• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/33

Click to flip

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