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170 Possible Causes for Immunoglobulin G Increased, Interstitial Pneumonitis

  • Infectious Mononucleosis

    In patients with AIDS, Epstein-Barr virus is associated with hairy leukoplakia, leiomyosarcoma, CNS lymphoma, and lymphoid interstitial pneumonitis in children.[] However, it may occasionally cause a syndrome of fever, interstitial pneumonitis, pancytopenia, and uveitis (ie, chronic active EBV).[]

  • Lymphocytic Interstitial Pneumonia

    Previous Contents Next Lymphocytic interstitial pneumonitis (LIP) LIP is a non-infectious pulmonary disorder caused by white cell infiltration into alveolae.[] Thirteen patients with lymphocytic interstitial pneumonitis were seen at the Mayo Clinic from 1966 through 1976.[] pneumonitis Plasma cell interstitial pneumonitis Interstitial lung disease Laboratory Studies Laboratory test results are nonspecific for lymphocytic interstitial pneumonia[]

  • Granulomatous Lung Disease

    The others: Non-specific interstitial pneumonia (NSIP) Organizing pneumonia (OP) Respiratory bronchiolitis (RB) Desquamative interstitial pneumonitis (DIP) Lymphocytic interstitial[] […] associated with BCG changes secondary to chronic aspiration pneumonitis lymphoproliferative lymphocytic interstitial pneumonitis lymphomatoid granulomatosis pulmonary Langerhans[] Eosinophilic granuloma (granulomas are a small component) Bronchocentric granulomatosis (granulomas are a small component) Churg-Strauss Syndrome Lymphocytic Interstitial[]

  • Necrotizing Alveolitis

    Desquamative interstitial pneumonia Nonspecific interstitial pneumonia Drug-induced pneumonitis Chronic presentation Nonspecific interstitial pneumonia Unusual interstitial[] Serum immunoglobulins (Ig) G and A were normal, while IgM fraction was increased (6.84 g/L; normal values 0.40-2.30 g/L).[] Idiopathic interstitial pneumonias The idiopathic interstitial pneumonias (IIPs) comprise a heterogenous group of disorders.[]

  • Sjogren's Syndrome

    Bronchiolitis and bronchiectasis are common airway manifestations but interstitial pneumonitis, and lymphocytic interstitial pneumonitis may also occur.[] There is also evidence for increased intrathecal immunoglobulin G (IgG) synthesis.[] interstitial pneumonitis 11 lymphoid interstitial pneumonia (LIP) focal lymphoid hyperplasia of the lung small airways disease 7,8 pulmonary amyloidosis : AL type 14 Mikulicz[]

  • Pulmonary Sarcoidosis

    However, the other patient exhibited usual interstitial pneumonia (UIP) in the lower lobe and sarcoidosis lesions in the upper lobe.[] The histological findings revealed usual interstitial pneumonia (UIP)-like lesions, whereas non-caseous granulomas were not detected.[] pneumonias (IIPs).[]

  • Rheumatoid Arthritis

    KEYWORDS: nonspecific interstitial pneumonia; overlap syndrome; rheumatoid arthritis; systemic sclerosis[] […] that the usual interstitial pneumonia (UIP) pattern is more common in this patient population.[] She had been treated with methotrexate and methylprednisolone for rheumatoid arthritis (RA) and interstitial pneumonia.[]

  • Pulmonary Lymphomatoid Granulomatosis

    The biopsy specimen was sent for consultation, and the diagnosis of cellular interstitial pneumonitis with features of lymphocytic interstitial pneumonitis was made.[] Our case represents another presentation of LG masquerading as interstitial pneumonitis clinically.[] A computed tomography-guided biopsy of 1 of the nodules revealed cellular interstitial pneumonitis.[]

  • Systemic Lupus Erythematosus

    pneumonia [UIP]).[] Previously, we found increased immunoglobulin (Ig)G levels against varicella-zoster virus (VZV) in SLE patients compared to controls, while antibody levels against diphtheria[] pneumonia (nonspecific) (usual) due to collagen vascular disease Interstitial pneumonia (nonspecific) (usual) in diseases classified elsewhere Organizing pneumonia due to[]

  • Immune Thrombocytopenic Purpura

    pneumonitis.[] Elevated serum immunoglobulin G (IgG) was detected, and tests for platelet-associated IgG and anti-nuclear antibody were positive.[] Wajeeha Razaq A diagnosis of immune thrombocytopenic purpura was made in this otherwise healthy young man and he was started on intravenous immunoglobulin G (IVIG) at a dose[]

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