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lymphoma
most common blood cancer and 3rd most common cancer of childhood
lymphoma
occurs when lymphocytes grow abnormally
lymphoma
lesions derived from precursor immature and mature lymphoid cells, B-cells, T-cells neoplasms
age
weak immune system
family history
infections
radiation
causes and risk factors of lymphoma
older than the age of 60
majority of people diagnosed are
children
disease develops when they have a pre-existing immune deficiency
HIV/AIDS
other illnesses/diseases like _____ make the body more susceptible to lymphoma
HIV/AIDS
Epstein-Barr virus
Hepatitis C
Helicobacter pylori
infections that increases risk
Hodgkin Lymphoma
marked by the presence of the Reed-Sternberg cell, a large cell that increases in number as the disease advances
Reed-Sternberg cell
a large cell that increases in number as the disease advances
Hodgkin Lymphoma
is highly curable with a survival rate that is considered very high
lymph tissue; lungs, bone marrow, blood
Hodgkin lymphoma affect the ________ in the lymphatic system but can spread to the __________
Non-Hodgkin Lymphoma
are of several types, characterized as fast or slow-growing an as originating from T-cells or B-cells
Non-Hodgkin Lymphoma
prognosis and treatment, depend on the stage and type of disease
45 um
diameter or Reed-Sternberg Cell may be up to
acidophilic
Reed-Sternberg Cell has an abundant _____ cytoplasm
binucleated, multinucleated, or polylobated
nucleus of Reed-Sternberg Cell
gigantic
Reed-Sternberg cell is _____, more than 5um in diameter, with large inclusion-like nucleoli
halo effect
Reed-Sternberg cell often has a clearing of the chromatin around the macronucleoli, resulting in a distinct ____
Hodgkin lymphoma
is a cancer of lymph tissue found in the lymph nodes, spleen, liver, bone marrow, and other sites
Hodgkin Lymphoma
a distinct primary solid malignancy of the immune system in which the exuberant production of cytokines and chemokines is associated with the abundance of a component of inflammatory cells that outnumber the recognized subpopulation of Hodgkin and Reed-Sternberg (H/RS) cells, derived from the germinal center B cells
germinal center B cells
Hodgkin and Reed-Sternberg cells are derived from
Hodgkin Lymphoma
was the first of the lymphomas to be recognition
lymphatic system
lymph vessels-network that branch to all tissue of the body
lymph
clear fluid that contains WBCs, especially lymphocytes such as B & T cells
lymph nodes
small round masses of tissue found in neck, underarms, chest, abdomen, groin
tonsils, thymus, spleen
lymphatic system other parts
spleens
____ involved by Hodgkin’s lymphoma may show a single or few large nodules
Thomas Hodgkin (1832)
described what he believed to be a primary yet benign disease of the lymphoid tissue
Samuel Wilkes (1865)
suggested that the disorder described by Hodgkin was a malignant process and was the first to apply the term Hodgkin disease
Sternberg (1898) & Reed (1902)
described the distinctive histological features of the disease, including the peculiar cell (R/S) cell, which now bears the name
unknown
causes of Hodgkin Lymphoma
15-30, 50-70
HL is common among ages
past infections with the Epstein-Barr virus
patients with HIV
HL risk factors
swollen glands
one symptom of HL in which there is a painless swelling of the lymph nodes in the neck, armpit, or groin
blood chemistry tests: protein levels, liver function tests, kidney function tests, uric acid level
bone marrow biopsy
CT scans of the chest, abdomen, pelvis
CBC to check for anemia & WBC
procedures usually done to detect HL
Modified Ann Arbor
staging system for HD
Stage 1
single lymph node region involved with the disease
stage 2
two or more lymph node regions involved on the same side of the diaphragm
stage 3
lymph node regions involved on both sides of the diaphragm
stage 4
diffuse involvement of an organ that is not considered part of the lymphatic system (lung or liver)
