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sizes of lymph nodes
vary in size from 2-30mm in length
size of a small kidney bean
spleen
largest mass of lymphatic tissue
manufactures B-lymphocytes for immunity
has no afferent lymphatic vessels and does not filter lymph
bone marrow and liver assume the spleen’s functions if removed
thymus
located along the trachea superior to he heart and posterior to he sternum in the upper thorax
site where T-lymphocytes mature
tonsils
protect against foreign body infiltration by producing lymphocytes
pharyngeal tonsils (adenoids) are located in the nasopharynx
palatine tonsils are in the posterior lateral wall of the oropharynx
lingual tonsils are at the base of the tongue in the oropharynx
lymphatic ducts
thoracic duct
approximately 35 to 45 cm in length
begins at about L2 at the cisterna chyli
drains all but the upper right quadrant of the body
right lymphatic duct
drains the upper right quadrant of the body
palpable lymph nodes
axillary
inguinal
cervical
popliteal or brachial (occasionally)
described seven cases in literature and distinguished these cases from leukemias and other lymphomas (person and year)
Thomas Hodgkin 1832
first controlled clinical trials radiation therapy for Hodgkin’s (person and year and location)
Henry Kaplan 1962 Stanford
symposium on staging Hodgkin’s (location and year)
Ann Arbor, Michigan 1971
epidemiology of Hodgkin’s (cases/deaths per year, incidence rate, peak incidence, median age, males vs females, countries)
8200 cases per year resulting in 1350 deaths
incidence is slowly increasing but unknown why
peak incidence: 11-30 years old
second peak in 70’s and 80’s
median age: 26
males have slight predominance and poorer prognosis
more common in developed countries
etiology of Hodgkin’s
infection
environmental
immunodeficiency - defective T-cell functioning is a risk factor
heredity - increased incidence in siblings of patients with Hodgkin’s
virus - Epstein-Barr Virus (EBV)
presentation and symptoms of Hodgkin’s
large painless mass in neck or supraclavicular region
enlarged lymph node supradiaphragmatic 90% of the time and civical region 60-80% of the time
adenopathy may produce local pain, lymphatic or venous obstruction, or airway narrowing
typically several weeks or months elapse between onset of signs/symptoms and diagnostic biopsy
detection/diagnosis for Hodgkin’s
patient history for B symptoms
physical exam
chest x-ray
lymph node biopsy
CT or MRI
bipedal lymphangiogram (LAG)
PET scan for imaging thoracic and abdominal nodes
bone marrow biopsy for higher risk patients with > stage II
staging laparotomy (exploratory abdominal surgery) was standard practice before advent of the CT scans
differences in pathology between lymphoma and Hodgkin’s
Reed-Sternberg cell - giant connective tissue cell containing one or two large nuclei
contiguous spread - “predictable” spread from one lymph node group to another
types of Hodgkin’s disease
lymphocyte predominant AKA lymphocyte rich HD
nodular sclerosing (NSHL)
lymphocyte depleted
mixed
lymphocyte predominant Hodgkin’s (AKA, origin, stages, prognosis)
AKA lymphocyte rich HD
B-cell origin
usually clinically localized disease - stage 1 or 2 and asymptomatic
excellent prognosis
nodular sclerosing Hodgkin’s (NSHL) (stages, appearance, epidemiology, prognosis)
most common - 60 to 80%
generally localized - stage 1 or 2
usually first appears in the lower cervical or supraclavicular region
typically occurs in the teenage years
good prognosis with high survival rate
lymphocyte depleted Hodgkin’s (epidemiology, prognosis)
tends to occur in patients who are older or have immune disorders (ex. HIV)
least common
worst prognosis
mixed cellularity Hodgkin’s (description, epidemiology)
mix of other cell types
2nd most common cell type
major lymph group pathways of Hodgkin’s
Waldeyer’s ring and cervical, preauricular, and occipital nodes
supraclavicular and infraclavicular
axillary
