History and exam
Key diagnostic factors
common
shortness of breath and fatigue
lymphadenopathy
Painless lymphadenopathy is common.[3]
Presence of lymphadenopathy can guide staging and treatment. See Diagnostic criteria and Management sections.
splenomegaly
Present in approximately 50% of cases.[4]
Presence of splenomegaly can guide staging and treatment. See Diagnostic criteria and Management sections.
uncommon
hepatomegaly
Present in approximately 14% of cases.[4]
Presence of hepatomegaly can guide staging and treatment. See Diagnostic criteria and Management sections.
Other diagnostic factors
uncommon
B symptoms
A minority of patients (approximately 10%) present with B symptoms (fever, drenching night sweats, unintentional weight loss) or other symptoms (e.g., chills, fatigue).[4]
Presence of B symptoms can guide treatment. See Management section.
recurrent infections
Due to dysfunctional lymphocytes and subsequent hypogammaglobulinemia.
May be present in patients with advanced disease.
epistaxis
Sign of thrombocytopenia.
May be present in patients with advanced disease.
pallor
Sign of anemia.
petechiae
Sign of thrombocytopenia.
Risk factors
strong
age over 60 years
Median age at diagnosis in the US is 71 years; approximately 70% of diagnoses occur in people age ≥65 years.[7]
weak
male sex
CLL is more common in men than in women (6.5 vs. 3.5 new cases per 100,000, respectively; 2019-2023, age-adjusted US data).[7]
white ethnicity
In the US, incidence of chronic lymphocytic leukemia (CLL) is greatest in non-Hispanic white people (8.2 new cases per 100,000 males and 4.4 new cases per 100,000 females, respectively; 2019-2023, age-adjusted US data).[7]
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