RBC Abnormalities: Poikilocytosis Flashcards

(31 cards)

1
Q

alterations or variations in shape

A

Poikilocytosis

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2
Q

ESR in poikolocytosis

A

ESR DECREASE

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3
Q

seen in patient with VITAMIN B12 AND FOLATE DEFICIENCIES (observed in erythrocytes and reticulocytes)

A

Oval Macrocytes (Oval or egg-like)

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4
Q
  1. Nuclear Maturation Lags behind Cytoplasmic Maturation
  2. IMPAIRED ABILITY OF CELLS TO SYNTHESIZED DNA
A

Asynchronous Development ; Megaloblastic Anemia

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5
Q

SECONDARY TO MEMBRANE DEFECTS:

Increase SPHINGOMYELIN over lecithin

A

Acanthocytes

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6
Q

SECONDARY TO MEMBRANE DEFECTS:

Also known as SPUR, Thorn cells ;

Severe Liver Disease
Neuroacanthocytosis
Mcleod Syndrome
Abetalipoprotenemia

A

Acanthocytes

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7
Q

SECONDARY TO MEMBRANE DEFECTS:

RBC with short projections ; distortion of OSMOTIC BALANCE

A

Echinocytes (Crenated, Sea Urchin)

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8
Q

SECONDARY TO MEMBRANE DEFECTS:

Burr Cells

A

Echinocytes

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9
Q

SECONDARY TO MEMBRANE DEFECTS:

seen in patient with
Uremia
Liver disease
Heparin Therapy
Pyruvate Kinase

A

Echinocytes (burr, sea urchin)

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10
Q

SECONDARY TO MEMBRANE DEFECTS:

Increased in surface to volume ratio; EXCESS CHOLESTROL
Hemoglobin concentration imbalance

A

Codocytes (Mexican hat, Target cells)

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11
Q

SECONDARY TO MEMBRANE DEFECTS:

Hemoglobinopathies
Thalassemia
Liver Disease

A

Codocytes (Mexican hat, Target)

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12
Q

SECONDARY TO MEMBRANE DEFECTS:

Thinner version of Codocytes seen in patient with:

Hepatic disorder
IDA
Thalassemia

A

Leptocytes

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13
Q

SECONDARY TO MEMBRANE DEFECTS:

No central palor
Defects of Red cell membrane protein (SPECTRIN)

A

Spherocytes

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14
Q

SECONDARY TO MEMBRANE DEFECTS:

Seen in patients with:

Hereditary spherocytosis
Immune Hemolytic Anemia
Extensive burns

A

Spherocytes

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15
Q

Hereditary Spherocytosis OFT result

A

Increase

“HIS”

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16
Q

SECONDARY TO MEMBRANE DEFECTS:

Slit Like area of central pallor
CATION IMBALANCE (Na/K)

A

Stomatocytes

“SS” - Stomato ; Sodium

17
Q

SECONDARY TO MEMBRANE DEFECTS:

Seen in patients with:

Hereditary stomatocytosis
RH NULL SYNDROME
Acquired (Liver disease, alcoholism)
Artifact

18
Q

SECONDARY TO MEMBRANE DEFECTS:

Cigar-shaped RBC
Defect is Cytoskeleton
DECREASED IN MEMBRANE PROTEIN BAND 4.1

19
Q

SECONDARY TO MEMBRANE DEFECTS:

Seen in patient with

Hereditary Elliptocytosis
Malignancy
Hb C disease
Hemolytic Anemia
IDA
Sickle cells trait
Thalassemia
Pernicious anemia

20
Q

SECONDARY TO MEMBRANE DEFECTS:

Egg-shaped RBC
Seen in patient with Macroovalocytes
MEGALOBLASTIC ANEMIA

21
Q

Hereditary Spherocytosis and Autoimmune Hemolytic Anemia has the same result with:

MCHC - Increased
OFT - Increased

What is the test used to differentiate the two?

A

Direct AHG Test (DAT)

22
Q

SECONDARY TO TRAUMA:

A
  1. Schizocytes
  2. Dacryocytes
  3. Microsperocytes, Pyropoikilocyte
  4. Semi-lunar bodies, Half-moon, Crescent cells
23
Q

SECONDARY TO TRAUMA:

Fragmented RBC

Seen in patient w/
Microangiopathic Hemolytic Anemia
Traumatic Cardiac Hemolysis
Extensive Burns

24
Q

SECONDARY TO TRAUMA:

Hornlike projections

A

Helmet Cells (Keratocyte)

25
SECONDARY TO TRAUMA: Pinched bottle appearance
Knizocytes
26
SECONDARY TO TRAUMA: Single pointed extension ; squeezing and fragmentation (Teardrop)
Dacryocytes
27
SECONDARY TO TRAUMA: Seen in patients with Primary Myelofibrosis Myelophthisic anemia Thalassemia Megaloblastic Anemia
Dacryocytes
28
SECONDARY TO TRAUMA: Abnormality in membrane protein; HEAT SENSITIVITY at 45 deg cel.
Microspherocyte Pyropoikilocyte
29
SECONDARY TO TRAUMA: Pale-pink staining of ghost cell; seen in malaria
Semi-lunar, Half-moon, Crescent cell
30
SECONDARY TO HEMOGLOBIN CONTENT: formed from gelation Hgb S Lowered Oxygen and Decreased pH (Shift Left)
Drepanocyte (sickle cells) Holly-Leaf Shape
31
SECONDARY TO Hgb Content: seen in patient with SICKLE CELL ANEMIA
Drepanocytes