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El infiltrado linfoide destruía el parénquima dejando aislados túbulos residuales con dudosas imágenes de lesión linfoepitelial (C: H&E, ×20). La celularidad era monomorfa, de pequeño tamaño, contorno nuclear irregular, con nucléolo poco evidente y sin actividad mitótica significativa (D: H&E, ×40).</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Enoc Merino García, María Pilar Pérez del Barrio, Josefa Borrego Hinojosa, Francisco J. Borrego Utiel, María Carmen Sánchez Perales" "autores" => array:5 [ 0 => array:2 [ "nombre" => "Enoc" "apellidos" => "Merino García" ] 1 => array:2 [ "nombre" => "María Pilar" "apellidos" => "Pérez del Barrio" ] 2 => array:2 [ "nombre" => "Josefa" "apellidos" => "Borrego Hinojosa" ] 3 => array:2 [ "nombre" => "Francisco J." 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Borrego Utiel, María Carmen Sánchez Perales" "autores" => array:5 [ 0 => array:4 [ "nombre" => "Enoc" "apellidos" => "Merino García" "email" => array:1 [ 0 => "enocmerino@gmail.com" ] "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">*</span>" "identificador" => "cor0005" ] ] ] 1 => array:2 [ "nombre" => "María Pilar" "apellidos" => "Pérez del Barrio" ] 2 => array:2 [ "nombre" => "Josefa" "apellidos" => "Borrego Hinojosa" ] 3 => array:2 [ "nombre" => "Francisco J." "apellidos" => "Borrego Utiel" ] 4 => array:2 [ "nombre" => "María Carmen" "apellidos" => "Sánchez Perales" ] ] "afiliaciones" => array:1 [ 0 => array:2 [ "entidad" => "Unidad de Gestión Clínica de Nefrología, Complejo Hospitalario de Jaén, Jaén, Spain" "identificador" => "aff0005" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "<span class="elsevierStyleItalic">Corresponding author</span>." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Infiltración renal linfomatosa en paciente con síndrome nefrótico" ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0005" "etiqueta" => "Fig. 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1084 "Ancho" => 1417 "Tamanyo" => 485371 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Histological characteristics of the lymphoid infiltrates that affected both the renal parenchyma (A: H&E, ×10) and the perirenal tissue (B: H&E, ×10). The lymphoid infiltrate had destroyed the parenchyma, leaving isolated residual tubules with images that may suggest lymphoepithelial lesion (C: H&E, ×20). Cells were monomorphic, small in size, with an irregular nuclear outline, barely visible nucleolus and no significant mitotic activity (D: H&E, ×40).</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">We describe the case of a patient with renal disease associated with a B-cell lymphoid infiltrate, with no associated systemic disease and with the presence of monoclonal IgM-kappa paraprotein.</p><p id="par0010" class="elsevierStylePara elsevierViewall">Renal involvement is known to be associated with lymphoplasmacytic neoplasia and is not considered rare (14–34% depending on whether the biopsy is <span class="elsevierStyleItalic">pre mortem</span> or <span class="elsevierStyleItalic">post mortem</span>), but it often goes undiagnosed due to the absence of symptoms and sometimes the lack of biopsies performed in these patients.<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> However, the occurrence of primary low-grade B-cell lymphoma of mucosa-associated lymphoid tissue (MALT) is considered unusual.<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">2</span></a> These tumours were initially described by Isaacson and Wright<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a> in the gastrointestinal tract, and later in the thyroids, lungs and salivary glands. More recently, B-cell MALT lymphomas have been reported in a large variety of locations, including the urogenital tract, although as mentioned, their occurrence is very rare.<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a> The presence of a glomerular lesion associated with lymphoplasmacytic neoplasia is not uncommon, and could be the direct result of the lymphoplasmacytic disorder through deposition of a paraprotein (amyloid) or monoclonal immunoglobulin, or its origin could be mediated by an immune mechanism that causes membranoproliferative, membranous or minimal change glomerulonephritis (GN).<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a> There are reported cases of isolated renal involvement with no evidence of systemic disease, haematological malignancy or associated autoimmune disease which are sometimes associated with a serum monoclonal IgG or IgM-kappa component.