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Català Bauset, M., Gilsanz Peral, A., Girbés Borràs, J., Zugasti Murillo, A., Moreno Esteban, B., Halperin Rabinovich, I., Obiols Alfonso, G., Picó Alfonso, A., Del Pozo Picó, C., et al. (2008) Clinical Practice Guideline for the Diagnosis and Treatment of Hypophysitis. Endocrinología y Nutrición, 55, 44-53. http://dx.doi.org/10.1016/S1575-0922(08)70634-X

has been cited by the following article:

• TITLE: A Case Report of Lymphocytic Hypophysitis Related to Pregnancy

  AUTHORS: Estrella Diego, Andreea Ciudin, Olga Simo-Servat, Angel Ortiz, Liliana Gutierrez-Carrasquilla, Jordi Mesa

  KEYWORDS: Hypophysitis, Pregnancy, Panhypopituitarism, Lymphocytic Hypophysitis

  JOURNAL NAME: Open Journal of Endocrine and Metabolic Diseases, Vol.5 No.12, December 9, 2015

  ABSTRACT: A 39-year-old woman consulted in the postpartum period because of agalactia, polyuria, polydipsia, and headache and decreased visual acuity. The initial analysis was compatible with a panhypopituitarism. The magnetic resonance (MRI) showed an expansive sellar and suprasellar lesion of high density in the basal study and enhancement after contrast administration, in contact with the optic chiasm, so urgent surgery was indicated. While waiting for the surgery, intravenous corticosteroids were initiated and the symptoms rapidly resolved. Most of the pituitary axes were recovered, except the diabetes insipidus. The control MRI showed complete resolution of the sellar mass. The surgery was canceled and the diagnosis of lymphocyte hypohpyisitis was made. Lymphocyte hypophysitis is an uncommon disease in which inflammation of the pituitary gland occurs. This results in a permanent or transient hormonal insufficiency. Lymphocyte hypophysitis is a very rare condition that occurs preferentially in women in the peripartum period. Early initiation of high doses of systemic corticosteroids may avoid unnecessary surgery in some cases.