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

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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

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3
Q
  • CD10, 18, 22, and TdT
  • Invade bone marrow
  • t(9;22) or (12;21)
A

Precursor B cell ALL

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4
Q
  • CD3, 7, and TdT
  • Thymic tumor
  • t(9;22) or (12;21)
A

Pre T cell ALL

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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

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6
Q
  • CD19, 20, 22, 79a, sIg
  • Cells overexpress bcl-6
  • Large cells
A

Diffuse Large B cell Lymphoma

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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

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8
Q
  • Mott cell (perinuclear clearning)
  • cIg (+)
  • Punched out bone lesions
A

Multiple Myeloma

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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

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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

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11
Q
  • CD19, 20, 22, 79a, sIgM
  • Associated with H. pylori infxn
A

Extranodal Marginal Cell Lymphoma

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12
Q
  • CD19, 20, 22, 79a, sIgM
  • Replaces white pulp germinal centers
A

Splenic Marginal cell lymphoma

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13
Q
  • Thin membrane protrusions (looks like hair)
  • CD103
  • Marrow fibrosis
  • Massive splenomegaly and pancytopenia
A

Hairy Cell Leukemia

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14
Q
  • CD4, 30
  • Anaplastic lymphoma kinase
  • Infiltration of dermis and generalized lymphadenopathy
A

Anaplastic Large Cell Lymphoma

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15
Q
  • HTLV-1 Provirus Positive
  • CD2, 3, 5
  • Hyperlobated nuclei
  • Bone and cutaneous lesions
A

Adult T cell Leukemia / Lymphoma

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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