Renal Involvement in Cystic Fibrosis: Diseases Spectrum and Clinical Relevance

被引:43
作者
Yahiaoui, Yasmina [1 ]
Jablonski, Mathieu [1 ]
Hubert, Dominique [2 ,3 ]
Mosnier-Pudar, Helen [4 ]
Noel, Laure-Helene [5 ]
Stern, Marc [6 ]
Grenet, Dominique [6 ]
Gruenfeld, Jean-Pierre [1 ]
Chauveau, Dominique [7 ,8 ]
Fakhouri, Fadi [1 ]
机构
[1] Univ Paris 05, Hop Necker, AP HP, Dept Nephrol, Paris, France
[2] Hop Cochin, AP HP, Dept Pulmonol, F-75674 Paris, France
[3] Hop Cochin, AP HP, Adult Cyst Fibrosis Ctr, F-75674 Paris, France
[4] Hop Cochin, AP HP, Dept Endocrinol, F-75674 Paris, France
[5] Hop Necker Enfants Malad, INSERM, U845, Paris, France
[6] Hop Foch, Dept Pulmonol, Suresnes, France
[7] Univ Toulouse 3, Dept Nephrol & Clin Immunol, CHU Rangueil, Ctr Reference Malad Renales Rares, F-31062 Toulouse, France
[8] Univ Toulouse 3, INSERM, CHU Rangueil, U563, F-31062 Toulouse, France
来源
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2009年 / 4卷 / 05期
关键词
MICROVASCULAR COMPLICATIONS; LUNG TRANSPLANTATION; GLOMERULONEPHRITIS; NEPHROPATHY;
D O I
10.2215/CJN.00750209
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background and objectives: Clinically relevant kidney involvement is uncommonly described in adult patients with cystic fibrosis (CF). We sought to report on a series of patients with CF and kidney biopsy- documented renal involvement. Design, setting, participants, & measurements: A retrospective study was undertaken in two referral centers for adult patients with CF in Paris, France. Patients who had undergone a biopsy of native kidneys between 1992 and 2008 were identified, and their medical records were reviewed. Results: We identified 13 adult patients with CF and renal disease. Proteinuria was present in all but two cases and was associated with progressive renal impairment in four patients (median serum creatinine 85 mu mol/L; range 53 to 144 mu mol/L). Renal biopsy disclosed a heterogeneous spectrum of nephropathies including AA amyloiclosis (n = 3), diabetic glomerulopathy (n = 3), FSGS (n = 2), minimal-change disease (n = 1), postinfectious glomerulortephritis (n = 1), IgA nephropathy related to Henoch-Schbnlein purpura (n = 1), membranous nephropathy (n = 1), and chronic interstitial nephropathy (n = 1). Chronic renal failure occurred in five patients, and one patient reached ESRD. Conclusions: Although rare, clinically significant renal disease may arise in young adult patients with CF. Given the wide spectrum of diseases that may be encountered, definite diagnosis by kidney biopsy is mandatory to optimize clinical treatment of these complex patients, particularly in the perspective of organ transplantation. Clin J Am Soc Nephrol 4: 921-928, 2009. doi: 10.2215/CJN.00750209
引用
收藏
页码:921 / 928
页数:8
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