Hypophysitis: A comprehensive overview

Presse Med. 2021 Dec;50(4):104076. doi: 10.1016/j.lpm.2021.104076. Epub 2021 Oct 21.

Abstract

Hypophysitis is defined as inflammation of the pituitary gland. It is a heterogeneous condition as it can originate from different parts of the pituitary gland, can be caused by different pathophysiological processes, and can be isolated or the manifestation of a underlying systemic disease. Hypophysitis usually presents with endocrine deficiencies, including diabetes insipidus, with varying patterns. A subset of patients presents with mass effects. The last decades major progress has been made in the understanding of this disease. New forms are now recognized, new diagnostics are being developed, and specific treatments are proposed. This review provides an overview of the current knowledge on hypophysitis using an aetiology-based approach and provides the clinician with a stepwise approach to the patient with (suspected) hypophysitis.

Publication types

  • Systematic Review

MeSH terms

  • Autoimmune Hypophysitis / diagnosis
  • Autoimmune Hypophysitis / etiology
  • Diabetes Insipidus / etiology
  • Endocrine System Diseases / diagnosis
  • Endocrine System Diseases / etiology
  • Erdheim-Chester Disease / complications
  • Histiocytosis, Langerhans-Cell / complications
  • Humans
  • Hypophysitis / diagnosis
  • Hypophysitis / diagnostic imaging
  • Hypophysitis / etiology*
  • Hypophysitis / therapy
  • Immune Checkpoint Inhibitors / adverse effects
  • Immunoglobulin G
  • Immunoglobulin G4-Related Disease / complications
  • Pituitary Gland / diagnostic imaging
  • Symptom Assessment / methods
  • Xanthomatosis / complications

Substances

  • Immune Checkpoint Inhibitors
  • Immunoglobulin G