immunohistochemistry showing positive stain for cyclin D1.</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Colon lymphoma is uncommon, representing only 0.2–1.2% of all colonic neoplasms. The most common histological subtype is mantle cell lymphoma, followed by large B-cell diffuse lymphoma, with other types being less common. Clinical manifestations are non-specific and the endoscopic appearance is highly variable, possibly presenting as diffuse infiltration, a single mass or polyps but also with normal mucosa. There is a high rate of morbidity and mortality.<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">We report a case of a 67-year-old female with previous medical history of diabetes mellitus and dyslipidemia who performed a screening colonoscopy, where multiple sessile polyps (at least 20) were found along all colon segments, from cecal region to rectum. These polyps were covered by normal mucosa and had diameter between 10–20<span class="elsevierStyleHsp" style=""></span>mm (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>A). One single polyp removed from ascending colon was histologically hyperplastic. She was asymptomatic and physical examination was normal. Hemogram, albumin, lactate dehydrogenase, urea, creatinine, electrolyte levels and coagulation studies were all normal. Her last colonoscopy performed 8 years earlier was normal. Two sisters had history of colorectal cancer. Because the cause of polyposis was not clear and there was family history of neoplasia, colonoscopy was repeated. At this time, three polyps from transverse colon and a large cecal polypoid lesion (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>B) were resected. Histopathological examination revealed diffuse nodular infiltration by small-sized atypical lymphoid cells with irregular nuclei and scant cytoplasm involving mucosa and submucosa (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>C). Immunohistochemical staining was positive for CD20, CD5 and cyclin D1 (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>D) and negative for CD3 and CD10. Diagnosis of mantle cell lymphoma presenting as multiple lymphomatoid polyposis was established. Computed tomography and positron emission tomography revealed involvement of intra- and extra-abdominal lymph nodes, spleen and Waldeyer's ring, besides gastrointestinal tract, consistent with stage IV of Ann-arbor staging system. She was referred for chemotherapy with rituximab plus bendamustine.</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Mantle cell lymphoma is a rare and aggressive B-cell non-Hodgkin lymphoma, characterized by chromosomal translocation t(11;14) and cyclin D1 overexpression. On immunohistochemistry, tumor cells are characteristically CD5 and pan B-cell antigen positive (CD19, CD20, CD22) and negative for the expression of CD10 and CD23. This type of lymphoma more commonly affects males and usually presents in the fifth or sixth decades of life.<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">Gastrointestinal involvement occurs in 5–20% of cases, usually as multiple lymphomatoid polyposis, with multiple polyps involved by lymphoproliferative disease along one or more segments of gastrointestinal tract.<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a> The most commonly affected segments are colon and rectum, followed by small intestine, stomach and duodenum.<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a> Less commonly, it may present as a single mass mimicking adenocarcinoma.<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a> Symptoms of abdominal pain, diarrhea or hematochezia are usually present. Most patients present at advanced stage with extra-intestinal involvement. The main extra digestive sites affected are the bone marrow, peripheral lymph nodes, Waldeyer's ring and liver.<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">The current therapeutic approach is based on clinical risk factors, symptoms, patient characteristics and stage of disease. For patients in good condition who are younger than 65 years of age, intensive frontline immunochemotherapy induction regimen combining rituximab with cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) and high dose of cytarabine followed by autologous stem cell transplantation is recommended. For the group of elderly patients or in poor health condition not eligible for autologous stem cell transplantation, conventional immunochemotherapy (e.g. R-CHOP) followed by maintenance with rituximab, appears to be ‘gold standard’.<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">3,4</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">Unfortunately, despite high response rate to intensive chemotherapy regimens which usually results in regression of macroscopic and sometimes microscopic lesions, remissions are usually short, relapse rate is high and median survival is only 3–4 years.<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a> Poor prognostic factors include unsatisfactory general clinical condition, involvement of multiple extranodal sites, advanced age (older than 70 years), elevated lactate dehydrogenase levels and bone marrow infiltration.