{"id":"00071cd4-506f-4fb6-97ba-e2b1e429aaff","slug":"utility-of-the-spinal-instability-neoplastic-score-to-identify-patients-with-gorham-stout-disease-requiring-spine-surgery","title":"Utility of the spinal instability neoplastic score to identify patients with Gorham-Stout disease requiring spine surgery","authors":["Chloe Gui","Brett Rocos","Laura-Nanna Lohkamp","Angela Cheung","Robert Bleakney","Eric Massicotte"],"abstract":"Background: Gorham-Stout disease (GSD) is a rare syndrome presenting with progressive osteolysis which in the spine can lead to cord injury, instability, and deformity. Here, the early spine surgery may prevent catastrophic outcomes. Case Description: A 25-year-old male with GSD involving the T2 to T6 levels presented with acute traumatic kyphoscoliosis at T3 and T4 and left lower extremity paraparesis. The CT scan 4 weeks before this showed progressing osteolysis versus the CT 5 years ago. Unfortunately, the patient underwent delayed treatment resulting in permanent neurological sequelae. Surgery included a laminectomy and vertebrectomy of T3/T4 with instrumented fusion from T1-10. The use of the spinal instability neoplastic score (SINS) is a useful tool to prompt early referral to spine surgeons. Conclusion: We recommend using the SINS score in GSD patients who develop spinal lesions to prompt early referral for consideration of surgery. Gorham-Stout disease (GSD) is rare; only approximately 300 cases have been reported.[ 11 ] The condition is attributed to the nonneoplastic proliferation and dilation of lymphatic channels resulting in destruction of the cortical ribbon in an average of 7.5 bones by the time of clinical presentation/diagnosis; these include (in descending frequency) ribs, cranium, clavicle, cervical spine, thoracic spine, humerus, and femur.[ 2 , 10 , 13 ] Although the osteolysis is progressive, it is occasionally spontaneously arrested or diminished following medical and/or radiation treatment.[ 3 , 9 , 12 , 14 ] Spinal involvement has been reported in 75 patients, 33 of which required surgery for fracture or deformity.[ 4 , 6 , 15 ] Here, we report a patient newly diagnosed with GSD who acutely presented with a T3/4 spinal deformity that was not managed in a timely fashion (i.e., C3, T4 corpectomy/ posterior fusion T1-T10) and resulted in a permanent paraparesis. A 25-year-old male with GSD presented with traumatic kyphoscoliosis centered at the T3-T4 level.[ 11 ] Previously, serial MR studies showed asymptomatic progressive fatty marrow replacement of the T4-T6 spinous processes and T2-T6 vertebral bodies/posterior elements; nothing had changed over 3 years [ Figure 1a - c ]. Four weeks before admission, the patient presented with a T3 spinous process fracture, and the CT showed osteolysis of the T2-T6 vertebral bodies and left T3-T8 facet joints; these findings had progressed compared to a CT of the thorax 5 years prior. On the current admission, the patient now had a significant paraparesis with a T4 sensory level. The MR showed spinal canal stenosis at T3-T4 with hyperintense signal in the cord on T2 sequences [ Figure 1d ]. The CT demonstrated a fracture of the T3 inferior endplate and T4 superior endplate with extension through the right superior facet and left inferior facet resulting in destruction of the posterior elements and 53° of kyphosis with levoscoliosis [ Figure 2a and b ]. Annual MR imaging of the thoracic spine over 3 years (a-c) demonstrates stability of the increased signal intensity of the T2-T6 vertebral bodies, which is consistent with the fatty marrow replacement seen in Gorham-Stout disease. Postinjury imaging (d) demonstrates severe kyphosis at T3-T4. Acute cord signal change is evident, in keeping with acute myelopathy (d). CT imaging shows the T3 spinous fracture (a) sustained 1 month before further pathologic kyphotic angulation deformity at T3-T4 with extensive destruction of the posterior elements (b). Postoperative CT imaging demonstrates instrumented fusion from T1-T10 with significant improvement in kyphotic deformity at T3-4 (c). The patient underwent a partial vertebrectomy at T3 and T4 and posterior instrumented fusion from T1 to T10 [ Figure 2c ]. The right T4 nerve root was sacrificed during the vertebrectomy, and a traumatic dural laceration sustained as a result of the fracture was repaired with an autologous duraplasty. The patient made an uneventful recovery, except for a persisting left pleural effusion, a known complication of GSD that was present preoperatively and unrelated to surgical intervention. At 3-month follow-up, the entire left leg was numb more consistent with a neurological level of T12 and below. A zone of partial preservation was observed from T6 to T12.","thumbnailUrl":"https://sni-digital-videos.s3.amazonaws.com/articles/00071cd4-506f-4fb6-97ba-e2b1e429aaff/featured/hero-1781562435574.png","publishDate":"2021-05-17T00:00:00.000Z","doi":"10.25259/SNI_311_2021","categories":["Spine","Case Report"],"fullTextUrl":"https://surgicalneurologyint.com/wp-content/uploads/2021/05/10812/SNI-12-227.pdf"}