Brown tumor due to primary hyperparathyroidism resulting in acute paraparesis: Case report and literature review

Author:

Shaaban Ahmed Taha Elsayed1,Ibrahem Mostafa1,Saleh Ahmed1,Haider Abdulrazzaq2,Alyafai Abdulnasser1

Affiliation:

1. Department of Neurosurgery, Hamad Medical Corporation, Hamad General Hospital, Doha, Qatar.

2. Department of Pathology, Hamad Medical Corporation, Hamad General Hospital, Doha, Qatar.

Abstract

Background: Brown tumor (Osteoclastoma) is a rare benign, focal, lytic bone lesion most commonly attributed to a parathyroid adenoma; it occurs in approximately 5% of patients with primary hyperparathyroidism, and 13% of patients with secondary hyperparathyroidism. Most tumors are located in the mandible, pelvis, ribs, and large bones; only rarely is it found in the axial spine. Case Description: A 37-year-old male with primary hyperparathyroidism presented with an MR-documented T4 and T5 brown tumor (Osteitis Fibrosa Cystica) resulting in an acute paraparesis. The patient successfully underwent excisional biopsy of an expansile, enhancing, bony destructive lesion at the T4-5 level. Subsequently, he required subtotal excision of a left upper parathyroid tumor. Conclusion: Patient with primary hyperparathyroidism may acutely present with paraparesis attributed to brown tumors of the spine warranting emergent operative decompression.

Publisher

Scientific Scholar

Subject

Clinical Neurology,Surgery

Reference10 articles.

1. Vertebral brown tumors causing neurologic compromise;Fargen;World Neurosurg,2013

2. Contribution of multimodality imaging for positive and aetiological diagnosis of multiple brown tumours;Gregoire;Ann Endocrinol (Paris),2012

3. Spinal cord compression secondary to brown tumor as first manifestation of primary hyperparathyroidism;Hammou;World Neurosurg,2020

4. Management of brown tumor of spine with primary hyperparathyroidism: A case report and literature review;Hu;Medicine (Baltimore),2019

5. Natural history and surgical treatment of brown tumor lesions at various sites in refractory primary hyperparathyroidism;Khalil;Eur J Med Res,2007

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