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Article
June 1991

Brown Tumor and Secondary Hyperparathyroidism

Author Affiliations

From the Division of Ophthalmology, The Mt Sinai Medical Center, Cleveland, Ohio (Drs Levine and Chu); the Departments of Ophthalmology (Dr Levine) and Pathology (Dr Abdul-Karim), Case Western Reserve University School of Medicine, Cleveland; and Oculoplastics Clinics, University Hospitals of Cleveland (Dr Levine).

Arch Ophthalmol. 1991;109(6):847-849. doi:10.1001/archopht.1991.01080060111036
Abstract

• Brown tumor is a focal, bony lesion of hyperparathyroidism that results from parathyroid hormone on bone increasing osteoclastic activity with bone resorption and trabecular fibrosis. This leads to microfractures and hemorrhage and the appearance of brown tumors, which are seen most commonly in primary hyperparathyroidism and less frequently in secondary hyperparathyroidism. Rarely do these tumors involve the orbit. We report the sixth case, to our knowledge, of orbital involvement, in a patient with chronic renal failure (secondary hyperparathyroidism) and review the literature.

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