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AJNR Awards, New Junior Editors, and more. Read the latest AJNR updates

Case of the Week

Section Editors: Matylda Machnowska1 and Anvita Pauranik2
1University of Toronto, Toronto, Ontario, Canada
2BC Children's Hospital, University of British Columbia, Vancouver, British Columbia, Canada

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Submit a Case Previous Cases ASPNR Pediatric Cases

January 19, 2015
  • Description
  • Legends
  • Legends 2
  • Histopathology
  • Companion Case
  • Companion Case Legends
  • Follow-up
  • Diagnosis
  • Appendix
  • Brain Teaser
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Brown Tumor of Hyperparathyroidism

  • Brown tumors (BT) are reactive osteolytic lesions caused by primary or secondary hyperparathyroidism.
  • BT can occur as solitary or multiple lesions. The lesions may appear in any bone but are most frequently found in facial bones and jaws, sternum, pelvis, ribs and femur.
  • Key Diagnostic Features
    • Expansile lytic lesions
    • The cortex may be thinned, fractured, or have a partial sclerotic rim.
    • MR imaging findings are nonspecific and dependent on the relative proportion of tissue components.
    • Hypointensity on T1WI, strong enhancement following contrast administration, and heterogeneous signal intensity on T2WI
    • T2-shortening effect by hemosiderin and fluid-fluid levels have been described.
  • DDx
    • Metastases
    • Epidermoid
    • Multiple myeloma
    • Leukemia
    • Lymphoma
    • Langerhans cell histiocytosis
  • Rx: Management of hyperparathyroidism and, rarely, surgery

Suggested Reading

Hong WS, Sung MS, Chun K-A, et al. Emphasis on the MR imaging findings of brown tumor: a report of five cases. Skeletal Radiol 2011;40:205–13, 10.1007/s00256-010-0979-0

Mateo L, Massuet A, Solà M, et al. Brown tumor of the cervical spine: a case report and review of the literature. Clin Rheumatol 2011;30:419–24, 10.1007/s10067-010-1608-y

Current Issue

American Journal of Neuroradiology: 46 (6)
American Journal of Neuroradiology
Vol. 46, Issue 6
1 Jun 2025
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