White Blood Cell Quiz Flashcards
1
Q
- Pro-lymphocytes (mitotically active) aggregate together forming proliferation centers
- Smudge Celll
- CD19, 20, 23, and 5 (T-cell marker)
- Location: Blood and marrow
A
CLL
2
Q
- Pro-lymphocytes (mitotically active) aggregate together forming proliferation centers
- Smudge Celll
- CD19, 20, 23, and 5 (T-cell marker)
- Location: Lymph nodes
A
SLL
3
Q
- CD10, 18, 22, and TdT
- Invade bone marrow
- t(9;22) or (12;21)
A
Precursor B cell ALL
4
Q
- CD3, 7, and TdT
- Thymic tumor
- t(9;22) or (12;21)
A
Pre T cell ALL
5
Q
- Nodular pattern of infiltration of tissue
- sIg, CD 19, 20, and CD79a (CD5 is not expressed)
- Stain for bcl-2 is (+)
- T(14;18)
A
Follicular Lymphoma
6
Q
- CD19, 20, 22, 79a, sIg
- Cells overexpress bcl-6
- Large cells
A
Diffuse Large B cell Lymphoma
7
Q
- CD10, 19, 20, 22, 79a, sIg, and bcl-6
- Translocation involves c-myc on chromosome 8
- Marophages with ingested debris
- Small cells
A
Burkitt Lymphoma
8
Q
- Mott cell (perinuclear clearning)
- cIg (+)
- Punched out bone lesions
A
Multiple Myeloma
9
Q
- CD19, 20, 22, 79a, surface IgM
- NOT CD5 or CD23 (distinguishes from B-CLL)
- Intranuclear inclusion, IgM
- Secretes M protein
- NO L-chains
A
Lymphoplasmacytic Lymphoma
10
Q
- Resemble normal B cells
- CD5, 19, 20, 22 and sIg (IgM)
- NO CD10 or 23
- Over expression of cyclin D1
- Painless lymphadenopathy
A
Mantle Cell Lymphoma
11
Q
- CD19, 20, 22, 79a, sIgM
- Associated with H. pylori infxn
A
Extranodal Marginal Cell Lymphoma
12
Q
- CD19, 20, 22, 79a, sIgM
- Replaces white pulp germinal centers
A
Splenic Marginal cell lymphoma
13
Q
- Thin membrane protrusions (looks like hair)
- CD103
- Marrow fibrosis
- Massive splenomegaly and pancytopenia
A
Hairy Cell Leukemia
14
Q
- CD4, 30
- Anaplastic lymphoma kinase
- Infiltration of dermis and generalized lymphadenopathy
A
Anaplastic Large Cell Lymphoma
15
Q
- HTLV-1 Provirus Positive
- CD2, 3, 5
- Hyperlobated nuclei
- Bone and cutaneous lesions
A
Adult T cell Leukemia / Lymphoma
16
Q
- CD4, 2, 3, 45RO, 5
- Cells form bands thru tissue
- Symptoms
- Inflammatory preneoplastic phase: like eczema
- Plaque phase
- Tumor phase: with ulcerations
A
Mycosis Fungoides
17
Q
- CD4, 2, 3, 45RO, 5
- cell with cerebriform shaped nucleus
- Erythroderma
- Lymphadenopathy
A
Seazary Syndrome
18
Q
- TCR, CD3, CD8
- Lymphocytosis
- Anemia
- Neutropenia
A
T cell variant Large Granular Lymphocytic Leukemia
19
Q
- CD56
- B symptoms
- Hepatosplenomegaly
- Anemia / Thrombocytopenia
A
NK cell variant Large Granular Lymphocytic Leukemia
20
Q
- CD2 and CD56
- Associated with EBV
- Invade small vessels
- ischemic necrosis
- Most commonly affects nose and sinuses
A
Extranodal NK / T cell Lymphoma
21
Q
- HRS Lacunar cells
- CD15+, CD30+, EBV-, CD20-
- Bands of collagen divide tissue into nodules
A
Nodular Sclerosis Hodgkins Lymphoma
Presents in Stage 1 or 2
22
Q
- Classic HRS and Mononuclear variants
- CD15+, CD30+, EBV+
A
Mixed Cellular HL
Presents in stage 3 or 4
23
Q
- Classic HRS cell and Mononuclear variants
- CD15+, CD30+
- 40% EBV+
- Infiltrate mostly T cells
A
Lymphocyte Rich HL
24
Q
- Hypocellular infiltrate
- CD15+, CD30+, EBV+
- Non-collagenous fibrosis
A
Lymphocyte Depletion HL
Presents in Stage 3 or 4
25
* Popcorn cell
* CD20+
* Able to produce Ig
* Inguinal node involvement
* Inflammatory infiltrate mostly B cells
Nodular Lymphocyte Predominant HL
Presents in stage 1 or 2
26
* Myeloid blasts \> 20% of bone marrow cells
* CD34, 33, some with CD15
* large nucleus with clear cytoplasm
AML, M1
27
* Myeloid blasts \> 20% of bone marrow cells
* CD34, 33, some with CD15
* large nucleus with fine, azurophilic peroxidase positive granules
AML, M2
28
* Myeloid blasts \> 20% of bone marrow cells
* CD34, 33, some with CD15
* large nucleus with Hypergranular, azurophilic peroxidase positive granules and Auer rods
AML, M3
29
* Myeloid blasts \> 20% of bone marrow cells
* CD34, 33, some with CD15
* large nucleus with basophilic granules in cytoplasm
AML, M4
30
* Myeloid blasts \> 20% of bone marrow cells
* CD34, 33, some with CD15
* large, folded or lobulated nucleus
* Peroxidase negative
* Esterase positive
AML, M5
31
* Circulating neutrophils, metamyelocytes, and myelocytes
* Marrow is ~100% cellular
* bcr-abl fusion gene
CML
32
* Hypercellular bone marrow
* erythrocytosis, granulocytosis, and thrombocytosis in periphery
* Increased red cell mass and hematocrit
* Low lvls of EPO
* Erythromelalgia
Polycythemia Vera
33
* Thrombocytosis with giant platelets
* Erythromelalgia
* Characteristics of other myeloproliferative diseases are absent
Essential thrombocytosis
Must be diagnosed by excluding other diseases
34
* Marrow fibrosis
* In marrow, megakaryocytes are large and clustered
* Peripheral blood shows nucleated erythroid progenitors, granulocytic progenitors, and teardrop shaped RBCs
Primary Myelofibrosis
Marrow converted to bone late in disease
35
* Cells express CD1, S-100, HLA-DR
* Birbeck granules with areas of dilation
Langerhans cell histiocytosis
36
What is the Hand Schuller Christian triad?
* In Langerhans Cell Histiocytosis
* Diabetes insipidus
* Exophthalmos
* Involvement of calvaria