Lymphoma powerpoint (slides 1-33) Flashcards
Where does leukemia originate?
bone marrow or blood
Where do lymphomas originate?
in the lymphatic system (lymphoreticular system)
What kind of treatment is used for leukemias and lymphomas?
systemic treatment
What are the two types of lymphoma?
Hodgkin’s and non-Hodkin’s
What is the lymphatic system?
the group of tissues and organs that
produce and store white blood cells that fight infection
What system does the lymphatic system work with and to what purpose?
circulatory system
The systems work together to transport nutrients and to
remove wastes and are intertwined throughout the bod
What does the lymphatic system include?
bone marrow, spleen, thymus,
lymph nodes, and lymphatic vessels
What organ is the largest lymphatic organ that recycles red blood cells and houses lymphocytes that help contest certain types of bacteria?
The spleen
____________ cells are eliminated by the lymphatic system and portions of the
__________ help produce lymph.
red blood
blood
Lymph fluid carries ________, _________, and ___________ throughout the
body and provides protection while filtering harmful particles that may give
rise to infection and disease
Antibodies
Nutrients
Lymphocytes
Lymph nodes become swollen when _________ are present and when the body
produces more lymphocytes to fight infection.
bacteria
Lymphocytes that grow abnormally are the origin of __________________ and compromise the body’s ability to fight infection
Hodgkin’s and Non-
Hodgkin’s lymphomas
What category of lymphoma is marked by the presence of a type of cell called the Reed- Sternberg cell?
Hodgkin’s lymphoma
Which category of lymphoma includes a large diverse group of cancers of immune system cells?
Non-Hodgkin’s Lymphoma
What are “natural killer cells”
T cells (lymphocytes)
_____________is the result of abnormal growth of __________ and ___________, which develop in the bone marrow and mature in the lymphatic organs.
Hodgkin’s lymphoma
T-cells
B-lymphocytes
Where do lymphocytes develop and mature?
Develop in bone marrow
Mature in the lymphatic organs
What are Reed-Sternberg cells?
Large lymphoid cells that contain multiple nuclei. B lymphocytes that failed to undergo apoptosis
HL spreads in a systematic manner from one lymph node group to the next in a
______________ _______________.
predictable pattern
HL is more prevalent in:
males, regardless of race
What is the age epidemiology of HL?
greatest in 20-34 years
rare occurrence in age below 5
What is a sign of HL?
A painless mass is most often discovered in lymph node
areas above the diaphragm
What are the virus risk factors to HL?
Epstein Barr Virus (EBV)
HIV
What are risk factors to HL?
Viruses
Weakened immune system
Age
-15-24 years old
-55+
Family History
-family members, especially siblings of HL patients have increased risk for developing HL
What are the signs/symptoms of HL?
painless swollen lymph nodes
(most common symptom)
Coughing
Chest pain
Fatigue
Splenomegaly
(enlarged spleen, in the case of advanced disease)
What are the B-symptoms of HL?
Weight loss – 10% of body weight in 6 months prior to diagnosis
Fevers – higher than 100.4 Fahrenheit
Night sweats
Itchy skin – generalized pruritus
Pain with alcohol ingestion
What imaging is used in detection and diagnosis of HL?
Chest x-rays
(swollen lymph nodes in chest)
CT
MRI
PET
How is HL detected in a history/ physical exam?
a physician checks for swollen lymph nodes in the neck,
underarms, and groin and checks for a swollen spleen or liver
What lab test is done for HL?
CBC to check the number of white blood cells
(platelet count, liver, and renal function tests)
Anemia, leukopenia, thrombocytosis, and lymphopenia can indicate _____________.
bone marrow involvement
1) Low blood albumin below___.
2) high erythrocyte ____________ rate
3) high white blood cells
count about _________.
4) low red blood cell count with hemoglobin level below ________.
5) low blood lymphocyte count below ______.
may indicate HL.
4
sedimentation
15,000
10.5
600
Bone marrow biopsies for HL are reserved for those with _________-stage disease and _______________
disease.
later
subdiaphragmatic
A ________ biopsy should be done if splenic involvement is found.
liver
What are the subcategories of HL and the percentage of incidence of each?
Classic Hodgkin Lymphoma
(95%)
Nodular Lymphocyte Predominant Hodgkin Lymphoma
(5%)
What are the subcategories of Classic Hodgkin Lymphoma (CHL)?
Nodular sclerosing HL
Mixed cellularity HL
Lymphocyte Rich HL
Lymphocytic Depleted HL
Which CHL is most common, usually involves nodes in the chest and neck, has greatest incidence in ages 20s-30s, and is typically diagnosed at an early stage?
Nodular Sclerosing CHL
Which CHL has an age diagnosis average of 38 years old and tends to be seen in those affected by HIV?
Mixed Cellularity CHL
Which CHL is found only in 5% of CHL cases, usually occurs in the upper body, and typically doesn’t occur in more than a few lymph nodes?
Lymphocytic Rich CHL
Which CHL is the rarest and usually presents with more advanced disease, therefore has the worst prognosis, and usually affects people in their 30s with HIV?
Lymphocytic Depleted CHL
In HL, the ___________ of spread is predictable, but not ____________ of spread.
pattern/route
rate
What is the typical spread pattern of HL?
Lymphatic drainage then spreading to other organs
What is considered local invasion in HL?
spread to surrounding viscera after spreading to adjacent lymph region
What is the most common site of metastasis in HL?
adjacent lymph nodes
What is the most common visceral involvement?
spleen, liver, and bone marrow
For HL, metastasis can also occur in the _______ and _________ system in late stages.
lungs
skeletal
What is the HL staging system?
The Ann Arbor Staging System
Explain ABES in the Ann Arbor Staging System
A: the patient does not have B symptoms
B: The patient has B symptoms
E: Extranodal disease is present
S- Disease is found in the spleen
What stage of HL is
involvement of two or more lymph node regions on the same side of the diaphragm or of one lymph node region and a extra-lymphatic site.
Stage II
What stage of HL is
involvement of a single lymph node region or single extra-lymphatic site
Stage I
What stage of HL is
involves disseminated disease of one or more extra-lymphatic organ.
Stage IV
What stage of HL is
involvement of lymph node regions on both sides of the diaphragm, which may include the spleen or an extra-lymphatic organ
Stage III
What can be said if patients have
clinical stage I or II disease without the
presence of B symptoms, less than 3 sites of
nodal involvement, and no markedly abnormal
lab results?
early favorable HL
True or false: HL that is advanced can still be considered favorable with stage III or IV and 3 or fewer risk factors.
True
____________ _______________ has stage III or IV and 4 or more risk factors.
Advanced unfavorable