Hong Chang Hwa, Lee Hong Seop, Lee Won Seok, Kim Hyun Kwon, Won Sung Hun, Yeo Eui Dong, Jung Ki Jin, Ryu Aeli, Kang Jin Ku, Lee Dhong Won, Kim Woo Jong
Department of Orthopaedic Surgery, Soonchunhyang University Hospital Cheonan, Dongam-gu, Cheonan.
Department of Foot and Ankle Surgery, Nowon Eulji Medical Center, Eulji University, Nowon-gu.
Medicine (Baltimore). 2020 Jun 26;99(26):e20893. doi: 10.1097/MD.0000000000020893.
Tarsal tunnel syndrome (TTS) is a compressive neuropathy of the posterior tibial nerve and its branches. Tarsal coalition is defined as a fibrous, cartilaginous, or osseous bridging of 2 or more tarsal bones. TTS with tarsal coalition is uncommon. Here, we present a rare example of successful surgical management of TTS with posterior facet talocalcaneal coalition.
A 74-year-old woman presented with hypoesthesia, numbness, and an intermittent tingling sensation on the plantar area over the right forefoot to the middle foot area. The hypoesthesia and paresthesia of the right foot began 6 years previously and were severe along the lateral plantar aspect. The symptoms were mild at rest and increased during daily activities. Tinel sign was positive along the posteroinferior aspect of the medial malleolus.
Lateral ankle radiography showed joint-space narrowing and sclerotic bony changes with a deformed C-sign and humpback sign. Oblique coronal and sagittal computed tomography revealed an irregular medial posterior facet, partial coalition, narrowing, and subcortical cyst formation of the posterior subtalar joint. Magnetic resonance imaging showed an abnormal posterior talocalcaneal coalition compressing the posterior tibia nerve. Electromyography and nerve conduction velocity studies were performed, and the findings indicated that there was an incomplete lesion of the right plantar nerve, especially of the lateral plantar nerve, around the ankle level.
Surgical decompression was performed. Intraoperatively, the lateral plantar nerve exhibited fibrotic changes and tightening below the posterior facet talocalcaneal coalition. The coalition was excised, and the lateral plantar nerve was released with soft-tissue dissection.
The patient's symptoms of tingling sensation and hypoesthesia were almost relieved at 4 months postoperatively, but she complained of paresthesia with an itching sensation when the skin of the plantar area was touched. The paresthesia had disappeared almost completely at 8 months after surgery. She had no recurrence of symptoms at the 1-year follow-up.
The TTS with tarsal coalition is rare. Supportive history and physical examination are essential for diagnosis. Plain radiographs and computed tomography or magnetic resonance imaging are helpful to determine the cause of TTS and verify the tarsal coalition. After diagnosis, surgical excision of the coalition may be appropriate for management with a good outcome.
跗管综合征(TTS)是胫后神经及其分支的一种压迫性神经病变。跗骨联合是指两块或多块跗骨之间的纤维性、软骨性或骨性连接。合并跗骨联合的TTS并不常见。在此,我们展示了一例成功手术治疗合并后关节面距跟骨联合的TTS的罕见病例。
一名74岁女性,右前足至中足区域足底出现感觉减退、麻木及间歇性刺痛感。右脚的感觉减退和感觉异常始于6年前,沿足底外侧较为严重。症状在休息时较轻,日常活动时加重。在内踝后下方Tinel征阳性。
踝关节外侧X线片显示关节间隙变窄及骨质硬化改变,伴有变形的C征和驼背征。斜冠状位和矢状位计算机断层扫描显示后关节面不规则、部分联合、变窄以及距下后关节皮质下囊肿形成。磁共振成像显示异常的距跟骨联合压迫胫后神经。进行了肌电图和神经传导速度研究,结果表明在踝关节水平右侧足底神经,尤其是足底外侧神经存在不完全损伤。
进行了手术减压。术中,足底外侧神经在距跟骨联合后关节面下方出现纤维化改变并被拉紧。切除联合部,并通过软组织分离松解足底外侧神经。
术后4个月患者的刺痛感和感觉减退症状几乎缓解,但她抱怨足底区域皮肤被触碰时有感觉异常伴瘙痒感。术后8个月时感觉异常几乎完全消失。1年随访时症状无复发。
合并跗骨联合的TTS很罕见。支持性的病史和体格检查对诊断至关重要。X线平片及计算机断层扫描或磁共振成像有助于确定TTS的病因并证实跗骨联合。诊断后,手术切除联合部可能是合适的治疗方法,效果良好。