Serviço de Cirurgia da Mão do Hospital Pequeno Príncipe, Curitiba, PR, Brazil.
Ambulatório Ortopedia Pediátrica, Rua Desembargador Motta, 1070 - Água Verde,, Curitiba, PR, 80250-060, Brazil.
Orphanet J Rare Dis. 2021 Sep 9;16(1):382. doi: 10.1186/s13023-021-01982-3.
Mucopolysaccharidosis consists of a group of diseases caused by the deficiency of lysosomal enzymes, which may lead to the compression of the median nerve in the carpal tunnel due to the accumulation of glycosaminoglycan, resulting in the hand disability. The study purpose is to present functional results of carpal tunnel release in mucopolysaccharidosis patients. Patients were selected from an enzyme replacement group in the Department of Pediatric Neurology. The legal guardians of the patients were informed about the likely functional change of the hands induced by compression of the median nerve. Clinical evaluation was performed in those patients who received their legal guardians' consent to participate and was included inspection, assessment of functional level, wrinkle test and the digital pinch function to manipulate small and large objects. Ultrasound and electromyography were performed to confirm the clinical median nerve compression. Bilateral extended opening technique was performed to access the carpal tunnel and analyze the anatomic findings of the median nerve and the flexed tendons of the fingers. After the surgical release of the carpal tunnel, the clinical evaluation was repeated. Subjective observations of the legal guardians were also considered.
Seven patients underwent bilateral surgical opening of the carpal tunnel; six boys, mean age of 9.5 (5 to 13), five of them presenting Type II mucopolysaccharidosis, 1 Type I and 1 Type VI. The average follow-up was 12 months (10-13 months). The functional results observed included the improvement in the handling of small and large objects in all children who underwent decompression of the median nerve. The comparison between the pre-operative and post-operative functional levels revealed that 2 patients evolved from Level II to IV, 3 from Level III to IV, 1 from Level IV to V and 1 patient remained in Level III. Tenosynovitis around the flexor tendons and severe compression of the median nerve in the fourteen carpal tunnels were observed during the surgical procedure. In 6 wrists, partial tenosynovitis was performed.
Despite the improvement in the overall function of the children' hands, we cannot conclude that only surgery was responsible for the benefit. Better designed studies are required.
黏多糖贮积症由一组溶酶体酶缺乏引起的疾病组成,由于糖胺聚糖的积累,可能导致正中神经在腕管中受压,从而导致手部残疾。本研究旨在介绍黏多糖贮积症患者腕管松解的功能结果。患者选自儿科神经病学部的酶替代治疗组。告知患者的法定监护人,由于正中神经受压可能导致手部功能发生变化。对那些获得法定监护人同意参与并进行了包括检查、功能水平评估、皱纹试验和手指捏力功能以操纵大小物体的患者进行了临床评估。进行超声和肌电图检查以确认临床正中神经受压。采用双侧伸展开口技术进入腕管,并分析正中神经和手指弯曲肌腱的解剖发现。行腕管松解术后,重复进行临床评估。还考虑了法定监护人的主观观察。
7 例患者行双侧腕管切开术;6 例男孩,平均年龄 9.5 岁(5-13 岁),其中 5 例为 II 型黏多糖贮积症,1 例为 I 型,1 例为 VI 型。平均随访时间为 12 个月(10-13 个月)。观察到的功能结果包括所有接受正中神经减压的儿童处理大小物体的能力均得到改善。术前和术后功能水平的比较显示,2 例患者从 II 级进展到 IV 级,3 例从 III 级进展到 IV 级,1 例从 IV 级进展到 V 级,1 例患者仍处于 III 级。在手术过程中,发现 14 个腕管中的屈肌腱周围腱鞘炎和正中神经严重受压。6 个腕关节行部分腱鞘炎松解术。
尽管儿童手部整体功能得到改善,但我们不能仅得出手术是唯一有益的结论。需要设计更好的研究。