Related Experiment Video
Updated: Jun 28, 2026

An In Vitro Model for the Study of Cellular Pathophysiology in Globoid Cell Leukodystrophy
Published on: October 21, 2014
Mind the gap: IgG4-related disease mimicking infectious cerebral mass lesions
Andrea De Maria1,2, Chiara Sepulcri3, Stefania Tutino3
1Clinica Malattie Infettive e Tropicali, DISSAL, University of Genoa, Largo R.Benzi 10, 16124, Genoa, Italy. De-maria@unige.it.
Insights
IgG4-related disease can mimic brain tumors and infections. This case highlights the importance of considering IgG4-related disease in the differential diagnosis of cerebral masses.
Area of Science:
- Neurology
- Immunology
- Pathology
Background:
- Cerebral intraparenchymal masses typically prompt evaluation for neoplastic or infectious causes.
- Diagnostic challenges arise when initial workups for common etiologies are inconclusive.
Observation:
- An 82-year-old male presented with seizures and cerebral masses, with a history of treated tuberculosis.
- Extensive workup excluded infectious and primary neoplastic origins.
- Histopathological examination of a resected lesion revealed IgG4-related disease.
Findings:
- The resected mass showed histiocytic granulomatous tissue with a significant IgG4-positive plasma cell component.
- The patient showed marked improvement following corticosteroid treatment.
Implications:
- IgG4-related disease should be considered in the differential diagnosis of single or multiple cerebral masses.
- This expands the known spectrum of IgG4-related disease presentations.
- Early recognition and treatment can lead to favorable patient outcomes.
Background:
Cerebral intraparenchymal masses represent usually a neoplastic, or infectious differential diagnostic workup in neurology or infectious disease units.
Case Presentation:
Our patient was an 82-year-old male presenting with seizures, cerebral masses and a history of past treated pulmonary tuberculosis. Initial workup included a differential diagnosis of an infectious mass/multiple abscess. After exclusion of infectious or primary neoplastic origins by negative HIV serology, the absence of immune suppression, endocarditic lesions, negative results of blood cultures and bronchoalveolar lavage, negative cerebrospinal fluid workout on spinal tap led to exclusion of infectious causes. A surgical procedure was performed to access one of the lesions. This yielded a firm, cyst-like mass of histiocytic granulomatous tissue with a conspicuous plasmacellular component and a relevant IgG4 plasmacellular component consistent with IgG4-related disease. Steroid treatment determined conspicuous improvement and led to discharge of the patient.
Conclusion:
Parenchymal IgG4-related disease may be included as a new entity in the differential diagnosis of single or multiple cerebral masses in addition to infectious or neoplastic etiology.
Related Concept Videos
Cryptococcal Meningitis
Bacterial Meningitis II: Pathophysiology
Encephalitis l: Introduction
Encephalitis ll: Pathophysiology
Brain Abscess l: Introduction
Cerebral Edema ll: Pathophysiology

