Revascularization of the necrotic femoral head after traumatic open anterior hip dislocation in a child: a case report
Avascular necrosis of the femoral capital epiphysis is the most serious complication after traumatic dislocation of the hip in children. This case report discusses the localization and revascularization of the necrotic femoral head following rarely experienced traumatic open anterior hip dislocation in children.
Our patient was an 11-year-old Japanese boy who had open anterior hip dislocation sustained in a traffic accident. Reduction of the hip joint was performed in an emergency operation, and he was evaluated using serial gadolinium-enhanced magnetic resonance imaging. T1-weighted magnetic resonance images showed two bands with low signal intensity in the femoral capital epiphysis on coronal and oblique axial planes, indicating the existence of avascular osteonecrosis of the femoral head. We observed gadolinium enhancement in the central region of the epiphysis, where the area between the two bands with low signal intensity was located. Serial assessment with enhanced magnetic resonance images during a non-weight-bearing period of 1.5 years after injury showed revascularization starting from the central region and converging toward the peripheral region. Although the patient had leg-length discrepancy due to the early epiphyseal closure, non-weight-bearing treatment for the avascular osteonecrosis of the femoral head achieved a favorable outcome without any hip joint dysfunction, pain, or sign of secondary osteoarthritic change within 4.5 years after injury.
We confirmed the revascularization process of the necrotic lesion in the femoral capital epiphysis in an 11-year-old boy using serial gadolinium-enhanced magnetic resonance imaging. Conservative non-weight-bearing treatment achieved a favorable outcome.
KeywordsRevascularization Ischemic osteonecrosis Femoral head Traumatic hip dislocation
Magnetic resonance imaging
Avascular necrosis of the femoral capital epiphysis is the most serious and feared complication after traumatic dislocation of the hip in children; treatment of the severely collapsed femoral head is challenging because it is often unsalvageable [1, 2, 3, 4, 5, 6, 7, 8, 9, 10]. Femoral head collapse causes pain and juvenile end-stage osteoarthritis, which leads to serious hip dysfunction. Therefore, postreduction treatment for ischemic necrosis plays a key role in preventing or minimizing development of femoral head collapse.
Herrera-Soto et al.  reported that children younger than age 12 years who develop osteonecrosis after traumatic hip dislocation will develop femoral head changes such as those seen with Legg-Calvé-Perthes disease [12, 13]. Kim et al. [14, 15] recently examined immature piglet models of ischemic osteonecrosis involving vascular disruption; furthermore, they evaluated the revascularization process in patients with Legg-Calvé-Perthes disease using gadolinium-enhanced magnetic resonance imaging (MRI). They concluded that local non-weight-bearing decreased the femoral head deformity and increased revascularization and resorption of the infarcted epiphysis. However, to the best of our knowledge, no previous report has demonstrated evaluations of the necrotic lesion and/or revascularization response following rarely experienced traumatic hip dislocation in children. We present a case of an 11-year-old boy with avascular necrosis of the femoral head and improvement in blood flow during non-weight-bearing according to serial gadolinium-enhanced MRI after traumatic open anterior hip dislocation.
Traumatic open anterior dislocation of the hip in children is associated with serious complications and could have a very poor prognosis [1, 5, 9, 10, 25, 26, 27, 28, 29]. In our patient’s case, bone scintigraphy after prompt reduction indicated reduced bone turnover on the femoral head due to the severity of the initial trauma [29, 30]. T1-weighted MR images at 2 months after injury showed two bands with low signal intensity in the femoral capital epiphysis, suggesting the existence of osteonecrosis. Gadolinium-enhanced MR images at 2 months showed nonenhanced area in the peripheral region of the femoral capital epiphysis, indicating disruption of artery of the ligamentum teres and branches of superior retinacular artery [17, 18].
Bohr et al.  examined the vascular supply to the femoral head following dislocation of the hip joint in newborn rabbits and showed that revascularization takes place through vessels from the trochanteric region and by vessels perforating the epiphyseal plate from the metaphyseal side. Conway et al.  reported that revascularization of the necrotic proximal femoral epiphysis in Legg-Calvé-Perthes disease can occur by rapid recanalization of existing vessels or by prolonged neovascularization through the development of new vessels. Kim et al. observed revascularization occurring from the periphery to the central region , which is different from our patient’s case. However, no previous report demonstrated the revascularization process of osteonecrosis after traumatic hip dislocation. In this case, serial MR images showed the gadolinium-enhanced region gradually spreading from the center of the epiphysis toward the peripheral region, indicating appreciable revascularization.
Weight-bearing within 6 weeks without accurately assessing either the necrotic area or revascularization might lead to premature breakdown of the hip joint in children with ischemic necrosis after traumatic hip dislocation [5, 9, 10, 14, 33]. Collapse of the necrotic femoral head could occur with earlier weight-bearing during the revascularization process due to the weakness of the affected head resulting from the mechanical stress . Kim et al. reported that joint loading due to muscle contractions can also contribute to the development of the femoral head deformity, but local non-weight-bearing could provide significantly better preservation of the round shape of the femoral head [14, 15]. They reported the gradual revascularization process of the femoral epiphysis in Legg-Calvé-Perthes disease using serial perfusion MRI and recommended that the non-weight-bearing period be based on a certain level of normalization of the signal intensity in the revascularized area due to reossification. In our patient’s case, repeated evaluation of the necrotic area and revascularization using gadolinium-enhanced MRI helped in the careful planning of appropriate time for weight-bearing. Although osteonecrosis in the anterior region caused slight collapse of articular surface of the femoral head, conservative treatment with non-weight-bearing for 1.5 years for the affected hip could achieve favorable outcomes within 4.5 years after injury.
Growth disturbances causing damage to the physis in the peripheral region including the perichondral structures, which play an essential role in the growth of the width and length , result in deformity of the proximal femur with leg-length discrepancy . Although long-term follow-up is necessary for early detection of hip arthritis, our patient returned to performing his normal activities without any limitation at 4.5 years after injury.
We confirmed the revascularization process of the necrotic lesion in the femoral capital epiphysis after traumatic open anterior dislocation of the hip joint in an 11-year-old boy using serial gadolinium-enhanced MRI. Although he had deformity of the proximal femur with leg-length discrepancy, non-weight-bearing treatment using a brace for 1.5 years achieved a favorable outcome without any hip joint dysfunction, pain, or sign of secondary osteoarthritic change within 4.5 years after injury.
KM, SH, GM, KK, TY, and YN contributed to the treatment of the patient. MK contributed to the image analysis. All authors read and approved the final version of the manuscript.
The authors received no funding.
Ethics approval and consent to participate
All procedures performed in studies involving human participants were in accordance with the ethical standards of our institution and the 1964 Helsinki declaration and its later amendments or comparable ethical standards.
Consent for publication
Written informed consent was obtained from the patient’s legal guardian(s) for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
The authors declare that they have no competing interests.
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