Balakrishnan G, Vijayaragavan S, Somesh B
Department of Plastic, Hand & Microsurgery, Right Hospitals, Kilpauk, Chennai, Tamil Nadu, India.
The Tamil Nadu Dr. MGR Medical University, Chennai, Tamil Nadu, India.
Indian J Plast Surg. 2020 Dec;53(3):349-356. doi: 10.1055/s-0040-1718858. Epub 2020 Nov 25.
Hypoplasia of thumb is the second common congenital difference of the thumb, next only to duplication. It may occur as an isolated hand difference or as a part of radial longitudinal deficiency. In approximately 60% of these children, the radius shows hypoplasia. The incidence of thumb hypoplasia is one in 100,000 live births. In 50% of these children, the other hand will also have similar deficiency, although variable in severity. Hypoplasia of thumb has been classified into five major categories, according to the increasing severity of hypoplasia. Type III hypoplasia of thumb is characterized by skeletal hypoplasia involving the first metacarpal and carpometacarpal joint, absent intrinsic muscles and rudimentary extrinsic muscles. It was further subclassified into types A, B & C. Type III B, described by Manske and McCarroll, involves extensive deficiency of extrinsic and intrinsic musculature with aplasia of the metacarpal base. Type III C, described by Buck-Gramcko, has hypoplastic metacarpal head. It is widely believed that reconstruction of Type III B & C hypoplastic thumb will not be functionally useful, and they are often included in the indications for pollicization in thumb hypoplasia. In India, we frequently come across parents, who are not willing to remove the hypoplastic digit. This forced us to find out a way to reconstruct the hypoplastic thumb into a functionally useful digit. We describe our surgical technique of reconstruction of hypoplastic thumbs and our experience in utilization of the technique in five children with Type III B & C hypoplasia of thumb. Carpometacarpal joint of thumb was reconstructed and stabilized with a toe phalangeal transfer in the first stage and an opponensplasty was done in the second stage to improve movement. In all the five operated children, our surgical technique yielded a stable thumb which was functional. The donor site morbidity was acceptable. The parents were satisfied with the appearance and functional improvement. Surgical reconstruction of hypoplastic thumbs of Type III B & C is possible, and conversion of these poorly developed remnants into a useful digit by our surgical technique is a gamechanger in the management of thumb hypoplasia.
拇指发育不全是拇指第二常见的先天性异常,仅次于多指畸形。它可能作为孤立的手部异常出现,也可能是桡侧纵列发育不全的一部分。在大约60%的这类患儿中,桡骨表现出发育不全。拇指发育不全的发病率为每10万例活产中有1例。在这些患儿中,50%的对侧手也会有类似的缺陷,尽管严重程度有所不同。根据发育不全的严重程度增加,拇指发育不全已被分为五大类。III型拇指发育不全的特征是骨骼发育不全,累及第一掌骨和腕掌关节,内在肌缺如,外在肌发育不全。它又进一步细分为A、B和C型。Manske和McCarroll描述的III B型,涉及外在和内在肌肉组织的广泛缺陷以及掌骨基部发育不全。Buck-Gramcko描述的III C型,掌骨头发育不全。人们普遍认为,III B型和III C型发育不全拇指的重建在功能上没有用处,它们通常被纳入拇指发育不全的拇指化手术适应症中。在印度,我们经常遇到不愿意切除发育不全手指的家长。这迫使我们找到一种方法,将发育不全的拇指重建为功能有用的手指。我们描述了我们重建发育不全拇指的手术技术,以及我们在5例III B型和III C型拇指发育不全患儿中应用该技术的经验。第一阶段用趾骨移植重建并稳定拇指腕掌关节,第二阶段进行对掌肌成形术以改善活动。在所有5例接受手术的患儿中,我们的手术技术产生了一个稳定且功能良好的拇指。供区并发症是可以接受的。家长们对外观和功能改善感到满意。III B型和III C型发育不全拇指的手术重建是可行的,通过我们的手术技术将这些发育不良的残端转化为有用的手指,在拇指发育不全的治疗中是一个重大改变。