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Myeloproliferative Disorders - Mahmoud Quiz Stats

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Score 0/39 Timer 15:00
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x x % Correct
This chromosome is present in 90% of patients with CMLphiladelphia
82.1%
this clinical disorder describes an abnormally elevated hemoglobin or hematocritpolycythemia vera
78.6%
This is the principle site of extramedullary hematopoiesisspleen
75%
These organs are most affected by PVHeart, spleen, kidney
71.4%
High Hct/Hb, splenomegaly, and increased RBC mass are major diagnostic criteria of:polycythemia vera
71.4%
this is the most dominant cell line affected by PVerythroid
67.9%
A mutation in this tyrosine kinase can lead to PVJAK2
67.9%
In MM, there is malignant proliferation of these platelet forming cells,megakaryocyte
67.9%
this type of cell is any leukocyte that is NOT a lymphocytemyeloid cell
64.3%
In regards to time, CML and PV are examples of this type of myeloproliferative disorderchronic
64.3%
the chronic phase of cml lasts for about this many years3-4 years
64.3%
Besides blast crisis, CML can also progress to this disorder, where bone marrow is replaced with scar tissuemyelofibrosis
64.3%
This disorder can result in a ruddy complexionpolycythemia vera
64.3%
Only blast cells are present in this myelogenous disorderacute myelogenous leukemia
60.7%
When JAK2 is mutated, cells become abnormally sensitive to this glycoprotein hormoneEPO
60.7%
In late PV, the bone marrow can become ____________fibrotic and hypocellular
60.7%
This disorder is characterized by a genetic abnormalitychronic myelogenous leukemia
57.1%
this acute condition occurs after the accelerated phase in CML patientsblast crisis
57.1%
in the accelerated phase of cml, there is an increase in this type of immature cellblast
57.1%
In this stage of cml, one can find nodular tumors on the skinblast crisis
57.1%
x x % Correct
This is the formation of stacks of RBCs observed in peripheral bloodRouleaux
57.1%
in this disorder, LAP levels are elevatedpolycythemia vera
57.1%
MMmyeloid metaplasia
53.6%
For a CML CBC, you can expect markedly increased levels of this cellwhite blood cell
53.6%
Look for decreased levels of this enzyme to differentiate cml from infectionleukocyte alkaline phosphatase
53.6%
Excessive histamine release can result in this GI diseasepeptic ulcer
53.6%
High rate of cell turnover can produce excessive amounts of this byproducturic acid
53.6%
This component of Virchow's Triad contributes to headachestasis
53.6%
Hepatic vein thrombosis is associated with this myeloproliferative disorder`polycythemia vera
50%
CML and MM share high levels of this purine byproducturic acid
50%
extramedullary hematopoiesis in the liver is characteristic of which diseasemyeloid metaplasia
50%
In CML the transformed pluripotent stem cells predominantly differentiate into this type of cellgranulocytic
46.4%
PV involves excessive release of this cytokinehistamine
46.4%
This is the most prominent picture of Myeloid metaplasiafibrosis
46.4%
Subcapsular infacts of the spleen are a characteristic finding of this disordermyeloid metaplasia
46.4%
in bone marrow, transformation into myelofibrosis marks the beginning of this phasespent phase
46.4%
This type of PV is a stem cell disorderabsolute
42.9%
in this myelogenous disorder, myeloid cells do not spill into the bloodmyelodysplastic
39.3%
This proper noun describes the three thrombolytic properties of PVVirchow's triad
39.3%

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Created Nov 30, 2010ReportNominate
Tags:disorder

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