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48 Cards in this Set

  • Front
  • Back
This is a cancer of the lymphocytes?
Lymphoma
Exact etiology is unknown
Family History
Association with Epstein-Barr Virus infection
In about 50% of cases, EBV proteins are identified in tumor cells
Mixed Cellularity 60-70%, Nodular Sclerosis 15-30%
Increase risk in patients with HIV/AIDS or post organ transplant
Hodgkin lymphoma
What are the five types of classic Hodgkin lymphoma?
Nodular Sclerosis
Mixed Cellularity
Lymphocytes Depleted
Lymphocyte Rich
Nodular Lymphocyte Predominant
Hodgkin Lymphoma Type:

More common in females than males, young adults
Usually affects the mediastinum & other supradiaphragmatic sites
Nodular Sclerosis
Hodgkin Lymphoma Type:

More common in males than females, older adults > young adults
Usually affects the abdominal lymph nodes & spleen
Observed most commonly in those with HIV
Mixed Cellularity
Hodgkin Lymphoma Type:

More common in males than females
Usually affects lymph nodes of the abdomen and pelvis
Associated with older age and HIV
Lymphocytes Depleted
Hodgkin Lymphoma Type:

Similar to MCHD
Lymphocyte Rich
Hodgkin Lymphoma Type:

More common in males > females, 3rd -5th decade
Usually affects nodes in the neck, chest & armpits
Reed Sternberg cells replaced by “Popcorn Cells” express CD 19 & CD 20 antigens
Nodular Lymphocyte Predominant
What is the classic presentation of Hodgkin lymphoma?
Persistent, painless enlarged lymph node
Neck (cervical/supraclavicular), armpit, groin
Apart from the classic presentation of Hodgkin lymphoma, what are the other presentations?
Pain in lymph nodes after consumption of alcoholic beverages

Mediastinal Mass: Discovered on CXR, Nonspecific chest pain, SOB, cough

Constitutional “B” Symptoms: Fever, night sweats, weight loss

Fatigue or Anemia, Frequent Infections, Increased Bruising or Bleeding

Generalized Pruritus, Edema

Splenomegaly or Hepatomegaly may be present with or without abdominal swelling, pain

Incidental enlarged lymph nodes on CXR or CT
In the diagnosis of Hodgkin lymphoma what are you looking for in the lymph node biopsy?
Reed Sternberg Cells -
Large multinucleated cancerous cells
Express CD30 & CD15 antigens
What other laboratories do you run with diagnosis of Hodgkin lymphoma?
CBC
Erythrocyte Sedimentation Rate (ESR)
Lactate Dehydrogenase (LDH)
Serum Creatinine
Alkaline Phosphatase
HIV
Bone Marrow Biopsy
Liver Function Tests
PT/INR/PTT
What diagnostic imaging do you order with Hodgkin lymphoma?
CXR
Chest, Abdomen & Pelvic CTs
What is the pattern of spread in Hodgkin lymphoma?
Hodgkin’s typically demonstrates an orderly pattern of spread
Lymph node progression from one group to the next
The disease rarely skips over an area of lymph nodes as it spreads
Hodgkin Lymphoma:

Classified I-IV
The higher the number, the more lymphoma has spread
Ann Arbor Staging
Hodgkin lymphoma:

What are the factors that are associated with unfavorable prognosis for Stage I & II patients?
Bulky disease
ESR >50mm/h, if the patient is asymptomatic
>3 sites of involvement
Presence of B symptoms
Presence of extranodal disease
What is the treatment for Hodgkin lymphoma?
Combination Chemotherapy and Radiation are more effective than either modality alone
Chemotherapy
ABVD: Doxorubicin (Adriamycin), Bleomycin, Vinblastine & Dacarbazine
Localized radiation
Increase risk of cancer later in life
Tx options for recurrence of Hodgkin lymphoma include?
Treatment options for recurrence include high-dose chemotherapy and bone marrow or stem cell transplant
What is involved with the follow up of Hodgkin Lymphoma?
Follow-up every 2-4 months for the first 1-2 years & every 3-6 months for next 3-5 years
H&P
CBC, Chemistry Panel, LDH, ESR
TSH
CXR & Chest, Abdominal, Pelvic CTs every 6-12 months in the first couple of years
PET scans
Females with chest irradiation-annual mammogram age 40 or 5-8 years following radiation
Vaccines: pneumococcus, H. influenzae, meningococcus, influenza
The following are risk factors for what?

Advancing Age
Chemical Exposure
Herbicides, Insecticides
Radiation Exposure
Immune System Deficiency
Organ transplant recipients
Autoimmune Diseases
RA, Lupus
Infections
Human T-Cell Leukemia/Lymphoma Virus, Epstein-Barr Virus, HIV, Helicobacter pylori, Hepatitis C
Non-Hodgkin Lymphoma
What are the clinical manifestations of Non-Hodgkin lymphoma?
Enlarged painless lymph nodes

Abdominal pain, tenderness, nausea, vomiting, ascites
Cough, difficulty breathing

Superior Vena Cava Syndrome

Swelling of arms, face, bluish discoloration of the head, arms & upper chest

Headache, difficulty thinking & concentrating, personality changes, movement disorders,

seizures

Skin lesions, generalized pruritus

Anemia (decreased RBCs),

Infections (decreased WBCs),

Increased Bruising or Bleeding (decreased platelets)

