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149 Possible Causes for Generalized Lymphadenopathy, Lactate Dehydrogenase Increased

  • 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[] IM is generally a self-limiting disease with symptoms resolving in a few weeks.[]

  • Angioimmunoblastic Lymphadenopathy

    A 55-year-old Japanese man presented with red papular lesions on the trunk and limbs, oedema, and generalized lymphadenopathy.[] Eosinophilia and hypergammaglobulinemia were not found whereas C-reactive protein, lactate dehydrogenase, β2-microglobulin and serum immunoglobulins were increased.[] Although complete remission of AML was achieved, fever persisted and atypical skin rash followed by generalized lymphadenopathy along with polyclonal hypergammaglobulinemia[]

  • Autoimmune Hemolytic Anemia

    She was found to have splenomegaly, generalized lymphadenopathy, pancytopenia, and acute hepatic failure.[] Unconjugated bilirubin is usually, but not always, elevated and urine urobilinogen is increased. Lactate dehydrogenase is usually elevated into the thousands.[] Abdomen was soft, lax with generalized tenderness and no hepatosplenomegaly. Apart from small right axillary lymph node, no lymphadenopathy could be detected clinically.[]

  • Cutaneous T-Cell Lymphoma

    This stage may last for years; neither hematological anomalies nor lymphadenopathy are generally encountered in these patients.[] No notable differences in rates of increased levels of serum lactate dehydrogenase (LDH) were observed (17 of 17 pEBVd( ) vs. 27 of 29 pEBVd(-)). pEBVd detection was associated[] Clinical Information A form of cutaneous t-cell lymphoma manifested by generalized exfoliative erythroderma; pruritus; peripheral lymphadenopathy, and abnormal hyperchromatic[]

  • Lassa Fever

    Although she was afebrile, generalized lymphadenopathy was still present, and a chest radiograph showed left-sided pleural effusion.[] High serum aspartate aminotransferase and lactate dehydrogenase (LDH) levels were remarkable in both patients.[] Viremia increased steadily and reached a plateau of approximately 10(8)-10(9) copies/ml 4 days before death, while IFN-gamma and TNF-alpha rose to extremely high levels only[]

  • Multiple Myeloma

    Abstract A 75-year-old male presented with generalized erythematous, scaly plaques and painless lymphadenopathy.[] Also, reflecting this aggressive clinical presentation, a higher proportion of patients with pPCL have significant leukocytosis, elevated lactate dehydrogenase (LDH) and β2[] This report highlights the dermatological manifestations of Rosai-Dorfman disease with generalized painless lymphadenopathy.[]

  • Non-Hodgkin Lymphoma

    Slow growing or indolent lymphomas usually present with lymphadenopathy, hepatomegaly, splenomegaly or different types of cytopenias.[] One indicator of the potential for tumor lysis syndrome is an elevated plasma lactate dehydrogenase level or hyperuricemia at the time of diagnosis.[] Most of the aggressive lymphomas present with a rapidly growing tumor mass, fever, night sweats, weight loss, and increased levels of serum lactate dehydrogenase and uric[]

  • Hairy Cell Leukemia

    […] nodes detected on CT scan, while one patient had generalized lymphadenopathy, and the others had either axillary or cervical nodes.[] Lactate dehydrogenase (LDH) is usually normal.[] However, the majority of patients complain of generalized fatigue and weakness.[]

  • Multicentric Castleman's Disease

    Abstract Multicentric Castleman's disease (MCD) is a rare disorder characterized by fever, polyclonal hypergammaglobulinemia, and generalized lymphadenopathy.[] lymphadenopathy and the proliferation of plasma cells.[] It is typically accompanied by generalized lymphadenopathy and multiorgan involvement.[]

  • T-Cell Lymphoma

    Abstract A 64-year-old woman presented with generalized lymphadenopathy and systemic manifestations.[] He developed graft-versus-host disease with skin and gastrointestinal involvement and generalized lymphadenopathy 4 months after transplantation.[] Clinical presentation The clinical spectrum includes high fevers, generalized lymphadenopathy, a skin rash, and hepatosplenomegaly.[]

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