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ABBEY MSII Unit 2 > Pathoma 6. > Flashcards

Pathoma 6. Flashcards

1
Q

Alkylating agents side effects? treat with?

A

neutropenia, also a risk factor for Acute Myeloid Leukemia arising from myelodysplastic dysplasia. Treat withGM–CSF and G–CSF

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2
Q

Gram negative sepsis can cause what in neutrophil count?

A

decrease due to mobilization to tissues

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3
Q

High cortisol state

A

Causes apoptosis of lymphocytes - Mobilization of marginal pool of leukocytes leading to release of neutrophils into bloodstream.

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4
Q

What cell line is most sensitive to whole body radiation?

A

Lymphocytes

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5
Q

Fc Receptors?

A

CD16

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6
Q

What distinguishes immature neutrophils?

A

Low expression of Fc receptors(CD16)

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7
Q

How does bacterial infection cause leukocytosis

A

mobilization of marginal pool

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8
Q

Monocytosis is seen in

A

chronic inflammatory state and malignancy

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9
Q

Eosinophilia is seen in

A

Allergic hypersensitivity, parasitic infection and Hodgkin’s Lymphoma

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10
Q

Mechanism of Eosinophilia in Hodgkin’s lymphoma…

A

increased IL–5 production

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11
Q

Basophilia

A

Chronic Myelogenous Leukemia(CML)

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12
Q

Lymphocytic Leukocytosis is seen in…

A

increased circulating lymphocytes caused by:\nviral infection and Bordetella Pertussis

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13
Q

Lymphocytic leukocytosis is a/w what BACTERIAL infection? MOA

A

Bordetella Pertussis–– produces lymphocytosis–promoting factor which blocks circulating lymphocytes from leaving the blood to enter lymph nodes. As such the lymphocytes are trapped in the blood

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14
Q

EBV infects?

A

–– Oropharynx, ––liver(hepatitis and hepatomegaly, elevated liver enzymes)–– B cells

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15
Q

atypical lymphocytes(which look like monocytes). They are reactive CD8+ T–cells that look like monocytes is characteristic of?

A

viral infection - EBV - T–cell hyperplasia causes:––Lymphadenopathy – paracortex(where T–cells reside)––Splenomegaly – Peri–arteriolar lymphatic sheath(PALS, where T–cells reside)

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16
Q

Monospot test. Interpretation?

A

Detects IgM heterophil antibodies that agglutinate RBCs from another animal. + means EBV. Confirm with viral capsid antigen. – with classic signs of mononucleosis could be infected with CMV

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17
Q

Splenic rupture?

A

infectious mononucleosis with EBV. Avoid contact sports for a year

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18
Q

Rash after penicillin

A

EBV

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19
Q

EBV risks

A

increase the risk of B–cell lymphoma, especially if immunocompromised

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20
Q

Characteristic marker for ALL?

A

TdT which is a DNA polymerase exclusive to lymphoblastic precursors

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21
Q

Characteristic marker for AML? Exceptions?

A

MPO and Auer Rods(crystallized MPO) are exclusive to AML- Acute Monocytic Leukemia and Acute Megakaryoblastic Leukemia usually lack MPO

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22
Q

Children over 5 with Down’s syndrome a/w

A

ALL

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23
Q

Most common type of ALL? Classic markers?

A

B–ALL- CD10, CD19, CD20

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24
Q

What prophylaxis do you need to administer in a case of B–ALL?

A

CSF and scrotum since they have a blood–brain blood–testis barrier that prevents medication from getting to them - B–ALL responds well to chemotherapy

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25
Q

T–ALL markers?

A

CD2 to CD8 - (CD2, CD3, CD4, CD7, CD8) - NOTABLY NO CD10

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26
Q

B–ALL chromosomal abnormalities?

A

t(12;21) translocation – good prognosis - t(9;22) translocation(Philadelphia chromosome) – poor prognosis - t(9;22) normally associated with CML but can also be seen with a poor prognosis form of B–ALL

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27
Q

Common presentation of T–ALL

A

mediastinal(thymic) mass in a teenager. Think T’s – Thymic Teenager T–ALL- Acute Lymphoblastic LymphOMA since it is a mass.

