Lymphoproliferative disorders Flashcards
How can lymphoma present?
lymphadenopathy or
extranodal disease or
bone marrow involvement
Systemic B symptoms
weight loss >10% in 6 months fever drenching night sweats pruritis fatigue
How to tell what type of lymphoma it is
biopsy - LN
How to tell where the lymphoma is
CT and clinical exam
Classification of “lymphoma”
Hodgkin
non Hodgkin - high grade and low grade
Lymphoproliferative disorders
ALL
CLL
Hodgkin lymphoma
non Hodgkin lymphoma
high grade NHL common type
diffuse large B cell lymphoma
low grade NHL common type
follicular
ALL - blood signs
high WCC, low Hb and low platelets
diagnosing ALL
> 20% lymphoblasts in the bone marrow
ALL - age
75% under 6 years
Are most ALL B or T cell lineages?
B
ALL - history of symptoms
bone marrow failure
bone/joint pain
Standard treatment for ALL
induction chemo
consolidation therapy
CNS directed treatment - intrathecal
maintenance treatment for 18 months
Who would receive a stem cell transplant for ALL?
high risk
newer therapies for ALL
bispecific T cell engagers - BiTe
CAR
problems with newer therapies for ALL
cytokine release syndrome
neurotoxicity
ALL poor risk factors
increasing age increasing WCC immunophenotyped cytogenetics - Philadelphia gene slow/poor response to treatment
CLL diagnosis
blood >5x10 9 lymphocytes, bone marrow >30% lymphocytes
Presentation of CLL
often asymptomatic
frequent findings = splenomegaly, bone marrow failure, lymphadenopathy, fever, sweats
less common = hepatomegaly, infections, weight loss
Associated findings with CLL
immunoparesis
haemolytic anaemia
Staging for CLL
binets
Indication for treatment - CLL
massive lymphadenopathy
progressive splenomegaly
progressive bone marrow failure
systemic symptoms
CLL treatment
often nothing
cytotoxic chemo
monoclonal ab
novel agent eg tyrosine kinase inhibitor