|
Name
|
Age
|
Characteristics
|
Less specific characteristics
|
Disease Process
|
|
Acute Lymphocytic Leukemia (ALL)
|
Peaks age 2-9, then again in older adults
|
Bone, joint, abdominal pain, CNS symptoms, increased ICP, hepatosplenomegaly, lymphadenopathy,
meningitis, transverse lines of rarefaction on epiphyses of
long bones
|
Fever, pallor, bleeding, anorexia, fatigue, weakness, weight loss
|
Proliferation of immature lymphocytes
|
|
Chronic myelogenous leukemia (CML)
|
Peaks around age 45, dx anywhere from 25-60
|
Increased sweating, splenomegaly with sternal tenderness, high platelet count early
in the disease, increase in polymorphonuclear neutrophils, normal lymphocytes and
monocytes, Philadelphia chromosome
|
Joint pain, bone pain, weakness, fever, fatigue
|
Excessive mature neoplastic granulocytes, Philadelphia chromosome
|
|
Chronic lymphocytic leukemia (CLL)
|
Between 50-70, rare before 30.
|
Richter’s syndrome, pain or paralysis from enlarge lymph nodes compression nerves,
pulmonary symptoms, splenomegaly, night sweats, hepatomegaly, lymphadenopathy, hypogammaglobinemia,
thrombocytopenia, frequent infections
|
Fatigue, weight loss, anorexia, fever
|
Production and accumulation of functionally
inactive but long-lived, mature appearing lymphocytes
|
|
Acute Myelogenous Leukemia (AML)
|
Between 60-70 (peak)
|
Sternal tenderness with NO splenomegaly, gingival hyperplasia, high LDH, hypercellular
bone dysplasia with myeloblasts
|
Fever, headache, anemia, fatigue, weakness, mouth sores, bleeding, infection.
|
Proliferation of myeloblasts
|