Case report
I. IDENTITY
Name : Mr. M
Age : 62years
Gender : Man
Religion
: Islam
Address : Arjawinangun
Main complaint : Can not urinate
Additional complaints : Pain when urinating
Sometimes bloody piss
History Disease Now:
Patients
come to hospitals with complaints Arjawinangun could not urinate since ± 2 days
SMRs. The patient began to feel the disturbance BAK since ± 2 months SMRs. When
you wish to urinat patient should wait longer straining and new urine out. Clear
yellow urine with poor stream but not branched and sometimes stops then out
again and sometimes blood-tinged miksion. After sometimes there dripping urine
and his bladder patients often feel incomplete. Low back pain, leg pain, a
sense of twisting, bladder stones, pubic pain threshold when urinating, fever,
raised lump in the groin and rectal bleeding accompanied denied. Patients also
denies decreased appetite and weight loss dramatically over bladder disorders
arise. smoothly.
Past
history of disease:
- Diabetes history indisputably
- History of high blood pressure is recognized
Family
history of disease:
No family member who suffers from the same disease
as the patient
III. PHYSICAL
EXAMINATION
Generalists
status
General
situation : Looks sick are
Awareness : Compos mentis
Vital signs : N : 86 x / min
RR : 24 x / min
S : 36.5 º C
TD : 160/90 mmHg
Head : Normocephal.
Eyes : Conjunctiva: Ananemis
Sclera: Anikterik
thoracic
Cast : Inspection: cardiac Iktus not visible
Palpation: no palpable cardiac Iktus
Percussion: Dim, limit of normal heart
Auscultation: I-II regular BJ, BJ additional (-)
Pulmo : Inspection: Symmetrical, under static and dynamic conditions.
Palpation:
Vocal fremitus on the right and left hemithorax symmetrical palpable.
Percussion: Sonor on both hemithorax.
Auscultation: Vesicular + / + N, crackles - / -, wheezing - / -
Abdomen : Inspection: Flat
Palpation:
Supple, NT / NK / NL -/-/-, liver and spleen not palpable enlarged
Percussion: Timpani in the entire field abdomen
Auscultation: normal BU
Extremities : Upper: Edema - / -, cyanosis - / -
Bottom : Edema - / -, cyanosis - / -
Urologist status
Right
Kidney Left
Kidney
CVA
Massa
- -
Ballotement
- -
Tenderness
- -
Pain
tap
- -
Supra
symphysis region
VU:
no palpable
Tenderness:
-
rectal toucher
-
Tonus sphincter ani: Good
-
Ampulla recti: No collapse
-
Rectal mucosa: Palpable slippery
-
Prostate: Prominent, consistency hard, uneven surface, nodules (+), tenderness
(+),
-
Handscoon: Slime (-), Blood (-), feces (-)
IV. EXAMINATION SUPPORT
Full Blood Lab
Leukosit : 11.000
mm³
Hb : 10,2 gr%/dl
Ht : 22,5gr%/dl
Plt : 457 mm³
VI. WORKING DIAGNOSE
Prostate cancer
VII. DIFERENTIAL DIAGNOSE
Benign Prostate Hiperplasia (BPH)
VIII. TREATMEN
-
Medikamentosa:
Cefoperazoniv
2x1 amp
Tramadol
iv 2x1 amp
Ranitidin iv 2 x1 amp
Amlodipin
1 x 10 mg
-
Prostatektomiradikaldenganpemeriksaan
PA
IX. PROGNOSIS
- Quo ad vitam : dubia ad bonam
- Quo ad functionam : ad malam
CARCINOMA PROSTATE
A.
Anatomy
and physiology
The
prostate is a gland found only in males. It is located in front of the rectum
and below the urinary bladder. The size of the prostate varies with age. In
younger men, it is about the size of a walnut, but it can be much larger in
older men.
