Immunoglobulin G4-related disease: case report and literature review

• Published in: Immunologic research 2021-10, Vol.69 (5), p.415-421
• Main Authors: Dong, Liang-Liang, Sheikh, Irfan Sahail, Huang, Ai-Hua, Wu, Xiao-Hong, Chen, En-Guo, Ying, Ke-Jing
• Format: Article
• Language: English
• Subjects: Aged; Allergology; Autoimmune diseases; Biomarkers; Biomedical and Life Sciences; Biomedicine; Biopsy; Brain - diagnostic imaging; Brain - pathology; Case reports; Central nervous system; Cerebrospinal fluid; Computed tomography; Diagnosis; Differential diagnosis; Disease Management; Disease Susceptibility; Fever; Humans; Immunoglobulin G; Immunoglobulin G4; Immunoglobulin G4-Related Disease - diagnosis; Immunoglobulin G4-Related Disease - etiology; Immunoglobulin G4-Related Disease - metabolism; Immunoglobulin G4-Related Disease - therapy; Immunoglobulins; Immunohistochemistry; Immunology; Immunosuppressive Agents - administration & dosage; Immunosuppressive Agents - therapeutic use; Inflammation; Internal Medicine; Literature reviews; Lung - diagnostic imaging; Lung - pathology; Lung diseases; Magnetic Resonance Imaging; Male; Medical imaging; Medicine/Public Health; Neuroimaging; Patients; Plasma cells; Prednisolone; Review; Signs and symptoms; Skull; Symptom Assessment; Tapering; Thickening; Tomography, X-Ray Computed; Treatment Outcome
• ISSN: 0257-277X; 1559-0755
• DOI: 10.1007/s12026-021-09215-2

Immunoglobulin (Ig) G4-related disease (IgG4-RD) is a rare and chronic progressive clinical entity, characterized by elevated serum IgG4 along with tissue infiltration by IgG4 + plasma cells. It is an immune-mediated fibro-inflammatory condition that can affect virtually any organ and tissue. IgG4-related lung disease (IgG4-RLD) occupies 14% of all IgG4-RD, with nonspecific symptoms and various abnormal radiographic patterns. Published data on IgG4-related hypertrophic pachymeningitis (IgG4-RHP), an increasingly recognized central nervous system manifestation of IgG4-RD, is also limited. Both lung and cranial dura involvement have not yet been reported until now. We further entail a review of the literature on the clinicopathologic features and differential diagnosis of this uncommon disease. We herein report an interesting case of a 70-year-old male patient admitted due to headache and fever. A magnetic resonance imaging (MRI) of the brain revealed extensive dural thickening with marked enhancement. Chest computed tomography (CT) scan showed nodular or mass-like consolidation and focal interstitial change. Thoracoscopic lung biopsy and lumbar puncture were conducted. After careful histopathological observation and consideration of alternative differential diagnoses, he was diagnosed with IgG4-related disease with lung and cranial dural involvement based upon significant elevation of serum and cerebrospinal fluid (CSF) IgG4 concentration. The patient was started on oral prednisolone 60 mg/day (1.0 mg/kg/day) for 14 days, and a tapering dose of 5 mg every 2 weeks followed by maintenance therapy at low dose for 3 months. His clinical manifestations, and serologic and imaging findings improved with steroid treatment. Currently, the patient remains well without disease progression. IgG4-RD should be considered as a differential when diagnosing other similar multisystemic lesions. Clinical examination, careful histological observation, and immunostaining for appropriate markers are essential in establishing the diagnosis. Clinicians should become familiar with this alternative differential diagnosis.