HEMA LEC - Erythrocyte Inclusions And Associated Diseases Flashcards

(30 cards)

1
Q

Usually orthochromic normoblasts (metarubricyte) but can appear in any erythrocytic stage of maturation

A

Nucleated RBCs (nRBCs, nucRBCs)

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2
Q

Indicate bone marrow stimulation or increased erythropoiesis

A

Nucleated RBCs (nRBCs, nucRBCs)

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3
Q

Associated with thalassemia major, sickle cell anemia, and other hemolytic anemias, erythroleukemia, and myeloproliferative disorders

A

Nucleated RBCs (nRBCs, nucRBCs)

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4
Q

Normal newborns can have a few

A

Nucleated RBCs (nRBCs, nucRBCs)

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5
Q

Healthy individuals should have none on a peripheral blood smear.

A

Nucleated RBCs (nRBCs, nucRBCs)

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6
Q

Small, round DNA fragments (0.5-1.0um in diameter) usually one per cell, but can be multiple which results from karyorrhexis or nuclear disintegration

A

Howell-Jolly bodies

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7
Q

Stain dark purple to black with Wright’s stain; positive (+) in Feulgen Reaction

A

Howell-Jolly bodies

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8
Q

Not seen in normal erythrocytes; normally pitted by splenic macrophages

A

Howell-Jolly bodies

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9
Q

karyorrhexis or nuclear disintegration

A

Howell-Jolly bodies

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10
Q

d. Seen in sickle cell anemia, beta-thalassemia major, and other severe hemolytic anemias, MEGALOBLASTIC ANEMIA, alcoholism, post-splenectomy, accelerated erythropoiesis

A

Howell-Jolly bodies

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11
Q

Multiple, tiny, fine, or coarse inclusion (ribosomal RNA remnants) evenly dispersed throughout the cell;

A

Basophilic stippling (punctuate basophilia)

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12
Q

“blueberry bagel” appearance

A

Basophilic stippling (punctuate basophilia)

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13
Q

Stain dark blue with Wright’s stain

A

Basophilic stippling (punctuate basophilia)

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14
Q

Seen in in thalassemias, megaloblastic anemias, sideroblastic anemia, LEAD POISONING, pyrimidine-5-nucleotidase deficiency, and alcoholism

A

Basophilic stippling (punctuate basophilia)

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15
Q

Small, irregular, dark-staining IRON granules usually clumped together at PERIPHERY of the cell

A

Pappenheimer bodies

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16
Q

Stain with Perl’s Prussian blue stain; appear dark violet with Wright’s stain

A

Pappenheimer bodies

17
Q

Caused by an accumulation of ribosomes, mitochondria, and iron fragments

A

Pappenheimer bodies

18
Q

Seen in sideroblastic anemia, hemoglobinopathies, thalassemia megaloblastic anemia, myelodysplastic syndrome (RARS)!!!

A

Pappenheimer bodies

19
Q

Thin, red-violet, single to multiple ringlike structures that may appear in lip or figure-eight shapes

20
Q

Seen in megaloblastic anemia, myelodysplastic syndromes, lead poisoning

21
Q

Composed of fragments of nuclear material, specifically, remnants of microtubules of mitotic spindle

22
Q

Condensed, intracellular, rod-shaped crystal, or hexagonal crystals with blunt ends and stains darkly

A

Hemoglobin C crystals

23
Q

Seen in hemoglobin C or SC disease, but not in trait

A

Hemoglobin C crystals

24
Q

1-2 blunt, fingerlike projection extending from the cell membrane

A

Hemoglobin SC crystals (Washington monument)

25
Seen in hemoglobin SC disease
Hemoglobin SC crystals (Washington monument)
26
Multiple inclusions ranging in size from 0.3 to 2.0um | Invisible with Wright’s stain; must use a supravital stain to visualize; usually crystal violet
Heinz bodies
27
Seen in G6PD deficiency, beta-thalassemia major, Hgb H disease, unstable hemoglobinopathies, drug-induced anemias
Heinz bodies
28
Represent denatured hemoglobin
Heinz bodies
29
include P. vivax, P, falciparum, P. malariae and P. ovale
Malarial parasite
30
protozoan inclusion (B. microti), transmitted from deer to humans by tick bite. RBC inclusion resembles that of P. falciparum rings which a characteristic “MALTESE CROSS” appearance
Babesia