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颈椎朗格汉斯细胞组织细胞增生症:单中心 30 例经验。

Langerhans cell histiocytosis of the cervical spine: a single Chinese institution experience with thirty cases.

机构信息

Departments of Orthopaedics, Peking University Third Hospital, Beijing, People's Republic of China.

出版信息

Spine (Phila Pa 1976). 2010 Jan 1;35(1):E8-15. doi: 10.1097/BRS.0b013e3181b8aa2d.

Abstract

STUDY DESIGN

A retrospective study of cervical Langerhans cell histiocytosis (LCH).

OBJECTIVE

To evaluate the safety and efficiency of the present diagnosis and treatment strategy.

SUMMARY OF BACKGROUND DATA

The diagnosis and treatment protocols are still controversial for the rarity of cervical LCH.

METHODS

Thirty patients with cervical LCH were diagnosed in the past 10 years. Biopsy was routinely performed to establish the final diagnosis before treatment. Immobilization was usually the first choice. Low-dose radiotherapy was suggested for cases with solitary marked bony erosion and/or soft tissue extension, and chemotherapy for cases with multiple lesions. Surgery was preserved for suspected malignancy, neurologic deficits, severe deformity, and/or instability.

RESULTS

The mean age at diagnosis was 14.2 (range: 1.5-41) years old. Neck pain (96.7%) was the most common symptom, followed by restricted motion (70%), neurologic symptoms (36.7%), and torticollis (30%). Four cases had multiple lesions. Fourteen cases had atlantoaxial lesion and 16 cases were subaxial. The lesion extended to paravertebral soft tissue in 40% cases, to epidural space in 30%, to pedicle and/or transverse process in 56.3%. One case had endplate destruction. The accuracy of percutaneous needle biopsy under CT guidance was 91.2%. Eighteen patients had conservative treatment and 12 underwent operation. Three cases involving C2 vertebral body had fixed atlantoaxial anterior dislocation. Another 3 cases with atlantoaxial lateral mass destruction had spontaneous fusion. Eighteen patients had conservative treatment (1 only by immobilization, 13 by radiotherapy, 2 by chemotherapy, and 2 by combined chemotherapy and radiotherapy) and 12 underwent operation. All the initial symptoms were resolved, and there was no recurrence. From retrospective view, the surgical procedure might be avoided in 60% cases. Twenty-five cases had an average 61.6-month follow-up. In cases with severe bony collapse, the vertebral height ratio increased from 20.0% to 44.9% and the lateral mass height ratio from 22.2% to 56.8%.

CONCLUSION

Cervical LCH lesions often extend to paravertebral soft tissue, epidural space, pedicles, and even to the endplate and lamina. Needle biopsy under CT guidance is safe and effective. The prognosis of cervical LCH is generally fair. Conservative treatment is usually enough and surgery should be reserved for major neurologic defects like myelopathy or monoparesis.

摘要

研究设计

回顾性研究颈椎朗格汉斯细胞组织细胞增生症(LCH)。

目的

评估目前诊断和治疗策略的安全性和有效性。

背景资料概要

由于颈椎朗格汉斯细胞组织细胞增生症罕见,其诊断和治疗方案仍存在争议。

方法

过去 10 年共诊断出 30 例颈椎 LCH 患者。治疗前常规行活检以明确最终诊断。颈椎 LCH 患者常首选固定治疗。对于孤立性明显骨侵蚀和/或软组织延伸的病例,建议采用低剂量放疗;对于多发病例,建议采用化疗。对于疑似恶性肿瘤、神经功能缺损、严重畸形和/或不稳定的病例,保留手术治疗。

结果

患者的平均年龄为 14.2 岁(范围:1.5-41 岁)。颈部疼痛(96.7%)是最常见的症状,其次是运动受限(70%)、神经症状(36.7%)和斜颈(30%)。4 例为多发病例。14 例累及寰枢椎,16 例为颈下区病变。40%的病例病变延伸至椎旁软组织,30%延伸至硬膜外间隙,56.3%延伸至椎弓根和/或横突。1 例有终板破坏。CT 引导下经皮穿刺活检的准确率为 91.2%。18 例患者接受保守治疗,12 例患者接受手术治疗。3 例累及 C2 椎体的患者出现寰枢椎前脱位固定。另外 3 例伴有寰枢椎侧块破坏的患者出现自发性融合。18 例患者接受保守治疗(1 例仅行固定治疗,13 例行放疗,2 例行化疗,2 例行化疗联合放疗),12 例患者接受手术治疗。所有患者的初始症状均得到缓解,且无复发。回顾性分析显示,60%的患者可避免手术。25 例患者的平均随访时间为 61.6 个月。对于严重骨塌陷的患者,椎体高度比从 20.0%增加到 44.9%,侧块高度比从 22.2%增加到 56.8%。

结论

颈椎 LCH 病变常延伸至椎旁软组织、硬膜外间隙、椎弓根,甚至终板和椎板。CT 引导下经皮穿刺活检安全有效。颈椎 LCH 的预后一般较好。保守治疗通常足够,对于脊髓病或单瘫等严重神经功能缺损,应保留手术治疗。

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