B Symptoms
Unexplained weight loss
Fever
Night Sweats
What are the three things you use to diagnose Non-Hodgkin Lymphoma?
Excisional biopsy of lymph nodes
Bone marrow biopsy
Lumbar puncture
What additional laboratory studies can you use in diagnosing Non-Hodgkin Lymphoma?
CBC
Lactate Dehydrogenase (LDH)
Liver Function Tests
Serum BUN and Creatinine
Coagulation Tests (PTT, PT/INR)
What imaging studies can you use in Non-Hodgkin Lymphoma?
CXR
Chest, Abdomen, Pelvic, Head & Neck CT
MRI of Brain & Spinal Cord
Positron Emission Tomography (PET)
Gallium Scan
Bone Scan
Ultrasound
Non-Hodgkin lymphoma can be classified as what?
B-Cell Lymphoma
Account for about 85%

or

T-Cell Lymphoma
Account for about 15%
Non-Hodgkin Lymphoma:

What are the Beta-Cell Lymphomas?
Primary mediastinal

Mantle Cell lymphoma

Marginal zone
Extranodal
Nodal
Splenic

Lymphoplasmacytic lymphoma

Hairy Cell leukemia

Burkitt's lymphoma

Primary central nervous system lymphoma
Non-Hodgkin Lymphoma:
Beta Cell Lymphoma:

Starts in the mediastinum
More common in women (mid-30s)
Fast growing but treatable, half are patients can be cured
Primary Mediastinal
Non-Hodgkin Lymphoma:
Beta Cell Lymphoma:

Average age at presentation is about 60
More frequent in men
Typically widespread when diagnosed: lymph nodes, bone marrow, spleen
Mantle Cell Lymphoma
Non-Hodgkin Lymphoma:
Beta Cell Lymphoma:

Extranodal (AKA Mucosa-Associated Lymphoid Tissue {MALT} Lymphomas)
Most occur in the stomach; associated with infection by Helicobacter pylori
Other sites: lung, skin, thyroid, salivary glands
Nodal
Splenic
Marginal Zone
Non-Hodgkin Lymphoma:
Beta Cell Lymphoma:

Lymphoma cells produce immunoglobulin M (IgM) antibody
Slow growing, isn’t considered to be curable
Lymphoplasmacytic Lymphoma (Waldenstrom Macroglobulinemia)
Non-Hodgkin Lymphoma:
Beta Cell Lymphoma:

Small B lymphocytes with projections causing a “hairy” appearance
Found in the bone marrow, spleen and circulating in blood
Slow growing, some patients may not require treatment
Hairy Cell Leukemia
Non-Hodgkin Lymphoma:
Beta Cell Lymphoma:

Fast growing
In African children it is associated with jaw and facial bone tumors
In US, the abdomen is the most common location, majority of those affected are men, half can be cured with chemotherapy
Burkitt’s Lymphoma
Non-Hodgkin Lymphoma:
Beta Cell Lymphoma:

Involves the brain, spinal cord, meninges
Tends to spread throughout the nervous system
More common in patients with AIDS
Primary Central Nervous System Lymphoma
What are the Non Hodgkin T-Cell lymphomas?
Mycosis fungoides

Precursor T-Lymphoblastic lymphoma/Leukemia

Peripheral T-Cell Lymphomas
Non Hodgkin T-Cell Lymphoma:

Most common cutaneous lymphoma
Usually occurring after the age of 50
Categorized as patch, plaque or tumor stage
Prognosis is related to stage
May be treated with radiation or chemotherapy if spread to organs or lymph nodes has occurred
Mycosis fungoides
Non Hodgkin T-Cell Lymphoma:

Considered either a lymphoma or leukemia depending upon the amount of bone marrow involvement
Often starts in the thymus gland & can develop into tumors of the mediastinum
Occurs more often in young adults, males > females
Fast growing
Once in the bone marrow, only half of patients are cured
Precursor T-Lymphoblastic Lymphoma/Leukemia
Non Hodgkin T-Cell Lymphoma:

Cutaneous T-Cell
Angioimmunoblastic
Extranodal Natural Killer
Enteropathy Type
Subcutaneous Panniculitis-like
Anaplastic Large Cell
Peripheral T-Cell Not Otherwise Specified
Peripheral T-Cell Lymphomas
Develop from mature T cells
NHL limited to 1 lymph node group
NHL in an organ or site other than the lymph nodes but has not spread
Ann Arbor Stage I NHL
NHL Limited to 2 lymph nodes groups on same side of the diaphragm

Limited to one extranodal site with spread to one or more lymph node groups on the same side of the diaphragm
Ann Arbor Stage II NHL
NHL Lymphoma on both sides of the diaphragm
Ann Arbor Stage III NHL
NHL Lymphoma spread outside of the lymph system to the bone marrow, liver, bone, spinal cord or lungs
Ann Arbor Stage IV
What are the principles of treatment for NHL?
Radiation
Chemotherapy
Surgery
Biological Therapy
Stem Cell or Bone Marrow Transplant
Principle of NHL TX:

May be primary treatment or used in conjunction with chemotherapy
Can also be used for palliation of symptoms
Radiation
Principle of NHL TX:

Can be primary treatment or used in conjunction with radiation
Several different regimens based on type and stage
Cyclophosphamide, Doxorubicin, Vincristine and Prednisone is a common regimen
Chemotherapy
Principle of NHL TX:

Rarely used as a treatment option
Surgery
Principle of NHL TX:

Monoclonal Antibodies: Rituximab (Rituxan), Ibritumomab tiuxetan (Zevalin), Tositumomab (Bexxar)
Biological Therapy
What is involved with the follow up for NHL?
Follow-up
Routine physicals every 2-3 months during the first year
Repeat laboratory work, CXR, CT
PET scans
What are the details of NHL and relapse?
Relapses can occur or new cancers can develop
Relapses are usually treated with high-dose chemotherapy followed by stem cell transplant
Potential for cure varies amongst the different types, stage and response to initial therapy