Lithium poisoning and proteinuria in the nephrotic range
Intoxicación por litio y proteinuria en rango nefrótico
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Polaina Rusillo, M.D. Sánchez Martos, G. Viedma Chamorro, I. Ruiz Ávila, V. Pérez Bañasco" "autores" => array:5 [ 0 => array:4 [ "Iniciales" => "M." "apellidos" => "Polaina Rusillo" "email" => array:1 [ 0 => "nefropolaina@yahoo.es" ] "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "affa" ] ] ] 1 => array:3 [ "Iniciales" => "M.D." "apellidos" => "Sánchez Martos" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "affa" ] ] ] 2 => array:3 [ "Iniciales" => "G." "apellidos" => "Viedma Chamorro" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "affa" ] ] ] 3 => array:3 [ "Iniciales" => "I." "apellidos" => "Ruiz Ávila" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "affa" ] ] ] 4 => array:3 [ "Iniciales" => "V." "apellidos" => "Pérez Bañasco" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "affa" ] ] ] ] "afiliaciones" => array:1 [ 0 => array:3 [ "entidad" => "Servicio de Nefrología. Servicio de Anatomía Patológica, Complejo Hospitalario de Jaén, Jaén, Jaén, España, " "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "affa" ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Intoxicación por litio y proteinuria en rango nefrótico" ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig1" "etiqueta" => "Fig. 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "copyright" => "Elsevier España" "figura" => array:1 [ 0 => array:4 [ "imagen" => "19218078_f1_p281.jpg" "Alto" => 203 "Ancho" => 259 "Tamanyo" => 14830 ] ] ] ] "textoCompleto" => "<p class="elsevierStylePara">Dear Editor:</p><p class="elsevierStylePara">The incidence of renal affectation in Systemic Sclerosis (SSc) is difficult to establish, because in the early stages and in its milder forms, the manifestations may be subclinical, and they may coincide with other pathologies, given the disease’s long evolution. We distinguish between three types of nephropathy: acute, chronic and overlap syndrome (associating scleroderma and other rheumatic illnesses).<span class="elsevierStyleSup">1-2</span></p><p class="elsevierStylePara"><span class="elsevierStyleBold">Clinical case</span></p><p class="elsevierStylePara">Male patient, aged 36 years with a history of SSc since 2000, bipolar disorder, terminal ileitis, consumer of alcohol and marijuana.</p><p class="elsevierStylePara">Underwent treatment with D-penicilamine for the SSc for several years, which was discontinued a year ago due to gastric distress. Usual treatment: nifedipine, deflazacort, lithium and olanzapine.</p><p class="elsevierStylePara">In January 2008, the patient was referred for renal failure (RF) study, due to recent presentation of plasma creatinine at about 2mg/dl, proteinuria 300mg/dl and hypoalbuminaemia 2.36g/dl.</p><p class="elsevierStylePara">Physical examination showed limited flexion of the fingers; the rest was normal. BP: 123/76mmHg.</p><p class="elsevierStylePara">Analytical tests showed: haemoglobin, 11.5g/dl; urea, 138; creatinine, 4.2; cholesterol 157mg/dl. Total proteins, 5.4; albumin 2.6g/dl. PTH, 119pg/mml. Widespectrum immunology screen negative except for ANCA-anti-MPO+. Proteinuria, 4.2g/día; sediment, 1,042 red blood cells per high-power field. Creatinine clearance 25ml/min. In studies prior to 2000, anti-scl 70 and ANA+ were prominent. The ultrasound showed kidneys measuring 11.5cm with an increase in cortical echogenicity.</p><p class="elsevierStylePara">Given the presence of RF and proteinuria in the nephrotic range, we started treatment with ramipril and recommended discontinuing the lithium.</p><p class="elsevierStylePara">15 days later, the patient came to the Emergency Room with nausea, vomiting, and abdominal pain that had been evolving over several days.He presented a lithaemia of 4.4 mEq/l,; crp 5.8; urea 178mg/dl. Hydration treatment was started, despite the fact that it increased lithaemia; for this reason, the patient underwent emergency haemodialysis. In subsequent checks, the lithaemia was below 1.5meq/l, so it was not necessary for him to undergo additional haemodialysis sessions.</p><p class="elsevierStylePara">As glomerular disease was suspected, we performed a kidney biopsy. The anatomical pathology showed 10 glomerules, of which two were sclerotic and six had focal and circumferential epithelial crescents and diffuse mesangial proliferation and capillary lumens obliteration with a mixed interstitial inflammatory infiltrate. Negative immunofluorescence test (figures 1 and 2).</p><p class="elsevierStylePara">We started immunosuppression with three methylprednisolone tablets, followed by 1mg prednisone/kg/day and 900mg of cyclophosphamide in a monthly bolus, and followed up on the patient.