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Welcome to the new AJNR, Updated Hall of Fame, and more. Read the full announcements.


AJNR is seeking candidates for the position of Associate Section Editor, AJNR Case Collection. Read the full announcement.

 

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

March 21, 2019
  • Description
  • Legends
  • Diagnosis
  • Brain Teaser
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Pituitary Abscess

  • Background
    • ​Pituitary abscess is a rare, but potentially life threatening condition unless promptly diagnosed and treated, and it accounts for less than 1% of all pituitary diseases.
    • Given the rare incidence and vague symptoms accompanying the disease, the majority of cases are diagnosed either post mortem or post operatively. 
    • Pituitary abscesses may occur in a normal pituitary gland in 70% of cases, or secondary to a preexisting lesion, such as craniopharyngioma, adenoma, or a Rathke cleft cyst.
    • It can be due to hematogenous spread of infection or direct spread such as from meningitis or sinusitis.
  • Clinical Presentation
    • ​Patients may present with headache, anterior pituitary dysfunction, diabetes insipidus, visual disorders, dizziness, fever, and non specific signs of infection.
  • Key Diagnostic Features
    • ​On CT, there may be enlargement of the sella turcica with a round, low attenuation mass with a peripheral rim of enhancement. 
    • The MRI findings are a cystic sellar mass that is isointense or hypointense on T1 weighted images and isointense or hyperintense on T2 weighted images.
    • After contrast administration, there is a peripheral rim of enhancement.
    • The mass shows restricted diffusion.
  • Differential Diagnosis
    • ​Cystic pituitary adenoma: A cystic pituitary adenoma may mimic a pituitary abscess but should not show diffusion restriction.
    • Rathke’s cleft cyst or intrasellar craniopharyngioma: Both craniopharyngiomas and Rathke’s cleft cysts may contain nodules which would help differentiate from a pituitary abscess.
      • Craniopharyngiomas typically are lobulated cystic/nodular masses. They may show instrinstic T1 hypersignal. They may have peripheral contrast enhancement but should not have diffusion restriction. 
      • Rathke’s cleft cysts may rarely have a rim of enhancement on post contrast images but should not have diffusion restriction. They may be T1 hyperintense and may have an internal low T2 signal nodule.
    • Pituitary apoplexy: Pituitary apoplexy may be indistinguishable from pituitary abscess but both would be treated surgically. Pituitary apoplexy may show heterogeneous internal signal and restricted diffusion due to blood products, and may have peripheral contrast enhancement.   
  • Treatment
    • ​Surgical drainage and antibiotic therapy

Suggested Reading

  1. Karagiannis AK, Dimitropoulou F, Papatheodorou A, et al. Pituitary abscess: A case report and review of the literature. Endocrinol Diabetes Metab Case Rep​ 2016;1, 10.1530/EDM-16-0014.
  2. Byun WM, Kim OL, Kim D. MR imaging findings of Rathke's cleft cysts: Significance of intracystic nodules. AJNR Am J Neuroradiol 2000;21:485–88.
  3. Rogg JM, Tung GA, Anderson G, et al. Pituitary apoplexy: early detection with diffusion-weighted MR imaging. AJNR Am J Neuroradiol 2002;23: 1240–45.

Current Issue

American Journal of Neuroradiology: 45 (12)
American Journal of Neuroradiology
Vol. 45, Issue 12
1 Dec 2024
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