Milton Camille K, O'Connor Kyle P, Smitherman Adam D, Conner Andrew K, Martin Michael D
Department of Neurosurgery, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma, United States.
Surg Neurol Int. 2020 Mar 21;11:51. doi: 10.25259/SNI_3_2020. eCollection 2020.
Spinal osteochondromas are rare, benign tumors arising from the cartilaginous elements of the spine that may appear as solitary lesions versus multiple lesions in patients with hereditary multiple exostoses. Here, we present a 15-year-old female with a solitary C3-C4 osteochondroma who presented with a progressive quadriparesis and hand contracture successfully managed with a laminectomy/posterior spinal fusion.
A 15-year-old female presented with a 3-month history of progressive quadriparesis and hand contracture secondary to a magnetic resonance (MR) documented C3-C4 cervical spine osteochondroma. The MR imaging revealed a solitary osseous extramedullary outgrowth arising from the left laminar cortex of the C-3 vertebral body extending to C-4. Due to the marked resultant canal stenosis, the patient underwent a cervical laminectomy of C3- C4 with posterior spinal fusion. Gross total resection was achieved, and the pathology confirmed an osteochondroma. The patient's myelopathy resolved, and 2 years later, she demonstrated no residual deficits or tumor recurrence.
Here, we report the successful management of a 15-year-old female with a C3-C4 osteochondroma and progressive quadriparesis through cervical laminectomy/fusion.
脊柱骨软骨瘤是一种罕见的良性肿瘤,起源于脊柱的软骨成分,在遗传性多发性骨软骨瘤患者中可表现为单发病变或多发病变。在此,我们报告一名15岁女性,患有孤立性C3 - C4骨软骨瘤,表现为进行性四肢瘫和手部挛缩,通过椎板切除术/后路脊柱融合术成功治疗。
一名15岁女性,有3个月进行性四肢瘫和手部挛缩病史,磁共振成像(MR)显示为C3 - C4颈椎骨软骨瘤。MR成像显示一个孤立的髓外骨性突起,起源于C3椎体左侧椎板皮质,延伸至C4。由于明显的椎管狭窄,患者接受了C3 - C4颈椎椎板切除术及后路脊柱融合术。实现了肿瘤全切,病理证实为骨软骨瘤。患者的脊髓病得到缓解,2年后,她没有残留神经功能缺损或肿瘤复发。
在此,我们报告通过颈椎椎板切除术/融合术成功治疗一名患有C3 - C4骨软骨瘤和进行性四肢瘫的15岁女性。