The
prostate is an organ consisting of
components glands, stroma and muscular. This
gland begins to grow at the age of 12 weeks
gestation due to the
effect of androgen hormones are derived from
fetus testis. The
prostate is a derivative of urogenital sinus
of embryonic tissue. Prostate gland lies side of
inferior fur jar,
wrap in front of the
rectum and posterior urethra. The average size of the prostate in older men 4 x 3 x 2.5 cm and weighs approximately
20 grams.
The
prostate's job is to make some of the fluid that protects and nourishes sperm
cells in semen, making the semen more liquid. Just behind the prostate are
glands called seminal vesicles that make most of the fluid for semen.
The urethra, which is the tube that carries urine and semen out of the
body through the penis, goes through the center of the prostate.
The
prostate starts to develop before birth. It grows rapidly during puberty,
fueled by male hormones (called androgens) in the body. The main
androgen, testosterone, is made in the testicles. The enzyme 5-alpha
reductase converts testosterone into dihydrotestosterone (DHT). DHT
is the main hormone that signals the prostate to grow. The prostate usually
stays at about the same size or grows slowly in adults, as long as male
hormones are present
B.
Defined
Prostate
cancer is cancer
that develops in the prostate,
a gland in
the male reproductive system. This
occurs when prostate cells mutate
and begin to grow out of control. These cells may spread from the prostate metastasis to other parts of the body,
especially the bones and lymph nodes. Prostate cancer
may cause pain, difficulty in urinating, erectile dysfunction
and other symptoms.
C.
Epidemiology
Other
than skin cancer, prostate cancer is the most common cancer in American men.
The latest American Cancer Society estimates for prostate cancer in the United
States are for 2012:
·
About 241,740 new cases of prostate cancer will be diagnosed
·
About 28,170 men will die of prostate cancer
About
1 man in 6 will be diagnosed with prostate cancer during his lifetime. Prostate
cancer occurs mainly in older men. Nearly two thirds are diagnosed in men aged 65
or older, and it is rare before age 40. The average age at the time of
diagnosis is about 67.
Possible pre-cancerous conditions
of the prostate
Some
doctors believe that prostate cancer starts out as a pre-cancerous condition, although
this is not yet known for sure.
-
Prostatic intraepithelial neoplasia (PIN)
In
this condition, there are changes in how the prostate gland cells look under
the microscope, but the abnormal cells don't look like they are growing into
other parts of the prostate (like cancer cells would). Based on how abnormal
the patterns of cells look,
they
are classified as:
· Low-grade PIN: the patterns of
prostate cells appear almost normal
· High-grade PIN: the patterns of
cells look more abnormal
PIN
begins to appear in the prostates of some men as early as their 20s. Almost
half of all men have PIN by the time they reach 50. Many men begin to develop
low-grade PIN at an early age but do not necessarily develop prostate cancer.
The importance of low-grade PIN in relation to prostate cancer is still
unclear. If a finding of low-grade PIN is reported on a prostate biopsy, the
follow-up for patients is usually the same as if nothing abnormal was seen.
-
Proliferative inflammatory atrophy (PIA)
This
is another finding that may be noted on a prostate biopsy. In PIA, the prostate
cells look smaller than normal, and there are signs of inflammation in the
area. PIA is not cancer, but researchers believe that PIA may sometimes lead to
high-grade PIN, or perhaps to prostate cancer directly.
D.
Etiology
Until
now still not
known for certain causes of prostate
ca: but some hypothesis
states that prostatic hyperplasia
is closely related to the hypothesis
that some suspected
as the cause of ca mammmae are:
1.
A change in the balance between testosterone and estrogen in the elderly.
2. The role of a growth factor (growth factor) as a driver of growth in the prostate gland stroma.
3. Increased long-life cells of the prostate due to reduced cell death
2. The role of a growth factor (growth factor) as a driver of growth in the prostate gland stroma.
3. Increased long-life cells of the prostate due to reduced cell death
4.
Stem cell theory
explains that the
abnormal proliferation of stem cells leading to
the production of stromal cells and epithelial
prostate gland as being excessive.
E.
