Borowski Andrzej, Grissom Leslie, Littleton Aaron G, Donohoe Maureen, King Marnie, Kumar S Jay
Department of Orthopaedics, Alfred I. duPont Hospital for Children, Nemours Children's Clinic, Wilmington, DE 19803, USA.
J Pediatr Orthop. 2008 Jun;28(4):466-70. doi: 10.1097/BPO.0b013e31816c4dd8.
Amyoplasia (type 1), characterized by quadrimelic limb involvement, is one of the most common types of arthrogryposis. In children with hyperextension or extension contracture of the knee, subluxation or dislocation of the knee joint with an associated subluxation or dislocation of the patella is frequently seen. Patellar malpositioning may be secondary to congenital hypoplasia of the patellar groove of the femur and/or dysplasia of the patellofemoral joint. A contracted quadriceps tendon and illiotibial band, as seen in extension contractures of the knee in arthrogryposis, may also contribute to patella alta and lateral subluxation of the patella. The aim of our study is to determine the position of the patella in children with quadrimelic arthrogryposis and knee extension contracture.
The inclusion criteria for this study were as follows: patients diagnosed with arthrogryposis multiplex congenita group 1, a knee extension contracture present from birth, follow-up from birth or early childhood, at least yearly physical examinations, and a knee ultrasonography or magnetic resonance imaging study performed. Patellar position was determined, and the cartilaginous femoral sulcus angle, as well as the osseous femoral sulcus angle, was measured.
Clinically, none of patella in any of the patients could be palpated before surgery. The patella was displaced superiorly and laterally in 16/16 knees as seen on ultrasonography. Magnetic resonance imaging also showed the patella to be displaced superior and laterally.
All patients in our series with extension contracture of the knee and type 1 arthrogryposis had a patella that was superior and lateral to the patellar groove. We found that quadricepsplasty and relocation of the patella improved knee flexion. All patients regained active knee extension in 6 months postsurgery.
Level III-diagnostic.
以四肢受累为特征的先天性多发性关节挛缩症1型(amyoplasia,type 1)是最常见的关节挛缩症类型之一。在患有膝关节过伸或伸直挛缩的儿童中,常可见膝关节半脱位或脱位,并伴有髌骨半脱位或脱位。髌骨位置异常可能继发于股骨髌股沟先天性发育不全和/或髌股关节发育异常。如先天性多发性关节挛缩症膝关节伸直挛缩所见,股四头肌腱和髂胫束挛缩也可能导致髌骨高位和髌骨外侧半脱位。本研究的目的是确定四肢关节挛缩症合并膝关节伸直挛缩患儿的髌骨位置。
本研究的纳入标准如下:诊断为先天性多发性关节挛缩症1型的患者,出生时即存在膝关节伸直挛缩,从出生或幼儿期开始随访,至少每年进行一次体格检查,并进行膝关节超声或磁共振成像检查。确定髌骨位置,并测量软骨性股骨沟角和骨性股骨沟角。
临床上,所有患者在手术前均无法触及髌骨。超声检查显示,16例患者的16个膝关节中,髌骨均向上和向外移位。磁共振成像也显示髌骨向上和向外移位。
我们系列研究中所有患有膝关节伸直挛缩和1型先天性多发性关节挛缩症的患者,其髌骨均位于髌股沟的上方和外侧。我们发现股四头肌成形术和髌骨复位可改善膝关节屈曲。所有患者术后6个月均恢复了主动膝关节伸直。
三级诊断性证据。