Baghla Davinder Ps, Shariff Sajid, Dega Raman
Hercies Road, Uxbridge, Middlesex, UB10 9LU, UK.
J Med Case Rep. 2010 Feb 23;4:66. doi: 10.1186/1752-1947-4-66.
Cases of acute tarsal tunnel syndrome are rare. To the best of our knowledge, we describe the only reported case of acute posterior tibial nerve compression resulting from adjacent haemotogenous pyogenic calcaneal osteomyelitis.
A previously healthy 38-year-old Caucasian woman developed symptoms of acute tarsal tunnel syndrome in her right foot over a six-day period. No antecedent trauma or systemic symptoms were noted. Magnetic resonance imaging and bone scan imaging, followed by surgical decompression and bone biopsy confirmed a diagnosis of Staphylococcus aureus calcaneal osteomyelitis. Her pain and paraesthesia disappeared after the operation, while her inflammatory markers normalised during a 12-week course of antibiotics. After four years she has remained asymptomatic without any indication of recurrence.
This case is not just unique in describing osteomyelitis as a cause of tarsal tunnel syndrome, because haemotogenous calcaneal osteomyelitis is in itself a rare pathology. We recommend considering infection as a differential diagnosis in patients presenting with acute tarsal tunnel syndrome.
急性跗管综合征病例罕见。据我们所知,我们描述了唯一一例因相邻血源性化脓性跟骨骨髓炎导致急性胫后神经受压的病例。
一名38岁既往健康的白人女性在六天内出现了右脚急性跗管综合征的症状。未发现先前的创伤或全身症状。磁共振成像和骨扫描成像,随后进行手术减压和骨活检,确诊为金黄色葡萄球菌性跟骨骨髓炎。术后她的疼痛和感觉异常消失,同时在为期12周的抗生素疗程中炎症指标恢复正常。四年后,她一直无症状,没有任何复发迹象。
该病例不仅在将骨髓炎描述为跗管综合征的病因方面具有独特性,因为血源性跟骨骨髓炎本身就是一种罕见的病理情况。我们建议对出现急性跗管综合征的患者考虑感染作为鉴别诊断。