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28
Q

What subtype of AML is associated with a chromosomal abnormality?

A

Acute Promyelocytic Leukemia has t(15;17) which involves translocation of retinoic acid receptor(RAR) on chromosome 17 to chromosome 15; RAR disruption blocks maturation and promyelocytes(blasts) accumulate. Since these blasts contain lots of Auer Rods which can activated coagulation, there is a risk for DIC.

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29
Q

APL puts you at risk for? How do you prevent this?

A

DIC due to Auer rods in blasts. all–trans–retinoic acid(ATRA, a vit A derivative). Binds altered receptors and causes the blasts to mature(and eventually die).

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30
Q

Acute Myeloid Leukemia arises predominantly in what demographic?

A

Older population, 50–60 yrs

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31
Q

leukemia with infiltration of gums. Notable lab feature?

A

Acute monocytic leukemia(AML subclassification) - usually lack MPO

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32
Q

leukemia that lack MPO

A

Acute megakaryoblastic leukemia(don’t need/use MPO) also, Acute monocytic leukemia

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33
Q

Children under 5 with Down’s syndrome a/w

A

Acute megakaryoblastic leukemia - lacks MPO

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34
Q

Hematopoietic Stem Cell expresses what receptor

A

CD34+

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35
Q

Chronic Leukemia is characteristic of what cell line?

A

Mature lymphocytes(B and T cells)

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36
Q

Chronic Lymphocytic Leukemia has what cells? What receptors are expressed?

A

b–cells. CD5 and CD20\n\nCD5 normally expressed on T–cells. Here it is aberrantly expressed

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37
Q

Small Lymphocytic Lymphoma

A

involvement of lymph nodes in CLL

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38
Q

Complications of CLL

A

–– Hypogammaglobulinemia: neoplastic B–cells won’t make Ig’s. If they do, the Ig’s suck and agglutinate self–RBCs causing… ––Autoimmune Hemolytic Anemia ––Possibility to transform to large B–cell lymphoma

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39
Q

What is a risk factor for large B–cell lymphoma

A

CLL(Richter Transformation)\nmarked clinically by a NEW ONSET enlarging lymph node or spleen with a history of stable enlarged lymph nodes.\n\nAlso, follicular lymphoma

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40
Q

Most common cause of death in CLL

A

infection due to defective Ig production

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41
Q

tartrate resistant acid phosphatase

A

TRAP…a/w Hairy Cell Leukemia\n\n\nsplenomegaly – notably, expansion of RED PULP. Dry Tap – bone marrow is fibrosed - NOTABLY lymphadenopathy is ABSENT because they are trapped in red pulp.

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42
Q

hairy cytoplasmic processes a/w what disease? clinical features?

A

Tartrate resistant acid phosphatase(Hairy Cell leukemia)\n\nsplenomegaly – notably, expansion of RED PULP. Dry Tap – bone marrow is fibrosed - NOTABLY lymphadenopathy is ABSENT because they are trapped in red pulp.

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43
Q

treatment of hairy cell leukemia?

A

2–CDA(cladribine) which is an adenosine deaminase inhibitor. Causes adenosine to accumulate to toxic levels in neoplastic B–cells

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44
Q

ATLL

A

Adult T–cell Leukemia\Lymphoma\nneoplastic proliferation of CD4+ T cells. Strongly associated with HTLV–1(retrovirus)

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45
Q

geographic associations with ATLL

A

Japan and the Caribbean. Neoplastic proliferation of CD4+

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46
Q

Clinical features of ATLL

A

rash, lytic(punched out) bone lesions with hypercalcemia and lymphadenopathy with hepatosplenomegaly. DO NOT CONFUSED WITH multiple myeloma(frequently associated with lytic bone lesion). Rash is a good distinguishing feature.

47
Q

Mycosis Fungoides – clinical symptoms?

