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Benign Disease of The Uterus
Khalid Sait (FRCSC)
Professor of Gynecological Oncology
Faculty of Medicine
King Abdulaziz University
Anatomy of the uterus
n  Endometrium
n  Myometrium
Both
are mesodermal in
origin Both
formed secondary to
fusion of mullarian
ducts ( 8-9 weeks
post ovulation)
Anatomy of the uterus
Endometrium
n  Cycle histological variation
Important in :
1- diagnose luteal phase defect
2- Documentation of ovulation
( change of proliferative endometrium to
secretary endometrium under influence of
progesterone
Benign disease of the
endometrium
n  Endometrial
Polyp
Localized
overgrowths of
endometrial tissue
covered by epithelium
and containing a variable
amount of glands ,stroma
and blood vessels
endometrial polyps.
n  a symptomatic
n  excessive bleeding during a menstrual period,
n  bleeding in between periods,
n  spotting after intercourse. Some women report a
few days of brown blood after a normal menstrual
period. If the polyp interferes with the egg and
sperm, it may make it hard to get pregnant.
n  slightly higher chance of miscarriage
n  could this be cancer?
endometrial polyps.
n  Sonohysterogram (water ultrasound) The
water opens the uterine cavity, allowing
the doctor to see if any polyps are
hanging around.
n  hysterosalpingogram (HSG)
n  hysteroscope
Benign disease of the
endometrium
n Inflammation
Acute : mostly related with pregnancy and
abortion ( multimicrobial )
Chronic non specific Endometrities:
1- pregnancy
2- PID
3-IUCD
4- Infarcted Polyps
5-Cancer
Chronic specific endometrities:
TB, Mycoplasma,Viral and Fungal
Benign disease of the
endometrium
n Endomtrial hyperplasia
Proliferation of a glands of irregular
size and shape with increase in the gland/
stroma ratio compared with proliferative
endometrium
Classification Of Endometrial Hyperplasia
WHO ( Kurman &Norris )
n  Simple ( Cystic ) Hyperplasia with and
with out atypia
n  Complex Hyperplasia with or with out
atypia
Benign disease of the
endometrium ( Endometrial hyperplasia……..)
n  Unopposed estrogen exposure
n  PCO and unovulation
n  Estrogen producing tumor
n  Estrogen therapy
n  Obesity .DM . HTN
n  2% of pt. with out atypia progress to
cancer
n  23 % of pt. with atypia progress to
Natural History of Endometrial
Hyperplasia
Type NO Mean age Regress
(%)
Progress
to
carcinoma
no
Mean
( years)
Follow up
( years)
Simple with
out atypia
93 42 74(80) 1 11 1-26.7
10 preg.
Complex
with out
atypia
29 39 23(79) 1 8.3 2-26
3 preg.
Atypical
hyperplasia
48 40 28(58) 11 4.1 1-25
3 preg.
Atypical
simple
13 9 1
Atypical
complex
35 20 10
Kurman et al(170 patients )
Young patients
( Endometrial Status)
No Atypia Atypia
simple complex Simple
Mild atypia
Complex
Moderate
Or severe
No
abnormal
bleeding
Abnormal
Bleeding
observe
Intermittent
Progestin
therapy
Intermittent
Or continues Progestin
therapy
Consider
6-month sample
Especially for
Abnormal bleeding
Continuous
High dose
Progestin
therapy
Sample 6 months
Uterine preservation is not required
( Old Patients)
Endometrial status
NO CYTOLOGIC
ATYPIA
ATYPIA
Intermittent or
continuous therapy
And sample in 6 months
OR
HYSTERECTOMY
Pt. Is not
surgical candida
Fit for surgery
Intermittent or
continuous therapy
And sample in 6 months
Hysterectomy
Medical Treatment
n  With out atypia:
1- Provera 10 mg for 10 days for 3 mos
2- OCP
n  Atypia pt: mild:
I) 10 mg bid continuously followed by intermittent therapy
14 days per month Or
OCP if contraception is required
n  MOD OR SEVER ATYPIA:
10 MG TID continuous for 6 mos
(SAMPLE IN 6 MONTHS)
Medical Treatment
n  PTS WANT TO CONCEIVE IS GIVEN GnRH agonist for 3 Months.
