WorksheetsLONG QUIZ
Total questions: 40
Worksheet time: 31mins
1. ___________ stoppage of blood flow.
Hematemesis
Hemolysis
Hemostasis
Hemophilia
Splenomegaly
Increased platelet
Decreased platelet
Platelet will not be affected
RBC increased
Splenectomy
Increased platelet
Decreased platelet
Platelet will not be affected
RBC increased
Is a glycoprotein hormone produced mainly by the liver and the kidney that regulates the production of platelets by the bone marrow.
Thrombopoietin
Ferritin
Hemoglobin
Fibrinogen
_____ Bleeding into a joint is and is an important cause of monoarticular joint pain and swelling. Hemarthrosis may be suspected on the basis of a suggestive history, physical examination, or imaging studies, but definitive diagnosis usually requires joint aspiration.
Hematemesis
Hemarthrosis
Ecchymosis
Purpura
A bleeding disorder associated with abnormal platelets, which are small blood cells involved in blood clotting. People with this condition tend to bruise easily and have an increased risk of nosebleeds (epistaxis).
GRAY PLATELET SYNDROME
HERMANSKY-PUDLAK
CHEDIAK-HIGASHI
WISKOTT-ALDRICH SYNDROME
A disorder characterized by a condition called oculocutaneous albinism, which causes abnormally light coloring (pigmentation) of the skin, hair, and eyes.
GRAY PLATELET SYNDROME
HERMANSKY-PUDLAK
CHEDIAK-HIGASHI
WISKOTT-ALDRICH SYNDROME
What are the different signs that forms the TRIAD for Wiskott-Aldrich Syndrome?
Give me 3 answers.
Hemophilia
Immunodeficiency
Eczema
Thrombocytopenia
The process by which bone marrow progenitor cells develop into mature megakaryocytes (MKs), which in turn produce platelets required for normal hemostasis.
HEMOSTASIS
HEMOPHILIA
MEGAKARYOPOIESIS
HEMATOPOIESIS
Last stage capable of endomitosis.
PROMEGAKARYO
CYTE
MEGAKARYOCYTE
PLATELETS
MATURE
MEGAKARYOCYTE
The stage where DMS Demarcating Membrane System is first formed.
PROMEGAKARYO
CYTE
MEGAKARYOCYTE
PLATELETS
MATURE
MEGAKARYOCYTE
The Lifespan of the platelet.
5 DAYS
15 DAYS
10 DAYS
21 DAYS
Purplish red pinpoint hemorrhagic spots in the skin caused by loss of capillary to withstand normal blood pressure and trauma.
PETECHIAE
PURPURA
ECCHYMOSIS
HEMATEMESIS
Based on the picture what do you call this type of disorder?
Hematemesis
Epistaxis
Melena
NOTA
Occurs as a result of skin fragility.
Devil’s pinches
Mechanical purpura
Senile purpura
Schamberg’s purpura
Seen in older individuals or in individuals undergoing corticosteroid therapy; purpuric lesion occurs on the hand and arms.
Devil’s pinches
Mechanical purpura
Senile purpura
Schamberg’s purpura
Occurs as a result of sudden increase in capillary pressure and usually manifests as petechiae.
Devil’s pinches
Mechanical purpura
Senile purpura
Schamberg’s purpura
A disorder of women that presents with recurrent purpura on the lower extremities and resultant hemosiderin staining of the skin similar to Schamberg’s.
HYPERVISCOSITY SYNDROME
CRYOGLOBULINEMIA
WALDENSTOM’S PURPURA
AMYLOIDOSIS
The process of achieving hemostasis via the interaction of plasma coagulation factors(the coagulation cascade).
Secondary hemostasis
Coagulation cascade
Primary hemostasis
Extrinsic Pathway
An abnormal and increased susceptibility to bleeding, often due to hypocoagulability.
Hemorrhagic diathesis
IgA vasculitis
Osler-Weber-Rendu syndrome
Thrombotic microangiopathy
An autosomal recessive disorder causing clotting factor XI deficiency. Results in a bleeding diathesis. Especially common in Ashkenazi Jews.
Factor XI deficiency
Factor IX deficiency
Factor VIII deficiency
Vitamin K deficiency
One of the main components of blood.
WBC
RBC
PLATELET
HEMOGLOBIN
●Examples of hemoglobinopathies include:
Give me 3 answers.
○sickle cell anemia
○hemoglobin C disease
○thalassemia
○hemophilia a
Sickle cell
Thalassemia
Hemoglobin C
Hereditary spherocytosis
It is a condition that affects red blood cells. People with this condition typically experience a shortage of red blood cells (anemia ), yellowing of the eyes and skin (jaundice), and an enlarged spleen (splenomegaly).
Sickle cell
Thalassemia
Hemoglobin C
Hereditary spherocytosis
A hereditary disorder of the red blood cells (RBCs). In this condition, the RBCs assume an elliptical shape, rather than the typical round shape. Blood is comprised of red blood cells, platelets, and various white blood cells. Elliptocytosis is a hereditary disorder of the red blood cells (RBCs).
Spherocytosis
Hemoglobin C
Elliptocytosis
Hemoglobin SC
Spherocytosis
Hemoglobin C
Elliptocytosis
Hemoglobin SC
Occurs when a person is missing or does not have enough of an enzyme called glucose-6-phosphate dehydrogenase. This enzyme helps red blood cells work properly.
Some common general symptoms of anemia include:
Give me 2 answers.
Common symptoms of hemolysis (increased red blood cell breakdown) include: Give me 3 answers.
●scleral icterus (yellow eyes)
●decreased exercise tolerance
●gallstones
●enlarged spleen
○A low dietary intake of iron or blood loss due to issues such as very heavy menstruation may cause _______. More serious causes include blood loss from internal bleeding in the gastrointestinal tract or cancers.
●Iron deficiency anemia
●Pernicious Anemia
●Aplastic Anemia
●Autoimmune Hemolytic Anemia
○Rare disorder in which the body has trouble using vitamin B-12, a key component in making RBCs. This may happen due to an autoimmune condition or other cause weakening the stomach lining, which makes cells that bind to vitamin B-12 so the intestines can digest them.
●Iron deficiency anemia
●Pernicious Anemia
●Aplastic Anemia
●Autoimmune Hemolytic Anemia
Acanthocyte
Elliptocyte
Dacryocyte
Echinocyte
Can occur in patients with Renal failure or malnutrition.
Acanthocyte
Elliptocyte
Dacryocyte
Echinocyte
Can be seen in ALCOHOLISM .
ACANTHOCYTE
ECHINOCYTE
STOMATOCYTE
SPHEROCYTE
Can be seen in patients with Iron deficiency thalassemia.
Stomatocyte
Schistocyte
Elliptocyte
Target Cell
This can be seen in patients with Wilson's disease.
Acanthocyte
Elliptocyte
Echinocyte
Spherocyte
WRITE DOWN YOUR HEMATOLOGY 2 TEACHER'S COMPLETE NAME.
(a)
