Lymphoplasmacytic hypophysitis associated with immunoglobulin G4

Peter Khong1, Alar Enno1, Balsam Darwish1

  • 1Liverpool Hospital, Elizabeth Street, Liverpool, NSW 2170, Australia.

Summary

A rare case of lymphoplasmacytic hypophysitis, associated with immunoglobulin G4 (IgG4), presented as an expanding sellar lesion in a 33-year-old woman. This condition mimicked a pituitary adenoma but was confirmed by histopathology.

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