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Preparation of Mouse Pituitary Immunogen for the Induction of Experimental Autoimmune Hypophysitis
Published on: December 17, 2010
Lymphoplasmacytic hypophysitis associated with immunoglobulin G4
Peter Khong1, Alar Enno1, Balsam Darwish1
1Liverpool Hospital, Elizabeth Street, Liverpool, NSW 2170, Australia.
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.
Area of Science:
- Endocrinology
- Neuroimaging
- Immunopathology
Background:
- Sellar lesions can present with varied etiologies, including pituitary adenomas and inflammatory conditions.
- Amenorrhea and sellar mass are common presenting symptoms requiring thorough differential diagnosis.
Observation:
- A 33-year-old woman presented with a 2-year history of amenorrhea and an expanding sellar lesion.
- Magnetic resonance imaging (MRI) revealed a pituitary fossa lesion initially suspected to be a pituitary adenoma.
- The lesion enlarged by 5mm over one year, with dural and pituitary stalk enhancement.
Findings:
- Histopathology demonstrated a lymphocytic and plasma cell inflammatory infiltrate.
- The findings were suggestive of lymphoplasmacytic hypophysitis.
- The condition was associated with immunoglobulin G4 (IgG4) deposition.
Implications:
- This case highlights IgG4-related hypophysitis as a rare differential diagnosis for sellar masses.
- Accurate diagnosis is crucial for appropriate management and to differentiate from neoplastic lesions.
- Understanding IgG4-related hypophysitis expands the spectrum of sellar pathology.
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