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12 years old girl, a known case of Neurofibromatosis Type 1, presented with shortening and deformity of Left leg since birth. Her Xrays revealed Left Congenital Pseudarthrosis of Tibia. She had undergone six surgeries elsewhere but her pseudarthrosis had failed to heal.


Congenital Pseudarthrosis of Tibia


She underwent surgery by our new comprehensive protocol for pseudarthrosis excision, fixation with rod and plate, and bone grafting.


Congenital Pseudarthrosis of Tibia


At two years post-operative, the pseudarthrosis has healed and deformity is corrected.





A one year old female child presents with antero-lateral bowing of Right tibia bone.


Congenital Pseudarthrosis of Tibia


The lesion progressed to a frank fracture (CPT) by age 2 years.



The child was operated by our new comprehensive protocol.


Congenital Pseudarthrosis of Tibia CPT


At 2 years post-operative, the pseudarthrosis has solidly healed, deformity if fully corrected and child is fully functional.


Congenital Pseudarthrosis of Tibia




Congenital Pseudarthrosis of Tibia (CPT) is an extremely rare condition and occurs in 1 in 1,50,000 children. In 50% cases, CPT is associated with a genetic condition called Neurofibromatosis Type 1.


In this condition, the leg bone (tibia) is usually bowed at birth but progresses to frank fracture (pseudarthrosis) by age of 2 years.


Treatment of CPT is always surgical. Traditional treatment methods were associated with significant difficulty in achieving union, and, multiple surgeries were often needed for achieving union.


However, in recent years, we have been using a new treatment protocol with excellent success rate. The results of our technique have been peer-reviewed and published in the Indian Journal of Orthopaedics (see Reference below).




Vaidya Sandeep V, Aroojis A, Mehta R, Agashe MV, Dhawale A, Bansal AV, Sarathy K. Short Term Results of a New Comprehensive Protocol for the Management of Congenital Pseudarthrosis of the Tibia. Indian J Orthop. 2019 Nov-Dec;53(6):736-744. doi: 10.4103/ortho.IJOrtho_155_19. PMID: 31673175; PMCID: PMC6804390.