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ASCP exam preparation (USA · MLS / MLT) – page 12

1200 practice MCQs for the ASCP medical laboratory exam. Level: Advanced.

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Q221EasyRBC indices & anemias

Intrinsic factor, needed for vitamin B12 absorption, is secreted by which cells?

Answer: D. Gastric parietal cells

Parietal cells of the stomach secrete both hydrochloric acid and intrinsic factor. Chief cells secrete pepsinogen, and the ileum is where the B12–intrinsic factor complex is absorbed.

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Q222EasyRBC indices & anemias

Dietary folate is absorbed mainly in which part of the gut?

Answer: D. Duodenum and jejunum

Folate is absorbed in the proximal small intestine (duodenum and jejunum). The terminal ileum is the site of vitamin B12 absorption.

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Q223EasyRBC indices & anemias

Hepcidin, the hormone that controls iron absorption and release, is produced mainly by the:

Answer: A. Liver

Hepcidin is made by hepatocytes. It blocks ferroportin, reducing iron absorption from the gut and iron release from macrophages.

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Q224EasyRBC indices & anemias

Which pattern of red cell indices describes a microcytic hypochromic anemia?

Answer: D. Low MCV and low MCH

Microcytic means a low MCV (small cells) and hypochromic means low hemoglobin per cell, shown by a low MCH (and often low MCHC). Iron deficiency is the classic example.

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Q225EasyRBC morphology & inclusions

Enlarged infected red cells with fine pink-red stippling (Schüffner dots) on a Giemsa-stained thin film suggest infection with:

Answer: A. Plasmodium vivax

Schüffner dots in enlarged red cells are typical of P. vivax (P. ovale shows similar dots). P. falciparum shows Maurer clefts, and P. malariae infects normal-sized cells without Schüffner dots.

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Q226EasyRBC morphology & inclusions

A red cell containing iron granules (Pappenheimer bodies) that stain with Prussian blue is called a:

Answer: B. Siderocyte

A siderocyte is a red cell that contains iron-positive granules. Spherocytes, stomatocytes and schistocytes are shape changes.

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Q227EasyWBC morphology & differential

A white cell slightly larger than a red cell, with a round dense nucleus and a thin rim of sky-blue cytoplasm, is a:

Answer: C. Small lymphocyte

This is the typical small lymphocyte. Monocytes are much larger with folded nuclei, and neutrophils and basophils have lobed nuclei and granules.

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Q228EasyWBC morphology & differential

The movement of neutrophils out of blood vessels, squeezing between endothelial cells into the tissues, is called:

Answer: A. Diapedesis

Diapedesis is the passage of leukocytes through the vessel wall. Chemotaxis is directed movement toward chemical signals, and margination is sticking to the vessel wall.

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Q229EasyWBC disorders & leukemias

Infectious mononucleosis is caused by which virus?

Answer: C. Epstein-Barr virus

Classic infectious mononucleosis is caused by Epstein-Barr virus, which infects B lymphocytes. The heterophile (Monospot) test supports the diagnosis.

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Q230EasyWBC disorders & leukemias

Acute promyelocytic leukemia is characterized by which translocation?

Answer: B. t(15;17)

APL carries t(15;17), which forms the PML::RARA fusion. t(9;22) is the Philadelphia chromosome, t(8;14) is typical of Burkitt lymphoma and t(14;18) of follicular lymphoma.

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Q231EasyWBC disorders & leukemias

Acute leukemia is best described as:

Answer: D. A rapid build-up of immature blast cells in the marrow and blood

In acute leukemia, maturation is blocked and blasts build up quickly, crowding out normal blood cell production. A slow rise of mature lymphocytes describes CLL.

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Q232EasyPlatelets

Which description fits a normal platelet on a Wright-stained smear?

Answer: B. A small anucleate cell fragment with fine purple granules

Platelets have no nucleus. They are fragments of megakaryocyte cytoplasm with purple-staining granules.

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Q233EasyPlatelets

During platelet aggregation, fibrinogen forms bridges between platelets by binding to which receptor?

Answer: A. GP IIb/IIIa

Activated GP IIb/IIIa (integrin αIIbβ3) binds fibrinogen, linking platelets together. GP Ib/IX/V binds von Willebrand factor for adhesion, and P2Y12 is an ADP receptor.

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Q234EasyPlatelets

Primary hemostasis ends with the formation of:

Answer: D. A platelet plug

Primary hemostasis is vessel constriction plus platelet adhesion and aggregation, forming a platelet plug. Secondary hemostasis (coagulation) then adds a stable fibrin mesh.

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Q235EasyHemostasis & coagulation

Coagulation factor IV is:

Answer: C. Calcium ions

Factor IV is calcium, which several clotting complexes need. Citrate and EDTA prevent clotting by removing it. Proaccelerin is factor V.

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Q236EasyHemostasis & coagulation

Which enzyme breaks down fibrin in a clot?

Answer: C. Plasmin

Plasmin, formed from plasminogen by tissue plasminogen activator, digests fibrin. Thrombin forms fibrin, and factor XIIIa cross-links it.

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Q237EasyHemostasis & coagulation

Which drug is given to reverse an overdose of unfractionated heparin?

Answer: B. Protamine sulfate

Protamine sulfate binds heparin and neutralizes it. Vitamin K reverses warfarin, and tranexamic acid inhibits fibrinolysis.

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Q238EasyHemostasis & coagulation

The first response of a blood vessel to injury is:

Answer: A. Vasoconstriction

Injured vessels constrict at once to reduce blood flow. Platelet plug formation and coagulation follow, and fibrinolysis comes last.

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Q239EasyHemolytic anemias & hemoglobinopathies

Which drug is an iron chelator used in transfusion-dependent thalassemia?

Answer: A. Deferoxamine

Deferoxamine (and oral agents such as deferasirox) binds excess iron so it can be excreted, preventing damage from transfusional iron overload.

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Q240EasyHemolytic anemias & hemoglobinopathies

The most common type of crisis in sickle cell disease is:

Answer: C. Vaso-occlusive (painful) crisis

Painful vaso-occlusive crises, caused by sickled cells blocking small vessels, are by far the most common. The other crises are less frequent but can be severe.

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