A

Neoplastic proliferation of CD4+ T–cells. Aggregates of neoplastic cells in the epidermis are called Pautrier microabscesses. Cells can spread to involve blood producing “Sezary syndrome” with characteristic lymphocytes with “cerebriform nuclei”(Sezary Cells) seen on blood smear.

48
Q

Demographic of Myeloproliferative Disorders\nBrief description of common symptoms?

A

late adulthood\nneoplastic proliferation of mature cells of myeloid lineage.\nCommon symptoms: –– Hyperuricemia and gout–– marrow fibrosis–– transformation to acute leukemia

49
Q

MOA of myeloproliferative symptom of hyperuricemia and gout

A

Hyperuricemia and gout –– increased turnover of cells result in activation of purine degradation pathway whose end metabolite is uric acid.

50
Q

Chronic Myeloid Leukemia. Characteristic chromosome abnormality? What cell type is characteristically increase?

A

Neoplastic proliferation of granulocytes. Predominant cell that is increased is basophils\nt(9;22) – philadelphia chromosome –– generates BCR–ABL protein that increases tyrosine kinase activity

51
Q

First line treatment for CML? MOA?

A

Imatinib which blocks the tyrosine kinase

52
Q

Worst complication of CML? Preceded by?

A

Acute Leukemia heralded by new onset enlargement of spleen. NOTABLY, transformation can turn into AML OR ALL since the mutation is in the HSC(CD34+).

53
Q

Distinguish between a leukemoid reaction(infection) and CML

A

CML will have the following findings:1.) Negative leukocyte alkaline phosphatase(LAP) stain 2.) Increased basophils 3.) t(9;22)\n\nLAP is an enzyme present in the secondary granules during inflammation. Therefore leukemoid reactions would be positive for this.

54
Q

JAK2 Kinase associations

A

Polycythemia Vera\nEssential Thrombocythemia\nMyelofibrosis

55
Q

Classic a/w Polycythemia Vera

A

most common cause of Budd–Chiari syndrome–– blockage of hepatic vein

56
Q

itching after bathing

A

Polycythemia Vera due to excessive mast cells

57
Q

treatment for polycythemia vera

A

1.) Phlebotomy\n2.) Hydroxyurea

58
Q

reactive polycythemia vs polycythemia vera

A

Reactive Polycythemia due to lung disease––> Decreased SaO2, increased EPO Polycythemia secondary to Renal Cell Carcinoma secreting EPO––> SaO2 normal, EPO high Polycythemia Vera ––> SaO2 normal, EPO low

59
Q

What is associated with excessive platelets?

A

Iron deficiency anemia - Essential Thrombocythemia

60
Q

Notable difference with Essential Thrombocythemia compared to other myelodysplastic syndromes?

A

No risk for hyperuricemia, gout or progression to acute leukemia. This is due to the fact there is not an increase in turnover of nuclear material since platelets are just pieces of megakaryocyte cytoplasm pinched off.

61
Q

JAK2 associated disorder associated with marrow fibrosis

A

myelofibrosis

62
Q

Clinical features of myelofibrosis. Mutation in? What cell predominates?

A

JAK2 Kinase mutation leading to proliferation of mature myeloid cells(esp. megakaryocytes). Splenomegaly due to extramedullary hematopoiesis\ntear–drop RBC’s, nucleated RBC’s(Howell Jowelly bodies), immature granulocytes)

63
Q

tear drop RBC’s a/w

A

myelofibrosis

64
Q

follicular lymphadenopathy

A

Rheumatoid arthritis and early HIV(due to dendritic cells expressing CD4+ receptors and hanging out in follicles) - follicles are habitated by B–cells

65
Q

Paracortex lymphadenopathy

A

viral infections

66
Q

Deep in medulla lymphadenopathy

A

LN draining tissue with cancer (hyperplasia of sinus histiocytes)

67
Q

Small B cell lymphoma’s

A

Follicular lymphoma - Mantle Cell Lymphoma - Marginal Cell lymphoma - Small Lymphocytic Lymphoma(CLL associated)

