| Literature DB >> 19558303 |
Dibyendu Kumar Ray1, Chun Po Yen, Mary Lee Vance, Edward R Laws, Beatriz Lopes, Jason P Sheehan.
Abstract
Lymphocytic hypophysitis is a relatively uncommon autoimmune inflammatory disorder affecting the pituitary gland. It most frequently occurs in women of child-bearing age. The authors report on their experience with a patient who presented with diplopia and marked enlargement of the pituitary gland. She underwent transsphenoidal surgery, and histopathological analysis confirmed the diagnosis of lymphocytic hypophysitis. The disease proved refractory to resection, and any attempt at withdrawal of corticosteroid therapy resulted in a return of the patient's symptoms and enlargement of the sellar contents. The patient underwent Gamma Knife surgery (GKS) to the sella and both cavernous sinuses. After GKS, the patient was able to discontinue steroid therapy without return of her symptoms. Follow-up MR images demonstrated no evidence of recurrence of lymphocytic hypophysitis. For persistent lymphocytic hypophysitis, GKS is a reasonable treatment option.Entities:
Mesh:
Year: 2010 PMID: 19558303 DOI: 10.3171/2009.6.JNS081176
Source DB: PubMed Journal: J Neurosurg ISSN: 0022-3085 Impact factor: 5.115