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Sharlotte Anne
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Cards (67)
Chronic Lymphoproliferative
Disorders
Chronic Lymphocytic
Leukemia
Pro-Lymphocytic
Leukemia
Hairy Cell
Leukemia
Chronic Lymphocytic Leukemia
Predominant cell:
Dormant B-cells
(cannot produce antibodies)
Less likely to undergo
blastic
transformation (chronic- acute)
Chronic
Granulocytic
L- can undergo blastic T.
Autoimmune
Hemolytic Anemia-
hemolysis (presence of autoantibodies)
Autoantibodies
Cell antibodies, can react with
RBC
> Complement activated= HEMOLYSIS (
decreased
RBC count)
Other Signs and Symptoms of Chronic Lymphocytic Leukemia
Lymphadenopathy
(enlargement of lymph nodes)
Splenomegaly
(enlargement of spleen why= hemolysis)
Hepatomegaly
Pruritus-
skin infection caused by
Herpes zoster
Reason for skin infection in Chronic Lymphocytic Leukemia
No
antibodies
Lab Findings for Chronic Lymphocytic Leukemia
Lymphocyte count:
10-150x 10
^
9/L
PBS: predominant of
SMUDGE
cells(
T
cells)
Hypogammaglobulinemia
(
decreased
antibodies)
Prognosis for Chronic Lymphocytic Leukemia
4
years
Treatment for Chronic Lymphocytic Leukemia
Leukapheresis
(transfusion of
granulocytes
as well as WBC) and regular injection with IgG (additional AB)
Hairy Cell Leukemia/ Lymphocytic Reticuloendotheliosis
Affected cell:
B-cells
Pancytopenia
(increased in all blood cells)
Splenomegaly-
Splenectomy (removal of spleen)
Characteristics of Hairy Cell Leukemia
40-60
yrs old (
Males 4x
more prone)
TRAP
Tartrazine
Resistant
Acid Phosphatase
Acid Phosphatase
Common seen in
prostate
(seminal fluid)
Pro-Lymphocytic Leukemia
Predominant cells:
prolymphocytes
Increase
promyelocytes
Prognosis for Pro-Lymphocytic Leukemia
<
1
year
Other Lymphocytic Neoplasms
Infection
/
viruses
Burkitt's Lymphoma
EBV
and
HIV
Translocation of
c-myc
on
chromosome
region
Mycosis Fungoides and Sezary Syndrome
Different stages of a single
neoplastic
disorder (neoplastic: new
cells
(abnormal))
T-helper cell (
lymphatic
tissues) – skin
Skin:
parakeratosis
Pautrier's microabscesses (
lymphocyte
clusters)
Lymph node: Sezary cells
Band-like
infiltrates
Plasma cell
B lymphocytes
(ANTIBODIES)
Multiple Myeloma
Plasma cell
Dysfunctional
50
% of IgG
20
% of IgA
15
% of lambda and gamma chain
Abnormal protein (BENCE JONES PROTEINS) not excreted = tends to accumulate; present in
80
% of MM px
How to know if there are BJP in the urine
Test for
solubility
(heat at 60-80C= will form precipitate) 150C-
DISSOLVE
Hyaline
cast
First cast that will form, made up of uromodulin/
Tamm–Horsfall
protein
Types of chains in Multiple Myeloma
Light
chain (
lambda
, gamma), gamma chain
Increased Protein
RBC
form
roulex
formation
ESR
Elevated
/
Increased
Flame cells
With
reddish
tinge of ribosomal
proteins
(IgA)
Dutcher bodies
Intranuclear
crystalline structures (
IgG
)
Russel Bodies
Accumulations of IgG
Grape
cell/Mott cell,
Morula
cell
Plasma cell that contains small colorless/
blue
/
pink
globules
Plasma Cell Leukemia
>
2x10
^
9/L
plasma cell count
Waldenstroms Macroglobulinemia
Increase production of
IgM
(>3 g/dL); Increase
protein
= Rouleux formation= Increase ESR
Heavy Chain Disease
Abnormal
synthesis (
Gamma
(IgG) or Alpha(IgA))
Causes of Lymphoma
Infections
(part. HIV/EBV)
Enlargement
of the lymph nodes
Signs and Symptoms of Hodgkin's Lymphoma
Fever
Night
sweats or
10
% weight loss in 6 months (it can be both)
Leukocytosis
Lymphocytopenia
Leukocytosis
Increased
in all WBC
Lymphocytopenia
Decrease
lymphocytes
Prognosis of Hodgkin's Lymphoma with Lymphocytopenia
Poor
prognosis
Diagnosis of
Hodgkin's
Lymphoma
Lymph node biopsy
(histopath) – presence of
REED- STERNBERG CELL
(lacunar histiocytes)
Reed-Sternberg cell
Giant multi/
binucleated
cell- hallmark finding for
Hodgkin's
lymphoma
Ann Harbor Staging System for Hodgkin's Lymphoma
I-IV
(locate region of lymph nodes)
A(no symptom
) or
B(presence of symptom
(suffix)
E (
extra lymphatic involvement-
organs affected) or
S(spreading)
(subscripts)
Stage 1 Hodgkin's Lymphoma
Single
lymph node
is affected (
axillary
area)
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