thorax (including hilar and mediastinal nodes)
abdominal cavity (including paraaortic nodes
pelvic cavity (including iliac nodes)
inguinal and femoral nodes
Waldeyer’s ring
tonsilar lymphatic tissue surrounding the nasopharynx and oropharynx
Ann Arbor staging for Hodgkin’s
stage I - involvement of a single node or site
stage II - involvement of 2 or more lymph nodes on same side of diaphragm
stage III - involvement of lymph nodes on both sides of the diaphragm
stage IV - diffuse involvement of one or more organs
H+ = liver (hepato)
L+ = lung
M+ = bone marrow
P+ = pleura
O+ = bone (osseous)
D+ = skin (dermis)
A vs B symptoms
A = asymptomatic
B = unfavorable prognosis
unexplained weight loss of more than 10% of body weight in last 6 months
unexplained fever w/ temps above 38C (100.5F) for 3 or more consecutive days
night sweats (sometimes w/ pruritus)
metastases tendency of Hodgkins
lungs and bones
treatment principles for Hodgkin’s
surgery only used for biopsy to grade and stage disease or debulk large tumors
stage I and II: definitive RTT with chemo
stage III and IV: definitive chemo with RTT
radiation technique for Hodgkin’s (types, position)
APPA mantle field
Akimbo position
Waldeyer’s ring if involved
subdiaphragmatic fields: para-aortic and inguinal nodes (inverted Y)
total nodal irradiation (TNI): mantle + inverted Y
mini-mantle: limited to cervical, supraclav, and/or axillary regions
subtotal lymphoid irradiation: mantle + para-aortics
lymph regions treated with mantle field
all major regions above the diaphragm
submandibular
occipital
cervical
supraclavicular
infraclavicular
axxillary
hilar
mediastinal
borders, field size, blocking, and dose for mantle field
superior border: line from mental point to mastoid tip
inferior border: xiphoid tip/diaphragm (T10)
lateral borders: include axilla
may require extended SSD for field sizes larger than 40×40
blocking
throat
humeral heads
lungs
spine (safety block)
sometimes, heart
dose: 35-44 Gy, 150-200 cGy/day
Waldeyer’s ring technique (border, fields, energy, dose)
abutts with superior border or mantle field
parallel-opposed portals (POP) or single lateral field
6-9 MeV electrons
dose: 36 Gy
subdiaphragmatic fields for Hodgkin’s (stages, fields, border)
used for late stages 3 or 4 or early stages w/ B symptoms
most commonly involve para-aortic and inguinal nodes via inverted Y field
field includes the spleen if intact or splenic pedicle if splenectomy
single or two fields
superior border of inverted Y abuts to the inferior border of mantle field
name of method used for irregular field calculations
Clarkson’s method
acute vs late symptoms of Hodgkin’s radiation treatment
acute
fatigue
occipital hair loss
skin erythema
sore throat/esophagitis
altered taste
transient dysphagia from esophagitis
dry cough
nausea
occasional vomiting
late
mild radiation pneumonitis
hypothyroidism (1/3 of patients)
herpes zoster
transient xerostomia
increased dental caries
radiation arteritis (fewer than 5%)
Lhermitt’es syndrome (numbness, tingling, electric shock like sensations)
patients are also at higher risk for lung, breast, and GI cancers after mantle
treatment
patients with secondary breast cancer tend to develop more aggressive breast cancers
treatment related malignancies and cardiac complications are the main causes of death in long-term survivors
chemotherapy for Hodgkin’s (types, children)
MOPP (less commonly used now)
Nitrogen Mustard
Oncovin (Vincristine)
Prednisone
Procarbazine
ABVD - new standard treatment with less complications and side effects such as secondary malignancies like leukemia and sterility
Adriamycin
Bleomycin
Vincristine (Oncovin)
Dacarbazine
treatment of choice for children to spare bone growth
prognosis for Hodgkin’s
80% overall 5 year survival
40-50% cure rate for widespread metastatic disease
stage and age of patient are biggest factors
older patients have poorer prognosis than younger patients
presence of B symptoms = worse prognosis