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PA BOARDS HEMATOLOGY CHEAT SHEET, HEMATOLOGY AND ONCOLOGY PANCE/PANRE, HEMATOLOGY PEARLS (1), HEMATOLOGY, HEMATOLOGY/ONCOLOGY WORD ASSOCIATIONS PANCE/PANRE EXAM QUESTIONS WITH VERIFIED ANSWERS 2024/2025 R213,95   Add to cart

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PA BOARDS HEMATOLOGY CHEAT SHEET, HEMATOLOGY AND ONCOLOGY PANCE/PANRE, HEMATOLOGY PEARLS (1), HEMATOLOGY, HEMATOLOGY/ONCOLOGY WORD ASSOCIATIONS PANCE/PANRE EXAM QUESTIONS WITH VERIFIED ANSWERS 2024/2025

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PA BOARDS HEMATOLOGY CHEAT SHEET, HEMATOLOGY AND ONCOLOGY PANCE/PANRE, HEMATOLOGY PEARLS (1), HEMATOLOGY, HEMATOLOGY/ONCOLOGY WORD ASSOCIATIONS PANCE/PANRE EXAM QUESTIONS WITH VERIFIED ANSWERS 2024/2025 Megaloblastic. Peripheral neuropathy MMA B12 Deficiency Megaloblastic. No neuro symptoms F...

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  • November 11, 2024
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  • 2024/2025
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PA BOARDS HEMATOLOGY CHEAT SHEET, HEMATOLOGY AND
ONCOLOGY PANCE/PANRE, HEMATOLOGY PEARLS (1),
HEMATOLOGY, HEMATOLOGY/ONCOLOGY WORD
ASSOCIATIONS PANCE/PANRE EXAM QUESTIONS WITH
VERIFIED ANSWERS 2024/2025

Megaloblastic. Peripheral neuropathy MMA

B12 Deficiency

Megaloblastic. No neuro symptoms

Folate Deficiency

Blood loss. Microcytic. Low ferritin.

Iron Deficiency

Increased LDH, reticulocyte, Indirect bilirubin. Decreased

haptoglobin.

Hemolysis

Pancytopenia Low retic count. Bone biopsy.

Aplastic Anemia

X-linked enzyme deficiency. Infection. Fava beans. Bite cells. Heinz body

G6PD deficiency

Most common bleeding disorder. Elevated aPTT. Von willebrand factor activity.

RIPA. Desmopressin

Von Willebrand

,X-linked recessive disorder. Hemarthrosis. Normal Platelets.

prolonged aPTT.

Hemophilia

Thrombophilia. DVT. PE. No screening.

Factor V Leiden

Anticardiolipin antibody. Recurrent pregnancy loss. Prolonged aPTT. Russel

Viper Venom test. DVT

Antiphospholipid Syndrome

4 > days. Thrombosis. ELISA. Venous limb gangrene

Heparin Induced Thrombocytopenia

Shiga Toxin producing E COLI 0157:H7. Quinine. Microangiopathic hemolytic

anemia and thrombocytopenia.

Immune Thrombocytopenia

65. Myeloid. Auer rod Phi bodies. M3 all-trans-retinoic acid. > 20% blasts

AML

Children. Lymphoid. > 20% blasts. TdT

ALL

Neutrophils. Basophilia. Leukocytosis. 9:22 translocation.

Philadelphia chromosome Tyrosine Kinase Inhibitor.

CML (Philadelphia cream cheese)

Non functioning B cells. Lymphadenopathy. Lymphocytosis Flow cytometry.

Rituximab.

CLL

,Painless cervical lymphadenopathy. B symptoms. Reed Sternberg cells.

Mediastinal mass. Excisional node biopsy

Hodgkin Lymphoma

Plasma cells. IgG, IgA. Bence Jones Protein Rouleaux Formation. > 10% clonal

plasma cells

Multiple Myeloma

Vaso occlusion. Hemolytic anemia. Cold, Hypoxia, alcohol,

infection. Howell Jolly bodies. Penicillin < 5 years of age. Hydroxyurea.

Sickle cell

Auer rods on peripheral smear indicate...

acute myeloblastic leukemia (AML)

60 year old male with severe anemia, decreased neutrophil count, and small,

abnormal B lymphocytes in the bone marrow (>30%) with levels at 90,000 per

cubic millimeter. Has painless cervical lymphadenopathy and

hepatosplenomegaly. Likely diagnosis?

Chronic lymphocytic leukemia (CLL)

Bone marrow aspiration and biopsy reveals the presence of the Philadelphia (Ph)

chromosome in dividing marrow cells. Likely diagnosis?

Chromic myeloblastic leukemia (CML)

Follicular, cleaved cell, lymphocytic, histolytic

Hodgkins Lymphoma

Reed Sternberg cell

Hodgkin's lymphoma

, Plasma cells, monoclonal protein

Multiple myeloma

What disease is characterized by abnormal monoclonal protein, anemia, and lytic

bone lesions?

Multiple myeloma

30 year old white male with 3 month history of painless enlargement of bilateral

cervical lymph nodes, fever, and night sweats. Likely diagnosis?

Hodgkin's disease

What hematologic measurement is abnormal in chronic heavy alcohol use?

Mean corpuscular volume

Most frequent cause of B12 deficiency in patients with classic pernicious anemia

Lack of intrinsic factor

In thalassemia anemia, what causes the anemia?

Shortened lifespan of RBCs

Teenage African American female presents with severe bone and joint pain. CBC

shows severe anemia and elevate leukocyte and platelet counts. Most likely

diagnosis?

Sickle cell disease

What 2 tests are used to confirm the diagnosis of homozygous sickle cell

disease?

Peripheral smear and hemoglobin electrophoresis

The most helpful test to distinguish megaloblastic from nonmegaloblastic

macrocytic anemia

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