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急性神经综合征并发继发性甲状旁腺功能亢进。

Acute neurological syndrome complicating secondary hyperparathyroidism.

作者信息

Patel Ravina, Wiederkehr Michael

机构信息

Division of Nephrology, Department of Internal Medicine, Baylor University Medical CenterDallasTexas.

Department of Internal Medicine, Texas A&M Health Science Center College of MedicineDallasTexas.

出版信息

Proc (Bayl Univ Med Cent). 2018 Sep 24;31(4):534-536. doi: 10.1080/08998280.2018.1499004. eCollection 2018 Oct.

Abstract

Longstanding severe hyperparathyroidism can lead to the formation of "brown tumors," benign but locally aggressive neoplasms. We present the case of a young woman with end-stage renal disease on hemodialysis with uncontrolled secondary hyperparathyroidism. The patient presented with progressive lower extremity weakness and back pain. Imaging showed multiple lytic bone lesions, the most impressive being a T3 spinal lesion causing cord compression. She underwent urgent neurosurgical resection of the tumor at T3 followed by subtotal parathyroidectomy. Our case touches upon the pathophysiology, consequences, and treatment of secondary hyperparathyroidism in patients with end-stage renal disease.

摘要

长期存在的严重甲状旁腺功能亢进可导致“棕色瘤”的形成,这是一种良性但具有局部侵袭性的肿瘤。我们报告了一例患有终末期肾病且接受血液透析的年轻女性病例,其继发性甲状旁腺功能亢进未得到控制。该患者出现进行性下肢无力和背痛。影像学检查显示多处溶骨性骨病变,最显著的是一个导致脊髓受压的T3椎体病变。她接受了T3椎体肿瘤的紧急神经外科切除术,随后进行了甲状旁腺次全切除术。我们的病例涉及终末期肾病患者继发性甲状旁腺功能亢进的病理生理学、后果及治疗。

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Acute neurological syndrome complicating secondary hyperparathyroidism.急性神经综合征并发继发性甲状旁腺功能亢进。
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