Risk
factors
-
Age
Prostate cancer is very
rare in men younger than 40, but the chance of having prostate cancer rises
rapidly after age 50. Almost 2 out of 3 prostate cancers are found in men over
the age of 65.
-
Race/ethnicity
-
Nationality
Prostate cancer is most
common in North America, northwestern Europe, Australia, and on Caribbean
islands. It is less common in Asia, Africa, Central America, and South America.
-
Family history
-
Genes
Some inherited gene
changes raise the risk for more than one type of cancer. For example, inherited
mutations of the BRCA1 or BRCA2 genes are the reason that breast and ovarian
cancers are much more common in some families. Mutations in these genes may
also increase prostate cancer risk in some men, but they account for a very
small percentage of prostate cancer cases.
-
Smoking
Most studies have not
found a link between smoking and the risk of developing prostate cancer. Some
recent research has linked smoking to a possible small increase in the risk of
death from prostate cancer, but this is a new finding that will need to be
confirmed by other studies.
-
Inflammation of the prostate
Some studies have
suggested that prostatitis (inflammation of the prostate gland) may be
linked to an increased risk of prostate cancer, but other studies have not
found such a link. Inflammation is often seen in samples of prostate tissue
that also contain cancer. The link between the two is not yet clear, but this
is an active area of research
-
Sexually transmitted infections
Researchers have looked
to see if sexually transmitted infections (like gonorrhea or chlamydia) might
increase the risk of prostate cancer, possibly by leading to inflammation of
the prostate. So far, studies have not agreed, and no firm conclusions have
been reached.
-
Vasectomy
Some earlier studies
had suggested that men who have had a vasectomy (minor surgery to make men
infertile) – especially those younger than 35 at the time of the procedure –
may have a slightly increased risk for prostate cancer. But most recent studies
have not found any increased risk among men who have had this operation. Fear
of an increased risk of prostate cancer should not be a reason to avoid a
vasectomy.
F.
Pathophysiology
Causes
of Prostate Ca
until now not known with certainty,
but several hypotheses
states that are closely related to
Prostate Ca hypothesis
suspected as the cause of Ca breast is a change in the balance between testosterone and estrogen in the elderly, this will interfere with the process of cell differentiation
and proliferation . This disrupted
cell differentiation that causes cancer
cells, another cause that is the factor of excessive
stromal growth and
increased longevity of prostate
cells due to reduced cell death that results in a change in the genetic material.
Changes prolife causing
stromal cell production and prostate gland
epithelial cells become
excessive, causing Ca Prostate (Price)
Cancer
will cause constriction
of lumen of the prostatic urethra
and will inhibit
the flow of urine. This situation
led to an emphasis intraavesikal, to be
able to dispense urine, the bladder must be
able to contract strongly against the
prisoner. Continuous contraction
causes anatomic changes
of the bladder detrusor
hypertrophy form, trabeculation, selula formation,
Sakula, and divetikel.
Detrusor muscle thickening
phase is called phase
compensation.
Structural
changes in the bladder is felt by the patient
as a complaint on the lower urinary tract
or lower urinary
track symptoms (LUTS)
formerly known as symptoms - symptoms prostatismus,
by increasing retention urethra, detrusor muscle
into dekompensaasi phase and ultimately
unable to again to contract
resulting in urinary retention. Intravesikal higher pressure
will be forwarded to all parts of the bladder into the ureter or
vesico-ureteric reflux
occurs. This situation if continued will
result in hydroureter, hydronephrosis, and even eventually be able to
fall into kidney
failure.
Continuous
development of tumors that can occur directly
to the expansion of the urethra, bladder neck and bladder semmininalis.
Prostate Ca can
also spread via
the hematogenous the pelvic bones of the
lumbar vertebrae, femur and ribs. Organ metastases are the
liver and lung.