68
Q

Intermediate sized b cells lymphoma

A

Burkitt lymphoma

69
Q

Most common form of non–hodgkin’s lymphoma

A

Diffuse large b cell lymphoma

70
Q

What receptor do small b–cells express

A

CD20+ - key marker for B–cells

71
Q

Chromosomal abnormality with follicular lymphoma

A

t(14;18) –– IgH, BCL2 translocation. overstabilization of mitochondria causes failure to for some b–cells to die during somatic hypermutation

72
Q

Treatment for follicular lymphoma

A

only for symptomatic peoples – use rituximab(anti–CD20 antibody) with low dose chemotherapy

73
Q

demographic of small b cell lymphomas

A

mostly late adulthood

74
Q

Important complication of follicular lymphoma. What else can progress to this?

A

progression to diffuse large b–cell lymphoma. Generally have lots of lymphomas, but if one spontaneously starts GROWING get worried for large b–cell. Similar to Chronic Lymphocytic Leukemia

75
Q

Distinguish follicular hyperplasia with follicular lymphoma

A

1.) disruption of architecture(follicles stay near cortex in normal tissue) 2.) lack of tangible body macrophages(somatic hypermutation leads to some apoptotic cells with macrophage consumption in normal tissue) 3.) Bcl2 expression(NOT expresses in reactive hyperplasia) 4.) Monoclonality – test with kappa:gamma ration being not 3:1(normal is 3:1)

76
Q

Mantle Cell lymphoma chromosomal abnormality. gene product?

A

t(11;14) which switches cyclin D gene with IgG. Cyclin D regulates progression from G1 ––> S

77
Q

Marginal Zone Lymphoma a/w?

A

Associated with chronic inflammatory states such as Hashimoto Thyroiditis, Sjogren Syndrome, and H. Pylori gastritis. MALToma is a marginal zone lymphoma… Marginal zone is only formed through activation of zone through germinal centers

78
Q

“Neoplastic proliferation of cells immediately adjacent to follicle”

A

Mantle Cell Lymphoma

79
Q

H. pylori gastritis can lead to

A

Gastric MALToma, which is a marginal zone lymphoma

80
Q

Burkitt Lymphoma presents in what demographic?

A

Presents in child/young adult as an extra nodal mass.

81
Q

Burkitt Lymphoma geographical associations?

A

African form a/w jaw Sporadic form a/w abdomen

82
Q

Burkitt’s lymphoma chromosomal abnormality?

A

t(8;14) results in translocation of c–myc to the IgH leading to overexpression of c–myc. c–myc is an oncogene and promotes cell growth. “starry sky” sky is rapidly growing cells, stars are dead cells cause they grow so fast

83
Q

Burkitt’s Lymphoma is a/w what infection?

A

EBV

84
Q

most common form of non–hodgkins lymphoma?

A

Diffuse large b–cell lymphoma

85
Q

demographic of diffuse large b–cell lymphoma

A

late adulthood as an enlarging lymph node. Arises sporadically or as a transformation(follicular lymphoma)

86
Q

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A

lacunar cells. special kind of reed–sternberg cell present in nodular sclerosis type of hodgkin’s lymphoma

87
Q

owls eye nuclei

A

reed–sternberg cell - hodgkin’s lymphoma

88
Q

Mixed cellularity hodgkin’s lymphoma is a/w?

A

eosinophilia and abundant eosinophils in tissue due to the production of IL–5 by reed–steinberg cells

89
Q

Multiple proliferation of plasma cells? What etiology?

A

Multiple Myeloma –– production of high IL–6 which is a stimulator of plasma cell growth and immunoglobulin production

90
Q

Multiple Myeloma clinical features?

A

1.) production of osteoclast activating factor causes lytic bone lesions(Remember ATLL) especially in vertebrae and skull 2.) M protein spike on electrophoresis due to neoplastic production of immunoglobulin. 3.) Primary AL amyloidosis occurs due to excess production of light chain which gets secreted into blood as AL amyloid, into the urine as Bence–Jones protein and causes renal failure in the kidneys.

