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Báo cáo y học: Light chain deposition disease presenting as paroxysmal atrial fibrillation: a case report
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Báo cáo y học: "Light chain deposition disease presenting as paroxysmal atrial fibrillation: a case report"Journal of Medical Case Reports BioMed Central Open AccessCase reportLight chain deposition disease presenting as paroxysmal atrialfibrillation: a case reportFabio Fabbian*1, Nevio Stabellini1, Sergio Sartori2, Paola Tombesi2,Arrigo Aleotti3, Maurizio Bergami1, Simona Uggeri1, Adriana Galdi1,Christian Molino2 and Luigi Catizone1Address: 1Renal Unit, St. Anna Hospital, Ferrara, Italy, 2Internal Medicine, University of Ferrara, Ferrara, Italy and 3Electron Microscopy Service§University of Ferrara, Ferrara, ItalyEmail: Fabio Fabbian* - hrfabbia@tin.it; Nevio Stabellini - sbn@unife.it; Sergio Sartori - srs@unife.it; Paola Tombesi - srs@unife.it;Arrigo Aleotti - cme@unife.it; Maurizio Bergami - m.bergami@ospfe.it; Simona Uggeri - simonauggeri@lycos.it;Adriana Galdi - nefrologia.ferrara@email.it; Christian Molino - clinicamedica@unife.it; Luigi Catizone - l.catizone@ospfe.it* Corresponding authorPublished: 29 December 2007 Received: 21 June 2007 Accepted: 29 December 2007Journal of Medical Case Reports 2007, 1:187 doi:10.1186/1752-1947-1-187This article is available from: http://www.jmedicalcasereports.com/content/1/1/187© 2007 Fabbian et al; licensee BioMed Central Ltd.This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0),which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Introduction: Light chain deposition disease (LCDD) can involve the heart and cause severe heart failure. Cardiac involvement is usually described in the advanced stages of the disease. We report the case of a woman in whom restrictive cardiomyopathy due to LCDD presented with paroxysmal atrial fibrillation. Case presentation: A 55-year-old woman was admitted to our emergency department because of palpitations. In a recent blood test, serum creatinine was 1.4 mg/dl. She was found to have high blood pressure, left ventricular hypertrophy and paroxysmal atrial fibrillation. An ACE-inhibitor was prescribed but her renal function rapidly worsened and she was admitted to our nephrology unit. On admission serum creatinine was 9.4 mg/dl, potassium 6.8 mmol/l, haemoglobin 7.7 g/dl, N- terminal pro-brain natriuretic peptide 29894 pg/ml. A central venous catheter was inserted and haemodialysis was started. She underwent a renal biopsy which showed kappa LCDD. Bone marrow aspiration and bone biopsy demonstrated kappa light chain multiple myeloma. Echocardiographic findings were consistent with restrictive cardiomyopathy. Thalidomide and dexamethasone were prescribed, and a peritoneal catheter was inserted. Peritoneal dialysis has now been performed for 15 months without complications. Discussion: Despite the predominant tubular deposition of kappa light chain, in our patient the first clinical manifestation of LCDD was cardiac disease manifesting as atrial fibrillation and the correct diagnosis was delayed. The clinical management initially addressed the cardiovascular symptoms without paying sufficient attention to the pre-existing slight increase in our patients serum creatinine. However cardiac involvement is a quite uncommon presentation of LCDD, and this unusual case suggests that the onset of acute arrhythmias associated with restrictive cardiomyopathy and impaired renal function might be related to LCDD. Page 1 of 4 (page number not for citation purposes)Journal of Medical Case Reports 2007, 1:187 http://www.jmedicalcasereports.com/content/1/1/187 tion showed monoclonal kappa light chain in the urine.IntroductionLight chain deposition disease (LCCD) is a systemic dis- Echocardiography detected substan ...
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Báo cáo y học: "Light chain deposition disease presenting as paroxysmal atrial fibrillation: a case report"Journal of Medical Case Reports BioMed Central Open AccessCase reportLight chain deposition disease presenting as paroxysmal atrialfibrillation: a case reportFabio Fabbian*1, Nevio Stabellini1, Sergio Sartori2, Paola Tombesi2,Arrigo Aleotti3, Maurizio Bergami1, Simona Uggeri1, Adriana Galdi1,Christian Molino2 and Luigi Catizone1Address: 1Renal Unit, St. Anna Hospital, Ferrara, Italy, 2Internal Medicine, University of Ferrara, Ferrara, Italy and 3Electron Microscopy Service§University of Ferrara, Ferrara, ItalyEmail: Fabio Fabbian* - hrfabbia@tin.it; Nevio Stabellini - sbn@unife.it; Sergio Sartori - srs@unife.it; Paola Tombesi - srs@unife.it;Arrigo Aleotti - cme@unife.it; Maurizio Bergami - m.bergami@ospfe.it; Simona Uggeri - simonauggeri@lycos.it;Adriana Galdi - nefrologia.ferrara@email.it; Christian Molino - clinicamedica@unife.it; Luigi Catizone - l.catizone@ospfe.it* Corresponding authorPublished: 29 December 2007 Received: 21 June 2007 Accepted: 29 December 2007Journal of Medical Case Reports 2007, 1:187 doi:10.1186/1752-1947-1-187This article is available from: http://www.jmedicalcasereports.com/content/1/1/187© 2007 Fabbian et al; licensee BioMed Central Ltd.This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0),which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Introduction: Light chain deposition disease (LCDD) can involve the heart and cause severe heart failure. Cardiac involvement is usually described in the advanced stages of the disease. We report the case of a woman in whom restrictive cardiomyopathy due to LCDD presented with paroxysmal atrial fibrillation. Case presentation: A 55-year-old woman was admitted to our emergency department because of palpitations. In a recent blood test, serum creatinine was 1.4 mg/dl. She was found to have high blood pressure, left ventricular hypertrophy and paroxysmal atrial fibrillation. An ACE-inhibitor was prescribed but her renal function rapidly worsened and she was admitted to our nephrology unit. On admission serum creatinine was 9.4 mg/dl, potassium 6.8 mmol/l, haemoglobin 7.7 g/dl, N- terminal pro-brain natriuretic peptide 29894 pg/ml. A central venous catheter was inserted and haemodialysis was started. She underwent a renal biopsy which showed kappa LCDD. Bone marrow aspiration and bone biopsy demonstrated kappa light chain multiple myeloma. Echocardiographic findings were consistent with restrictive cardiomyopathy. Thalidomide and dexamethasone were prescribed, and a peritoneal catheter was inserted. Peritoneal dialysis has now been performed for 15 months without complications. Discussion: Despite the predominant tubular deposition of kappa light chain, in our patient the first clinical manifestation of LCDD was cardiac disease manifesting as atrial fibrillation and the correct diagnosis was delayed. The clinical management initially addressed the cardiovascular symptoms without paying sufficient attention to the pre-existing slight increase in our patients serum creatinine. However cardiac involvement is a quite uncommon presentation of LCDD, and this unusual case suggests that the onset of acute arrhythmias associated with restrictive cardiomyopathy and impaired renal function might be related to LCDD. Page 1 of 4 (page number not for citation purposes)Journal of Medical Case Reports 2007, 1:187 http://www.jmedicalcasereports.com/content/1/1/187 tion showed monoclonal kappa light chain in the urine.IntroductionLight chain deposition disease (LCCD) is a systemic dis- Echocardiography detected substan ...
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