Reactive Leukocyte Disorders Flashcards

1
Q

Define neutropenia and agranulocytosis and list important causes for each.

A

Neutropenia is defined as absolute neutrophils count (ANC) of less than 1800/microliters. Agranulocytosis is defined as ANC less than 500.It can be due inadequate production or ineffective production:
* Suppression of hematopoietic stem cells - Aplastic anemia, radiation Suppression of committed granulocytic precursors Drugs Dose dependent –alkylating agents, antimetabolites. This is often reversible.
Idiosyncratic –chloramphenicol, aminopyrine, sulfonamides, chlorpromazine, phenylbutazone, thiouracil. This is often non reversible.

  • Large granular lymphocyte leukemia
  • Congenital
  • Ineffective hematopoiesis - Megaloblastic anemia, myelodysplastic syndromes
    Or it can be due to increased destruction:
  • Immune mediated -idiopathic, drug-induced.
  • Splenic sequestration
  • Increased margination
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2
Q

Define neutrophilia and list important causes for it

A

Absolute neutrophil count (ANC) >7000/μLIncreased granulopoiesis:
* Infections –primarily bacterial Immunological inflammatory
* Neoplasia Myeloproliferative neoplasms Paraneoplastic
* Drugs –colony stimulating factors
Increased release from marrow stores
* Endotoxemia
* Infection
* Hypoxia Decreased margination
* Exercise
* Catecholamines Decreased extravasation into tissues
* Glucocorticoids

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3
Q

Discuss the pathophysiology of leukocyte adhesion deficiency, chronic granulomatous disease, Chediak-Higashi syndrome, and myeloperoxidase deficiency

A
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4
Q

Enumerate the three main histologic types of lymph node hyperplasia with examples

A
  • Follicular hyperplasia
  • Paracortical (interfollicular) hyperplasia
  • Sinus histiocytosis
  • Mixed pattern of hyperplasia
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5
Q

Discuss the pathologic features of lymphadenopathy related to toxoplasmosis

A

We see a mixed pattern of hyperplasia, there is marked follicular hyperplasia, epitheloid granulomas and sinusoidal dilation with monocytoid B cells.Epitheloid granulomas consists of small and large histiocytic aggregates with germinal centersand interfollicular areas.

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6
Q

Explain the possible reasons that can give rise to eosinophilia.

A
  • Allergic disorders
  • Parasitic infections
  • Malignant neoplasms
  • Drugs (IL-2)
  • Collagen vascular disorders
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7
Q

Explain the possible reasons that may give rise to basophilia in a patient.

A
  • Neoplasms - CML
  • Allergic disorders
  • Inflammation
  • Endocrine disorders
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8
Q

Explain the possible reasons that can lead to the development of monocytosis.

A
  • Chronic infections
  • Inflammation
  • Collagen vascular disorders
  • Neoplasms
  • Inflammatory bowel disease
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9
Q

What is the definition of lymphocytosis?

A

Absolute lymphocyte count > 4000/μL (adults) or > 7000/µL (children) or > 9000/µL (infants)

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10
Q

What are the most common reasons for the development of lymphocytosis in patients?

A
  • Viral infections
  • Acute bacterial infection - only with whooping cough
  • Chronic bacterial infections - only with TB and brucellosis
  • Lymphoproliferative diseases
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11
Q

What are atypical lymphocytes?

A

Aka Downey cells, these are seen in viral infections such as EBV. They have a characteristic appearence.Atypical lymphocytes are clinically seen in a variety of viral illnesses but as far as STEP is concerned it is only associated with EBV.

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12
Q

How can we differentiate between a basophil and an atypical lymphocyte?

A

Basophils has a much higher nucelus to cytoplasm ratio as shown.

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13
Q

Define lympohocytopenia and explain why does it develop?

A

Absolute lymphocyte count < 1500/μL (adults) or < 3000/µL (children)Usually due to decrease in CD4+ helper T-cells

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14
Q

Explain the possible etiologies for the development of lymphocytopenia.

A

Decreased production

  • Congenital and acquired immunodeficiency syndromes
  • Hodgkin lymphoma Increased destruction
  • Radiation, chemotherapy
  • Antilymphocyte globulin
  • Steroids, ACTH
  • AIDS Increased loss of lymphocytes
  • Damage to lymphatics and loss of lymph –protein losing enteropathy, Whipple disease, increased central venous pressure
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15
Q

Explain follicular hyperplasia.How does it look like?

A

Increased number of and larger size of secondary follicles

  • Infection Systemic inflammatory disorders
  • Rheumatoid arthritis
  • Drug reaction
  • AIDS
  • Differential diagnosis includes follicular lymphoma
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16
Q

How can we differentiate between follicular lymphoma and follicular hyperplasia?

A

BCL2 gene is overexpressed in follicular lymphoma, making the B cells non apoptotic, we can stain for this protein to differentiate between the 2

17
Q

Explain paracortical hyperplasia and how does it look like?

A

Aka interfollicular hyperplasia,expansion of paracortex by a heterogeneous reactive cell population

  • Viral infection –CMV, EBV, measles, varicella
  • Immunologic disorders
  • SLE
  • Drug reaction
18
Q

What is sinus histiocytosis?

A

Increase in macrophages in sinuses In lymph nodes during infection, cancerSinus histiocytosis is associated with massive lymphadenopathy