Cell morphologies and causes Flashcards

(19 cards)

1
Q

Macrocytosis

A

Definition:
* RBC size > 100 fL (Mean Corpuscular Volume, MCV)

Common Causes (M/c/c):
* Alcoholism
* Vitamin B12 deficiency
* Folate deficiency
* Myelodysplastic syndrome**

Uncommon Causes:
* Reiculocytosis
* Liver disease (non-alcoholic or alcoholic)
* Multiple myeloma
* Acute leukemia
* Hypothyroidism

mnemonic- RML Hospital

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2
Q

Nucleated RBCs

A

Key Concept:
* Indicates bone marrow (B.M.) stress or immaturity of RBC production
* B.M. may be:
* Struggling to keep up with losses
* Lacking sufficient resources (e.g. nutritional deficiencies)
* Stimulated erythropoiesis (emergency production)

  1. Problem in Production:
    • Malignant infiltration of B.M.
    • Anemia
    • Extramedullary hematopoiesis
    • Stimulated erythropoiesis
  2. Problem in Maintenance:
    • Hypoxia (↑ demand)
    • Nutritional deficiencies
    • Sepsis (↑ demand)
    • Liver disease
  3. Decreased Destruction:
    • Post-splenectomy
    • Hemolysis
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3
Q

Rouleaux formation

A
  • Stacks of RBCs are formed due to bridging of macromolecules.

Mechanism:
* Bridging occurs between RBCs and macromolecules due to:
* High levels of circulating acute phase proteins
* Increased “stickiness” of RBCs

Causes:
* Infection
* Inflammation
* Dehydration
* Hyperviscosity
* Malignancy
* Multiple myeloma (paraproteinemia)
* Chronic liver disease
* Autoimmune conditions

MAMC-Malignancy, Autoimmune conditions, Multiple myeloma, CLD

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4
Q

Polychromasia

A

Definition:
* A disorder of erythrocyte maturation.
* Applies only to Giemsa stain.

Staining Characteristics:
* Immature RBCs stain blue-gray due to retained genetic material.
* Mature RBCs stain orange.
* The blue-gray color indicates residual RNA/DNA.
* Serves as a nonspecific marker of bone marrow stress.

Causes of Polychromasia:

  1. Response to Red Cell Loss:
    • Hemorrhage
    • Hemolysis
  2. Recovery of Marrow Function:
    • Iron infusion
    • Vitamin B12 replacement
    • Erythropoietin injection
    • Recovery following chemotherapy
  3. Failure of Marrow to Sustain Function:
    • Myelofibrosis
  4. Failure of RBC Quality Control:
    • Postsplenectomy
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5
Q

Leucoerythroblastic picture

A

Presence of immature forms of cells of Myeloid series seen in circulation

Causes:
-Sepsis
-Trauma
- rebound following BM suppression
_ Myeloproliferative disorders
- Myelofibrosis
- Malignant infilteration of BM

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6
Q

Target cells

A

Definition:
* RBCs with too much membrane relative to hemoglobin (Hb) content
* Opposite of spherocytes

Most Common Cause (M/c/c):
* Hemoglobinopathies

Other Causes:
* Failure to remove abnormal RBCs from circulation:
* Iron deficiency
* Thalassemia
* Sickle cell anemia
* Other hemoglobin disorders
* Splenectomy

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7
Q

Dimorphic red cells

A
  • Presence of two morphologically distinct populations of red blood cells (often varying in size or hemoglobin content)
    Causes:
    1. Iron deficiency anemia — post iron transfusion
    2. Mixed deficiency anemia — Iron + Vitamin B12/folate deficiency
    3. EPO-induced erythropoiesis
    4. Delayed transfusion reaction*
    5. Myelodysplastic syndromes (MDS)**
    6. Myeloproliferative disorders*
    7. Ribavirin anemia — associated with* ringed sideroblasts
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8
Q

Echinocytes

A

Liver disease
Splenectomy

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9
Q

Acanthocytes

A

Liver dis
splenectomy
Renal failure

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10
Q

Tear Drop Cells

A

Thalassemia
Myelofibrosis
Extramedullary haematopoesis

MET!!

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11
Q

Schistiocytes

A

Fragmented RBCs

Causes:
Mechanical valves
Extracorporeal circuit
TTP/MAHA
DIC

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12
Q

Blister Cells

A

Indicate Oxidative damage
* Dapsone
*Primaquine
*G6PD deficiency

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13
Q

Heinz Bodies

A

Definition:
* Denatured hemoglobin (Hb)
* Marker of oxidative stress

*	Seen in RBC metabolism disorders and hemoglobinopathies
*	Rapidly cleared by splenic macrophages Causes of Heinz Bodies:

I. Oxidative Stress
* Drugs:
* Primaquine
* Quinidine

II. Unstable Hemoglobin
* Methemoglobinemia
* Alpha-thalassemia**
* Chronic liver disease**

III. Deranged RBC Metabolism
* G6PD deficiency
* Dapsone toxicity
* Bactrim (trimethoprim-sulfamethoxazole)

IV. Impaired Red Cell Clearance
* Splenectomy

5 conditions: G6pd def, Meth haemoglobinemia, Thalassemia, splenectomy, Chronic Liver disease
5 Drugs: Methylene Blue, Primaquine, Dapsone, Bactrim, Quinidine.

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14
Q

Dohle bodies

A
  • found in Neutrophils
  • consist of ER and Ribosomes
    #seen in:
    -Infections
    -Trauma
    -Burns
    -Leukemoid reactions
    -Foll. GCSF

whenever cell turnover increases

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15
Q

Howell Jolly bodies

A

Erythrocytes with bits of DNA
Causes:
* Splenectomy
* Pernicious anemia
* Macrocytosis(all causes)
*corticosteroids

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16
Q

Pappenheimer bodies

A

Hemosiderin containing granules
Causes:
Sideroblastic anemia
Splenectomy

17
Q

Basophilic stippling

A

They are altered Ribosomes in cytoplasm
Causes:
-Lead poisoning
-Thalassemia
-Alcohol abuse

18
Q

Leukemoid Reaction

A

Def:
Hyperproliferation of leukocytes with immature cells released into the bloodstream; WBC count may reach 30,000–50,000/µL.

Common Causes:

=> Infections:
* Pneumonia
* Tuberculosis

=> Inflammation:
* Empyema

=> Metabolic conditions:
* Diabetic ketoacidosis (DKA)

=> Ischemia of large organs:
* Liver
* Bowel
* Kidney

=> Malignancy

=> Drugs:
* Steroids
* ATRA (All-trans retinoic acid)
* G-CSF (Granulocyte-colony stimulating factor)

=> Hematologic conditions:
* Myeloproliferative disorders
* Myeloid leukemia

19
Q

Leukoerythroblastic Picture

Left Shift

Toxic changes

A

= Definition: Presence of: immature forms of cells of myeloid series
- Granulocytic left shift (immature granulocytes eg- band cells)
-Nucleated red blood cells (RBCs) on the same blood film

=>Causes:GLIM

*	Sepsis
*	Inflammation
*	G-CSF
*	Leukemia
*	Myelofibrosis
*	Myocardial infarction (MI)
*	Chronic lung disease

Left Shift
* Indicates immature granulocytes (mostly neutrophils)
* Normal band cells: 2–5%
* Any increase above this = left shift
* Suggests:
* Sepsis
* Hemorrhage
* Anemia

Toxic Changes
≥2 of the following 3:
1. Toxic granules → Indicate immature cells
2. Toxic vacuoles → Suggest phagocytosis
3. Döhle bodies → Remnants of endoplasmic reticulum