Common Peroneal Nerve and Tarsal Tunnel Release Surgery in an Adolescent Male with Hunter Syndrome: Illustrative Case.

Rhode Island medical journal (2013) Pub Date : 2024-05-02
Elijah M Persad-Paisley, Belinda Shao, Vinay Rao, Loree K Kalliainen
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Abstract

Background: Children with Hunter syndrome have a high prevalence of nerve compression syndromes given the buildup of glycosaminoglycans in the tendon sheaths and soft tissue structures. These are often comorbid with orthopedic conditions given joint and tendon contractures due to the same pathology. While carpal tunnel syndrome and surgical treatment has been well-reported in this population, the literature on lower extremity nerve compression syndromes and their treatment in Hunter syndrome is sparse.

Observations: We report the case of a 13-year-old male with a history of Hunter syndrome who presented with toe-walking and tenderness over the peroneal and tarsal tunnel areas. He underwent bilateral common peroneal nerve and tarsal tunnel releases, with findings of severe nerve compression and hypertrophied soft tissue structures demonstrating fibromuscular scarring on pathology. Post-operatively, the patient's family reported subjective improvement in lower extremity mobility and plantar flexion.

Lessons: In this case, peroneal and tarsal nerve compression were diagnosed clinically and treated effectively with surgical release and postoperative ankle casting. Given the wide differential of common comorbid orthopedic conditions in Hunter syndrome and the lack of validated electrodiagnostic normative values in this population, the history and physical examination and consideration of nerve compression syndromes are tantamount for successful workup and treatment of gait abnormalities in the child with Hunter syndrome.

一名患有亨特综合征的青少年男性的腓总神经和跗骨隧道松解手术:示例病例。
背景:由于腱鞘和软组织结构中糖胺聚糖的堆积,亨特综合征患儿的神经压迫综合征发病率很高。由于同样的病理原因导致关节和肌腱挛缩,这些症状通常会合并骨科疾病。虽然腕管综合征和手术治疗在这一人群中已有大量报道,但有关亨特综合征的下肢神经压迫综合征及其治疗的文献却很少:我们报告了一例有亨特综合征病史的 13 岁男性病例,他出现了脚趾行走以及腓骨和跗骨隧道区域的压痛。他接受了双侧腓总神经和跗骨隧道松解术,术后发现神经严重受压,软组织结构肥大,病理显示为纤维肌性瘢痕。术后,患者家属表示下肢活动能力和跖屈能力得到了主观改善:在本病例中,腓总神经和跗神经压迫经临床确诊,并通过手术松解和术后踝关节石膏固定得到了有效治疗。鉴于亨特综合征常见合并骨科疾病的广泛差异,以及缺乏该人群的有效电诊断标准值,病史和体格检查以及神经压迫综合征的考虑对于亨特综合征患儿步态异常的成功检查和治疗至关重要。
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