Hematopathology III Flashcards

1
Q

What is the main difference in acute and chronic leukemias?

A

Acute will have blast cells and chronic will have more differentiated cells

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2
Q

What is the typical patient of Diffuse Large B-cell Lymphoma?

A

Older adults - median age is 60

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3
Q

How does Diffuse Large B-cell Lymphoma present?

A

Rapidly enlarging, symptomatic mass at single or extranodal site

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4
Q

What are the distinct subtypes of Diffuse Large B-cell Lymphoma?

A

Germinal Center B-cell (GCB)

Activated B-cell (ABC)

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5
Q

What is the difference in outcomes of Diffuse Large B-cell Lymphoma in GCB VS ABC?

A

GCB has much better survival and prognosis that ABC - different treatments are used for each type

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6
Q

Translocation of Diffuse Large B-cell Lymphoma

A
  • t(14;18) in 30% of patients
  • BCL6 rearrangement in 30-40%

VERY rare will have MYC translocations alongside one of the other two - “double hit”

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7
Q

What biomarkers will Diffuse Large B-cell Lymphoma express?

A

CD20

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8
Q

What is the appearance of the spleen in Diffuse Large B-cell Lymphoma?

A

“Fish flesh” appearance of a large expansile mass

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9
Q

What happens to the lymphocytes in Diffuse Large B-cell Lymphoma?

A

They become much larger than normal

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10
Q

What is the presentation of Peripheral T-Cell Lymphoma?

A

Lymphadenopathy, eosinophilia, pruritis, fever and weight loss

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11
Q

What is the biomarker of Peripheral T-Cell Lymphoma?

A

CD3+

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12
Q

What are the cells like in Peripheral T-Cell Lymphoma?

A

Polymorphic and heterogeneous often with eosinophilia

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13
Q

What are the patients of Hodgkin lymphoma?

A

Bimodal - in young adults and the in older adults

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14
Q

What is the spread of Hodgkin lymphoma?

A

Spreads in contiguous fashion thorough the lymphoid tissue

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15
Q

What is the characteristic cell of Hodgkin lymphoma?

A

Reed-Sternberg Cells

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16
Q

What type of cells does Hodgkin lymphoma arise from?

A

B cells

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17
Q

What is a common mechanism for the activation of classical Hodgkin lymphoma?

A

NF-kB activation can occur via infection by EBV is a common mechanism for Hodgkin lymphoma

18
Q

What is the appearance of Reed-Sternberg cells?

A

Owl eyes - binucleated

19
Q

What do the classical Hodgkin lymphoma cells have as biomarkers?

A

CD15/30

20
Q

What are the biomarkers of nodular lymphocyte predominant Hodgkin lymphoma?

A

CD20/45

21
Q

What is the most common class of Hodgkin lymphoma?

A

Nodular sclerosis

22
Q

What are the classes of Hodgkin lymphoma?

A
  • Lymphocyte rich
  • Mixed cellularity
  • Lymphocyte Depleted
  • Nodular Sclerosis
  • Nodular Lymphocyte Predominant
23
Q

Lymphocyte rich Histology

A

Reactive small lymphocytes predominate, few mononuclear or classic Reed-Sternberg cells

24
Q

Mixed cellularity

A

Reed-Sternberg cells and variants on a mixed cellular background including eosinophils, plasma cells, T- lymphocytes, histiocytes

25
Q

Lymphocyte Depleted

A

Paucity of lymphocytes and relative abundance of Reed-Sternberg cells

26
Q

Nodular Sclerosis

A

Fibrous nodular pattern, lacunar cells

27
Q

Nodular Lymphocyte Predominant

A

Nodularity with predominance of mature lymphocytes and popcorn cell or L & H variant of RS cells

28
Q

What morphology of cells are seen in nodular lymphocyte predominant Hodgkin lymphoma?

A

“Popcorn-like” cells

29
Q

What is the most common plasma cell neoplasm?

A

Monoclonal Gammopathy of Undetermined Significance (MGUS)

30
Q

Waldenstrom’s Macrogloobulinemia

A

High levels of IgM M-spike and symptoms due to hyperviscocity of blood from high protein levels in the blood (most commonly associated with lymphoplasmacytic lymphoma)

  • Visual distrubances
  • Bleeding
31
Q

Multiple Myeloma

A

The presence of monoclonal plasma cell proliferation involving bone marrow and typically skeleton at multiple sites

32
Q

What is the proliferation of plasma cells in MM dependent upon?

A

Cytokines - mainly IL-6

33
Q

What are serum and urine indications of MM?

A

Monoclonal protein in serum

IgG or IgA in the urine

34
Q

What can be found in the bone marrow in MM patients?

A

Bone marrow showing clonal plasmacytosis or presence of a plasmacytoma

35
Q

What are the symptoms of MM? (CRAB)

A

hyperCalcemia, Renal insufficiency, Anemia, Bone lesions/Back pain

36
Q

What is seen in the skull in MM?

A

Punched out regions due to secretions of cytokines that increase osteoclastic activity

37
Q

How does electrophoresis tell you about the MM diagnosis?

A

It can show a single strong band which is indicative of a monoclonal protein - i.e. the monoclonal antibody of MM

38
Q

What are some of the complications of MM?

A
  • Bone resorption: hypercalcemia, fractures
  • Suppression of humoral immunity leading to recurrent infections
  • Renal insufficiency - Bence-Jones proteinuria of light chains which are toxic to renal tubular epithelium
  • Amyloidosis
39
Q

What is the main patient population of MM?

A

Elderly - over 70 years old

40
Q

What is the patient population of Monoclonal Gammopathy of Undetermined Significance (MGUS)?

A

Older patients ~50 years

41
Q

What is done for MGUS?

A

Nothing as most patients are asymptomatic - only 1% develop symptomatic plasma cell neoplasms within a year - only treat with symptoms