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难治性原发性甲状旁腺功能亢进症不同部位棕色瘤病变的自然史及外科治疗

Natural history and surgical treatment of brown tumor lesions at various sites in refractory primary hyperparathyroidism.

作者信息

Khalil P N, Heining S M, Huss R, Ihrler S, Siebeck M, Hallfeldt K, Euler E, Mutschler W

机构信息

Department of Surgery, Downtown Medical Centre, Ludwig-Maximilians-University, 80336 Munich, Germany.

出版信息

Eur J Med Res. 2007 May 29;12(5):222-30.

PMID:17513195
Abstract

OBJECTIVE

Nowadays, the occurrence of brown tumor lesions or osteitis fibrosa cystica caused by long-lasting primary hyperparathyroidism are very rare, since measuring serum calcium became available routinely in the mid-1970s. It is a tumor-like lesion that may affect the entire skeleton, often presenting with diffuse focal bone pain or by pathological fracture.

METHODS

We describe our experience of brown tumor lesions at different skeletal sites that were treated at our trauma centre within the last two years. This included surgical therapy for the indications (i) pain at the pelvis, (ii) increased risk for pathological fracture at the tibia and (iii) acute radicular symptoms at the lumbar spine. The literature was reviewed for the current understanding of the pathophysiology as well as therapy of brown tumor lesions in primary hyperparathyroidism.

RESULTS

Curettage of a left-sided iliac crest brown tumor terminated focal pain. A less invasive stabilisation system and bone cement decreased both patient pain and the fracture risk of brown tumor lesion sites of the shinbone; and internal fixator including laminectomy at the lumbar spine ended radicular symptoms.

CONCLUSION

Patients with refractory primary hyperparathyroidism should be monitored closely by endocrinologists and the patient's serum calcium level should be adjusted as far as possible. Radiography is required only if focal bone pain or pathological fractures or radicular symptoms occur. Surgery should be considered if large bone defects with spontaneous fracture risk or increasing pain are present. Tumor curettage, Palacos plombage and less invasive stabilisation systems have proved to be acceptable surgical options.

摘要

目的

如今,由于自20世纪70年代中期开始常规检测血清钙,由长期原发性甲状旁腺功能亢进引起的棕色肿瘤病变或纤维囊性骨炎已非常罕见。它是一种肿瘤样病变,可能影响整个骨骼,常表现为弥漫性局部骨痛或病理性骨折。

方法

我们描述了过去两年在我们创伤中心治疗的不同骨骼部位棕色肿瘤病变的经验。这包括针对以下指征的手术治疗:(i)骨盆疼痛;(ii)胫骨病理性骨折风险增加;(iii)腰椎急性神经根症状。回顾文献以了解原发性甲状旁腺功能亢进中棕色肿瘤病变的病理生理学及治疗的当前认识。

结果

刮除左侧髂嵴棕色肿瘤缓解了局部疼痛。一种侵入性较小的稳定系统和骨水泥减轻了患者疼痛并降低了胫骨棕色肿瘤病变部位的骨折风险;包括腰椎椎板切除术的内固定器消除了神经根症状。

结论

难治性原发性甲状旁腺功能亢进患者应由内分泌科医生密切监测,尽可能调整患者的血清钙水平。仅当出现局部骨痛、病理性骨折或神经根症状时才需要进行放射检查。如果存在有自发骨折风险的大骨缺损或疼痛加剧,则应考虑手术。肿瘤刮除术、帕拉科斯骨腔填充术和侵入性较小的稳定系统已被证明是可接受的手术选择。

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