IgG4-negative pituitary inflammatory pseudotumor with sphenoidal involvement resembling a macroadenoma

Br J Neurosurg. 2023 Dec;37(6):1886-1892. doi: 10.1080/02688697.2020.1834509. Epub 2020 Oct 16.

Abstract

Background: Inflammatory pseudotumors (IPTs) are rare benign conditions of unknown etiology that can affect any part of the body. IPTs are most commonly associated with Immunoglobulin G4 (IgG4)-related disease. Central nervous system IPTs, especially with pituitary involvement, are even rarer entities. The presence of an IgG4-negative pituitary IPT with simultaneous extracranial involvement has not been reported.

Case report: We present the case of a 41-year-old female with past medical history of rheumatoid arthritis and a diagnosis of pituitary IPT with coexisting sphenoidal (extracranial) involvement mimicking a pituitary macroadenoma at presentation. The patient underwent multiple consecutive biopsies, and an extensive workup prior to establishing the diagnosis. Laboratory work-up showed normal serum IgG4 and unremarkable liver function tests.

Conclusion: Pituitary lesions with simultaneous sphenoidal involvement in patients with IgG4-negative systemic inflammatory disease should raise the clinical suspicion for intracranial IPTs, as these tumors can mimic aggressive counterparts causing adjacent bony erosion, and local invasion.

Keywords: Intracranial inflammatory pseudotumor; pituitary mass; pituitary pseudotumor; sellar pseudotumor; sphenoiditis.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Diagnosis, Differential
  • Female
  • Granuloma, Plasma Cell* / diagnostic imaging
  • Granuloma, Plasma Cell* / pathology
  • Humans
  • Immunoglobulin G
  • Immunoglobulin G4-Related Disease*
  • Pituitary Diseases* / diagnosis

Substances

  • Immunoglobulin G