Frikha R, Dahmene J, Ben Hamida R, Chaieb Z, Janhaoui N, Laziz Ben Ayeche M
Service d'Orthopédie, CHU Sahloul, route de Ceinture, 4054 Sousse, Tunisie.
Rev Chir Orthop Reparatrice Appar Mot. 2005 Nov;91(7):642-8. doi: 10.1016/s0035-1040(05)84468-x.
The purpose of this work was to present a descriptive analysis of eight cases of congenital agenesia of the anterior cruciate ligament (ACL). Congenital absence of the ACL is rare. The few series reported in the literature have been limited to sporadic cases all associated with diverse malformations. We report a series of eight cases knees in five patients presenting congenital knee laxity. These patients were all members of the same family, raising the question of an inherited condition. We describe the characteristic features and natural history of ACL agenesia compared with post-traumatic loss of the ACL.
This descriptive study included five patients (eight knees) with agenesia of the ACL. There were four men and one woman, mean age 46 years. All five patients had a common ancestor.
The main symptom was medial femorotibial and patellofemoral pain, present in all patients. Physical examination revealed major anterior laxity (positive pivot test, Trillat Lachman test) involving the posterior capsule and ligament structures and an abnormal knob on the anterior tibial tubercle. Plain x-rays demonstrated an abnormal aspect of the tibial spines, suggestive of ACL agenesia. The spines were flat in three knees, smooth in three, and dome shaped in two. On the lateral view, the femoral condyles presented an abnormal rounded posterior curvature in all of the affected knees. The tibial slope was increased in all knees, 20.6 degrees on average. MRI and arthroscopy confirmed the diagnosis in three knees.
Examining our cases and the data in the literature led to the following remarks. The family pedigree in our patients suggested autosomal dominant inheritance. Episodes of serious laxity are rare in subjects with congenital absence of the ACL compared with posttrauma patients, probably due to adaptation since infancy. Hypoplasia of the tibial spine and the lateral femoral condyle are characteristic consequences of ACL agenesia. In comparison with posttrauma cases, the natural history of ACL agenesia is characterized by better functional tolerance and inevitable progression to osteoarthritis due to the permanent anterior laxity. Degenerative disease may develop late and more slowly than after traumatic injury of the ACL. Unlike common arthrosis, the lateral femorotibial and patellofemoral compartments are preserved longer.
Though rare, congenital absence of the ACL should be evoked as a possibility in patients with chronic anterior laxity without trauma. The radiological aspect is highly suggestive of the diagnosis which can be confirmed by MRI or arthroscopy. Study of the present series enabled a description of the natural history of ACL agenesia, which is different from that of traumatic ACL tears because of the lack of secondary meniscal lesions and the later progression of osteoarthritic degeneration.
本研究旨在对8例先天性前交叉韧带(ACL)发育不全病例进行描述性分析。先天性ACL缺如较为罕见。文献中报道的少数病例系列仅限于散发病例,且均伴有各种畸形。我们报告了5例患者的8个膝关节出现先天性膝关节松弛的病例系列。这些患者均为同一家族成员,这引发了关于遗传性疾病的疑问。我们描述了ACL发育不全的特征性表现及自然病程,并与创伤后ACL损伤进行了比较。
本描述性研究纳入了5例ACL发育不全患者(8个膝关节)。其中男性4例,女性1例,平均年龄46岁。所有5例患者有一个共同祖先。
主要症状为所有患者均存在的股胫内侧和髌股疼痛。体格检查发现主要为前向松弛(阳性轴移试验、Trillat拉赫曼试验阳性),累及后关节囊和韧带结构,胫骨结节前方有异常隆起。X线平片显示胫骨棘形态异常,提示ACL发育不全。3个膝关节的胫骨棘扁平,3个光滑,2个呈圆顶状。在侧位片上,所有患膝的股骨髁均呈现异常的圆形后凸。所有膝关节的胫骨坡度均增加,平均为20.6度。MRI和关节镜检查在3个膝关节中证实了诊断。
对我们的病例及文献数据进行研究后得出以下结论。我们患者的家族谱系提示为常染色体显性遗传。与创伤后患者相比,先天性ACL缺如的患者很少出现严重的松弛发作,这可能是由于自幼适应的结果。胫骨棘和股骨外侧髁发育不全是ACL发育不全的特征性后果。与创伤后病例相比,ACL发育不全的自然病程的特点是功能耐受性较好,但由于永久性前向松弛,不可避免地会发展为骨关节炎。退行性疾病可能比ACL创伤后发病晚且进展缓慢。与常见的关节病不同,股胫外侧和髌股关节间隙保留时间更长。
虽然罕见,但对于无创伤的慢性前向松弛患者,应考虑先天性ACL缺如的可能性。放射学表现高度提示诊断,可通过MRI或关节镜检查确诊。对本病例系列的研究使得能够描述ACL发育不全的自然病程,由于缺乏继发性半月板损伤以及骨关节炎退变进展较晚,其与创伤性ACL撕裂不同。