<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">In conclusion, although uncommon, lymphoproliferative diseases should be considered in the differential diagnosis of gastrointestinal polyposis, especially at advanced age. This case demonstrates that advanced stage lymphomas may present as multiple lymphomatous polyposis without producing gastrointestinal symptoms and that other types of polyps may occasionally develop in the middle of lymphomatous polyps. Therefore, absence of symptoms and incidental finding of a benign polyp do not preclude this ominous diagnosis.</p></span>" "pdfFichero" => "main.pdf" "tienePdf" => true "multimedia" => array:1 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1197 "Ancho" => 1500 "Tamanyo" => 315438 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">A Multiple small yellowish polyps covered by normal mucosa were found along all colonic segments, from cecal region to rectum. B. A large polypoid lesion with approximately 25<span class="elsevierStyleHsp" style=""></span>mm was identified at the cecum and removed by endoscopic mucosal resection. C. A monomorphic infiltration of mucosa and submucosa by small-sized atypical lymphoid cells may be seen. These cells are characterized by irregular nuclei and scant cytoplasm and demonstrate a nodular infiltrative growth pattern (HE, 200×). D. Immunohistochemistry showing positive stain for cyclin D1.</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0015" "bibliografiaReferencia" => array:5 [ 0 => array:3 [ "identificador" => "bib0030" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Colon lymphomas: an analysis of our experience over the last 23 years" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:6 [ 0 => "V. Martin Dominguez" 1 => "J. 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Oliveira" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1016/j.bjhh.2016.11.005" "Revista" => array:6 [ "tituloSerie" => "Rev Bras Hematol Hemoter" "fecha" => "2017" "volumen" => "39" "paginaInicial" => "73" "paginaFinal" => "76" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/28270353" "web" => "Medline" ] ] ] ] ] ] ] ] 3 => array:3 [ "identificador" => "bib0045" "etiqueta" => "4" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Extensive colorectal lymphomatous polyposis complicated by acute intestinal obstruction: a case report" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "J. Waisberg" 1 => "A.D.V. Anderi" 2 => "P.A.S. Cardoso" 3 => "J.H.M. Borducchi" 4 => "D.E. Germini" 5 => "M.I.F. Franco" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1186/s13256-017-1340-1" "Revista" => array:5 [ "tituloSerie" => "J Med Case Rep" "fecha" => "2017" "volumen" => "11" "paginaInicial" => "190" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/28705174" "web" => "Medline" ] ] ] ] ] ] ] ] 4 => array:3 [ "identificador" => "bib0050" "etiqueta" => "5" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Primary gastrointestinal tract mantle cell lymphoma as multiple lymphomatous polyposis" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:2 [ 0 => "A. Ruskone-Fourmestraux" 1 => "J. Audouin" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1016/j.bpg.2009.12.001" "Revista" => array:6 [ "tituloSerie" => "Best Pract Res Clin Gastroenterol" "fecha" => "2010" "volumen" => "24" "paginaInicial" => "35" "paginaFinal" => "42" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/20206107" "web" => "Medline" ] ] ] ] ] ] ] ] ] ] ] ] ] "idiomaDefecto" => "en" "url" => "/02105705/0000004400000005/v1_202104280833/S0210570520303307/v1_202104280833/en/main.assets" "Apartado" => array:4 [ "identificador" => "9030" "tipo" => "SECCION" "es" => array:2 [ "titulo" => "Cartas científicas" "idiomaDefecto" => true ] "idiomaDefecto" => "es" ] "PDF" => "https://static.elsevier.es/multimedia/02105705/0000004400000005/v1_202104280833/S0210570520303307/v1_202104280833/en/main.pdf?idApp=UINPBA00004N&text.app=https://www.elsevier.es/" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0210570520303307?idApp=UINPBA00004N" ]
| Year/Month | Html | Total | |
|---|---|---|---|
| 2024 November | 19 | 4 | 23 |
| 2024 October | 71 | 0 | 71 |
| 2024 September | 50 | 2 | 52 |
| 2024 August | 50 | 7 | 57 |
| 2024 July | 65 | 3 | 68 |
| 2024 June | 31 | 8 | 39 |
| 2024 May | 49 | 4 | 53 |
| 2024 April | 34 | 5 | 39 |
| 2024 March | 54 | 2 | 56 |
| 2024 February | 69 | 3 | 72 |
| 2024 January | 54 | 3 | 57 |
| 2023 December | 42 | 0 | 42 |
| 2023 November | 55 | 5 | 60 |
| 2023 October | 50 | 6 | 56 |
| 2023 September | 14 | 1 | 15 |
| 2023 August | 21 | 0 | 21 |
| 2023 July | 11 | 1 | 12 |
| 2023 June | 24 | 2 | 26 |
| 2023 May | 43 | 0 | 43 |
| 2023 March | 2 | 1 | 3 |
| 2022 December | 1 | 0 | 1 |
| 2022 November | 3 | 3 | 6 |
| 2022 October | 6 | 5 | 11 |
| 2022 September | 5 | 4 | 9 |
| 2022 August | 5 | 5 | 10 |
| 2022 July | 2 | 2 | 4 |
| 2022 June | 1 | 2 | 3 |
| 2021 September | 1 | 0 | 1 |
| 2021 July | 1 | 0 | 1 |
| 2021 June | 1 | 0 | 1 |
| 2021 May | 1 | 1 | 2 |
| 2021 April | 4 | 4 | 8 |
Show all
