White Blood Cell Disorders 1 Flashcards

1
Q

drug induced neutropenia is often due to suppression of ________

A

suppression of committed myeloid precursors

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2
Q

what are some causes for peripheral loss of neutrophils resulting in neutropenia

A
  • immune related
  • splenic sequestration
  • increased consumption of neutrophils
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3
Q

the most common cause of severe neutropenia is _____

A

drug induced (chemotherapy)

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4
Q

for predictable neutropenia caused by chemotherapy, treating includes a _____ (drug: ____)

A

G-CSF (granulocyte colony stimulating factor)

drug: filgrastim

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5
Q

what are some reactive changes in neutrophils in a patient with bacterial sepsis that you can see on histology?

A

Dohle bodies which are small blue cytoplasmic patches of dilated ER

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6
Q

which lymphomas are often associated with eosinophilic leukocytosis

A
  • Hodgkin’s

- T cell

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7
Q

which skin diseases are associated with eosinophilic leukocytosis

A
  • bulls pemphigus and pemphigoid

- dermatitis herpetiformis

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8
Q

Dohle bodies, seen in ______ is indicative of _____

A

neutrophils (Dohle bodies are small cytoplasmic inclusions)

indicative of a patient with bacterial sepsis

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9
Q

if you see basophilic leukocytosis on histology, it almost alway syndicates which myeloproliferative neoplasm?

A

CML

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10
Q

viral infections from EBV, Hep A and CMV are causes for reactive monocytosis/lymphocytosis

A

reactive lymphocytosis

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11
Q

inflammatory bowel diseases such as ulcerative colitis is a cause of reactive monocytosis/lymphocytosis

A

monocytosis

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12
Q

infectious mononucleosis is the most common example of reactive ______

A

atypical lymphocytes

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13
Q

in the lymph node, most of the B cell activity occurs in the _________

A

follicle (cortical region)

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14
Q

paracortical hyperplasia of the lymph node is associated with _____

A

T cell response

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15
Q

what do you see in the medulla of the lymph node?

A

mainly plasma cells

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16
Q

it is hard to tell the difference from the peripheral blood between: reactive increase in granulocytes aka neutrophils (leukmoid reaction) vs _____

A

CML

17
Q

a child presents to the office with axillary lymphadenopathy, what should be done?

A
  • because it is a child, lymphadenopathy is often due to meeting with pathogens (reactive)
  • no need to rush for a biopsy. just have them come back after some time and see if it has gotten smaller
18
Q

general categories of causes of WBC malignancies

A
  • pro growth mutations: tyrosine kinase mutations, MYC translocation
  • ↑ self renewal: MLL translation, PML-RARA fusion gene
  • ↓ apoptosis (pro survival): BCL2 tranlocation
19
Q

what is the difference between leukemia and lymphoma

A
  • leukemia: neoplasia involves predominantly the bone marrow and peripheral blood at the time of presentation
  • lymphoma: neoplasia from discreet tissue masses at the time of presentation
20
Q

almost all of ______ lymphomas present with ____ lymph node enlargement
(tender/nontender)

A

HODGKIN’S

NON TENDER

21
Q

lymphoid leukemias present with _____

A

cytopenias because symptoms and signs are related to bone marrow replacement

22
Q

in the lymphoid lineage, plasma cell neoplasms usually present with ______

A

bone destruction leading to bone pain due to pathological fractures

23
Q

extra nodal enlargement and thus GI symptoms and local symptoms are common in ______ lymphoma

A

NON HODGKINS

24
Q

B/T cell neoplasms show light chain restriction by expression either kappa or lambda chains

A

B cell neoplasms

25
Q

the _____ or ____ chains in B cell neoplasms can be detectable via ____ or _____

A

kappa or lambda;

flow cytometry or immunohistochemical stains

26
Q

what translocation is associated with follicular lymphoma?

A

t(14,18)

27
Q

what translocation is associated with mantle cell lymphoma

A

t(11,14)

28
Q

what translocation is associated with MALToma

A

t(11,18)

29
Q

t(8.14)

A

Burkitt’s lymphoma