| Literature DB >> 23325962 |
Hitesh Shah1, Marie Rousset, Federico Canavese.
Abstract
Congenital pseudarthrosis of the tibia (CPT) is a rare pathology, which is usually associated with neurofibromatosis type I. The natural history of the disease is extremely unfavorable and once a fracture occurs, there is a little or no tendency for the lesion to heal spontaneously. It is challenging to treat effectively this difficult condition and its possible complications. Treatment is mainly surgical and it aims to obtain a long term bone union, to prevent limb length discrepancies, to avoid mechanical axis deviation, soft tissue lesions, nearby joint stiffness, and pathological fracture. The key to get primary union is to excise hamartomatous tissue and pathological periosteum. Age at surgery, status of fibula, associated shortening, and deformities of leg and ankle play significant role in primary union and residual challenges after primary healing. Unfortunately, none of invasive and noninvasive methods have proven their superiority. Surgical options such as intramedullary nailing, vascularized fibula graft, and external fixator, have shown equivocal success rate in achieving primary union although they are often associated with acceptable results. Amputation must be reserved for failed reconstruction, severe limb length discrepancy and gross deformities of leg and ankle. Distinct advantages, complications, and limitation of each primary treatment as well as strategies to deal with potential complications have been described. Each child with CPT must be followed up till skeletal maturity to identify and rectify residual problems after primary healing.Entities:
Keywords: Congenital pseudarthrosis of the tibia; children; complications; surgery; treatment
Year: 2012 PMID: 23325962 PMCID: PMC3543877 DOI: 10.4103/0019-5413.104184
Source DB: PubMed Journal: Indian J Orthop ISSN: 0019-5413 Impact factor: 1.251
Figure 1Anteroposterior and lateral radiographs of a patient with CPT. Radiographs show thin and atrophic tibial bone, with a pointed distal fragment. The false joint is in the distal third of the shaft. The fibula is affected
Figure 2Anteroposterior radiographs of a patient with untreated CPT
Figure 3Pre (a, b) and postoperative (c, d) anteroposterior and lateral radiographs of a patient with CPT treated by intramedullary rod. Intramedullary rod provides stability and does not disturb distal tibial epiphysis
Figure 4Clinical photographs showing potential complications of CPT: Ankle valgus (a) and valgus of the distal tibial shaft (b)
Figure 5Flow chart showing treatment options according to the age at surgery: Less than 2 years, between 2 and 8 years, and over 8 years
Figure 6The flow chart showing the surgical options when dealing with normal and abnormal fibula (Pseudarthrosis or hypoplasia of the fibula is associated with CPT in two-thirds of the cases)