<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">This patient was a 71-year-old man admitted because oedema. He had a 1-year history of hypertension and post-traumatic subdural haematoma drained 6 years earlier. Due to the presence of renal failure (serum creatinine 2.5<span class="elsevierStyleHsp" style=""></span>mg/dL) with of nephrotic syndrome (albumin: 1.9<span class="elsevierStyleHsp" style=""></span>g/dL; total cholesterol: 315<span class="elsevierStyleHsp" style=""></span>mg/dL; urinary protein: 6.6<span class="elsevierStyleHsp" style=""></span>g/24<span class="elsevierStyleHsp" style=""></span>h) and normal-sized kidneys by ultrasound, a renal biopsy was performed. Other additional tests showed elevated beta-2 microglobulin and lactate dehydrogenase, serum protein electrophoresis and immunofixation with the presence of monoclonal IgM-kappa gammopathy (monoclonal component 0.2<span class="elsevierStyleHsp" style=""></span>g/dL) and urine negative for Bence-Jones protein. During hospitalisation, the patient presented a deterioration in renal function (Cr 3.8<span class="elsevierStyleHsp" style=""></span>mg/dL). Treatment was therefore initiated with oral prednisone at a dose of 1.5<span class="elsevierStyleHsp" style=""></span>mg/kg/day plus diuretics (furosemide and spironolactone) and angiotensin II receptor blockers in an attempt to control the proteinuria.</p><p id="par0020" class="elsevierStylePara elsevierViewall">The renal biopsy (<a class="elsevierStyleCrossRefs" href="#fig0005">Figs. 1 and 2</a>) revealed the presence of: (1) dense lymphoid infiltrates, immunophenotypically atypical, suggestive of a low-grade B cell lymphoproliferative process, and (2) mesangioproliferative glomerulonephritis, with few exudative changes and no demonstrable immune deposits.</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">Given the biopsy findings and the presence of monoclonal IgM-kappa gammopathy, the haematology department was consulted to assess the presence of a possible chronic lymphoproliferative process that had associated renal infiltration, as the most likely cause of the symptoms. Iliac crest biopsy was performed, with a diagnosis of mixed mature B and T cell lymphoid infiltrate, probably reactive.</p><p id="par0030" class="elsevierStylePara elsevierViewall">The patient recovered renal function quickly with oral prednisone and diuretics, achieving normal renal function (1.1<span class="elsevierStyleHsp" style=""></span>mg/dL) and a reduction of proteinuria to 260<span class="elsevierStyleHsp" style=""></span>mg/day in 2 months, despite persistence of the monoclonal IgM-kappa component (0.1<span class="elsevierStyleHsp" style=""></span>g/dL). After 9 months of follow-up by nephrology and haematology departments, he continues to have no evidence of progression of the lymphoproliferative process, with normal renal function and persistence of the monoclonal IgM-kappa component (0.1–0.2<span class="elsevierStyleHsp" style=""></span>g/dL).</p><p id="par0035" class="elsevierStylePara elsevierViewall">In our case, there was no evidence (clinical, analytical or imaging tests) that made us suspect renal lymphoma. The biopsy was suggestive of a low-grade B cell lymphoproliferative process together with mesangioproliferative glomerulonephritis with no demonstrable immune deposits. The literature describes the association of lymphomas with numerous forms of glomerulonephritis: membranous GN,<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a> membranoproliferative GN<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">4,5</span></a> and minimal change GN.<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a> In many cases, like ours, the clinical presentation is determined by the renal disease associated with the lymphoproliferative process, presenting nephrotic proteinuria with or without associated renal insufficiency.<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a> Our patient started with nephrotic syndrome secondary to the presence of mesangioproliferative GN; therefore, the initiation of steroid treatment from the time at which we performed the renal biopsy and a favourable response to steroids resulted in the rapid recovery of renal function (Cr 1.1<span class="elsevierStyleHsp" style=""></span>mg/dL) with disappearance of the proteinuria (260<span class="elsevierStyleHsp" style=""></span>mg/day) in only 2 months.</p><p id="par0040" class="elsevierStylePara elsevierViewall">Following the result of the renal biopsy, the haematology department was consulted. Having ruled out an associated chronic lymphoproliferative process, and given the absence of symptoms, we decided to adopt a watch and wait approach with close follow up of the patient's clinical progress. After 9 months, the patient remained asymptomatic, with normal renal function and no proteinuria, with persistence of the monoclonal IgM-kappa component. Although the initial diagnosis suggested a poor short-term prognosis, the absence of systemic involvement seems to have contributed to a favourable outcome.