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CLL is usually first suspected by a diagnosis of lymphocytosis, an increase in a type of white blood cell, on a complete blood count test. This frequently is an incidental finding on a routine physician visit.
Diagnosis is usually based on repeated complete blood counts and a bone marrow examination following observations of the symptoms. Sometimes, blood tests may not show that a person has leukemia, especially in the early stages of the disease or during remission.
Diagnosis. Diagnosing ALL begins with a thorough medical history, physical examination, complete blood count, and blood smears. While many symptoms of ALL can be found in common illnesses, persistent or unexplained symptoms raise suspicion of cancer.
Diagnosis Laboratory findings. The requisite lymphocytosis of this disease is typically 2-20x10 9 /L. Immunoglobulin derangements including hypergammaglobulinemia, autoantibodies, and circulating immune complexes are commonly seen. Peripheral blood
The diagnosis of MBL in these patients depends on finding 0.5-5x10 9 monoclonal B cells that express the makers characteristic of CLL/SLL MLB, atypical CLL/SLL MLB, non-CLL/SLL MLB, or MLB-MZ. However, individuals with CBL-MZ commonly present with B-cell blood counts that are extremely high (>4.0x10 9 ; range 3.0x10 9 /L to 37.1x10 9 /L); [2 ...
- Neutrophil - Wikipediawikipedia.org
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The diagnosis of HCL may be suggested by abnormal results on a complete blood count (CBC), but additional testing is necessary to confirm the diagnosis. A CBC normally shows low counts for white blood cells, red blood cells, and platelets in HCL patients.
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