Fanconi syndrome associated with a non-ossifying fibroma of bone

A 20-year-old man presenting with osteomalacia was found to have the Fanconi syndrome, as evidenced by hypophosphatemia with hyperphosphaturia, glycosurla in the presence of normoglycemia, and generalized aminoaciduria. After removal of a non-ossifying fibroma of the left tibia, the renal tubular ab...

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Veröffentlicht in:	The American journal of medicine 1985-04, Vol.78 (4), p.708-710
Hauptverfasser:	Leehey, David J., Ing, Todd S., Daugirdas, John T.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult Biological and medical sciences Bone Neoplasms - blood Bone Neoplasms - complications Bone Neoplasms - surgery Diseases of the osteoarticular system Fanconi Syndrome - etiology Fibroma - blood Fibroma - complications Fibroma - surgery Humans Male Medical sciences Osteomalacia - etiology Phosphates - blood Tibia - surgery Tumors of striated muscle and skeleton
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Zusammenfassung:	A 20-year-old man presenting with osteomalacia was found to have the Fanconi syndrome, as evidenced by hypophosphatemia with hyperphosphaturia, glycosurla 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.
ISSN:	0002-9343 1555-7162
DOI:	10.1016/0002-9343(85)90419-X