Severe lymphocytic adenohypophysitis with selective disappearance of prolactin cells: a histologic, ultrastructural and immunoelectron microscopic study

Citation
E. Horvath et al., Severe lymphocytic adenohypophysitis with selective disappearance of prolactin cells: a histologic, ultrastructural and immunoelectron microscopic study, ACT NEUROP, 101(6), 2001, pp. 631-637
Citations number
25
Categorie Soggetti
Neurosciences & Behavoir
Journal title
ACTA NEUROPATHOLOGICA
ISSN journal
00016322 → ACNP
Volume
101
Issue
6
Year of publication
2001
Pages
631 - 637
Database
ISI
SICI code
0001-6322(200106)101:6<631:SLAWSD>2.0.ZU;2-1
Abstract
We report the first documented example (case 1) of lymphocytic adenohypophy sitis (LAH) associated with selective destruction of prolactin cells. The m orphologic data are compared to those obtained in another, more typical cas e (case 2). Case 1 was a 35-year-old woman with remote history of pregnancy who presented with headache, oligomenorrhea and visual disturbances. The b lood prolactin level was nearly undetectable, but no deficiency of other pi tuitary hormones was evident. A sellar and parasellar mass compressing the optic chiasm was removed transsphenoidally. Histology demonstrated massive infiltration with lymphocytes, plasma cells and macrophages causing marked destruction of pituitary acini. Part of the gland was fibrotic. Immunocytoc hemistry documented all pituitary hormones, but only few cells, probably ma mmosomatotrophs, were immunoreactive for prolactin. Electron microscopy and immunoelectron microscopy using double gold labeling for growth hormone an d prolactin detected no prolactin cells. A striking ultrastructural finding was the prominence of folliculostellate cells in areas of active cell dest ruction supporting the presumed immune role of these cells. LAH in case 2 ( 24-year-old woman) became manifest during late pregnancy, causing pituitary enlargement and visual field defects. Pituitary tests showed no major horm onal deficits. Moderate hyperprolactinemia was appropriate for her pregnanc y status. A sellar mass, thought to be adenoma, was removed. Histology demo nstrated multifocal LAH without major destruction of acinar structures. Imm unocytochemistry and electron microscopy documented all pituitary cell type s including the marked abundance of prolactin-producing cells, resultant of gestational prolactin cell hyperplasia. In addition to prolactin cells and growth hormone cells, immunoelectron microscopy showed several bihormonal mammosomatotrophs, also appropriate for pregnancy.