plasmacelldyscrasias Flashcards

1
Q

what are some plasma cell dyscasias

A

MGUS, multiple myeloma, plasmacytoma, amyloidosis, waldenstroms macroglobuninmia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what is a multiple myeloma

A

cancer of plasma cells that produce antibodies and immune function. Looking for a monoclonal cancer M cell common in males, AA ad over 65.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what is mgus

A

monoclonal gammopathy of undetermined significance we dont know what is causing it. Precancerous condition no symptoms 1% chance per year of becoming a myeloma.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what are the symptoms of myeloma

A

various body systems, bone/fractures numbness/tingling in the lower back/legs , wieght loss, weakness altered mental status, short breath fatigue unrinary issues.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

tell me about the chains in myelomas

A

IgG most common and then IgA d and e are rare, in the heavy chains and kappa and lambda are the light chains third most common in the light chain only myeloma. EX: IgG Kappa or IgA lambda

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

how do you diagnoses multiple myeloma

A

presence of serum or urinary monoclonal protein more than 3% in the blood, and presence of clonal plasma cells in the bone marrow greater than 10%, and presence of end organ damage such as calcium concentration lytic bone lesions anemia or renal failure, you need all three of these to diagnos this.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what is smoldering myeloma

A

when you do not have the end organ damage but the other two symptoms

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what is the staging of multiple myeloma

A

Stage 1 B2M [meta 2 microglobulin test] less than 3.5 and serum albumin more than 3.5, stage 2 neither stage 1 or 3, stage 3 B2M more than 5.5, prognosis per stage 1. 62, 2. 44, 3. 29 months.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what are the cytogenetics for multiple myeloma

A

Chromosome 14 for the heavy chains and a mutation or trans-location will change the risk and prognosis.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

how do you treat multiple myeloma

A

smoldering just wait and watch, normal myelomas, chemo steroids immunomodulators, bone marrow transplant and bisphosphonates and radiation.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what is the screen for amylodosis associated with multiple myeloma

A

Congo red stian is the definitive test but you can also do MPEV but absence does not mean its not there.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what is amylodiosis

A

protein confomation disorder asociaed with clonal plasma cell dyscrasia, extracellular deposition of light chain fragments in abnormal insoluble form.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what percent of patients with myeloma have amyloidosis

A

10% most common in the kidney heart liver periorbital

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what are the prognostic factors of amyloidosis

A

Cardiac 6 months, most important factor is if its in the heart. But also poor if in the liver.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what is the treatment of amyloidosis

A

treatment aid is to retard further deposition because you cannot cure it.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

tell me about waldenstroms macroglobuninemia

A

excess IgM specific. And this is more of a low grade lymphoma IgM found in the blood but markers in the bone marrow.

17
Q

what are the symptoms of waldenstroms

A

large size leads to , GI bleed, coombs positive anemia, cryoblobunlinemia, hyperviscosity,

18
Q

how do you diagnose waldenstroms

A

any monoclonal IgM in the blood. In the bone marrow more than 10% monoclonal lymphocytes and plasma cell differentiation,

19
Q

what are the treatments of waldenstroms

A

asymptomatic observe only, symptomatic chemo plasmapheresis. Incurable and greatest risk of progression in years 1-5