Immunoglobulin G Increased Causes & Reasons

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Immunoglobulin G Increased Symptom Checker: Possible causes include Third Trimester Pregnancy. Check the full list of possible causes and conditions now! Talk to our Chatbot to narrow down your search.

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Possible Causes

Third Trimester Pregnancy

The concomitant phenomenon of a third trimester pregnancy with a significant degree of pelvic organ prolapse is extremely rare. We report on a patient with pelvic organ prolapse complicating third trimester pregnancy treated by concomitant cesarean hysterectomy and abdominal sacrocolpopexy. A 30-year-old woman,[…] [ncbi.nlm.nih.gov]

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Hashimoto Thyroiditis

Electromicroscopy shows deposits of immunoglobulin (Ig) G and Tg along the basement membranes of follicular cells. Both B and T cells infiltrate the thyroid. [hormones.gr]

Increased expression of Th1-related cytokines such as IFNg, interleukin-2 and CD25 reportedly occurs in intrathyroidal T cells from patients with HT. [hormones.gr]

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Infectious Mononucleosis

The objective is to report a case of atypical acute infectious mononucleosis in a juvenile ankylosing spondylitis patient who was treated with infliximab. A 20-year-old man was hospitalized for the evaluation of lymphadenopathy and systemic symptoms. His symptoms developed at the eighth week of the infliximab[…] [ncbi.nlm.nih.gov]

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Non-Hodgkin Lymphoma

We report a rare case of non-Hodgkin lymphoma presented as an ileocecal mass. The patient was a 77-year-old man with history of symptoms of partial bowel obstruction, intermittent right iliac fossa pain, loss of weight, vomiting and fatigue. Clinical signs included moderate abdominal tenderness with a palpable mass in[…] [ncbi.nlm.nih.gov]

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Portal Cirrhosis

Laennec's cirrhosis Specialty Gastroenterology Laennec's cirrhosis, also known as portal cirrhosis, alcoholic cirrhosis, fatty cirrhosis, or atrophic cirrhosis,[1] is named after René Laennec,[2] a French physician and the inventor of the stethoscope. It is a disease of the liver in which the normal lobular architecture[…] [en.wikipedia.org]

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Rheumatoid Arthritis

Please log in to edit this article. Edit Synonym: chronic polyarthritis (CP) Lay term: rheumatism German : Rheumatoide Arthritis 1 Definition Rheumatoid arthritis is a chronic inflammation system disease, which occurs in the interior skin ( synovium ), of a joint and causes a clinical picture of a polyarthritis.[…] [flexikon.doccheck.com]

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Celiac Disease

G; IgA, immunoglobulin A; AGA, anti-gliadin antibodies; EMA, endomysial antibodies; tTG, tissue transglutaminase. [dx.doi.org]

Valletta E., Fornaro M., Pecori S., Zanoni G. Selective immunoglobulin A deficiency and celiac disease: Let’s give serology a chance. J. Investig. Allergol. Clin. [ncbi.nlm.nih.gov]

Recognition of the coeliac iceberg has also contributed to increased detection of cases of coeliac disease (Fig. 1 ). 12 This concept demonstrates the clinical variability [dx.doi.org]

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Heroin Dependence

Addict Biol. 2014 Jan;19(1):111-21. doi: 10.1111/j.1369-1600.2012.00445.x. Epub 2012 Apr 13. Nelson EC 1, Lynskey MT, Heath AC, Wray N, Agrawal A, Shand FL, Henders AK, Wallace L, Todorov AA, Schrage AJ, Madden PA, Degenhardt L, Martin NG, Montgomery GW. Author information 1 Department of Psychiatry, Washington University[…] [ncbi.nlm.nih.gov]

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Macronodular Cirrhosis

BACKGROUND/AIMS: Incomplete septal cirrhosis (ISC) is a form of macronodular cirrhosis characterized by slender, incomplete septa that demarcate inconspicuous nodules. Its clinical features have not been investigated in a large series. The aims of this study were to review the clinical symptoms and evolution of ISC in[…] [ncbi.nlm.nih.gov]

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Cryptogenic Cirrhosis

Abstract Some patients diagnosed with cryptogenic cirrhosis may have "burned-out" nonalcoholic fatty liver disease (NAFL). To test this hypothesis, we used our liver transplant database (November 1984 to November 1998) to assess the incidence of NAFL in patients with cryptogenic cirrhosis after orthotopic liver[…] [ncbi.nlm.nih.gov]

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Multiple Myeloma

Consistent with a hypomorphic effect, we find that the MM risk allele also associates with reduced levels of immunoglobulin A (IgA) and G (IgG) in healthy subjects ( P 8.6 [dx.doi.org]

(Ig) G or IgA of at least 30 g/L or urinary monoclonal protein of at least 500 mg per 24 hours. [web.archive.org]

10 9 and P 6.4 10 3, respectively) and, potentially, with an increased risk of bacterial meningitis (OR 1.30; P 0.0024). [dx.doi.org]

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Systemic Lupus Erythematosus

Previously, we found increased immunoglobulin (Ig)G levels against varicella-zoster virus (VZV) in SLE patients compared to controls, while antibody levels against diphtheria [ncbi.nlm.nih.gov]

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Sjögren Syndrome

There is also evidence for increased intrathecal immunoglobulin G (IgG) synthesis. [epilepsy.com]

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Nephrotic Syndrome

Immunoglobulin G (IgG)-λ type M protein was detected, and the levels of free λ chain was significantly increased. [ncbi.nlm.nih.gov]

Risk of infection may be increased in INS because of low immunoglobulin (Ig)G levels, which do not appear to be the result of urinary losses. [emedicine.com]