91
Q

What types of Ig is produced by multiple myeloma?

A

IgG and IgA

92
Q

Increased serum protein decreases charge between RBCs causing them to stick together…

A

Rouleaux formation of RBCs due to multiple myeloma

93
Q

Most common cause of death in multiple myeloma?

A

increased risk for infection due to overproduction of useless Ig(lacks antigenic diversity)

94
Q

What is diagnostic of Monoclonal Gammopathy of undetermined significance?

A

A finding of M–protein spike in electrophoresis but lacking any other feature of multiple myeloma… NO AL amyloid in blood - NO bence–jones protein in urine - NO hypercalcemia or lytic bone lesions - Common in elderly

95
Q

Waldenstrom’s Macroglobulinemia

A

B–cell lymphoma that produces monoclonal IgM(it’s a BIG Ig) - patients present with generalized lymphadenopathy. There will be M–spike due to IgM. No lytic bone lesions. Causes serum viscosity leading to defective platelet aggregation - Treat with plasmaphoresis

96
Q

What receptors on Hodgkin’s lymphoma?

A

It is a B–cell lymphoma but NOTABLY does not have CD20 receptor. It has CD15 and CD30 and contains Reed–Sternberg cells which are associated with “owl’s eye”

97
Q

classic presentation of nodular sclerosis hodgkins?

A

young adult female with cervical or mediastinal lymph node

98
Q

What are langherhan’s cells?

A

specialized dendritic cells that are found predominantly in the skin that derive from bone marrow monocytes.

99
Q

What is characteristic of langherhan’s cells? What receptors are they positive for?

A

Birbeck granules on electron microscopy. - CD1a+ and S100+

100
Q

Chronic leukocytic leukemias

A

B–cell Leukemia’s - Chronic Lymphocytic Leukemia(CLL)\nHairy Cell Leukemia - T–Cell Leukemia’s(CD4+) - Adult T–Cell Leukemia/Lymphoma(ATLL) - Mycosis Fungoides

101
Q

Myeloproliferative Disorders

A

Chronic Myeloid Leukemia(CML) - Polycythemia Vera(PV) - Essential Thrombocythemia - Myelofibrosis

102
Q

Lymphadenopathy

A

Can be chronic(painLESS) or acute(painFUL)

103
Q

Name all the important Lymphomas

A

Non–hodgkins ––Follicular Lymphoma––Mantle Cell Lymphoma––Marginal Zone Lymphoma––Small Lymphocytic Lymphoma––Burkitt Lymphoma–– Diffuse Large B–cell lymphoma - Hodgkin’s Lymphoma

104
Q

Small Lymphoma(s)

A

––Follicular Lymphoma––Mantle Cell Lymphoma––Marginal Zone Lymphoma

105
Q

Large Lymphoma(s)

A

––Diffuse Large B cell lymphoma

106
Q

Intermediate Lymphoma(s)

A

–– Burkitt’s Lymphoma

107
Q

someone with CLL that has an acutely enlarging lymph node/spleen

A

Richter transformation –– progression of CLL to Diffuse large B–cell lymphoma

108
Q

skin rash with lytic bone lesions

A

ATLL

109
Q

lytic bone lesions

A

multiple myeloma

110
Q

“starry sky”

A

burkitt’s lymphoma

111
Q

most common PRIMARY malignancy of bone?

A

multiple myeloma – malignant proliferation of plasma cells in the bone marrow

112
Q

These diseases will have M spikes on serum protein elecrophoresis…

A

Multiple Myeloma; Waldenstroms Macroglobulinemia; Monoclonal Gammopathy of undetermined significance

113
Q

Most common subtype of hodgkin’s lymphoma? What are other subtypes?

A

Nodular Sclerosis Lymphocyte–rich Mixed cellularity Lymphocyte–depleted

ABBEY MSII Unit 2 (19 decks)

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