Hematology / Oncology - Specific Findings Flashcards

1
Q

PT

A

Tests function of common extrinsic coagulation pathway, factors I, II, V, VII, and X

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2
Q

PTT

A

Tests function of common intrinsic coagulation pathway, all factors EXCEPT for VII and XIII

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3
Q

Follicular Lymphoma - Gene Translocation

A

t(14;18) - translocation of heavy-chain Ig (14) and BCL-2 (18)

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4
Q

DIC - Lab Findings

A

Elevated D-dimer / decreased fibrinogen
Decreased factors V and VIII / elevated PT and PTT
Decreased platelet count
Schistocytes seen on smear - RBCs are damaged by passage through obstructed vessel lumen

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5
Q

Reed-Sternberg Cells

A

Classic finding in Hodgkin Lymphoma; neoplastic cells of B-cell origin

CD15+, CD30+
Bi-nucleated / bi-lobed with “Owl Eye” appearance

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6
Q

Burkitt Lymphoma - Gene Translocation

A

t(8;14) - translocation of c-myc (chromosome 8) and Ig heavy chain (chromosome 14)

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7
Q

Diffuse large B-cell lymphoma - Gene Translocation

A

t(14;18)

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8
Q

Mantle Cell Lymphoma - Gene Translocation

A

t(11;14) - translocation of cyclin D1 (chromosome 11) and Ig heavy chain (chromosome 14)

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9
Q

“Starry Sky”

A

Describes the appearance of lymph nodes seen in Burkitt’s lymphoma; characterized by sheets of lymphocytes interspersed with macrophages

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10
Q

Basophilic Stippling of RBCs

A

Seen in lead poisoning

Pb inhibits ribonucleases in RBCs causing accumulation of rRNA, which appears basophilic on smear

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11
Q

Burton Lines

A

Seen in lead poisoning

Evident at the metaphyses of long bones on X ray

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12
Q

Amyloidosis - Staining

A

Congo red stain shows amyloid (Ig light chain) deposits with apple green birefringence under polarized light

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13
Q

M-spike on serum protein electrophoresis

A

Represents high levels of monoclonal Ig light chain in the serum

Finding in Monoclonal Gammopathy of Undetermined Significance (<3g/dL) and Multiple Myeloma

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14
Q

Bence-Jones Protein

A

Monoclonal Ig light chain in the urine

Finding in multiple myeloma

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15
Q

Osmotic Fragility Test

A

Positive osmotic fragility test seen in Hereditary Spherocytosis

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16
Q

Which clotting factors are monitored by PT/INR?

A

Common & Extrinsic Pathway factors:

I
II
V
VII
X 

Affected by Warfarin

17
Q

Which clotting factors are monitored by PTT?

A

Common & Intrinsic Pathway Factors:

(All except VII and XIII)

Affected by Heparin

18
Q

Prolonged PTT - NOT correctable by 1:1 mixing with FFP

A

Anti-phospholipid antibody syndrome (“Lupus anticoagulant”)

19
Q

Which HLA type is associated with psoriatic arthritis, ankylosing spondylitis, arthritis of inflammatory bowel disease, and reactive arthritis?

A

HLA-B27

20
Q

Which HLA types are associated with SLE?

A

HLA-DR2

HLA-DR3

21
Q

Which HLA type is associated with rheumatoid arthritis?

A

HLA-DR4

22
Q

Sunburst pattern on long bone X ray

A

Osteosarcoma

23
Q

Which autoantibody is most specific for SLE? What other autoantibodies are seen?

A

anti-dsDNA is the most SPECIFIC

anti-nuclear antibodies (ANA)
anti-Smith antibodies
anti-cardiolipin antibodies - false positive on tests for syphilis, prolonged PTT
anti-histone antibodies - sensitive for drug-induced lupus

24
Q

Libman-Sacks endocarditis

A

Wart-like (non-infectious) vegetations on both sides of a valve

Commonly seen in SLE

25
Q

How do gout crystals look under microscopy?

A

Uric acid crystals from aspirated joint fluid are needle-shaped and negatively bi-refringent (yellow under parallel light, blue under perpendicular light)

26
Q

M-spike on serum protein electrophoresis - IgG or IgA

A

Multiple Myeloma

27
Q

M spike on serum protein electrophoresis - IgM

A

Waldenstrom macroglobulinemia

28
Q

5 “Ps” - Painful abdomen, port-wine colored urine, polyneuropathy, pyschiatric disturbances, precipitated by drugs, alcohol, starvation

A

Acute Intermittent Porphyria

Deficiency of porphobilinogen deaminase with accumulation of porphobilinogen in blood and urine

29
Q

“Soap bubble” on X-ray

A

Giant Cell Tumor - benign tumor of bone, usually seen at the epiphyseal ends of long bones (distal femur, proximal tibia)

30
Q

Heinz Body

A

Precipitates of hemoglobin seen within the RBCs of patients with hemolytic anemia due to G6PD Deficiency upon exposure to oxidizing agents

31
Q

TdT

A

Marker of pre-T and pre-B cells

Positive in acute lymphoblastic leukemia (ALL)

32
Q

CD10

A

Marker of pre-B cells

Positive in acute B-ALL

33
Q

Direct Coomb’s Test

A

i.e. used to diagnose warm agglutinin hemolysis

anti-Ig antibody is added to patient’s serum; if patient’s own RBCs are coated with Ig then agglutination occurs

34
Q

Indirect Coomb’s Test

A

i.e. used to asses blood compatibility before transfusion

Normal RBCs are added to patient’s serum; RBCs will agglutinate if patient’s serum as anti-RBC surface Ig

35
Q

Oat Cells

A

Neoplastic proliferation of neuroendocrine Kulchitsky cells; small, blue cells resembling lymphocytes but 2x bigger

Stain chromogranin A +

36
Q

Target Cells

A

DDx = HALT

Heboglobin C Disease
Asplenia
Liver Disease
Thalassemias

37
Q

Sarcoidosis - Lab findings

A

Elevated serum ACE levels
Elevated CD4 / CD8 ratio
Hypercalcemia

38
Q

Sarcoidosis - Imaging findings

A

Bilateral hilar lymphadenopathy

Coarse reticular opacities

39
Q

Sarcoidosis - Other associated clinical findings

A

Restrictive lung disease (interstitial fibrosis)
Erythema nodosum
Bell’s palsy
Uveitis