radiation therapy, chemotherapy, or both
Stages I and II (limited disease) can be treated with
chemotherapy alone, or a combination of radiation therapy and chemotherapy
stage III is treated with
chemotherapy alone
stage IV (extensive disease) is most often treated with
radiation therapy
use of radiation or high-energy x-rays to kill cancer cells, keep them from growing or regrowing but may result to suppression of the immune system and blood count
chemotherapy
use of powerful drugs to kill cancer cells; may cause low WBC, RBC, and platelet count
adriamycine
bleomycin
vinblastine
dacarbazine
ABVD is an example of a chemotherapy drug for Hodgkin lymphoma, it stands for
transfusion of blood products
fight low platelet count and anemia
antibiotics
fight infection, especially if fever occurs
stem cell transplantation
patients own stem cells are harvested, stored, and returned after chemotherapy
biological therapy / immunotherapy
takes advantage of the body’s natural immunity against pathogens
monoclonal antibodies
Abs made in the lab to find and attach itself to a specific antigen; help kill tumor cells directly or indirectly
cytokines
naturally occurring chemicals or produced artificial life and administered in large doses
vaccines
do not prevent disease, rather stimulate the immune system to mount a specific response against cancer or create a memory of the cancer to prevent development of new tumor
men
are at greater risk for relapse
interleukin 10
interleukin 6
soluble CD 30
serologic markers such as elevations of
leukemia, infertility, heart disease
possible complications in treatment
classic hodgkin — 95%
predominant hodgkin — 5%
2 main types of Hodgkin Disease
nodular sclerosing hodgkin lymphoma
mixed cellularity hodgkin lymphoma
lymphocyte depleted hodgkin lymphoma
lymphocyte-rich classic hodgkin
classic hodgkin 4 subtypes
nodular lymphocytes predominant hodgkin
diffuse lymphocyte predominant hodgkin
2 subtypes of predominant hodgkin
nodular sclerosing hodgkin lymphoma
the most common type of hodgkin lymphoma and affects 60-80% of people in developed countries
common in females and mostly affects younger people-adolescent and young adults
birefringent collagenous sclerosis
classic R-S crlls
lacunar cell
histopathological features of NSHD
lacunar cell
a distinctive R-S variant cell
mixed cellularity hodgkin disease
15-30%
all ages
male = females
mixed cellularity hodgkin disease
affects abdomen and spleen, less likely the chest
nodular scelorsing hodgkin disease
disease mainly affects the nodes on the neck, armpits, and chest
mixed cellularity hodgkin disease
associated with those positive for HIV and EBV
heterogeneous mixture of cells: lymphocytes, histiocytes, plasma cells, eosinophils, R-S cells, and R-S variants
histopathological features or MCHD
lymphocyte depleted hodgkin disease
very rare, 1%
older people
HIV sufferers/patients
men
lymphocyte depleted hodgkin disease
affects abdomen and pelvis
sparse lymphocytes
irregular sclerosis
histopathological features of LDHD
lymphocyte-rich classic hodgkin disease
uncommon, 5-6%
males: 30s to 40s
most are diagnosed in early stages and response to treatment is excellent
Reed-Sternberg cell in cellular and stromal background
histopathologic features of LRCHD
cellular and stromal background
bg that determines the subcategory to which the lesion belongs
nodular lymphocyte predominant hodgkin disease
5%
3x more common in men
young adults: 30s-50s
nodular lymphocyte predominant hodgkin disease
affects peripheral lymph nodes (underarm, neck, ear, groin)
large, circular meshwork of cell
L&H cells
popcorn cells
B-cells, scattered T-cells
histopath features of NLPHD
diffuse lymphocyte predominant hodgkin disease
extremely rare
not well defined
spread-out arranged T-cells
histopath features of DLPHD
frequent handwashing
safe sex
not sharing of needles or other personal items
support groups
lymphoma prevention