Olson Samantha N, Harbaugh Thaddeus D, Stoltzfus Mason T, Majid Sonia S, Mrowczynski Oliver D
Neurosurgery, Penn State Health Milton S. Hershey Medical Center, Hershey, USA.
Cureus. 2024 Jul 29;16(7):e65650. doi: 10.7759/cureus.65650. eCollection 2024 Jul.
Carpal and cubital tunnel syndromes are the two most common compressive neuropathies, but both carpal and cubital tunnel syndromes are extremely rare in children. Therefore, the combination of carpal and cubital tunnel syndrome in the pediatric population is even more uncommon. These neuropathies have multiple causes, with the three main categories being mechanical injury, metabolic, and idiopathic. Here, we present the unique case of a 15-year-old female with no known genetic or physical risk factors who was diagnosed with atraumatic combined carpal and cubital tunnel syndrome with severe, chronic nerve entrapment and damage. After nearly two years of conservative management, the patient had a cubital tunnel and carpal tunnel release simultaneously. The transverse carpal ligament was grossly thickened intraoperatively, leading to difficulty in the identification of the median nerve. The ulnar nerve was severely compressed and flattened. Following decompression, both nerves continued to be erythematous and inflamed. After surgery, the patient had barriers to getting appropriate postoperative care. Specifically, the patient was unable to attend physical and hand therapy appointments, possibly leading to continued weakness, numbness, and intermittent pain. In our patient, the preoperative workup did not illuminate the severity of the median and ulnar nerve damage, possibly delaying surgical intervention. In addition to our case, we utilized the TriNetX database (TriNetX, Inc., Cambridge, Massachusetts, United States) to investigate the rate and treatment of compressive neuropathies in the pediatric population. The database was queried for pediatric patients who underwent carpal tunnel release, cubital tunnel release, and pediatric patients with both carpal and cubital tunnel syndrome diagnoses in childhood. We found that there were 20,819,207 pediatric patients on the TriNetX database, of whom 503 (0.002%) were diagnosed with both carpal and cubital tunnel syndrome. Based on our case and the current literature, a thorough history of pediatric patients with suspected carpal or cubital tunnel syndrome should include an evaluation of family history and activity level for pertinent risk factors. Widening the scope of the patient history could allow for more timely surgical intervention and improve long-term outcomes for the pediatric population. When evaluating children for either carpal tunnel or cubital tunnel syndrome, we recommend that healthcare providers evaluate both neuropathies simultaneously.
腕管综合征和肘管综合征是两种最常见的压迫性神经病变,但在儿童中,腕管综合征和肘管综合征都极为罕见。因此,小儿人群中同时出现腕管综合征和肘管综合征的情况更为少见。这些神经病变有多种病因,主要分为三类:机械性损伤、代谢性和特发性。在此,我们报告一例独特病例,一名15岁女性,无已知遗传或身体风险因素,被诊断为无创伤性合并腕管和肘管综合征,伴有严重、慢性神经卡压和损伤。经过近两年的保守治疗后,患者同时接受了肘管和腕管松解术。术中发现腕横韧带明显增厚,导致正中神经辨认困难。尺神经严重受压并变扁平。减压后,两条神经仍有红斑和炎症。术后,患者在获得适当的术后护理方面存在障碍。具体而言,患者无法参加物理治疗和手部治疗预约,这可能导致持续的无力、麻木和间歇性疼痛。在我们的患者中,术前检查未能明确正中神经和尺神经损伤的严重程度,可能延误了手术干预。除了我们的病例,我们还利用TriNetX数据库(TriNetX公司,美国马萨诸塞州剑桥)调查小儿人群中压迫性神经病变的发生率和治疗情况。在该数据库中查询接受腕管松解术、肘管松解术的小儿患者,以及童年时期诊断为腕管和肘管综合征的小儿患者。我们发现TriNetX数据库中有20819207名小儿患者,其中503名(0.002%)被诊断为腕管和肘管综合征。基于我们的病例和当前文献,对于疑似腕管或肘管综合征的小儿患者,全面的病史应包括对家族史和活动水平进行相关风险因素评估。拓宽患者病史范围可使手术干预更及时,并改善小儿人群的长期预后。在评估儿童的腕管综合征或肘管综合征时,我们建议医疗保健提供者同时评估这两种神经病变。