Literature DB >> 18512082

Nephronophthisis-like nephritis associated with fibrous dysplasia of bone.

Justine Bacchetta1, Roland Chapurlat, Raymonde Bouvier, Corinne Antignac, Laurence Dubourg, Rémi Kohler, Pierre D Delmas, Pierre Cochat.   

Abstract

Nephronophthisis is a chronic tubulointerstitial nephritis with autosomal recessive inheritance whose evolution to end-stage renal disease is insidious but constant. Fibrous dysplasia of bone is characterized by focal replacement of normal bone and marrow with abnormal bone and fibrous tissue. We report on a young boy initially diagnosed with fibrous dysplasia of bone, who underwent renal investigation because of treatment with pamidronate. He presented with mild proteinuria (albuminuria/creatininuria 19 mg/mmol) and decreased glomerular filtration rate (GFR) (79 ml/min per 1.73 m(2) body surface area) leading to kidney biopsy, which showed nephronophthisis-like lesions, but neither NPHP1 gene deletion nor UMOD (uromodulin) mutation were identified. No association between fibrous dysplasia of bone and nephronophthisis has yet been described. Nephronophthisis-like nephritis associated with fibrous dysplasia of bone might represent a possible new syndrome in the nephronophthisis and medullary cystic kidney disease complex. However, a fortuitous association between these two conditions is also possible.

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Year:  2008        PMID: 18512082     DOI: 10.1007/s00467-008-0850-x

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.714


  19 in total

1.  Pamidronate treatment of bone fibrous dysplasia in nine children with McCune-Albright syndrome.

Authors:  R Lala; P Matarazzo; S Bertelloni; F Buzi; F Rigon; C de Sanctis
Journal:  Acta Paediatr       Date:  2000-02       Impact factor: 2.299

Review 2.  Fibrous dysplasia as a stem cell disease.

Authors:  Mara Riminucci; Isabella Saggio; Pamela Gehron Robey; Paolo Bianco
Journal:  J Bone Miner Res       Date:  2006-12       Impact factor: 6.741

3.  Hypophosphataemic osteomalacia in fibrous dysplasia.

Authors:  C E Dent; J M Gertner
Journal:  Q J Med       Date:  1976-07

Review 4.  Fibrous dysplasia. Pathophysiology, evaluation, and treatment.

Authors:  Matthew R DiCaprio; William F Enneking
Journal:  J Bone Joint Surg Am       Date:  2005-08       Impact factor: 5.284

5.  Sonographic measurements and appearance of normal kidneys in children.

Authors:  B K Han; D S Babcock
Journal:  AJR Am J Roentgenol       Date:  1985-09       Impact factor: 3.959

6.  Expression of FGF23 is correlated with serum phosphate level in isolated fibrous dysplasia.

Authors:  Keisuke Kobayashi; Yasuo Imanishi; Hiroyuki Koshiyama; Akimitsu Miyauchi; Kenichi Wakasa; Takehisa Kawata; Hitoshi Goto; Hirotsugu Ohashi; Hajime M Koyano; Ryuichi Mochizuki; Takami Miki; Masaaki Inaba; Yoshiki Nishizawa
Journal:  Life Sci       Date:  2005-12-07       Impact factor: 5.037

Review 7.  Minireview: GNAS: normal and abnormal functions.

Authors:  Lee S Weinstein; Jie Liu; Akio Sakamoto; Tao Xie; Min Chen
Journal:  Endocrinology       Date:  2004-08-26       Impact factor: 4.736

8.  Treatment of fibrous dysplasia of bone with intravenous pamidronate: long-term effectiveness and evaluation of predictors of response to treatment.

Authors:  R D Chapurlat; P Hugueny; P D Delmas; P J Meunier
Journal:  Bone       Date:  2004-07       Impact factor: 4.398

Review 9.  Pamidronate-induced nephrotoxic tubular necrosis--a case report.

Authors:  S Smetana; A Michlin; E Rosenman; A Biro; M Boaz; Z Katzir
Journal:  Clin Nephrol       Date:  2004-01       Impact factor: 0.975

10.  Renal phosphate wasting in fibrous dysplasia of bone is part of a generalized renal tubular dysfunction similar to that seen in tumor-induced osteomalacia.

Authors:  M T Collins; C Chebli; J Jones; H Kushner; M Consugar; P Rinaldo; S Wientroub; P Bianco; P G Robey
Journal:  J Bone Miner Res       Date:  2001-05       Impact factor: 6.741

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  1 in total

1.  A human ciliopathy with polycystic ovarian syndrome and multiple subcutaneous cysts: A rare case report.

Authors:  Kangan Tan; Peng Liu; Lili Pang; Wanna Yang; Fengqin Hou
Journal:  Medicine (Baltimore)       Date:  2018-12       Impact factor: 1.817

  1 in total

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