</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: Merino García E, Pérez del Barrio MP, Borrego Hinojosa J, Borrego Utiel FJ, Sánchez Perales MC. Infiltración renal linfomatosa en paciente con síndrome nefrótico. Nefrologia. 2018;38:92–94.</p>" ] ] "multimedia" => array:2 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Fig. 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1084 "Ancho" => 1417 "Tamanyo" => 485371 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Histological characteristics of the lymphoid infiltrates that affected both the renal parenchyma (A: H&E, ×10) and the perirenal tissue (B: H&E, ×10). The lymphoid infiltrate had destroyed the parenchyma, leaving isolated residual tubules with images that may suggest lymphoepithelial lesion (C: H&E, ×20). Cells were monomorphic, small in size, with an irregular nuclear outline, barely visible nucleolus and no significant mitotic activity (D: H&E, ×40).</p>" ] ] 1 => array:7 [ "identificador" => "fig0010" "etiqueta" => "Fig. 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 1769 "Ancho" => 2333 "Tamanyo" => 1121028 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">The lymphoid population expressed CD20 and bcl-2, with negative staining for CD10 and other B lymphoid lineage markers. (A–C: immunohistochemistry technique indicated in figure, ×20). In preserved normal renal parenchyma, it can see lobular glomeruli with increased matrix and, to a lesser extent some mesangial cellularity with occasional images of endocapillary proliferation (D: H&E, ×40; E: PAS-diastase, ×40).</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" => "The spectrum of kidney involvement in lymphoma: a case report and review of the literature" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:4 [ 0 => "L.J. Cohen" 1 => "H.G. Reenke" 2 => "J.P. Laubach" 3 => "B.D. 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Year/Month | Html | Total | |
---|---|---|---|
2024 November | 7 | 8 | 15 |
2024 October | 52 | 38 | 90 |
2024 September | 76 | 22 | 98 |
2024 August | 80 | 60 | 140 |
2024 July | 70 | 26 | 96 |
2024 June | 58 | 33 | 91 |
2024 May | 87 | 29 | 116 |
2024 April | 72 | 42 | 114 |
2024 March | 92 | 18 | 110 |
2024 February | 82 | 39 | 121 |
2024 January | 69 | 23 | 92 |
2023 December | 64 | 34 | 98 |
2023 November | 74 | 42 | 116 |
2023 October | 71 | 30 | 101 |
2023 September | 102 | 28 | 130 |
2023 August | 64 | 26 | 90 |
2023 July | 102 | 32 | 134 |
2023 June | 72 | 24 | 96 |
2023 May | 90 | 33 | 123 |
2023 April | 67 | 21 | 88 |
2023 March | 60 | 29 | 89 |
2023 February | 53 | 36 | 89 |
2023 January | 69 | 28 | 97 |
2022 December | 85 | 54 | 139 |
2022 November | 88 | 51 | 139 |
2022 October | 84 | 59 | 143 |
2022 September | 97 | 59 | 156 |
2022 August | 63 | 57 | 120 |
2022 July | 48 | 44 | 92 |
2022 June | 60 | 41 | 101 |
2022 May | 80 | 49 | 129 |
2022 April | 88 | 61 | 149 |
2022 March | 66 | 70 | 136 |
2022 February | 46 | 49 | 95 |
2022 January | 63 | 38 | 101 |
2021 December | 48 | 48 | 96 |
2021 November | 62 | 33 | 95 |
2021 October | 56 | 53 | 109 |
2021 September | 77 | 33 | 110 |
2021 August | 45 | 45 | 90 |
2021 July | 63 | 33 | 96 |
2021 June | 38 | 28 | 66 |
2021 May | 58 | 48 | 106 |
2021 April | 123 | 58 | 181 |
2021 March | 60 | 58 | 118 |
2021 February | 43 | 31 | 74 |
2021 January | 41 | 25 | 66 |
2020 December | 40 | 16 | 56 |
2020 November | 30 | 14 | 44 |
2020 October | 34 | 23 | 57 |
2020 September | 28 | 21 | 49 |
2020 August | 36 | 26 | 62 |
2020 July | 31 | 21 | 52 |
2020 June | 21 | 22 | 43 |
2020 May | 48 | 19 | 67 |
2020 April | 28 | 15 | 43 |
2020 March | 28 | 12 | 40 |
2020 February | 41 | 24 | 65 |
2020 January | 38 | 22 | 60 |
2019 December | 47 | 19 | 66 |
2019 November | 45 | 17 | 62 |
2019 October | 26 | 13 | 39 |
2019 September | 29 | 17 | 46 |
2019 August | 35 | 23 | 58 |
2019 July | 32 | 26 | 58 |
2019 June | 31 | 26 | 57 |
2019 May | 36 | 14 | 50 |
2019 April | 91 | 49 | 140 |
2019 March | 44 | 20 | 64 |
2019 February | 48 | 22 | 70 |
2019 January | 46 | 20 | 66 |
2018 December | 127 | 42 | 169 |
2018 November | 219 | 22 | 241 |
2018 October | 154 | 14 | 168 |
2018 September | 95 | 22 | 117 |
2018 August | 84 | 16 | 100 |
2018 July | 76 | 15 | 91 |
2018 June | 83 | 18 | 101 |
2018 May | 92 | 11 | 103 |
2018 April | 67 | 11 | 78 |
2018 March | 93 | 12 | 105 |
2018 February | 72 | 8 | 80 |
2018 January | 44 | 6 | 50 |
2017 December | 49 | 4 | 53 |
2017 November | 47 | 9 | 56 |