Pathologic
process is the accumulation of
collagen and elastin
tissue between smooth
muscle contraction resulting in
muscle weakness. In
addition there is degeneration of the nerve cells that
innervate smooth muscle. This can result in hypersensitivity
post-functional, neurotransmitter
imbalance, and decreased
sensory input, so
the unstable detrusor muscle. Because abnormal
bladder muscle function, then an increase in residual urine causing hydronephrosis
and upper urinary
tract dysfunction.
G. Grading
prostate cancer
Pathologists
grade prostate cancers according to the Gleason system. This system assigns
a
Gleason grade, using numbers from 1 to 5 based on how much the cells in the
cancerous tissue look like normal prostate tissue.
· If the cancerous tissue looks much like normal prostate
tissue, a grade of 1 is assigned.
· If the cancer cells and their growth patterns look
very abnormal, it is called a grade 5 tumor.
· Grades 2 through 4 have features in between these
extremes.
Today,
most biopsies are grade 3 or higher, and grades 1 and 2 are not often used.
Since prostate cancers often have areas with different grades, a grade is
assigned to the 2 areas that make up most of the cancer. These 2 grades are
added together to yield the Gleason score (also called the Gleason sum)
between 2 and 10.
There
are some exceptions to this rule. If the highest grade takes up most (95% or
more) of the biopsy, the grade for that area is counted twice as the Gleason
score. Also, if 3 grades are present in a biopsy core, the highest grade is
always included in the Gleason score, even if most of the core is taken up by
areas of cancer with lower grades.
· Cancers with a Gleason score of 6 or less are often
called well-differentiated or lowgrade.
· Cancers with a Gleason score of 7 may be called moderately
differentiated or intermediate-grade.
· Cancers with Gleason scores of 8 to 10 may be called
poorly differentiated or highgrade.
The
higher the Gleason score, the more likely it is that your cancer will grow and
spread quickly.
H. Signs
and symptoms of prostate cancer
Early
prostate cancer usually causes no symptoms. Some advanced prostate cancers can
slow or weaken your urinary stream or make you need to urinate more often,
especially at night. But non-cancerous diseases of the prostate, such as benign
prostatic hyperplasia (BPH) cause these symptoms more often.
If
the prostate cancer is advanced, you might have blood in your urine (hematuria)
or trouble getting an erection (impotence). Advanced prostate cancer
commonly spreads to the bones, which can cause pain in the hips, back (spine),
chest (ribs), or other areas. Cancer that has spread to the spine can also
press on the spinal nerves, causing weakness or numbness in the legs or feet,
or even loss of bladder or bowel control. Other diseases can also cause many of
these same symptoms. It is important to tell your doctor if you have any of
these problems so that the cause can be found and treated, if needed.
I.
Diagnosis
Most
prostate cancers are first found during screening with a prostate-specific
antigen (PSA) blood test and or a digital rectal exam (DRE). (See "Can
prostate cancer be found early?") Early prostate cancers usually do not
cause symptoms, but more advanced cancers are sometimes first found because of
symptoms they cause. Whether cancer is suspected based on screening tests or
symptoms, the actual diagnosis can only be made with a prostate biopsy.
Imaging
tests
If
you are found to have prostate cancer, your doctor will use your digital rectal
exam (DRE) results, prostate-specific antigen (PSA) level, and Gleason score to
figure out how likely it is that the cancer has spread outside your prostate.
This information is used to decide which other tests (if any) need to be done
to look for possible cancer spread in the body. Men with a normal DRE result, a
low PSA, and a low Gleason score may not need any other tests because the
chance that the cancer has spread is so low.
Transrectal
ultrasound (TRUS)
Transrectal
ultrasound (TRUS) uses sound waves to make an image of the prostate on a video
screen. For this test, a small probe that gives off sound waves is placed into
the rectum. The sound waves enter the prostate and create echoes that are
picked up by the probe. A computer turns the pattern of echoes into a black and
white image of the prostate.
Bone scan
If
prostate cancer spreads to distant sites, it often goes to the bones first.
(Even when prostate cancer spreads to the bone, it is still prostate cancer,
not bone cancer.) A bone scan can help show whether cancer has reached the
bones.
