Primary granulomatous hypophysitis: a case report and literature review.

@article{Su2011PrimaryGH,
  title={Primary granulomatous hypophysitis: a case report and literature review.},
  author={Shao-bo Su and Da-jian Zhang and Shu-yuan Yue and Jianning Zhang},
  journal={Endocrine journal},
  year={2011},
  volume={58 6},
  pages={467-73}
}
Primary granulomatous hypophysitis (PGH) is a rarely occurred inflammatory disease of unknown etiology. We retrospective review a case of PGH treated by microsurgical transsphenoidal approach and review the appropriately documented cases of PGH collected from the literatures. The patient was a 56-year-old female who presented with 4 months history of headache and 2 months history of polyuria and polydipsia. Clinic examination did not find remarkable neurological signs, except endocrinological… CONTINUE READING