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985 Possible Causes for Generalized Lymphadenopathy, Polyclonal Hyperglobulinemia

  • Castleman Disease

    CD can present with localized (unicentric CD or UCD) or generalized lymphadenopathy (multicentric CD or MCD).[] The disease is characterized by fever, weight loss, anemia, polyclonal hyperglobulinemia, splenomegaly, thrombocytosis and peripheral lymphadenopathy.[] , hypoalbuminemia, polyclonal hypergammaglobulinemia, leukocytosis, thrombocytosis or splenomegaly. 1,4 In contrast to the localized form, the clinical course of the multicentric[]

  • Rosai-Dorfman Disease

    A provisional diagnosis of fever with generalized lymphadenopathy was made and the patient was admitted for further evaluation.[] hyperglobulinemia.[] The typical clinical features of this disease include bilateral painless lymphadenopathy, fever, and polyclonal hyperglobulinemia.[]

  • Multicentric Castleman's Disease

    Multicentric Castleman's disease (MCD) is a rare disorder characterized by fever, polyclonal hypergammaglobulinemia, and generalized lymphadenopathy.[] hyperglobulinemia, elevated transaminases and renal disease. 2 , 5 , 7 Dispenzieri et al. 8 analyzed the clinical spectrum of Castleman’s disease in 113 patients.[] Multicentric Castleman's Disease (MCD) is a systemic disease characterized by generalized lymphadenopathy and the proliferation of plasma cells.[]

  • Toxoplasmosis

    Physical examination findings will reveal mainly lymphadenopathy, cervical and suboccipital.[] In an immunocompetent host, infection is generally asymptomatic, but toxoplasmosis in pregnancy can cause birth defects.[] Asymptomatic lymphadenopathy is the most usual presentation. The main lymph nodes involved are cervical and suboccipital.[]

    Missing: Polyclonal Hyperglobulinemia
  • Infectious Mononucleosis

    lymphadenopathy, including cervical lymphadenopathy tonsillar enlargement possible hepatomegaly Treatment and prognosis Symptomatic therapy is usually sufficient.[] There is an increase in mononuclear white blood cells and other atypical lymphocytes, generalized lymphadenopathy, splenomegaly, and occasionally hepatomegaly with hepatitis[] Imaging is usually not necessary, but certain findings on imaging can be suggestive: CT splenomegaly possible splenic rupture splenic infarction has been reported 3 generalized[]

    Missing: Polyclonal Hyperglobulinemia
  • Non-Hodgkin Lymphoma

    Slow growing or indolent lymphomas usually present with lymphadenopathy, hepatomegaly, splenomegaly or different types of cytopenias.[] Common examples are follicular lymphoma and marginal zone lymphoma.Few subtypes of Non-Hodgkin lymphoma may also present with rash, pruritus, generalized aches and pains.[]

    Missing: Polyclonal Hyperglobulinemia
  • Chronic Fatigue Syndrome

    Ten patients with self diagnosed enlarged lymph glands were referred to a general medicine outpatient clinic and careful examination did not confirm lymphadenopathy.[]

    Missing: Polyclonal Hyperglobulinemia
  • Herpes Zoster

    Cited by 37 Crossref Citations This article has been cited by the following publications. This list is generated based on data provided by CrossRef. You, Joyce H. S. Ming, Wai-kit Tsang, Owen Tak-yin Chan, Paul Kay-sheung and van Wouwe, Jacobus P. 2019. Optimal gender-specific age for cost-effective vaccination with[…][]

    Missing: Polyclonal Hyperglobulinemia
  • Skin Cancer

    Authors' conclusions: Some preventative treatments may benefit people at high risk of developing NMSC, but the ability to draw firm conclusions is limited by small numbers of trials, often with one trial per intervention or with inconsistent results between studies. Read the full abstract... Background: Some groups of[…][]

    Missing: Polyclonal Hyperglobulinemia
  • Graves Disease

    Justine Huart, Stéphanie Grosch, Christophe Bovy, Michel Moutschen and Jean-Marie Krzesinski , IgG4-related membranous glomerulonephritis and generalized lymphadenopathy without[] There was no cervical, supraclavicular, epitrochlear, axillary, or inguinal lymphadenopathy.[] Physical examination revealed a calm, well-nourished man with scleral icterus and generalized jaundice.[]

    Missing: Polyclonal Hyperglobulinemia

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