Computed
tomography (CT)
The
CT scan (also known as a CAT scan) is a special kind of x-ray test that
gives detailed, cross-sectional images of your body. Instead of taking one
picture, like a standard x-ray, a CT scanner takes many pictures of the part of
your body being studied as it rotates around you. A computer then combines
these pictures into images of slices of the part of your body being studied.
Unlike a regular x-ray, a CT scan creates detailed images of the soft tissues
in the body. This test can sometimes help tell if prostate cancer has spread
into nearby lymph nodes. If your prostate cancer has come back after treatment,
the CT scan can often tell whether it
is
growing into other organs or structures in your pelvis.
On
the other hand, CT scans rarely provide useful information about newly
diagnosed prostate cancers that are likely to be confined to the prostate based
on other findings (DRE result, PSA level, and Gleason score). CT scans are not
as useful as magnetic resonance imaging (MRI) for looking at the prostate gland
itself.
Magnetic
resonance imaging (MRI)
MRI
scans use radio waves and strong magnets instead of x-rays. The energy from the
radio waves is absorbed by the body and then released in a pattern formed by
the type of body tissue and by certain diseases. A computer translates the
pattern into a very detailed image of parts of the body. Like a CT scan, a
contrast material might be injected, but this is done less often. Because the
scanners use magnets, people with pacemakers, certain heart valves, or other
medical implants may not be able to get an MRI.
MRI
scans can be helpful in looking at prostate cancer. They can produce a very
clear picture of the prostate and show whether the cancer has spread outside
the prostate into the seminal vesicles or other nearby structures. This
information can be very important for your doctors in planning your treatment.
But like CT scans, MRI scans may not provide useful information about newly
diagnosed prostate cancers that are likely to be confined to the prostate based
on other factors.
Lymph node biopsy
In
a lymph node biopsy, also known as lymph node dissection or lymphadenectomy,
one or more lymph nodes are removed to see if they contain cancer cells. This
is sometimes done to find out whether the cancer has spread from the prostate
to nearby lymph nodes. If cancer cells are found in a lymph node, surgery is
not likely to cure the cancer, so other treatment options are considered
Surgical biopsy
The
surgeon may remove lymph nodes through an incision in the lower part of your abdomen.
This is often done in the same operation as the radical prostatectomy. (See the
section, "Surgery for prostate cancer" for information about radical
prostatectomy.) If there is more than a very small chance that the cancer might
have spread (based on factors such as a high PSA level or a high Gleason
score), the surgeon may remove some lymph nodes before attempting to remove the
prostate gland.
J.
Penatalaksanaan
Modern
methods of detection and treatment mean that many prostate cancers are now
found earlier and can be treated more effectively. If you are diagnosed this
year, your outlook may be better than the numbers reported above. Depending on
the situation, the treatment options for men with prostate cancer may include:
· Expectant management (watchful waiting) or active
surveillance
· Surgery
· Radiation therapy
· Cryosurgery (cryotherapy)
· Hormone therapy
· Chemotherapy
· Vaccine treatment
These
treatments are generally used one at a time, although in some cases they may be
combined.
Medicines
Some
drugs may help reduce the risk of prostate cancer.
5-alpha
reductase inhibitors
5-alpha
reductase is the enzyme in the body that changes testosterone into dihydrotestosterone
(DHT), the main hormone that causes the prostate to grow. Drugs called 5-alpha
reductase inhibitors block the enzyme and prevent the formation of DHT.
Two
5-alpha reductase inhibitors are already in use to treat benign prostatic
hyperplasia (BPH), a non-cancerous growth of the prostate:
· Finasteride (Proscar®)
· Dutasteride (Avodart®)
Surgery
for prostate cancer
Surgery
is a common choice to try to cure prostate cancer if it is not thought to have
spread outside the gland (stage T1 or T2 cancers). The main type of surgery for
prostate cancer is known as a radical prostatectomy. In this operation,
the surgeon removes the entire prostate gland plus some of the tissue around
it, including the seminal vesicles. A radical prostatectomy can be done in
different ways.
