Create issue ticket

47 Possible Causes for Hyperglobulinemia, Lymph Node Hyperplasia

  • Castleman Disease

    […] most common of these are anemia, fever, diaphoresis, weight loss, night sweating and fatigue. 1,2,9 Patients with M-PCV may have an elevated erythrocyte sedimentation rate, hyperglobulinemia[scielo.br] Castleman's disease (also known as angiofollicular lymph node hyperplasia or benign giant lymph node hyperplasia), first described by Benjamin Castleman in 1956, 1 is a rare[archbronconeumol.org] Castleman disease also is referred to as: Castleman's disease Angiofollicular lymph node hyperplasia Giant lymph node hyperplasia[medicinenet.com]

  • Lymphoproliferative Syndrome 1

    […] mechanism D89 ICD-10-CM Diagnosis Code D89 Other disorders involving the immune mechanism, not elsewhere classified 2016 2017 2018 Non-Billable/Non-Specific Code Type 1 Excludes hyperglobulinemia[icd10data.com] Histopathological analysis of lymph nodes showed lymphadenitis with paracortical hyperplasia.[casereports.bmj.com] Lymph nodes showed marked paracortical hyperplasia.[thedoctorsdoctor.com]

  • Rosai-Dorfman Disease

    Although the histopathology is fairly distinctive, the laboratory abnormalities are not; past reports note elevated erythrocyte sedimentation rate, anemia, and polyclonal hyperglobulinemia[journals.lww.com] There were 8 hilar lymph nodes measuring 4–8 mm in diameter. All were diagnosed as reactive hyperplasia. Fig. 2.[rc.rcjournal.com] The typical clinical features of this disease include bilateral painless lymphadenopathy, fever, and polyclonal hyperglobulinemia.[jdrntruhs.org]

  • Ankylosing Spondylitis

    node syndrome (also known as mucocutaneous lymph node syndrome and Kawasaki disease) Lymphoid hamartoma (also known as angiofollicular lymph node hyperplasia, Castleman’s[skbthrive.wordpress.com] node hyperplasia (Castleman’s disease, giant lymph node hyperplasia, lymphoid hamartoma) Ankylosing spondylitis (AS, Bekhterev’s disease, Marie-Strümpell disease) Anti-GBM[autoimmunecoach.co.uk] node hyperplasia (also known as Castleman’s disease, giant lymph node hyperplasia, and lymphoid hamartoma) Ankylosing spondylitis (AS; also known as Bekhterev’s disease and[skbthrive.wordpress.com]

  • Primary Myelofibrosis

    Polyclonal hyperglobulinemia may be present. Patients with sporadic idiopathic or familial pulmonary hypertension have significant marrow fibrosis.[patient-help.com] node hyperplasia, 354 vitamin D-deficiency rickets, 355–358 Langerhans cell histiocytosis, 359 acute promyelocytic leukemia, 360,361 and malignant histiocytosis. 362 Correction[patient-help.com] […] hypereosinophilic syndrome, 347,348 kala azar, 349 primary thrombocytopenic purpura, 350 thrombotic thrombocytopenic purpura, 351 tretinoin administration, 352 neuroblastoma, 353 giant lymph[patient-help.com]

  • Measles

    Measles, also known as rubeola, is one of the most contagious infectious diseases. It is a viral infection commonly affecting the pediatric population. The disease can be prevented by receiving vaccination against it. Preliminary signs and symptoms of measles begin to show effect after the 8 – 12 days of exposure to[…][symptoma.com]

  • Systemic Amyloidosis

    Biopsy of the submandibular mass revealed angiofollicular lymph node hyperplasia consistent with a diagnosis of Castleman's disease.[karger.com] First is Castleman disease, also known as angiofollicular lymph node hyperplasia. 38 Extensive involvement of the AA amyloid can occur, even with unicentric Castleman disease[bloodjournal.org] Keller AR, Hochholzer L, Castleman B: Hyaline-vascular and plasma-cell types of giant lymph node hyperplasia of the mediastinum and other locations.[karger.com]

  • Lyme Disease

    Lyme disease is a form of tick–borne illness first recognized in the year 1975. The disease is more prevalent in North America and Europe. In the preliminary stages, Lyme disease manifests as skin rashes and flu like symptoms. When the individual is first bitten by ixodid tick, a small red bump may develop in the[…][symptoma.com]

  • Gamma-Heavy Chain Disease

    . : A case of mu heavy-chain disease associated with hyperglobulinemia, anemia, and a positive Coombs test. Ann Hematol 1998, 77:231–234.[link.springer.com] node hyperplasia in a patient with impaired T cell function. ( 6811785 ) Okuda K....Sugai S. 1982 45 The pathology of gamma heavy chain disease: report of a case with morphologic[malacards.org] A case of mu heavy-chain disease associated with hyperglobulinemia, anemia, and a positive Coombs test. Ann Hematol. 1998;77:231-4. 37.[cancernetwork.com]

  • Temporal Arteritis

    node hyperplasia, and abnormal liver function, mesenteric ischemia, sore throat, choking sensation.[physio-pedia.com] […] eight percent of those with the condition include: pleural effusion, coronary vasculitis, pericarditis, myocarditis, peripheral neuropathy, hearing loss, renal arteritis, lymph[physio-pedia.com]

Further symptoms

Similar symptoms