Hematology/Oncology Flashcards

1
Q

Four causes of microcytic anemia

A

TICS-Thalassemia. Iron deficiency anemia of Chronic disease, and Sideroblastic anemia

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2
Q

An elderly man with hyppochromic, microcytic anemia is asymptomatic. Diagnostic tests?

A

Fecal occult blood test and sigmoidoscopy; suspect colorectal cancer

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3
Q

Precipitants of hemolytic crisis in patients with G6PD deficiency

A

Sulonamides, antimalarial drugs, fava beans

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4
Q

The most common inherited caurse of hypercoagulability

A

Factor V Leiden mutation

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5
Q

The most common inherited bleeding disorder

A

von Willebrand disease

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6
Q

The most common ingerited hemolytic anemia

A

Hereditory spherocytosis

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7
Q

Diagnostic test for hereditary spherocytosis

A

Osmototic fagility test

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8
Q

Pure RBC aplasia

A

Diamond - Blackfan anemia

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9
Q

Aneia associated with absent radii and thumbs, diffuse hyperpigmentation, caf2 au lait spots, microcephaly, and pancytopenia

A

Fanconi anemia

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10
Q

Medications and viruses that lead to aplastic anemia

A

Chlorampheniicol, sulfonamides, radiation, HIV, chemotherapeutic agents, hepatitis, parvovirus B19, EBV

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11
Q

How to distinguish polycythemia vera from 2° polycythemia

A

Both have elevated hematocrit and RBC mass, but polycythemia vera should have normal O2 saturation and low erythropoietin levels

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12
Q

Thrombotic thrombocytopenic purpura (TTP) pentad?

A

“FAT RN”: Fever Anemia Thrombocytopenia, Renal dysfunction, Neurologic abnormalities

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13
Q

Hemolytic uremic syndroma (HUS) triad?

A

Anemia, thrombocytopenia, and acute renal failure

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14
Q

Treatlabt for TTP

A

Emergent large-volume plasmaphereseis, corticosteroids, antiplatelet drugs. Platelet transfusion is contraindicated!

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15
Q

Treatment for idiopathic thrombocytopenic purpura (ITP) in children

A

Usually resolves spontanea-ously; may require IVIG and/or corticosteroids

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16
Q

Which of the following are elevated n DIC; fibrin split products, D-dimer, fibrinogen, platelets and hematocrit?

A

Fibrin split products and D-dimer are eevated; platelets, fibrinogen and hematocrit are lowered

17
Q

An 8-year-old girl presents with prolonged bledding after dental surgery and with menses, normal PT, normal or elevated PTT and elevated bleeding time Diagnosis? Treatmant?

A

von Willebrand disease; treat with desmopressin , FFP , or cryoprecipitate

18
Q

A 60-year old African American man presents with bone pain. What might a workup for multiple myoloma reveal?

A

Monoclonal gammopaty, Bence Jones proteinuria, and “punched-out” lesions on radiographs of the skull and long bones

19
Q

Reed-Sternberg cells

A

Hodgkin lymphoma

20
Q

A 10-year-old boy presents with fever, meight loss and night sweats. Examination shows an anterior mediastinal mass. Suspected diagnosis?

A

Non-Hodgkin lymphoma

21
Q

Microcytic anemiawith lowered serum iron, lowered total iron-biniding capacity (TIBC) and normal or elevated ferritin

A

Anemia of chronic desease

22
Q

Microcytic anemia with lowered serum iron , lowered ferritin , and elevated TIBC

A

Iron-deficiency anemia

23
Q

An 80-year_old man presents with fatigue, lymphadenopaty, splenomegaly, and isolated lyphocytosis. What is the suspected diagnosis?

A

Chronic lymphocytic leukemia (CLL)

24
Q

Patient with fatigue is found to have a lowered hemoglobin and elevated mean corpuscular volume. What are potential causes for this anemia?

A

Lowered B12 (pernicious anemia, vegetarian diet, Crohn/GI disorders) or folate (alcoholics)

25
A late, life-threatening complication of chronic myelogenous leukemia (CML)
Blast crisis (fever, bonoe pain, splenomegaly, pancytopenia)
26
Auer rods on blood smear
Acute myelogenous leukemia (AML)
27
AML subtype associated with DIC. Treatment?
M3, Retinoic acid
28
Electrolyte-changes in tumor lysis syndrome
Lowered Ca2+, Elevated K+, elevated phospate, elevated uric acid
29
A 50-year-old man presents with early satiety, splenomegaly, and bleeding. Cytogenetics show t(9,22) Diagnosis?
CML
30
A patiënt on the chemotherapy service with an absolute neutrophil count (ANC) of 1000 is noted to have a fever of 38°8C Next best step?
Neutropenic, fever is a medical emergency. Start broad-spectrum antibiotics
31
Virus associated with aplastic anemia in patients with sickle cell anemia
Parvovirus B19
32
A 25-year - old African American man with sickle cell anemia has sudden onset of Bone pain. Management of pain crisis?
O2, analgesia, hydration and , if severe , transfusion
33
A significant cause of morbidity in thalassemia patients. Treatment?
Iron overload; use deferoxamine