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and later in the thyroids&#44; lungs and salivary glands&#46; More recently&#44; B-cell MALT lymphomas have been reported in a large variety of locations&#44; including the urogenital tract&#44; although as mentioned&#44; their occurrence is very rare&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a> The presence of a glomerular lesion associated with lymphoplasmacytic neoplasia is not uncommon&#44; and could be the direct result of the lymphoplasmacytic disorder through deposition of a paraprotein &#40;amyloid&#41; or monoclonal immunoglobulin&#44; or its origin could be mediated by an immune mechanism that causes membranoproliferative&#44; membranous or minimal change glomerulonephritis &#40;GN&#41;&#46;<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&#44; haematological malignancy or associated autoimmune disease which are sometimes associated with a serum monoclonal IgG or IgM-kappa component&#46;<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&#46; He had a 1-year history of hypertension and post-traumatic subdural haematoma drained 6 years earlier&#46; Due to the presence of renal failure &#40;serum creatinine 2&#46;5<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#41; with of nephrotic syndrome &#40;albumin&#58; 1&#46;9<span class="elsevierStyleHsp" style=""></span>g&#47;dL&#59; total cholesterol&#58; 315<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#59; urinary protein&#58; 6&#46;6<span class="elsevierStyleHsp" style=""></span>g&#47;24<span class="elsevierStyleHsp" style=""></span>h&#41; and normal-sized kidneys by ultrasound&#44; a renal biopsy was performed&#46; Other additional tests showed elevated beta-2 microglobulin and lactate dehydrogenase&#44; serum protein electrophoresis and immunofixation with the presence of monoclonal IgM-kappa gammopathy &#40;monoclonal component 0&#46;2<span class="elsevierStyleHsp" style=""></span>g&#47;dL&#41; and urine negative for Bence-Jones protein&#46; During hospitalisation&#44; the patient presented a deterioration in renal function &#40;Cr 3&#46;8<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#41;&#46; Treatment was therefore initiated with oral prednisone at a dose of 1&#46;5<span class="elsevierStyleHsp" style=""></span>mg&#47;kg&#47;day plus diuretics &#40;furosemide and spironolactone&#41; and angiotensin II receptor blockers in an attempt to control the proteinuria&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">The renal biopsy &#40;<a class="elsevierStyleCrossRefs" href="#fig0005">Figs&#46; 1 and 2</a>&#41; revealed the presence of&#58; &#40;1&#41; dense lymphoid infiltrates&#44; immunophenotypically atypical&#44; suggestive of a low-grade B cell lymphoproliferative process&#44; and &#40;2&#41; mesangioproliferative glomerulonephritis&#44; with few exudative changes and no demonstrable immune deposits&#46;</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&#44; the haematology department was consulted to assess the presence of a possible chronic lymphoproliferative process that had associated renal infiltration&#44; as the most likely cause of the symptoms&#46; Iliac crest biopsy was performed&#44; with a diagnosis of mixed mature B and T cell lymphoid infiltrate&#44; probably reactive&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">The patient recovered renal function quickly with oral prednisone and diuretics&#44; achieving normal renal function &#40;1&#46;1<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#41; and a reduction of proteinuria to 260<span class="elsevierStyleHsp" style=""></span>mg&#47;day in 2 months&#44; despite persistence of the monoclonal IgM-kappa component &#40;0&#46;1<span class="elsevierStyleHsp" style=""></span>g&#47;dL&#41;&#46; After 9 months of follow-up by nephrology and haematology departments&#44; he continues to have no evidence of progression of the lymphoproliferative process&#44; with normal renal function and persistence of the monoclonal IgM-kappa component &#40;0&#46;1&#8211;0&#46;2<span class="elsevierStyleHsp" style=""></span>g&#47;dL&#41;&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">In our case&#44; there was no evidence &#40;clinical&#44; analytical or imaging tests&#41; that made us suspect renal lymphoma&#46; The biopsy was suggestive of a low-grade B cell lymphoproliferative process together with mesangioproliferative glomerulonephritis with no demonstrable immune deposits&#46; The literature describes the association of lymphomas with numerous forms of glomerulonephritis&#58; membranous GN&#44;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a> membranoproliferative GN<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">4&#44;5</span></a> and minimal change GN&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a> In many cases&#44; like ours&#44; the clinical presentation is determined by the renal disease associated with the lymphoproliferative process&#44; presenting nephrotic proteinuria with or without associated renal insufficiency&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a> Our patient started with nephrotic syndrome secondary to the presence of mesangioproliferative GN&#59; therefore&#44; 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 &#40;Cr 1&#46;1<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#41; with disappearance of the proteinuria &#40;260<span class="elsevierStyleHsp" style=""></span>mg&#47;day&#41; in only 2 months&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Following the result of the renal biopsy&#44; the haematology department was consulted&#46; Having ruled out an associated chronic lymphoproliferative process&#44; and given the absence of symptoms&#44; we decided to adopt a watch and wait approach with close follow up of the patient&#39;s clinical progress&#46; After 9 months&#44; the patient remained asymptomatic&#44; with normal renal function and no proteinuria&#44; with persistence of the monoclonal IgM-kappa component&#46; Although the initial diagnosis suggested a poor short-term prognosis&#44; the absence of systemic involvement seems to have contributed to a favourable outcome&#46;</p></span>"
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Letter to the Editor
Renal lymphomatous infiltration in patient with nefrotic syndrome
Infiltración renal linfomatosa en paciente con síndrome nefrótico
Enoc Merino García
Corresponding author
enocmerino@gmail.com

Corresponding author.
