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首页> 外文期刊>Internet Journal of Orthopedic Surgery >Developmental Dysplasia Of The Hip At Five Years Of Age Treated With Open Reduction And Femoral Osteotomy: A Case Report
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Developmental Dysplasia Of The Hip At Five Years Of Age Treated With Open Reduction And Femoral Osteotomy: A Case Report

机译:开放复位复位股骨截骨术治疗5岁髋关节发育异常一例

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Developmental dysplasia of the hip when presenting late is always a great challenge for orthopaedicians. Once the diagnosis is made by A.P. & lateral view radiographs; operative treatment should preferably include osteotomy on pelvic side with open reduction and femoral shortening. We describe 3 cases who presented late and were treated with open reduction, femoral shortening and pemberton osteotomy. Salter and Pemberton osteotomy are the commonly done procedures on pelvic side in these cases. In our centre earlier we were using Salter osteotomy. The present case report details the usage of the Pemberton osteotomy in 3 cases of developmental dysplasia of the hip who presented late, when treated with Pemberton osteotomy resulted in a good reduction of the acetabular head. We thus strongly recommend Pemberton osteotomy over Salter osteotomy. Introduction Normal hip development depends on proportionate growth of the acetabular triradiate cartilages and the presence of a concentrically located femoral head. Various genetic factors, hormonal factors, intrauterine mal-positioning and postnatal factors play a role in etiology of the developmental dysplasia of the hip (DDH). A child may be born with acetabular dysplasia without dislocation of the hip, and the latter may develop weeks or months later.Westin et al. reported the late development of dislocation of the hip in children with normal neonatal clinical and radiographic examinations; they termed this developmental dysplasia as opposed to congenital dysplasia of the hip. Diagnosis based on clinical suspicion that is limitation of abduction, asymmetrical skin folds, positive Galezzi sign, waddling or Trendelenburg gait and followed by radiographs taken in anteroposterior (AP) view and lateral view (frog leg position). In AP view approximate position of cartilaginous head is ascertained by following the ossified femoral neck. Lateral view gives idea regarding the anteversion of the neck. DDH when diagnosed at birth and treated at earliest results in normal development of the hip without any surgical intervention, but for delayed presentation surgery is required. Treatment options start with conservative treatment to keep the head within the acetabulum for plastic modulation in position of abduction and flexion. If detection is late various surgical options available are reduction of the head with femoral or innominate or acetabular surgeries. There is no doubt that open reduction and femoral shortening with capsulorraphy can relocate the head but there is always the scope of reorientation of the acetabulum to improve head coverage and acetabular index1, 2, 3.Salter and Pemberton osteotomy are the commonly done procedures on the pelvic side2, 3. The present case report details the usage of Pemberton osteotomy in 3 cases of developmental dysplasia of the hip who presented late. When treated with Pemberton osteotomy they resulted in a good reduction of the acetabular head. Case report 3 females (2.5, 3, and 3.5 year old) presented to our institution with a limp of the affected side. After history, clinical examination and necessary investigation, they were diagnosed having developemental dysplasia of the hip with the head either subluxated or dislocated and with a high riding head. [Figure-1] The patients were taken up for surgical reduction and Pemberton type osteotomy was done in each one.In all the 3 cases reduction of the femoral head was done through anterior approach through bikini incision. After incision along the iliac crest, sub-perisoteal dissection of the gluteal muscle followed by retraction the rectus femoris, the capsule was opened. Femoral shortening in the sub-trochantric region was done through another incision and reduction of the femoral head into the acetabulum was done. A femur bone segment equal to overlapping of fragments was removed and fixation of femoral fragments with plating was done and graft removed from pelvic osteotomy was put at the shortening site. T
机译:迟到时髋关节发育不良始终是骨科医师的巨大挑战。一旦通过A.P.和侧面X射线照片做出诊断;手术治疗最好包括骨盆侧截骨,切开复位和股骨缩短。我们描述了3例迟发并经切开复位,股骨缩短和彭伯顿截骨术治疗的病例。在这些情况下,Salter和Pemberton截骨术是骨盆侧常见的手术。早些时候在我们中心,我们正在使用Salter截骨术。本病例报告详细介绍了在3例出现迟发的髋关节发育不良病例中使用彭伯顿截骨术的情况,当接受彭伯顿截骨术治疗后,髋臼头得到了很好的复位。因此,我们强烈建议Pemberton截骨术优于Salter截骨术。引言正常髋关节的发育取决于髋臼三辐射软骨的成比例生长以及同心定位的股骨头的存在。各种遗传因素,激素因素,子宫内定位不良和产后因素在髋部发育不良(DDH)的病因学中起作用。一个孩子可能出生时髋臼发育不良而没有髋关节脱位,后者可能在数周或数月后发展。报告了新生儿,临床和影像学检查正常的儿童髋关节脱位的晚期发展;他们将这种发育异常称为先天性髋关节发育不良。根据临床怀疑进行诊断,包括外展受限,皮肤不对称褶皱,阳性Galezzi征,蹒跚步态或特伦德伦堡步态,然后在前后位(AP)视图和侧面(青蛙腿位置)拍摄X线照片。在AP视图中,通过跟踪骨化的股骨颈来确定软骨头的大致位置。侧面视图给出了关于颈部前倾的想法。 DDH在出生时被诊断并尽早得到治疗,可导致髋关节正常发育,无需任何外科手术干预,但对于延迟提呈手术则需要进行。治疗选择从保守治疗开始,以使头部保持在髋臼内,以在外展和屈曲位置进行塑性调节。如果发现较晚,可用的各种外科手术选择是通过股骨或无创或髋臼手术来减少头部。毫无疑问,囊袋切开术和股骨缩短术可以使头部复位,但总有重新定位髋臼的范围,以改善头部覆盖度和髋臼指数1、2、3。Salter和Pemberton截骨术是通常的手术方法。骨盆侧2,3。本病例报告详细介绍了彭伯顿截骨术在3例晚期髋关节发育不良患者中的使用。当用彭伯顿截骨术治疗时,可有效减少髋臼头。病例报告3名女性(2.5岁,3岁和3.5岁)向我们的机构就诊,患侧side行。经过病史,临床检查和必要的调查后,他们被诊断为髋关节发育异常,头部半脱位或脱位,骑行头高。 [图1]对患者进行手术复位,每例均行Pemberton截骨术。在这3例中,均通过比基尼切口通过前入路复位股骨头。沿the切开后,臀肌的骨膜下解剖,然后缩回股直肌,打开胶囊。转子下区域的股骨缩短是通过另一个切口完成的,股骨头复位到髋臼中了。去除等于碎片重叠的股骨段,并用平板固定股骨碎片,并将骨盆切开术中取出的移植物放置在缩短部位。 Ť

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