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Lymphocytic hypophysitis: report of an unusual case of a rare disorder.

Authors :
Durán Martínez M
Santonja C
Pavón de Paz I
Monereo Megías S
Source :
Journal of endocrinological investigation [J Endocrinol Invest] 2001 Mar; Vol. 24 (3), pp. 190-3.
Publication Year :
2001

Abstract

A 36-year-old non-pregnant woman presented with a four-month history of progressive visual deterioration and amenorrhea. The latest gestation was 6 years earlier. Hormonal study revealed central diabetes insipidus, hypopituitarism, and slightly increased prolactin level. Ophthalmologic examination showed bilateral hemianopsia. In the magnetic resonance imaging an intrasellar mass with supra and retrosellar extension was found. The mass showed a polylobular aspect with heterogeneous signal within the tissue. The normal neurohypophysis could not be identified. Pterional craniotomy was performed. The pathological examinations revealed fibrous tissue with heavy inflammatory infiltrate composed of lymphocytes and plasma cells, islands of eosinophilic epithelial cells stained positively for chromogranin, GH, ACTH, and PRL and negatively for antibodies directed against HLA-II antigens. This case of lymphocytic hypophysitis was not related to pregnancy and involved the neurohypophysis. We discuss the features that can help to make a preoperative differential diagnosis.

Details

Language :
English
ISSN :
0391-4097
Volume :
24
Issue :
3
Database :
MEDLINE
Journal :
Journal of endocrinological investigation
Publication Type :
Academic Journal
Accession number :
11314750
Full Text :
https://doi.org/10.1007/BF03343842