, María Pilar Pérez del Barrio, Josefa Borrego Hinojosa, Francisco J. Borrego Utiel, María Carmen Sánchez Perales
Unidad de Gestión Clínica de Nefrología, Complejo Hospitalario de Jaén, Jaén, Spain
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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Histological characteristics of the lymphoid infiltrates that affected both the renal parenchyma &#40;A&#58; H&#38;E&#44; &#215;10&#41; and the perirenal tissue &#40;B&#58; H&#38;E&#44; &#215;10&#41;&#46; The lymphoid infiltrate had destroyed the parenchyma&#44; leaving isolated residual tubules with images that may suggest lymphoepithelial lesion &#40;C&#58; H&#38;E&#44; &#215;20&#41;&#46; Cells were monomorphic&#44; small in size&#44; with an irregular nuclear outline&#44; barely visible nucleolus and no significant mitotic activity &#40;D&#58; H&#38;E&#44; &#215;40&#41;&#46;</p>"
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    "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&#44; with no associated systemic disease and with the presence of monoclonal IgM-kappa paraprotein&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">Renal involvement is known to be associated with lymphoplasmacytic neoplasia and is not considered rare &#40;14&#8211;34&#37; depending on whether the biopsy is <span class="elsevierStyleItalic">pre mortem</span> or <span class="elsevierStyleItalic">post mortem</span>&#41;&#44; but it often goes undiagnosed due to the absence of symptoms and sometimes the lack of biopsies performed in these patients&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">1</span></a> However&#44; the occurrence of primary low-grade B-cell lymphoma of mucosa-associated lymphoid tissue &#40;MALT&#41; is considered unusual&#46;<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&#44; and later in the thyroids&#44; lungs and salivary glands&#46; More recently&#44; B-cell MALT lymphomas have been reported in a large variety of locations&#44; including the urogenital tract&#44; although as mentioned&#44; their occurrence is very rare&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">3</span></a> The presence of a glomerular lesion associated with lymphoplasmacytic neoplasia is not uncommon&#44; and could be the direct result of the lymphoplasmacytic disorder through deposition of a paraprotein &#40;amyloid&#41; or monoclonal immunoglobulin&#44; or its origin could be mediated by an immune mechanism that causes membranoproliferative&#44; membranous or minimal change glomerulonephritis &#40;GN&#41;&#46;<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&#44; haematological malignancy or associated autoimmune disease which are sometimes associated with a serum monoclonal IgG or IgM-kappa component&#46;<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&#46; He had a 1-year history of hypertension and post-traumatic subdural haematoma drained 6 years earlier&#46; Due to the presence of renal failure &#40;serum creatinine 2&#46;5<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#41; with of nephrotic syndrome &#40;albumin&#58; 1&#46;9<span class="elsevierStyleHsp" style=""></span>g&#47;dL&#59; total cholesterol&#58; 315<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#59; urinary protein&#58; 6&#46;6<span class="elsevierStyleHsp" style=""></span>g&#47;24<span class="elsevierStyleHsp" style=""></span>h&#41; and normal-sized kidneys by ultrasound&#44; a renal biopsy was performed&#46; Other additional tests showed elevated beta-2 microglobulin and lactate dehydrogenase&#44; serum protein electrophoresis and immunofixation with the presence of monoclonal IgM-kappa gammopathy &#40;monoclonal component 0&#46;2<span class="elsevierStyleHsp" style=""></span>g&#47;dL&#41; and urine negative for Bence-Jones protein&#46; During hospitalisation&#44; the patient presented a deterioration in renal function &#40;Cr 3&#46;8<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#41;&#46; Treatment was therefore initiated with oral prednisone at a dose of 1&#46;5<span class="elsevierStyleHsp" style=""></span>mg&#47;kg&#47;day plus diuretics &#40;furosemide and spironolactone&#41; and angiotensin II receptor blockers in an attempt to control the proteinuria&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">The renal biopsy &#40;<a