Panhypopituitarism apparently caused by hypophysitis masking a rapid development of a craniopharyngioma. A case report

  • P. Joosen
  • , P. Abrams
  • , J. Verhelst
  • , P. M. Parizel
  • , R. Salgado
  • , R. Abs

Research output: Contribution to journalArticlepeer-review

Abstract

We report the case of a 39-year old male presenting with panhypopituitarism and diabetes insipidus. MR imaging showed focal thickening of the pituitary infundibulum and infiltration of the anterior pituitary lobe, suggesting hypophysitis. Hormonal replacement therapy induced a pronounced amelioration of general well-being. Eight months later the subject developed visual disturbances. MR imaging now showed a cystic sellar mass. Surgical drainage was performed. A second operation was necessary six weeks later because of recurrent visual field defects. Diagnosis of papillary craniopharyngioma was finally made. This case demonstrates the remarkably rapid development of a craniopharyngioma, which initial radiological appearance was suggestive of hypophysitis. It also emphasizes the need of repeat MR examination in 1 case of unusual presentation of hypopituitarism.

Original languageEnglish
Pages (from-to)133-135
Number of pages3
JournalActa Clinica Belgica
Volume65
Issue number2
DOIs
Publication statusPublished - 2010
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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