Non-regenerative Anemia / Polycythemia Flashcards

1
Q

what do we see, broadly, in the case of a primary bone marrow disorder?

A

-generalized depression
-multiple cytopenias

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2
Q

what do we see, broadly, in the case of a secondary bone marrow disorder?

A

selective red cell depression

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3
Q

how can primary bone marrow disease arise?

A

Progenitor cells can be injured by exposure to chemicals, drugs, toxins, irradiation, viruses and through immune-mediated mechanisms. Usually these injuries are not cell-line specific or occur early enough in differentiation that common stem cells are affected; the result is that multiple cell lines are affected

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4
Q

what do we see in the peripheral blood in cases of primary one marrow disease?

A

nonregenerative anemia, leukopenia, and thrombocytopenia

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5
Q

what 4 broad categories of primary bone marrow disease are there?

A

-hypoplasia or aplasia
-myelodysplasia
-leukemia
-other reasons for myelophthisis

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6
Q

what can cause bone marrow hypoplasia or aplasia?

A

-Infectious – eg. FeLV, ehrlichiosis
-Drug/chemical toxicity
-Immune-mediated

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7
Q

what are some examples of drugs/chemicals that can result in bone marrow aplasia or hypoplasia?

A

◦ Estrogen
◦ Phenobarbital
◦ Griseofulvin
◦ Cephalosporins
◦ Chemotherapeutic agents

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8
Q

what are some factors that can result in estrogen toxicity?

A

-Exogenous administration
-Sertoli cell tumors
-Persistent estrus in ferrets

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9
Q

what are the criteria for diagnosis of Myelodysplasia/Myelodysplastic
Syndrome

A

◦ Peripheral blood cytopenia(s)
◦ Normal to hypercellular bone marrow
◦ Dysplastic features

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10
Q

what is leukemia?

A

Myeloproliferative disease is used interchangeably with leukemia to denote hematopoietic neoplasia arising from bone marrow cells

-Tumor of developing red cells, white cells (except lymphs) or platelets
-Can replace normal marrow with neoplastic cells

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11
Q

what is myelophthisis?

A

displacement of hemopoietic bone-marrow tissue by fibrosis, tumors, or granulomas. The word comes from the roots myelo-, which refers to bone marrow, and phthysis, shrinkage or atrophy.
- leading to peripheral cytopenias

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12
Q

what is myelofibrosis and what is its cause?

A

-proliferation of fibroblasts within the bone marrow cavity caused by:
 FeLV-related
 Marrow necrosis
 Neoplasia
 Chronic hemolytic anemia
=> often the cause in unknown

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13
Q

what are dacrocytes and when do we see them?

A

These tear drop cells are found primarily in diseases with bone marrow fibrosis, such as: primary myelofibrosis, myelodysplastic syndromes during the late course of the disease, rare form of acute leukemias and myelophthisis caused by metastatic cancers

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14
Q

what do we see in the blood in a case of primary bone marrow disease?

A

Non-regenerative anemia
Leukopenia +/- abnormal cells
Thrombocytopenia

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15
Q

what do we in the blood in a case of secondary bone marrow disease?

A

Non-regenerative anemia
Normal or increased leukocytes
Normal or increased platelets

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16
Q

what 5 factors are often the cause of secondary bone marrow disease?

A

-chronic inflammation
-endocrine disease
-FeLV related
-metastatic neoplasia
-renal disease

17
Q

what causes anemia of chronic disease? What are its charactieristics?

A

-Inflammation (infectious/non-infectious) & neoplasia
-Due to poor iron availability, suppressive cytokines
-Usually mild-moderate
◦ E.g dog: HCT usually between .20 and .30 (ref int.
.37-.55)
-Normocytic, normochromic anemia

18
Q

what hormone deficiencies can cause anemia of endocrine disease?

A

◦ Cortisol
◦ Androgens
◦ Thyroxine
◦ Growth hormone

19
Q

what are the characteristics of anemia that results from FeLV infection?

A

Anemia can be normocytic or macrocytic
Can cause nonregenerative anemia via:
◦ Anemia of chronic disease
◦ Myelophthisis from hematologic neoplasia
◦ Pure red cell aplasia (PRCA)

20
Q

what are the characteristics of anemia of renal disease? what are its characteristics?

A

Usually a moderate anemia, may be worse if bleeding or decreased platelet function
Due to:
• Decreased red cell life span
• Decreased Epo production
• Decreased marrow responsiveness to Epo

21
Q

what can Rubricytosis, Lead Toxicity, or Vitamin & Mineral
Deficiencies lead to

A

anemia due to secondary bone marrow disease

22
Q

with polycythemia, how will RBC, Hgb, and Hct values be impacted?

A

increased

23
Q

what is polycythemia? what are the broad categorizations?

A

increased number of red cells in the blood, due to primary disease or a secondary condition
-Relative polycythemia: normal red cell mass
-Absolute polycythemia: increased red cell mass

24
Q

what are the types of absolute polycythemia?

A

Primary: Decreased-Normal Epo, Normal PO2
Secondary: Increased Epo, Low PO2

25
Q

what causes primary absolute polycythemia?

A

 Myeloproliferative disease: polycythemia vera or erythrocytosis

26
Q

what causes secondary absolute polycythemia?

A

Many causes (Cariopulmonary disease, high altitude, hormone excess, renal masses, paraneoplastic)

27
Q

what is the most common cause of polycythemia?

A

dehydration

28
Q

what causes relative polycythemia? what are its identifying characteristics?

A

dehydration or splenic contraction
No change in Epo or PO2

29
Q

what is polycythemia vera

A

PV is a myeloproliferative disease involving neoplastic transformation of an erythroid stem cell. The red cells are morphologically normal

30
Q

what do we sometimes see in long-standing cases of absolute polycythemia and why?

A

there will be increased demand for iron. For this reason, microcytosis and hypochromia are sometimes observed in long-standing cases of absolute polycythemia