Open
approaches to prostatectomy
In
the more traditional approach to doing a prostatectomy, the surgeon operates
through a single long incision to remove the prostate and nearby tissues. This
is sometimes referred to as an open approach.
Radical
retropubic prostatectomy
For
this operation, the surgeon makes a skin incision in your lower abdomen, from
the belly button down to the pubic bone. You will be either under general
anesthesia (asleep) or be given spinal or epidural anesthesia (numbing the
lower half of the body) along with sedation during the surgery.
If
there is a reasonable chance the cancer may have spread to the lymph nodes
(based on your PSA level, DRE, and biopsy results), the surgeon may remove
lymph nodes from around the prostate at this time. The nodes are usually sent
to the pathology lab to see if they have cancer cells (it takes a few days to
get results), but in some cases the nodes may be looked at right away. If this
is done during surgery and any of the nodes have cancer cells, which means the
cancer has spread, the surgeon may not continue with the surgery. This is
because it is unlikely that the cancer can be cured with surgery, and removing
the prostate could still lead to serious side effects.
Radical perineal
prostatectomy
In
this operation, the surgeon makes the incision in the skin between the anus and
scrotum (the perineum), as shown in the picture above. This approach is used
less often because the nerves cannot easily be spared and lymph nodes can't be
removed. But it is often a shorter operation and might be an option if you
don't want the nerve-sparing procedure and you don't require lymph node
removal, and is often easier to recover from.
It
also might be used if you have other medical conditions that make retropubic
surgery difficult for you. It can be just as curative as the retropubic
approach if done correctly. The perineal operation usually takes less time than
the retropubic operation, and may result in less pain afterward.
Laparoscopic radical
prostatectomy
For
a laparoscopic radical prostatectomy (LRP), the surgeon makes several small
incisions, through which special long instruments are inserted to remove the
prostate. One of the instruments has a small video camera on the end, which lets
the surgeon see inside the abdomen.
Laparoscopic
prostatectomy has some advantages over the usual open radical prostatectomy,
including less blood loss and pain, shorter hospital stays (usually no more
than a day), and faster recovery times (although the catheter will be needed
for about the same amount of time).
Surgical risks
The
risks with any type of radical prostatectomy are much like those of any major
surgery, including risks from anesthesia. Among the most serious, there is a
small risk of heart attack, stroke, blood clots in the legs that may travel to
your lungs, and infection at the incision site.
If
lymph nodes are removed, a collection of lymph fluid (called a lymphocele)
can form and may need to be drained.
Because
there are many blood vessels near the prostate gland, another risk is bleeding
during and after the surgery. You may need blood transfusions, which carry
their own small risk. Rarely, part of the intestine might be cut during
surgery, which could lead to infections in the abdomen and might require more
surgery to correct. In extremely rare cases, people die because of
complications of this operation. Your risk depends, in part, on your overall
health, your age, and the skill of your surgical team.
Side effects
The
major possible side effects of radical prostatectomy are urinary incontinence
(being unable to control urine) and impotence (being unable to have erections).
It should be noted that these side effects can also occur with other forms of
treatment for prostate cancer, although they are described here in more detail
-
Urinary
incontinence
-
Impotence
(erectile dysfunction)
-
Changes in
orgasm
-
Loss of
fertility
-
Lymphedema
-
Change in
penis length
-
Inguinal
hernia
K. The
AJCC TNM staging system
The
TNM system for prostate cancer is based on 5 key pieces of information:
· The extent of the primary tumor (T category)
· Whether the cancer has spread to nearby lymph nodes
(N category)
· The absence or presence of distant metastasis (M
category)
· The PSA level at the time of diagnosis
· The Gleason score, based on the prostate biopsy (or
surgery)
T
categories (clinical)
There
are 4 categories for describing the local extent of a prostate tumor, ranging
from T1 to T4. Most of these have subcategories as well.
