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UTERI
GEDE NANDA SURYA WIJAYA
DEFINITIONS
Unknown
Each individual myoma is unicellular in origin
Estrogens no evidence that it is a causative factor , it
has been implicated in growth of myomas
Myomas contain estrogen receptors in higher
concentration than surrounding myometrium
Myomas may increase in size with estrogen therapy & in
pregnancy & decrease after menopause
They are not detectable before puberty
Progestrone increase mitotic activity & reduce apoptosis
There may be genetic predisposition
Theory : Stimulation theory, and Cellnest or genitoblas
theory
TERMINOLOGY & LOCATION
ANATOMIC LOCATION
CLASSIFICATION
SUBMUCOSAL
Submucosal myomas
These myomas derive from myometrial cells just below
the endometrium.
These neoplasms protrude into the uterine cavity.
SUBMUCOSAL
Intramural myomas
These myomas develop from within the uterine wall.
They may enlarge sufficiently to distort the uterine cavity
or serosal surface.
Some fibroids can be transmural and extend from the
serosal to the mucosal surface.
SUBSEROSAL
Subserosal myoma
These myoma originate from the myometrium at the
serosal surface of the uterus.
They can have a broad or pedunculated base and may
be intraligamentary (ie, extending between the folds of
the broad ligament).
SUBSEROSAL
Cervical myoma
These leiomyomas are located in the cervix, rather than
the uterine corpus
RISK FACTORS
Estrogen
- Estrogen plays an important role for the occurrence of
uterine myoma
- it is associated with: myomas never found before
menarkhe, commonly found in reproduction, growth faster
myomas in pregnant women and will shrink at menopause
- estrogen receptors in myomas more available than normal
myometrium
Obesity
- Most studies show a relationship between fibroids and
increasing body mass index. The relationship is complex
and is likely modified by other factors, such as parity, and
may be more related to change in body habitus as an adult.
RISK FACTORS
AGE
- Women diagnosed with myoma uteri mostly in their 40s
- Myoma uteri occurs in 20-25% of women of productive age
with a unknown factor
- Myoma uteri is rare in women before the age of puberty, is
heavily influenced by reproductive hormones
Menstruation Cycle
- Myoma uteri is most common in women aged 35-45 years
who are still menstruating
- decreases after menopause
- Myoma is commonly found in women of reproductive age,
and has never been reported before menarkhe
RISK FACTORS
Family History
- Women with first-degree lineage with myoma uteri patients
have an increased risk 2.5 times more likely to suffer from
myoma uteri compared with women without lineage patients
with myoma uteri.
- has 2 times the power of expression of VEGF- (a myoma-
related growth factor) compared with patients with myoma
who do not have a family history of uterine myoma
Ethnic
- African-American ethnic groups have the possibility of risk to
suffer 2.9 times as high as myoma uteri
- African-American women suffer from myoma uteri in younger
age and have myomas and larger as well as clinical symptoms
RISK FACTORS
Hormonal contraception
Use of low dose oral contraceptives (OCs) does not cause
fibroids to grow, therefore administration of these drugs
is not contraindicated in women with fibroids
Long acting progestin-only contraceptives (eg, depot
medroxyprogesterone) protect against development of
myoma
CLINICAL MANIFESTATIONS
Reproductive dysfunction
Myoma that distort the uterine cavity (submucosal or
intramural with an intracavitary component) result in
difficulty conceiving a pregnancy and an increased risk of
miscarriage.
Adverse pregnancy outcomes (placental abruption, fetal
growth restriction, malpresentation, and preterm labor
and birth)
DIAGNOSIS
Pelvic exam
Bimanual pelvic examination, an enlarged, mobile uterus
with an irregular contour
Infrequently, on speculum exam, a prolapsed submucosal
fibroid may be visible at the external cervical os
DIAGNOSIS
Imaging
Ultrasound
Transvaginal ultrasound has high sensitivity (95 to 100
percent) for detecting myomas in uteri less than 10 weeks'
size
Most widely used modality due to its availability and cost-
effectiveness
MRI
Best modality for visualizing the size and location of all
uterine myomas. Due to the expense of this modality, its
use is best reserved for surgical planning for complicated
procedures
DIFRENTIAL DIAGNOSIS
Medical therapy
Gonadotropin-releasing hormone agonists
Most effective medical therapy for uterine myomas.
