Pongmanee Suthipas, Kaensuk Sitthikorn, Suppagornmongkol Worapat, Liawrungrueang Wongthawat
Department of Orthopaedics, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Department of Orthopaedics, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Int J Surg Case Rep. 2021 Dec;89:106622. doi: 10.1016/j.ijscr.2021.106622. Epub 2021 Nov 24.
Symptomatic retro-odontoid pseudotumor (ROP) caused by cervical compression and myelopathy is rare. Pathological diagnosis is recommended for differential diagnosis including the following: inflammatory disease, primary bone tumor, metastatic disease and calcium pyrophosphate dihydrate deposition (CPPD) also known as "crowned dens syndrome". The authors report a rare case of ROP caused by CPPD deposition combined with multilevel cervical spondylotic myelopathy (MCSM) which was treated by tumor resectioning using a transoral approach combined with posterior decompression and fusion.
A 66-year-old male presented with progressive neck pain and spastic gait with no history of trauma. Radiographic imaging revealed degenerative change involving the atlanto-axial and atlanto-occipital joints with calcified enhancing soft tissue around the odontoid process causing cord compression and cervical instability at the C1-C2 level combined with MCSM and spinal cord compression at C3 to C7. Microscopic assisted transoral tumor resection combined with posterior decompression and fusion was performed at the occiput to T2. The pathology report describes a rhomboid-shaped crystal caused by calcium pyrophosphate dihydrate deposition (CPPD) disease. At the 6-month follow-up following the operation, the patient's neck pain and spastic gait were improved compared to the preoperative examination.
Cervical compression and myelopathy from ROP causing CPPD combined with MCSM is rare. Pathology diagnosis and surgical management are highly recommended.
In this case, a combined surgical approach: tumor resection using a transoral approach and a posterior approach for decompression and fusion at occiput to T2 was an effective option for this condition.
由颈椎压迫和脊髓病引起的症状性齿突后假瘤(ROP)较为罕见。建议进行病理诊断以进行鉴别诊断,包括以下疾病:炎症性疾病、原发性骨肿瘤、转移性疾病以及焦磷酸钙二水合物沉积(CPPD),也称为“齿突冠综合征”。作者报告了一例罕见的由CPPD沉积引起的ROP病例,该病例合并多节段颈椎脊髓型颈椎病(MCSM),采用经口入路肿瘤切除术联合后路减压融合术进行治疗。
一名66岁男性,无外伤史,出现进行性颈部疼痛和痉挛性步态。影像学检查显示寰枢关节和寰枕关节退变,齿突周围有钙化强化的软组织,导致C1-C2水平脊髓受压和颈椎不稳,合并MCSM以及C3至C7脊髓受压。在枕骨至T2节段进行了显微镜辅助经口肿瘤切除术联合后路减压融合术。病理报告描述为焦磷酸钙二水合物沉积(CPPD)病引起的菱形晶体。术后6个月随访时,与术前检查相比,患者的颈部疼痛和痉挛性步态有所改善。
由ROP引起的CPPD合并MCSM导致的颈椎压迫和脊髓病较为罕见。强烈建议进行病理诊断和手术治疗。
在本病例中,联合手术方法:经口入路肿瘤切除术和枕骨至T2节段后路减压融合术是治疗这种情况的有效选择。