class="elsevierStyleCrossRefs" href="#fig0005">Figs&#46; 1 and 2</a>&#41; revealed the presence of&#58; &#40;1&#41; dense lymphoid infiltrates&#44; immunophenotypically atypical&#44; suggestive of a low-grade B cell lymphoproliferative process&#44; and &#40;2&#41; mesangioproliferative glomerulonephritis&#44; with few exudative changes and no demonstrable immune deposits&#46;</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&#44; the haematology department was consulted to assess the presence of a possible chronic lymphoproliferative process that had associated renal infiltration&#44; as the most likely cause of the symptoms&#46; Iliac crest biopsy was performed&#44; with a diagnosis of mixed mature B and T cell lymphoid infiltrate&#44; probably reactive&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">The patient recovered renal function quickly with oral prednisone and diuretics&#44; achieving normal renal function &#40;1&#46;1<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#41; and a reduction of proteinuria to 260<span class="elsevierStyleHsp" style=""></span>mg&#47;day in 2 months&#44; despite persistence of the monoclonal IgM-kappa component &#40;0&#46;1<span class="elsevierStyleHsp" style=""></span>g&#47;dL&#41;&#46; After 9 months of follow-up by nephrology and haematology departments&#44; he continues to have no evidence of progression of the lymphoproliferative process&#44; with normal renal function and persistence of the monoclonal IgM-kappa component &#40;0&#46;1&#8211;0&#46;2<span class="elsevierStyleHsp" style=""></span>g&#47;dL&#41;&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">In our case&#44; there was no evidence &#40;clinical&#44; analytical or imaging tests&#41; that made us suspect renal lymphoma&#46; The biopsy was suggestive of a low-grade B cell lymphoproliferative process together with mesangioproliferative glomerulonephritis with no demonstrable immune deposits&#46; The literature describes the association of lymphomas with numerous forms of glomerulonephritis&#58; membranous GN&#44;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a> membranoproliferative GN<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">4&#44;5</span></a> and minimal change GN&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">4</span></a> In many cases&#44; like ours&#44; the clinical presentation is determined by the renal disease associated with the lymphoproliferative process&#44; presenting nephrotic proteinuria with or without associated renal insufficiency&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">5</span></a> Our patient started with nephrotic syndrome secondary to the presence of mesangioproliferative GN&#59; therefore&#44; 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 &#40;Cr 1&#46;1<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#41; with disappearance of the proteinuria &#40;260<span class="elsevierStyleHsp" style=""></span>mg&#47;day&#41; in only 2 months&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Following the result of the renal biopsy&#44; the haematology department was consulted&#46; Having ruled out an associated chronic lymphoproliferative process&#44; and given the absence of symptoms&#44; we decided to adopt a watch and wait approach with close follow up of the patient&#39;s clinical progress&#46; After 9 months&#44; the patient remained asymptomatic&#44; with normal renal function and no proteinuria&#44; with persistence of the monoclonal IgM-kappa component&#46; Although the initial diagnosis suggested a poor short-term prognosis&#44; the absence of systemic involvement seems to have contributed to a favourable outcome&#46;</p></span>"
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        "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as&#58; Merino Garc&#237;a E&#44; P&#233;rez del Barrio MP&#44; Borrego Hinojosa J&#44; Borrego Utiel FJ&#44; S&#225;nchez Perales MC&#46; Infiltraci&#243;n renal linfomatosa en paciente con s&#237;ndrome nefr&#243;tico&#46; Nefrologia&#46; 2018&#59;38&#58;92&#8211;94&#46;</p>"
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Article information
ISSN: 20132514
Original language: English
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Idiomas
Nefrología (English Edition)
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