Hypophysitis

Evidence-based neurology checklist on hypophysitis: Pathological types Lymphocytic Granulomatous Xanthomatous IgG4 antibody-related Drug-induced Risk factors Endocrine features Headache features Other features Lymphocytic hypophysitis

Pathological types

  • Lymphocytic
  • Granulomatous
  • Xanthomatous
  • IgG4 antibody-related

Drug-induced

Risk factors

Endocrine features

Headache features

Other features

Lymphocytic hypophysitis

References

  1. Levy A. Pituitary disease: presentation, diagnosis, and management. JNNP 2004; 75(Suppl III):iii47-iii52.
  2. Bellastella A, Bizzarro A, Coronella C, Bellastella G, Sinisi AA, De Bellis A. Lymphocytic hypophysitis: a rare or underestimated disease? Eur J Endocrinol 2003; 149:363-376.
  3. Motte J, Kreitschmann-Andermahr I, Fisse AL, et al. Trigemino-autonomic headache and Horner syndrome as a first sign of granulomatous hypophysitis. Neurol Neuroimmunol Neuroinflamm 2017; 4:e332. 
  4. Hunn BH, Martin WG, Simpson S Jr, Mclean CA. Idiopathic granulomatous hypophysitis: a systematic review of 82 cases in the literature. Pituitary 2014; 17:357-365. 
  5. Hanna B, Li YM, Beutler T, Goyal P, Hall WA. Xanthomatous hypophysitis. J Clin Neurosci 2015; 22:1091-1097. 
  6. And 4 more. Subscribe to see the full list

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