</p><p class="elsevierStylePara">We arrived at the clinical opinion that it was probably overlap syndrome scleroderma/vasculitis with ANCA-anti-MPO+ with stage IV CKD secondary to proliferative mesangial glomerulonephritis with extracapillary proliferation.</p><p class="elsevierStylePara"><span class="elsevierStyleBold">Discussion</span></p><p class="elsevierStylePara">Hybrid forms of scleroderma/ANCAvasculitis, sometimes associated with glomerulonephritis, are described in up to 10% of all cases. This overlap syndrome may occur after a period of treatment with D-penicilamine which varies from five months to five years. For some authors, this association represents a new entity that is related with this drug.Although our patient had gone at least a year without taking it, we can establish the hypothesis that the D-penicilamine could have acted latently as an antigenic factor, and then triggered the extracapillary form of vasculitis.<span class="elsevierStyleSup">3-7</span></p><p class="elsevierStylePara"><a href="grande/19218078_f1_p281.jpg" class="elsevierStyleCrossRefs"><img src="19218078_f1_p281.jpg"></img></a></p><p class="elsevierStylePara">Figure 1. </p><p class="elsevierStylePara"><a href="grande/19218078_f2_p281.jpg" class="elsevierStyleCrossRefs"><img src="19218078_f2_p281.jpg"></img></a></p><p class="elsevierStylePara">Figure 2. </p>" "pdfFichero" => "P-E-S-A192-EN.pdf" "tienePdf" => true "multimedia" => array:2 [ 0 => array:7 [ "identificador" => "fig1" "etiqueta" => "Fig. 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "copyright" => "Elsevier España" "figura" => array:1 [ 0 => array:4 [ "imagen" => "19218078_f1_p281.jpg" "Alto" => 203 "Ancho" => 259 "Tamanyo" => 14830 ] ] ] 1 => array:7 [ "identificador" => "fig2" "etiqueta" => "Fig. 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "copyright" => "Elsevier España" "figura" => array:1 [ 0 => array:4 [ "imagen" => "19218078_f2_p281.jpg" "Alto" => 210 "Ancho" => 260 "Tamanyo" => 16357 ] ] ] ] "bibliografia" => array:2 [ "titulo" => "Bibliography" "seccion" => array:1 [ 0 => array:1 [ "bibliografiaReferencia" => array:7 [ 0 => array:3 [ "identificador" => "bib1" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Tomioka M, Hinoshita F, Miyauchi N, Et al. ANCA-related crescentic glomerulonephritis in a patient with scleroderma without marked dermatological change and malig-migra hypertension. Intern Med 2004;43:496-502. <a href="http://www.ncbi.nlm.nih.gov/pubmed/15283187" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 1 => array:3 [ "identificador" => "bib2" "etiqueta" => "2" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Arnaud L, Huart A, Plaiser E, et al. Anca-relatec crescentic glomerulonephritis in systemic sclerosis: revisiting the normotensive scleroderma renal crisis. Clin Nephrol 2007;68:165-70. <a href="http://www.ncbi.nlm.nih.gov/pubmed/17915619" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 2 => array:3 [ "identificador" => "bib3" "etiqueta" => "3" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "NanKe Y, Akama H, Terai C, et al. Rapidly progressive glomerulonephritis with D-penicillamine. Am J Med 2000;320:398-402." "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 3 => array:3 [ "identificador" => "bib4" "etiqueta" => "4" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "García Porrua C, González Gay MA, Bouza P. D-penicillamine induced crescentic glomerulonephritis in a patient with scleroderma. Nephron 2000;84:101-2. <a href="http://www.ncbi.nlm.nih.gov/pubmed/10644924" target="_blank">[Pubmed]</a>" "contribucion" => array:1 [ 0 => null ] "host" => array:1 [ 0 => null ] ] ] ] 4 => array:3 [ "identificador" => "bib5" "etiqueta" => "5" "referencia" => array:1 [ 0 => array:3 [ "referenciaCompleta" => "Arunachalam R, Thiraviam K, Tholappan R, et al. Scleroderma with crescentic glomerulonephritis: a case report. J Med Case Reports 2008;13:151-5." 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| 2017 August | 33 | 9 | 42 |
| 2017 July | 28 | 16 | 44 |
| 2017 June | 27 | 7 | 34 |
| 2017 May | 37 | 15 | 52 |
| 2017 April | 30 | 26 | 56 |
| 2017 March | 27 | 38 | 65 |
| 2017 February | 19 | 5 | 24 |
| 2017 January | 15 | 4 | 19 |
| 2016 December | 46 | 10 | 56 |
| 2016 November | 48 | 10 | 58 |
| 2016 October | 52 | 10 | 62 |
| 2016 September | 90 | 3 | 93 |
| 2016 August | 141 | 3 | 144 |
| 2016 July | 104 | 6 | 110 |
| 2016 June | 111 | 0 | 111 |
| 2016 May | 121 | 0 | 121 |
| 2016 April | 75 | 0 | 75 |
| 2016 March | 58 | 0 | 58 |
| 2016 February | 77 | 0 | 77 |
| 2016 January | 85 | 0 | 85 |
| 2015 December | 80 | 0 | 80 |
| 2015 November | 57 | 0 | 57 |
| 2015 October | 54 | 0 | 54 |
| 2015 September | 54 | 0 | 54 |
| 2015 August | 63 | 0 | 63 |
| 2015 July | 64 | 0 | 64 |
| 2015 June | 37 | 0 | 37 |
| 2015 May | 39 | 0 | 39 |
| 2015 April | 5 | 0 | 5 |
Show all
