Bobinski Lukas, Tachtaras Evangelos, Hedström Erik
Department of Orthopedics, Umeå University Hospital, Umeå, Sweden.
Department of Diagnostics and Intervention, Orthopedics, Umeå University, Umeå, Sweden.
Eur Spine J. 2025 Feb;34(2):643-649. doi: 10.1007/s00586-024-08625-8. Epub 2024 Dec 30.
Hereditary Multiple Osteochondromas (HMO), previously known as Multiple Hereditary Exostoses (MHE), is a genetic disorder characterized by the formation of multiple, benign, exostoses (osteochondromas) growing from the metaphyseal region of long bones as well as from the axial skeleton. Lesions originating from the lumbar spine region are rare, and are most common growing from the posterior element of the vertebrae. HMO associated osteochondromas are difficult to treat due to continuous and incontrollable growth of these lesions and a lifetime risk for malignant transformation.
We describe a case of a 16-year old patient with known HMO who developed a giant ilio-lumbo-sacral osteochondroma. The tumor protruded into the L4-S1 intraspinal foramina with exophytic expansion to the right psoas muscle and lumbar plexus with compression of the right common iliac vein. To plan and execute the resection and minimize the risk of complications, we used a 3D printed model of the lesion with intraabdominal vessels. The patient was operated during a two-stage procedure - first by mini-open, transabdominal, navigated resection of the lesion, followed by delayed posterior, mini-invasive, navigated resection. The outcome was uneventful and there were no signs of regrowth or malignant transformation during 4 years of follow-up.
We describe a 360-degree surgical resection with application of a 3D printed model, navigation, and mini-invasive techniques. Our report may be useful and inspire spine surgeons to apply similar techniques to treat complex spine lesions.
遗传性多发性骨软骨瘤(HMO),以前称为多发性遗传性外生骨疣(MHE),是一种遗传性疾病,其特征是在长骨干骺端区域以及中轴骨骼上形成多个良性外生骨疣(骨软骨瘤)。起源于腰椎区域的病变很少见,最常见于从椎体后部生长。由于这些病变持续且无法控制地生长以及存在恶性转化的终生风险,HMO相关的骨软骨瘤难以治疗。
我们描述了一例16岁已知患有HMO的患者,其发生了巨大的髂腰骶骨骨软骨瘤。肿瘤突入L4 - S1椎间孔,向外生长并累及右侧腰大肌和腰丛,压迫右侧髂总静脉。为了规划和实施切除并将并发症风险降至最低,我们使用了带有腹内血管的病变3D打印模型。患者接受了两阶段手术——首先通过迷你开放经腹导航切除病变,然后延迟进行后路微创导航切除。结果顺利,在4年的随访期间没有复发或恶性转化的迹象。
我们描述了一种应用3D打印模型、导航和微创技术的360度手术切除方法。我们的报告可能会对脊柱外科医生有所帮助,并激励他们应用类似技术治疗复杂的脊柱病变。