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  Česky / Czech version Čes.-slov. Pediat., 58, 2003, No. 8, p. 503-506.
 
Idiopathic Osteolysis 
Schejbalová A., Trč T. 

Ortopedická klinika 2. LF UK a FN Motol - dětská a dospělá ortopedie a traumatologie, Praha přednosta doc. MUDr. T. Trč, CSc.
 


Summary:

       The authors present a survey of the idiopathic osteolysis syndrome. The case of a 14-year boy with idiopathic osteolysis of proximal half of the right humerus is described. The injury, reported in anamnesis occurred on the already pathologically changed terrain. The fracture was not healing: in contrast there was a gradual resorption of the bone. No hereditary disposition to the disease or to kidney affection was demonstrated, tumorous or inflammatory processes were excluded. Even hemangiomatosis or angiomatosis, which accompany the Gorham- Stout’s syndrome were not demonstrated. Eight months after the beginning of the disease a treatment with Calcitonin followed the progress of osteolysis to come to the halt. Paresis of brachial plexus of upper type was an accompanying clinical manifestation. The authors report that after several months there were no signs of reparation and a radical solution became necessary in the form of substitution of proximal half of humerus by the patient’s own fibula with proximal epiphysis being saved. The graft gradually healed up, the muscular strength improved and the paresis diminished. Four years later the patient is completely without complaints and no relapse of the disease occurred.

        Key words: idiopathic osteolysis, Gorham-Stout syndrome, therapy
       

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