Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
33 Cards in this Set
- Front
- Back
Leukemoid Rxn
|
- due to infxn (appendicitis, whooping cough, cutaneous larva migrans)
- Inc. LAP not leukemia |
|
Hodgkins vs NHL
|
Hodgkins
- RS cells; localized single group of nodes; "B" symptoms; 50% assoc. w/ EBV; young and old; Men>Female EXCEPT in NODULAR SCLEROSING; fish flesh on cut section; EtOH pain and hyperkeratosis NHL - HIV or immunosuppression - multiple peripheral nodes; majority are B cells; 20-40yrs old |
|
good prognosis in hodgkins
|
lots of lymphs
and dec. RS |
|
Reed-Sternberg
|
CD30+ and CD15+ B cell origin
- necessary for diagnosis of Hodgkins |
|
Nodular Sclerosing
|
Hodgkin
- MC type (65%) - Females - Collagen banding in lymph nodes - lucunar variant RS (pale cell look like artifact) - primarily young adults RS + Lymphocyte +++ excellent prognosis |
|
Mixed Cellularity
|
Hodgkin
Men - 25% -Numerous RS cells, EBV assoc RS ++++ Lymphocyte +++ intermediate prognosis |
|
Lymphocyte predominant
|
hodgkin
6% Males younger than 35 - L and H variant RS (large and pale) RS + Lymphocyte ++++ Excellent prognosis |
|
Lymphocyte depleted
|
rare
- Older males w/ disseminated disease RS: high relative to lymphocytes Lymphs: + Poor prognosis |
|
Burkitt's
|
NHL
- young - t(8;14) cmyc next to heavy chain Ig (14) - Starry sky - EBV assoc - Jaw in africa, pelvis or abdomen in sporadic |
|
Diffuse large B-cell lymphoma
|
NHL
MCC of adult NHL older males, but sometimes kids -Come from germinal center - can be mature T cell origin |
|
Mantle cell
|
NHL - B cell
older males - t(11; 14) - Poor Prognosis - CD5+ |
|
Follicular lymphoma
|
NHL - B cell origin
adults - t(14;18) BCL-2 expression - difficult to cure; indolent course |
|
Adult T-cell lymphoma/leukemia
|
HTLV-1
- activation of TAX which inhibits p53 - TdT negative and CD4+ - monoclonal CD4 T cell expansion - Cutaneous lesions - lytic bone lesions - Japan, West Africa, and Caribbean - Aggressive |
|
Mycosis fungoides/Sezary syndrome
|
NHL - t cell type
- cutaneous patches/nodule - Indolent CD4+ sezary when it becomes lymphoma/leukemia |
|
Multiple Myeloma
|
blacks>white
M>F FRIED EGG appearance Large amounts of IgG less common IgA - Rouleux formation; Pancytopenia and Cachexia CRAB: hyperCalcemia (due to cytokines), Renal insufficiency, Anemia; Bone lesions |
|
MM association
|
- in susceptibility to infxn
- primary AL - Punch-out lesions (IL-1, clast stimulator and blast inhibitor) - M spike - Ig light chains in urine |
|
Waldenstroms
|
M spike
due to inc IgM hyperviscosity symptoms - NO LYTIC BONE LESIONS generalized lymphadenopathy not present in MM |
|
MGUS
|
Plasma cell expansiom w/o symptoms of MM
- small IgG spik - no BJ |
|
Leukemia ages
|
ALL: til 14
AML: 14-39 and 40-60 (60% of cases) CML; 40-60 (40% of cases in age range) CLL: >60 |
|
Acute vs Chronic leukemia
|
Serum: WBC acute lots of blasts and chronic less than 10%
BM: hypercellular w/ Acute >20% blasts and chronic < 20% blasts |
|
Myeloid Neoplasms
|
Chronic myeloproliferative disorders
Myelodysplastic syndromes AML |
|
Chronic Myeloproliferative disorders
|
PV, CML, Myeloid metaplasia w/ myelofibrosis
- splenomegaly - progress to spent phase and transformation to acute leukemia |
|
ALL
Acute lymphoblastic leukemia/lymphoma |
BM in children or Mediastinal mass in adolescent males (T cell)
- BM replaced by LOTS of lymphoblasts = TdT + (marker of pre-T and pre-B cells) = CALLA + aka CD10 (Common ALL antigen) - Spread to CNS and testes (Bcell types)/Tcell types Ant mediastinum = t(12;21) better prognosis = Tcell ALL = CD10 neg, but TdT + |
|
Small lymphocytic lymphoma/ Chronic lymphocytic leukemia (CLL)
|
- older adults (>60)
- often asymptomatic; = SMUDGE CELLS and WARM Antibody AUTOIMMUNE HA - B cells can't become plasma cells = Hypogammaglobinemia |
|
Hairy Cell leukemia
|
- splenomegaly
- no lymphadenopathy - Elderly = MATURE B-Cell tumor in elderly = FILAMENTOUS HAIRLIKE project = stains TRAP POSITIVE |
|
AML
|
Adults
Auer Rods = M2 and M3 (APL) - Inc Myelooblasts on peripheral smear - Gum infiltration |
|
APL
|
AML type M3
- auer rods - DIC t(15;17) PML/RARa - abnormal retinoic acid metabolism = high dose all-trans retinoic acid induces differentiation by maturing cells |
|
CML
|
40-60 yr old
- subtype of Chronic myeloproliferative disorders = Philadelphia t(9:22), BCR-ABL = inc neuts, metamyelocytes, basophils = can transform into AML (2/3) or ALL (1/3) -> blast crisis = differentiation from AML b/c no auer rods = VERY LOW LAP vs leukemoid rxn = IMATINIB (inhibits BCR-ABL tyrosine kinase) Thrombocytosis |
|
Auer Rods
|
Peroxidase positive inclusions in granulocytes and myeloblasts
= fused azurophilic granules - seen in APL (M3) - tx of APL releases auer rods which cause DIC |
|
t: (9;22)
t: (8:14) (14;18) (15:17) 11;22) 11; 14 12;21 |
(9;22) = philadelphia; CML (bcr-abl)
(8;14) = Burkitt's (c-myc) (14;18) = Follicular Lymphoma (BCL-2 activation) NHL (15;17) = APL (PML/RARa) (11;22) = Ewing's sarcoma (11;14) = Mantle cell lymphoma 12;21 = ALL good prognosis |
|
Langerhans histiocytosis
|
-dendritic/langerhans proliferation
express S-100 and CD1a = birbeck granules "tennis rackets" on EM |
|
RBCs WBCs Platelets Philadelphia chromosome LAP JAK2 mutation
PV ET Myelofibrosis CML |
RBCS WBCs Platelets Philadelphia LAP JAK2 mutation
PV= inc. inc inc negative >100 yes ET = norm norm inc negative yes Myelofibrosis = dec RBCs Negative philadelphia; normal LAP; Positive JAK2 mutation CML= dec RBCs; inc WBCs; Inc Platelets; Pos philadelphia; dec LAP; negative JAK2 |
|
Polycythemia Vera
|
- inc. plasma vol, inc RBC mass, normal 02 and DECREASED EPO
= RCC, WILM'S, HCC, HYDRONEPHROSIS - puritus after bathing |