HEMA LEC - Erythrocyte Inclusions And Associated Diseases Flashcards

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

A

Cabot rings

20
Q

Seen in megaloblastic anemia, myelodysplastic syndromes, lead poisoning

A

Cabot rings

21
Q

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

A

Cabot rings

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
Q

Seen in hemoglobin SC disease

A

Hemoglobin SC crystals (Washington monument)

26
Q

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

A

Heinz bodies

27
Q

Seen in G6PD deficiency, beta-thalassemia major, Hgb H disease, unstable hemoglobinopathies, drug-induced anemias

A

Heinz bodies

28
Q

Represent denatured hemoglobin

A

Heinz bodies

29
Q

include P. vivax, P, falciparum, P. malariae and P. ovale

A

Malarial parasite

30
Q

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

A

Babesia