Work by initially increasing the release of gonadotropins,
followed by desensitization and downregulation to a
hypogonadotropic, hypogonadal state that clinically
resembles menopause.
Most women will develop amenorrhea, improvement in
anemia and a significant reduction (35 to 60 percent) in
uterine size within three months of initiating this therapy.
MANAGEMENT
Surgical therapy
Myomectomy
Myomectomy is an option for women who have not
completed childbearing or otherwise wish to retain their
uterus.
Disadvantage of this procedure is the risk that more
leiomyomas will develop from new clones of abnormal
myocytes
Hysteroscopic myomectomy is the procedure of choice
for removing intracavitary myomas
MANAGEMENT
Surgical therapy
Hystrectomy
Women with acute hemorrhage who do not respond to other
therapies
Women who have completed childbearing and have current
or increased future risk of other diseases.
Women who have failed prior minimally invasive therapy for
leiomyomas
Women who have completed childbearing and have
significant symptoms, multiple leiomyomas, and a desire for
a definitive end to symptomatology.
IDENTITY
Name : Ny. N
Age : 21 tahun
Address : Sunan Ampel Street
Religion : Muslim
Ethnic group : Java
Job : Personel Dental Laboratory
Edification : Senior High School
Inpatient date : 10-01-2017, 15.00
SUBYEKTIF
Chief Complaint : Patients come to the hospital as an elective
patients
Anamnese : Patients come to the hospital as an elective
patients complaining of occasional pains in the lower abdomen
and menstruation is not reguler. Patients complain of menstrual
noncurrent / outside of the menstrual cycle. Initially the patient
complained of menses is not reguler at the beginning of october,
mens patients in October starting on October 5 to 12, then the
patient says more blood out as menses on October 19, out only
once on the day and not come out again until the menstrual
cycle in the next month. In November, the patient mens starting
at 1 to 6 november, on November 15, patients get more blood
out of his genital, now out of blood mixed with mucus bit and
not feel pain at all. And then patients consult a doctor Sp.OG
and athen diagnosed of myoma uteri.
In March 2014, patients experiencing vaginal
discharge, and then patient went to the doctor and was told
that there was a cyst measuring 3 cm, then got drugs to
remove cyst. Patients have history of vaginal discharge from
2014, but intermittent. Patients also have history that she
was used IUD from 13 years ago, in 2015 had been bleeding
and eventual removal of an IUD and also have diabetes
mellitus since 5 years ago. Patients also said that the
families who suffered like this. During these days, the
patient does not feel any complaints, did not feel any lump
in the abdomen, did not feel any changes that happen to
her and did not know that suddenly she have myoma uteri
in her body.
OBSTETRIC ANAMNESE
Obstetric Anamnese : P2001 Ab0 with Myoma Uteri
Menstrual period : Regular, 1 time a month, every 28 days, for 5-6 days,
dismennorrea before menstruation
Fluor albus : (+) early 2014 until 2016, the colour is white, smelly (-), itchy (-), make
little wet the underwear
Past Disease history : DM (+) , HT (-), Asthma (-), Patological bleeding (+)
Family disease history : DM (-) , HT (-), Asthma (-), family with Mioma Uteri (+)
S : Patients feel nausea to vomiting, the patient also complained of his body limp, and a
little pain in the scar, a little blood out of shyness. There is no complaint about
defecation and urination.
S : Patients feel nausea to vomiting, the patient also complained of his body limp, and a
little pain in the scar, a little blood out of shyness. There is no complaint about
defecation and urination.
S : Patients no nausea, and a little pain in the scar, no blood outcome from genital. There is
no complaint about defecation and urination. Appetite is good.