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Original Articles

Necrotizing infundibulo-hypophysitis: case-report and literature review

ORCID Icon, , , , , & show all
Pages 613-616 | Received 29 Jan 2021, Accepted 07 Jun 2021, Published online: 21 Jun 2021

References

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  • Cacic M, Marinkovic J, Kruljac I, et al. Ischemic pituitary apoplexy, hypopituitarism and diabetes insipidus: a triad unique to necrotizing hypophysitis. Acta Clin Croat 2018; 57:768–71.
  • Honegger J, Schlaffer S, Menzel C, Pituitary Working Group of the German Society of Endocrinology, et al. Diagnosis of primary hypophysitis in Germany. J Clin Endocrinol Metab 2015;100:3841–9.
  • Fukuoka H. Hypophysitis. Endocrinol Metab Clin North Am 2015;44:143–9.
  • Gutenberg A, Caturegli P, Metz I, et al. Necrotizing infundibulo-hypophysitis: an entity too rare to be true? Pituitary 2012;15:202–8.
  • Ahmed SR, Aiello DP, Page R, et al. Necrotizing infundibulo-hypophysitis: a unique syndrome of diabetes insipidus and hypopituitarism. J Clin Endocrinol Metab 1993; 76:1499–504.
  • Onigata K, Yagi H, Ogawa R, et al. A child with necrotizing infundibulo-hypophysitis? Clin Pediatr Endocrinol 1994;3:223–4.
  • Ayuk J, McGregor EJ, Mitchell RD, et al. Acute management of pituitary apoplexy-surgery or conservative management? Clin Endocrinol (Oxf) 2004;61:747–52.

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