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Immune Thrombocytopenic Purpura

Elevated serum immunoglobulin G (IgG) was detected, and tests for platelet-associated IgG and anti-nuclear antibody were positive. [ncbi.nlm.nih.gov]

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 [healio.com]

In short, idiopathic thrombocytopenic purpura is an autoimmune disorder caused by immunoglobulin G (IgG) auto-antibodies on the platelet surface. [sanevax.org]

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Viral Hepatitis

Abstract The commonest causes of acute pancreatitis are cholelithiasis and alcohol. Rare causes include various viral infections, among which mumps is the commonest. Hepatitis A, hepatitis B and, recently, hepatitis E have been reported to cause acute but mild pancreatitis in patients with acute viral hepatitis. This[…] [ncbi.nlm.nih.gov]

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Primary Immune Deficiency Disorder

This article needs to be updated. Please update this article to reflect recent events or newly available information. (March 2019) Primary immunodeficiencies are disorders in which part of the body's immune system is missing or does not function normally. To be considered a primary immunodeficiency (PID), the cause[…] [en.wikipedia.org]

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Sarcoidosis

Intern Med. 2017 Oct 1;56(19):2583-2588. doi: 10.2169/internalmedicine.8768-16. Epub 2017 Sep 6. Author information 1 Department of Gastroenterology and Hepatology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Japan. 2 Saito Clinic, Japan. 3 Department of General Medicine,[…] [ncbi.nlm.nih.gov]

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Autoimmune Hepatitis

It is characterized by inflammatory liver histology, elevated transaminase level, circulating nonorgan-specific autoantibodies, and increased level of immunoglobulin G in [ncbi.nlm.nih.gov]

Elevated serum immunoglobulin G (IgG) was detected, and tests for platelet-associated IgG and anti-nuclear antibody were positive. [ncbi.nlm.nih.gov]

LABORATORY FEATURES • Lab Feature • Elevated AST • Hypergammaglobulinemia • Increased immunoglobulin G level • Hyperbilirubinemia • ALP 2 fold normal • Immunoserologic Markers [de.slideshare.net]

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Intraperitoneal Abscess in the Right Lower Quadrant

Fabrizio Michelassi, Jeffrey W. Milsom Springer Science & Business Media, ٠٦‏/١٢‏/٢٠١٢ - 515 من الصفحات Operative strategies in inflammatory small bowel disease, provides a thorough review of the operative techniques as well as the indications, and long term results for the surgical treatment of ulcerative colitis and[…] [books.google.com]

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Abdominal Visceral Abscess

Abstract This review describes the microbiology, diagnosis, and management of intra-abdominal abscesses (including subphrenic, hepatic, splenic, and retroperitoneal abscesses) in children. They often occur as a complication of local or generalized peritonitis, commonly secondary to appendicitis, necrotizing enterocolitis,[…] [ncbi.nlm.nih.gov]

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Subphrenic Abscess

A case of left-sided subphrenic abscess, secondary to perforation of a carcinoma of stomach, is described. The patient presented with a palpable spleen which was shown to be normal in size but displaced by the subphrenic collection. The importance of correct interpretation of this physical sign is discussed. [ncbi.nlm.nih.gov]

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Autoimmune Hemolytic Anemia

While conventional Coombs' tests were negative, the level of red blood cell (RBC)-bound immunoglobulin G (IgG) was increased. [ncbi.nlm.nih.gov]

Changing the RBC transfusion strategy to D- increased his Hb level to 6.7 g/dL on Day 10. [ncbi.nlm.nih.gov]

Definitions Treatment response was defined as at least a 1.5 g/dL increase of hemoglobin concentration (Hb) together with a 50% reduction of absolute reticulocyte count, observed [doi.org]

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Infectious Mononucleosis Hepatitis

Commonly, patients and physicians equate increased EBV immunoglobulin G (IgG) VCA antibody titers with chronic infectious mononucleosis or CFS because more than 90% of the [emedicine.medscape.com]

[…] population has increased EBV IgG VCA antibodies. [emedicine.medscape.com]

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Primary Biliary Cirrhosis

Further lab tests ( Table I ) showed increased levels and titers of antinuclear antibodies (ANA) speckled pattern and anti-smooth muscle antibodies (immunoglobulin G [IgG] [consultant360.com]

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Necrotizing Alveolitis

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). [clinicalcasereports.jacobspublishers.com]

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Diffuse Scleroderma

Chest. 1983 Nov;84(5):546-50. Abstract The pulmonary function and chest roentgenograms were evaluated in 88 patients with the CREST syndrome variant of progressive systemic sclerosis (PSS or scleroderma). Seventy-two percent of the patients had abnormal pulmonary function. An isolated decrease in diffusing[…] [ncbi.nlm.nih.gov]

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Cystic Fibrosis

Cystic fibrosis (mucoviscidosis) is an autosomal recessive genetic disorder of the exocrine glands. It is characterized by the production of abnormally viscous mucus by the affected glands. Cystic fibrosis is usually recognized in infancy or early childhood. The clinical manifestations of cystic fibrosis are typically[…] [symptoma.com]

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Granulomatosis with Polyangiitis

Granulomatosis with polyangiitis (GPA) is a systemic necrotizing small vessel vasculitis associated with circulating anti-neutrophil cytoplasmic antibodies (ANCAs). Skin manifestations, mostly represented by palpable purpura, papulonodular lesions and livedo reticularis, are present in up to 50% of the cases. Ulcerations[…] [ncbi.nlm.nih.gov]

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Sickle Cell Disease

Sickle RBCs have increased immunoglobulin G (IgG) on the cell surface. [emedicine.com]

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