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Mostly in kids and young adults; 80% of childhood leukemia
Almost twice as common in whites and more common in boys
Lymphadenopathy (from leukemic infiltration), hepatosplenomegaly (also leukemic infiltration), and infiltration of other organs (especially the brain and testicles) is common
May have a mediastinal mass reflecting thymic involvement with T cell ALL
Morphologic classification (FAB)
ALL L1
Homogenous population of small lymphoblasts (lymphoblasts = precursor B or T cells) with scant cytoplasm and variable basophilia
Nuclei are round and clefted with homogenous chromatin; inconspicuous or absent nucleoli
85% of all childhood ALL
Often have PAS “block” positivity
ALL L2
Heterogeneously sized population of relatively large lymphoblasts with moderately abundant cytoplasm and variable basophilia
Multiply cleaved nuclei with prominent nucleoli and clumped chromatin
15% of childhood ALL; most frequent adult ALL
PAS
ALL L3
Homogenous population of intermediate sized cells (L1 <>
Cytoplasm is abundant, deeply basophilic, and vacuolated (vacuoles are oil red O (+))
Nuclei are round to oval with 1+ prominent nucleoli
This is a leukemic manifestation of Burkitt’s lymphoma
If it’s first and most prominently manifested in the blood it’s leukemia
If it’s first and most prominently manifested in the nodes it’s lymphoma
1-2% of childhood ALL
Immunologic classification
80% are of B cell origin; those that are of T cell origin are arrested in the early intrathymic stages
Prognosis related to immunophenotype
Best with early precursor B cell ALL
Intermediate with immature T cell and pre-B cell ALL
Poorest with mature B cell ALL (ALL L3; leukemic Burkitt’s)
ALL in kids 2-10 YOA with early pre-B phenotype and hyperdiploidy carries the best prognosis
Adults (no matter phenotype) and kids with mature B phenotype have a very poor prognosis
Category: Medical Subject Notes , Pathology Notes
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