FINAL Flashcards
What type of parasite is Malaria?
Obligate intracellular protozoan
What type of cells does plasmodium sporozite infect first?
Liver Cells –> matures into schizont form –> rupture and release merozoite stage into blood
What do merozoites infect?
Erythrocytes
Through **ring cell stage **back to schizont
What is a hallmark symptom of Malignant tertian of plasmodium falciparum
Black Water Fever
due to capillary blockage;
Convulusions, coma, cardiac failure,
MALARIA Diagnosis
What do you see on a peripheral smear?
RING FORM
What other pathogen has ring-forms in RBC?
Plasmodium and Babesiosis
First line treatment for Malaria
Chloroquine
if restistant: quinine sulfate, atovoquone/proguanil, mefloquine
Name the pathogen
Double Stranded DNA virus
aka Human Herpes Virus-4 (HHV4)
EBV
How is EBV transmitted?
Close Saliva contact (Kissing disease)
resp. droplets/blood transfusion
What symptoms are seen with MONO?
Fever, Pharyngitis, fatigue, and rash
Hepatosplenomegaly is caused by what?
Lymphocyte infilitration
What test is done to diagnose EBV?
Monospot Test
EBV serology
Peripheral Smear: Atypical lymphocytes
A patient with EBV was misdiagnosed and treated for strep throat with Penicillin or Amoxicllin…What does the patient present with?
Diffuse Maculopapular Rash
CD4 Count > 500 v. < 100
> 500 = oral hairy leukoplakia
<100 Non hodgkin B Cell lymphoma, CNS lymphopma
Which of the following is seen in EMV infectious mononucleosis?
Atypical lymphocytes
What are Dohle Bodies?
RER remnants
When evaluating bone marrow, what is the normal myeloid:erythroid ratio?
3:1
Patient presents with >20% myeloid blast cells in bone marrow .. What is your diagnosis
Acute Myelogenous Leukemia (AML)
Patient is diagnosed with Acute Myelogenous Leukemia … you see abnormal azurophilic granules in a bone marrow aspirate, which are called what?
Auer Rods
What chromosome indicates an unfavorable progonsis in Acute Myelogenous Leulemia?
Philadephia Chromosome (9:22)t
Mutated constitutively activated tyrosine kinases results in
excessive proliferation
What mutation is seen in Chronic myelogenous leukemia?
Philadelphia chromosome (9,22) –> BCR-ABL Fusion Gene
What mutation is seen in Polycythemia vera, Primary myelofibrosis and essential thrombocytothemia?
JAK2 Point Mutations
t(9;22)
Philadelphia Chromosome
What do BCR-ABL fusion genes cause?
accelerated automatic cellular divison
What are the 2 phases of polycythemia vera?
too many RBCs
Polycythemic and Spent Phases
In Essential thrombocytosis, patients have elevated counts of ?
What about polycythemia and marrow fibrosis
Elevated PLATELETS
no polycthemia/marrow fibrosis
What group do these belong to?
CML: CNL, CEL
PV
ET
MF
MYELOPROLIFERATIVE SYNDROMES
Hallmarks of MPS?
Clonal
Malignant
Natural Progression
What type of somatic mutations do you see in patients with MPS?
JAK2, CALR, MPL
what mutation is responsible for loss of inhibition of kinase domains causing cell proliferation?
JAK2
secondary causes of Polycythemia Vera
COPD, sleep apnea, obseity, high altitude
treatment goal of polycythemia vera
Control the symptoms
Which MFS has a normal life expectancy but INCREASES the risk of thrombosis/vascular events?
Essential Thrombosis
This treatment is used for Myelofibrosis and is a JAK inhibitor
Decreased spleen sie/INC quality of life
Ruxolitinib
What is the treatment for chronic eosinophilic leukemia
Pemigatinib
in a protein electropheresis of a myeloma, what region shows a monoclonal spike?
GAMMA region
plasma cell neoplasms secrete what type of protein?
Paraprotein (M-Protein = Ig)
What is the pre-malignant condition of a myeloma?
Monoclonal Gammopathy of Undetermined Significane (MGUS)
1% risk of progression to MM per year
In Smoldering Multiple myeoloma, what is the % of risk of progressing each year?
no CRAB
10% vs 1% (MGUS)
What does CRAB indicate?
Ca;cium
Renal Impairment
Anemia
Bone Lesions
seen in patients with multiple myeoloma
Patient with multiple myeolma has a blood smear done, what do you see?
Rouleaux Formation = stacking Of RBC
Multiple Myeoloma
Bone survey is the gold standard, but what diagnostic mode is more sensitive to lytic lesions and is preferred?
CT without contrast of whole body
AL Systemic Amyloidosis
Plasma cell neoplasms are associated with what?
production of monoclonal Ig light chain (Lambda > Kappa)
Hallmark clinical features of AL Systemic Amyloidosis:
Periorbital purpura (Guaxinin eyes)
Macroglossia
Proteinuria
Precursor B Cell Neoplasms
Immature B cells
ALL
Peripheral B Cell Neoplasms
Mature B Cells
CLL, SLL
Follicular Lymphoma
Multiple Myeoloma
What is the definitive diagnosis of ALL?
>35% of blasts in marror/circulation
>Detection of B and or T lymphocyte-specific markers
ALL
What are the precursors for B-cell tumors
TdT, CD10, CD19
What disease has SMUDGE cells?
CLL