Abstract
We hereby present a case of massive allografting of the tibia in a 9-year-old girl with McCune-Albright syndrome. Total replacement of the diaphysis and preservation of growth plates on both ends of the tibia was performed. After 5 years of follow-up, the graft is still intact and growth plates are active. We discuss the current knowledge about this syndrome, intervention modalities, as well as advantages and disadvantages of massive allografting.
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