Literature DB >> 3985044

Fanconi syndrome associated with a non-ossifying fibroma of bone.

D J Leehey, T S Ing, J T Daugirdas.   

Abstract

A 20-year-old man presenting with osteomalacia was found to have the Fanconi syndrome, as evidenced by hypophosphatemia with hyperphosphaturia, glycosuria in the presence of normoglycemia, and generalized aminoaciduria. After removal of a non-ossifying fibroma of the left tibia, the renal tubular abnormalities promptly resolved with subsequent healing of the osteomalacia. A humoral factor released from the tumor may have caused the disorder in proximal renal tubular cell transport.

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Year:  1985        PMID： 3985044     DOI： 10.1016/0002-9343(85)90419-x

Source DB:  PubMed          Journal:  Am J Med        ISSN： 0002-9343            Impact factor:   4.965


  2 in total

1.  Oncogenic osteomalacia, raised FGF-23, and renal Fanconi syndrome.

Authors:  A G W Norden; R J C Laing; P Rowe; R J Unwin; O Wrong; A J Crisp
Journal:  QJM       Date:  2011-12-16

2.  Neurofibromatosis Type 1 With Cherubism-like Phenotype, Multiple Osteolytic Bone Lesions of Lower Extremities, and Alagille-syndrome: Case Report With Literature Survey.

Authors:  Reinhard E Friedrich; Jozef Zustin; Andreas M Luebke; Thorsten Rosenbaum; Martin Gosau; Christian Hagel; Felix K Kohlrusch; Ilse Wieland; Martin Zenker
Journal:  In Vivo       Date:  2021 May-Jun       Impact factor: 2.155
  2 in total

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