T1:
Your
doctor can't feel the tumor or see it with imaging such as transrectal
ultrasound.
· T1a: Cancer is found
incidentally (by accident) during a transurethral resection of the prostate
(TURP) that was done for benign prostatic hyperplasia (BPH). Cancer is in no
more than 5% of the tissue removed.
· T1b: Cancer is found during
a TURP but is in more than 5% of the tissue removed.
· T1c: Cancer is found by
needle biopsy that was done because of an increased PSA.
T2:
Your
doctor can feel the cancer with a digital rectal exam (DRE) or see it with imaging
such as transrectal ultrasound, but it still appears to be confined to the
prostate gland.
· T2a: The cancer is in one
half or less of only one side (left or right) of your prostate.
· T2b: The cancer is in more
than half of only one side (left or right) of your prostate.
· T2c: The cancer is in both
sides of your prostate.
T3:
The
cancer has begun to grow and spread outside your prostate and may have spread into
the seminal vesicles.
· T3a: The cancer extends
outside the prostate but not to the seminal vesicles.
· T3b: The cancer has spread
to the seminal vesicles.
T4:
The
cancer has grown into tissues next to your prostate (other than the seminal vesicles),
such as the urethral sphincter (muscle that helps control urination), the
rectum, the bladder, and/or the wall of the pelvis.
N
categories
N
categories describe whether the cancer has spread to nearby (regional) lymph
nodes.
NX:
Nearby
lymph nodes were not assessed.
N0:
The
cancer has not spread to any nearby lymph nodes.
N1:
The
cancer has spread to one or more nearby lymph nodes in the pelvis.
M
categories
M
categories describe whether the cancer has spread to distant parts of the body.
The most common sites of prostate cancer spread are to the bones and to distant
lymph nodes, although it can also spread to other organs, such as the lungs and
liver.
M0:
The
cancer has not spread past nearby lymph nodes.
M1:
The
cancer has spread beyond the nearby lymph nodes.
· M1a: The cancer has spread
to distant (outside of the pelvis) lymph nodes.
· M1b: The cancer has spread
to the bones.
· M1c: The cancer has spread
to other organs such as lungs, liver, or brain (with or without spread to the
bones).
L.
Prognosis
Survival
rates are often used by doctors as a standard way of discussing a person's prognosis
(outlook). Some patients with cancer may want to know the survival statistics for
people in similar situations, while others may not find the numbers helpful, or
may even not want to know them. If you would rather not read the survival rates,
skip to the next section.
The
5-year survival rate refers to the percentage of patients who live at least
5 years after their cancer is diagnosed. Of course, many of these people
live much longer than 5 years (and many are cured).
Five-year
relative survival rates, such as the numbers below, assume that some
people will die of other causes and compare the observed survival with that
expected for people without the cancer. This is a better way to see the impact
of the cancer on survival.
According
to the most recent data, when including all men with prostate cancer:
· The relative 5-year survival rate is nearly 100%
· The relative 10-year survival rate is 98%
· The 15-year relative survival rate is 91%
Keep
in mind that 5-year survival rates are based on patients diagnosed and first
treated more than 5 years ago, and 10-year survival rates are based on patients
diagnosed more than 10 years ago.
Referensi
Lap / UPF Ilmu Bedah. 1994. Pedoman
Diagnosa dan Terapi. Surabaya: Fakultas Kedokteran Airlangga.
Mansjoer, Arif. 2000. Kapita Selekta Kedokteran,
edisi 3 jilid kedua. Jakarta: Media Aesculapius FKUI.
Price, S. 1995. Patofisiologi. Konsep Klinis Proses-Proses Penyakit. Edisi
4. Jakarta: EGCPurnomo, Basuki B. 2000. Dasar – dasar urologi. Malang: CV Infomedika.
Sjamsuhidayat, R (et.al). 1997. Buku Ajar Bedah. Jakarta: Penerbit buku kedokteran, EG
herry setya yudha utama ,surgeon, dokter spesialis bedah, in www.dokterbedahherryyudha.com
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