Create issue ticket

205 Possible Causes for Immunodeficiency Is Progressive, Leukocytosis, Thrombocytosis

  • Adult-Onset Still Disease

    Both patients had marked leukocytosis with neutrophil predominance, thrombocytosis, elevated liver enzymes and elevated acute phase rectants.[] Collapsing glomerulopathy is a new pattern of renal disease that emerged with the human immunodeficiency virus (HIV) epidemic in the 1970s—HIV-associated nephropathy.[] AOSD) is a systemic inflammatory disease characterized by high-fevers, articular involvement, maculopapular rash, hepatosplenomegaly, lymphadenopathy, and a neutrophilic leukocytosis[]

  • Chronic Phase of Chronic Myeloid Leukemia

    Extreme thrombocytosis was present, although no evidence of acquired von Willebrand disorder was found.[] According to some investigators there is a reservoir of primitive progenitors that are capable of self-renewal or progression in vitro or in vivo in immunodeficient mice.[] CP-CML patients are generally asymptomatic and diagnosis of the disease is based on the incidental detection of hematological alterations: While leukocytosis 50*10 9/l is[]

  • Chronic Myeloid Leukemia

    A 10-year-old boy presented with spontaneous bruising and was found to have extreme thrombocytosis without neutrophilia/shift to immaturity, basophilia or eosinophilia.[] According to some investigators there is a reservoir of primitive progenitors that are capable of self-renewal or progression in vitro or in vivo in immunodeficient mice.[] Her disease was managed during pregnancy using interferon-α alone despite persistent leukocytosis.[]

  • Rheumatoid Arthritis

    FBC: normochromic, normocytic anaemia and reactive thrombocytosis are common in active disease.[] Host components which affect tumor progression. Tumor cell components which protect it from the immune system.[] Similarly, the platelet count is usually normal but thrombocytosis occurs in response to inflammation.[]

  • Familial Myelofibrosis

    […] lymphoid neoplasms or other malignancy Minor criteria: Leukoerythroblastosis Increased serum LDH (lactate dehydrogenase) Anemia Splenomegaly Laboratory Anemia, leukocytosis, thrombocytosis[] Myelofibrosis refers to the progressive replacement of functional bone marrow by connective tissue.[] A correlation between leukocytosis and risk of acute leukemia has been recently reported in patients with PV. 24 These data indicate that PV patients with leukocytosis are[]

  • Cecal Adenocarcinoma

    He was recently diagnosed as seropositive for human immunodeficiency virus, stage A1, with a viral load of 120000 copies/ml.[] A 77-year-old woman was transferred to our institution for abdominal pain, fever, and leukocytosis.[] He presented with asthenia and 10-day progression of abdominal pain, nausea, vomiting, absence of bowel transit, and great abdominal distension.[]

  • Promyelocytic Leukemia

    The peripheral smear showed normochromic, normocytic anemia (Hgb 8.6 g/dL, mean corpuscular hemoglobin concentration [MCHC] 35.2%, MCV 90 fL), mild thrombocytosis (platelets[] Progressive multifocal leukoencephalopathy (PML) was a rare disease until the era of human immunodeficiency virus (HIV) infection, when the number of cases of PML markedly[] The dynamic changes in leukocytosis showed a single peak wave in all the patients, and the median time to peak was 10 (range 2-26) days.[]

  • Systemic Amyloidosis

    Her past medical history was remarkable for membranoproliferative glomerulonephritis, hypertension, pulmonary hypertension, and anemia of thrombocytosis.[] Guy Pratt, Oliver Goodyear and Paul Moss, Immunodeficiency and immunotherapy in multiple myeloma, British Journal of Haematology, 138, 5, (563-579), (2007). O.[] Vincent Rajkumar, Monoclonal gammopathy of undetermined significance and smouldering multiple myeloma: emphasis on risk factors for progression, British Journal of Haematology[]

  • Myeloid Neoplasm Associated with FGFR1 Rearrangement

    : Myelodysplastic/myeloproliferative neoplasm with ring sideroblasts and thrombocytosis Considered full entity under MDS/MPN The name RARS-T is changed to MDS/MPN-RS-T.[] Reactive Lymphadenopathy Normal Lymph Node B-cell development Anatomy and cells Immunostaining patterns Primarily Follicular Pattern Reactive follicular hyperplasia Progressive[] Case 93 was from a 66-year-old man who had leukocytosis and circulating blasts (30%) and no eosinophilia.[]

  • Non-Hodgkin Lymphoma

    In the first case, the laboratory tests showed anemia, thrombocytosis, elevated inflammatory biomarkers, a low level of iron, and hypoproteinemia.[] The initial therapy and therapeutic response, details of remission, progression, or relapse, and subsequent therapies and follow-up were tabulated in each case.[] Thrombocytosis and lymphocytosis may also occur. Renal function and electrolytes: obstructive nephropathy, hypercalcaemia. LFTs. Serology: HIV, HTLV-1, hepatitis C.[]

Similar symptoms