Heme/Lymph (10/5/2013) Flashcards

10 of 10 Rekaps & Refs

1
Q
  1. What 3 symptoms may key you into a patient with Hodgkin disease?
A

(1) Painless LAD (2) Night sweats (3) Generalized pruritis

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2
Q
  1. What major histology finding alerts you to a patient with Hodgkin disease?
A

Large cells with prominent nucleoli (Reed-Sternberg, or RS, cells)

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3
Q
  1. What pathophysiologic effect can Vitamin K deficiency have in a newborn?
A

Results in defective gamma-carboxylation of glutamate residues of factors II, VII, IX, & X

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4
Q
  1. What hematological test/value is elevated in Vitamin K deficiency? What condition related to this finding can result?
A

Results in elevated PT, leading bleeding diathesis (hemorrhagic disease of newborns)

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5
Q
  1. What does ITP stand for? What is the pathophysiology of this disorder?
A

Idiopathic thrombocytopenic purpura (ITP); Chronic autoimmune disorder in which antibodies against platelet glycoproteins cause platelet destruction and removal by reticuloendothelial system

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6
Q
  1. Under what conditions can a diagnosis of ITP be made?
A

Only when secondary thrombocytopenia (lupus, viral, infections, drugs) have been ruled out can ITP diagnosis be made

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7
Q
  1. What type of cells are essential for Hodgkin lymphoma diagnosis? Are they pathognomonic?
A

RS cells essential for Hodgkin lymphoma diagnosis but not pathognomic

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8
Q
  1. What are the distinguishing features of classic RS cells?
A

Large with abundant cytoplasm and s+ oval lobulated nuclei with large nucleoli

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9
Q
  1. What cell is associated with Nodular sclerosing type of Hogkin disease? What characterizes this cell?
A

Lacunar cell (variant RS) with retraction of plate cytoplasm producing an empty space (lacuna)

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10
Q
  1. What are 3 conditions in which target cells are seen?
A

Seen in thalassemia, HbC disease, and liver disease

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11
Q
  1. How is sickle cell anemia related to the spleen? What consequences may this have?
A

Cause repeated splenic infarctions leading to splenic atrophy; Patients susceptible to infection with encapsulated microorganisms (e.g., Pneumococcus). Pneumococcal vaccine is required.

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12
Q
  1. What characterizes and/or accompanies DIC?
A

Characterized by excessive consumption of coagulation factors and clot formation throughout body, accompanied by diffuse bleeding and elevated PT/aPTT

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13
Q
  1. When considering DIC, what is used to rule out a functional deficiency of coagulation factors?
A

Low fibrinogen levels

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14
Q
  1. What 2 lab values/tests are used to confirm a DIC diagnosis?
A

High level of FDP and D-dimer confirm DIC, which can occur as a complication of sepsis

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15
Q
  1. What is the origin and clinical utility of D-dimer versus FDPs?
A

D-dimer formed only from degradation of fibrin, whereas FDP can result from degradation of either fibrin or fibrinogen = D-dimer much more specific indicator of both thrombin and plasmin activity; In patient with diffuse coagulopathy, increased D-dimer signifies simultaneous activity of both plasmin and thrombin, which is virtually diagnostic of DIC; D-dimer also useful screen for patient with suspected DVT or PE (as product of blood clot)

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16
Q
  1. In what patient population is Infectious mononucleosis usually manifested? What are 4 key characteristics in the typical presentation of Infectious mononucleosis?
A

Manifested in young adults, by fever, malaise, LAD, & splenomegaly

17
Q
  1. What test is used to diagnose Infectious mononucleosis? What is another name for this test?
A

Dx w/ heterophile antibody test (Monospot)

18
Q
  1. What pathogen causes heterophile-positive Mononucleosis?
A

EBV (Epstein-Barr virus)

19
Q
  1. How is Type M3 AML typically characterized upon histology?
A

Type M3 Acute myelogenous leukemia (AML) characteristically has Auer rods in cytoplasm of leukemic cells

20
Q
  1. What are Auer rods? What is an example of a setting in which they may be released ?
A

Auer rods are composed of enzymes found in azurophilic granules; Their rapid release during chemotherapy can trigger DIC