Minimal-invasive, image guided, 360-degree resection of ilio-lumbo-sacral ostechondroma, planned on the 3D model in a child with hereditary multiple ostechondroma (HMO).

IF 2.6 3区 医学 Q2 CLINICAL NEUROLOGY European Spine Journal Pub Date : 2025-02-01 Epub Date: 2024-12-30 DOI:10.1007/s00586-024-08625-8
Lukas Bobinski, Evangelos Tachtaras, Erik Hedström
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Abstract

Background: 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.

Case report: 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.

Conclusion: 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.

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微创,图像引导,360度切除髂-腰-骶骨骨软骨瘤,计划在儿童遗传性多发性骨软骨瘤(HMO)的3D模型。
背景:遗传性多发性骨软骨瘤(HMO),以前称为多发性遗传性外生骨瘤(MHE),是一种遗传性疾病,其特征是长骨干骺端和中轴骨骼形成多发性良性外生骨瘤(骨软骨瘤)。起源于腰椎区域的病变是罕见的,最常见的是从椎骨后部生长。HMO相关的骨软骨瘤是难以治疗的,因为这些病变的持续和不可控的增长和终身恶性转化的风险。病例报告:我们描述了一个病例16岁的患者已知HMO谁发展了一个巨大的髂-腰-骶骨软骨瘤。肿瘤突入L4-S1椎间孔,外生扩张至右侧腰肌和腰丛,压迫右侧髂总静脉。为了计划和执行切除并将并发症的风险降至最低,我们使用了带有腹内血管病变的3D打印模型。患者的手术分为两个阶段,首先是小切口经腹导航切除病变,然后是延迟后路微创导航切除。结果是平稳的,在4年的随访中没有再生或恶性转化的迹象。结论:我们描述了应用3D打印模型、导航和微创技术进行360度手术切除。我们的报告可能是有用的,并启发脊柱外科医生应用类似的技术来治疗复杂的脊柱病变。
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来源期刊
European Spine Journal
European Spine Journal 医学-临床神经学
CiteScore
4.80
自引率
10.70%
发文量
373
审稿时长
2-4 weeks
期刊介绍: "European Spine Journal" is a publication founded in response to the increasing trend toward specialization in spinal surgery and spinal pathology in general. The Journal is devoted to all spine related disciplines, including functional and surgical anatomy of the spine, biomechanics and pathophysiology, diagnostic procedures, and neurology, surgery and outcomes. The aim of "European Spine Journal" is to support the further development of highly innovative spine treatments including but not restricted to surgery and to provide an integrated and balanced view of diagnostic, research and treatment procedures as well as outcomes that will enhance effective collaboration among specialists worldwide. The “European Spine Journal” also participates in education by means of videos, interactive meetings and the endorsement of educative efforts. Official publication of EUROSPINE, The Spine Society of Europe
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