- Case report
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A case report: white cord syndrome following anterior cervical discectomy and fusion: importance of prompt diagnosis and treatment
BMC Musculoskeletal Disorders volume 21, Article number: 157 (2020)
Objective: White cord syndrome is extremely rare and search of the literature has revealed very few cases. Postoperative MR scan revealed hyperintense intrinsic cord signal changes within cord ischemia and edema. It is thought to be caused by reperfusion injury of the spinal cord. This is called white cord syndrome. This report is very rare case of ‘White Cord Syndrome’ with paraplegia after anterior cervical discectomy and fusion (ACDF).
A 49-year-old woman presented with neck pain lasting for several months and second and third finger radiating pain. Severe cervical herniated intervertebral disc findings could be identified at C6–7 level on C-spine MRI. ACDF C6–7 surgery was performed. Immediately after the operation, physical examination revealed paraplegia and emergency MRI was performed. On MR images, T2 high signal myelopathy suspected as reperfusion injury at C6–7 level, and emergency surgery was performed under diagnosis of white cord syndrome. After the emergency operation, the paraplegic problem was gradually resolved. Before discharge, motor power and sensory deficit of bilateral lower extremity were fully recovered.
Surgeons should explain the possibility of white cord syndrome before cervical decompression surgery and should perform a neurological examination immediately after surgery. We recommend that the importance of early recognition and prompt treatment of white cord syndrome.
Anterior cervical discectomy and fusion (ACDF) is a common surgical procedure for cervical spine surgery and has resulted in good clinical results. The most serious complication after cervical spine surgery is neurologic deficit such as paralysis or paraplegia. This paraplegia is reported to be mostly caused by hematoma or iatrogenic injury. However, there is paraplegia that cannot be explained by these things, which can be caused by reperfusion injury, so called ‘white cord syndrome’ . White cord syndrome is extremely rare and search of the literature has revealed very few cases. Postoperative MR scan revealed hyperintense intrinsic cord signal changes within cord ischemia and edema. It is thought to be caused by reperfusion injury of the spinal cord. Although the mechanism of the disease is not clear, it is believed that free radical oxygen damages the spinal cord [2,3,4]. We report a case of this complication after ACDF.
This 49-year-old woman presented with neck pain lasting for several months and second and third finger radiating pain. She had no neurological deficit except for severe radiating pain of C6 dermatome. And the myelopathic neurologic examinations were uneventful, such as Hoffman’s sign, knee jerk, and ankle clonus. There was no past history other than hypertension and no relevant past medical interventions. On the C-spine MRI, we were able to confirm that the cord was compressed by extrusion of the large central disc at the C6–7 level (Fig. 1a, b). ACDF C6–7 surgery was performed and the cord was decompressed by removing the C6–7 disc material. The interbody cage was inserted into the C6–7 disc space and the plate (Vectra™, Depuy Synthes, CH) was fixed on the C6–7 body anterior surface. On immediately postoperative physical examination, the upper extremity motor and sensory nerves were normal however, ankle clonus 4+, knee jerk 4+, sensory deterioration, and bilateral lower extremity motor grade 0 were confirmed. C-spine MRI was taken immediately. Wide spreading high signal intensity in sagittal STIR (Short tau inversion recovery) MR image was observed at C6–7 level (Fig. 2a). In axial T2-weghted MR, anterior bilateral symmetric ovoid foci of high signal intensity (the snake-eyes sign) was observed (Fig. 2b). She was started high dose steroid (Methylprednisolone 30 mg/kg/15 min + 5.4 mg/kg/23 h) was administered under white cord syndrome diagnosis and emergency operation was performed. She underwent laminoplasty (Centerpiece™, Medtronic, USA) operation at C4–5–6-7 levels. The T2 weighted MR scan was repeated 1 week later as seen in Fig. 3a, b. After surgery, motor and sensory deficits were gradually resolved. Before discharge, motor power and sensory deficit of bilateral lower extremity were fully recovered. However, mild tingling sensation was remained at bilateral L5, S1 dermatome area. The patient had been discharged at 14 days postoperatively, and the preoperative symptoms almost disappeared (Table 1).
Discussion and conclusions
White cord syndrome is extremely rare and search of the literature has revealed very few cases. Chin at al . reported the case of a 59-year-old man affected by C5–6 severe cord compression, who underwent C4–5 and C5–6 ACDF surgery. Tetraplagia occurred in the patient after surgery, and he was treated with more extensive decompression and steroids immediately. The patient was partially improved. And Giammalva et al.  reported the case of a 64-year-old man affected by C4–6 severe cord compression, who underwent C3–4 and C5–6 ACDF. Tetraparesis occurred in the patient after surgery, and the patient was immediately started only high-dose steroid protocol (NASCIS III). The patient was partially improved. Antwi et al.  reported the case of a 68-year-old man affected by C4–6 severe cervical stenosis, who underwent C3–7 posterior decompression surgery. This was the first white cord syndrome case caused by posterior cervical operation. Hemiparesis occurred in the patient after surgery, and the patient was immediately started high-dose steroid protocol. But, the patient was partially improved. The precise mechanism of development of the white cord syndrome has not been reported. However, it is presumed that reperfusion injury occurs in chronically ischemic tissue caused by free radical oxygen. Hall E . reports that the use of high-dose steroids inhibits the attack of free radical oxygen.
In our case, the patient had chronic severe cord compression, and the result of cord decompression was an unexpected neurological deficits. Postoperative T2-weighted MRI showed intramedullary hyperintensity and cord swelling. So we used high-dose steroids to reduce oxidative damage and performed extensive decompression to relieve localized cord expansion. However, there is insufficient evidence to suggest that this has helped the patient improve symptoms. So we performed immediately surgery as laminoplasty at C4–5–6-7. The reason for choosing laminoplasty was to perform a quick operation and to decompress more widely while saving the neck motion (Table 2). We were convinced that there was no injury during surgical procedure, and we could conclude that neurological deficit occurred as an unknown cause, that is, reperfusion mechanisms. This is mentioned in some literature and is due to oxidative stress, although the exact cause is not known.
In conclusion, High-dose steroids and extensive decompression surgery in post-operative white cord syndrome is controversial but we think it is one of the available treatments. And also surgeons should adequately explain and give warning the possibility of complication, such as white cord syndrome before surgery and check the neurological examination immediately after surgery in patient with severe cord compression. We recommend that the importance of early recognition and prompt treatment of white cord syndrome.
Availability of data and materials
The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.
Anterior cervical discectomy and fusion
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This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
Ethics approval and consent to participate
This study was approved by the institutional review board of Gachon University Gil Medical Center (ethics approval code: GAIRB No. 2019–354). The need for consent was waived by the institutional review board of Gachon University Gil Medical Center (ethics approval code: GAIRB No. 2019–354). Radiologic images are entirely unidentifiable and there are no details on individuals reported within the manuscript.
Consent for publication
We obtained our institutional review board (GAIRB No.: 2017–354). And written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.
The authors declare that they have no competing interests.
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Jun, D.S., Baik, JM. & Lee, SK. A case report: white cord syndrome following anterior cervical discectomy and fusion: importance of prompt diagnosis and treatment. BMC Musculoskelet Disord 21, 157 (2020). https://doi.org/10.1186/s12891-020-3162-3
- Huge disc, discectomy
- White cord syndrome