Followed by Ovulation Induction
n  LONG TERM PROGESTERONE : MEGACE 40-160 MG DAILY
n  ALTERNATIVE:
DEPOPROVERA 200 MG IM FOLLOWED BY
100 MG EVERY 2 WEEKS TWO TIMES AND THEN
100 MG MONTHLY FOR 6 MONTH
Benign disease of the
Uterus
n Congenital anomalies
Congenital Uterine Anomaly
n  Precise incidence is unknown (range from 1-2 %)
n  Clinical presentation:
1 Usually asymptomatic
2 Menstrual disorder
3 Dysmenorrhea
4 Recurrent abortion ( decrease intrauterine volume and
vascularity, increase uterine irritability and cervical
incompetance )
5 Premature labor
6 Abnormal presentation
7 Primary infertility
Congenital Uterine Anomaly
n  Diagnosis:
History
Pelvic exam
Hysterosalpingography
U/S
MRI
Laproscopy
Hysteroscopy
IVP or U/S (Exclude Renal anomaly )
Congenital Uterine Anomaly
n  Treatment:
1- Double uterus (didelphic uterus): no need to treat.
2- Bicornate ut. --------- Strassmann
procedure ( if indicated )
3- Ut. Septum --------- (BCP
for dysmenorrhea ), Tompkins metroplasty or
Hysteroscopic resection of septum )
4- Unicornate ut.
-------- Surgery indicated if there is blind horn which
cause symptom----- surgical resection of blind horn.
Benign disease of the
Myometrium
n Leiomyoma
n Adenomyosis
Q5
What Is Fibroids?
Are benign clonal tumours that arise from the
smooth-muscle cells of the human uterus.
Most uterine leiomyomas are asymptomatic.
Uterine leiomyoma locations;
Incidance 25-50%
Complication Of Fibroid
n  Symptoms
n  Infertility
n  Degeneration
Symptomatic Asymptomatic
Want future
pregnancy
Exclude other.
Med.
Surg. myom.
Ut.a. emb.
Depened on size.
<12 week F.U
>12week
myomectomy
Not want future
pregnancy
Exclude other.
Med.
Surg.myom.,TAH.
Ut.a.emb.
Depened on size.
<12week F.U
>12 week
Myom.,TAH.
MANEGMENT
MEDICAL MANEGMENT:
oral-contraception.
nsaids.
antifibrinolytic agents.
danazole.
Gnrh agonist.
progesterone antagonist.
SURGICAL MANEGMENT
Benign disease of the
endometrium
n DUB
Abnormal uterine bleeding resulting from
derangement in the magnitude or duration
of estrogen and progestron on the
endometrium. It is a clinical term used to
describe bleeding not attributable to an
underlying organic pathological condition
Benign disease of the
endometrium ( DUB……)
n  Condition has to be excluded
before making the diagnosis of
DUB:
1-Systemic causes
2-Local Cause
3-Pregnancy related
Benign disease of the uterus
Benign disease of the uterus

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Benign disease of the uterus

  • 1. Benign Disease of The Uterus Khalid Sait (FRCSC) Professor of Gynecological Oncology Faculty of Medicine King Abdulaziz University
  • 2.
  • 3. Anatomy of the uterus n  Endometrium n  Myometrium Both are mesodermal in origin Both formed secondary to fusion of mullarian ducts ( 8-9 weeks post ovulation)
  • 4.
  • 5. Anatomy of the uterus Endometrium n  Cycle histological variation Important in : 1- diagnose luteal phase defect 2- Documentation of ovulation ( change of proliferative endometrium to secretary endometrium under influence of progesterone
  • 6. Benign disease of the endometrium n  Endometrial Polyp Localized overgrowths of endometrial tissue covered by epithelium and containing a variable amount of glands ,stroma and blood vessels
  • 7. endometrial polyps. n  a symptomatic n  excessive bleeding during a menstrual period, n  bleeding in between periods, n  spotting after intercourse. Some women report a few days of brown blood after a normal menstrual period. If the polyp interferes with the egg and sperm, it may make it hard to get pregnant. n  slightly higher chance of miscarriage n  could this be cancer?
  • 8.
  • 9. endometrial polyps. n  Sonohysterogram (water ultrasound) The water opens the uterine cavity, allowing the doctor to see if any polyps are hanging around. n  hysterosalpingogram (HSG) n  hysteroscope
  • 10.
  • 11. Benign disease of the endometrium n Inflammation Acute : mostly related with pregnancy and abortion ( multimicrobial ) Chronic non specific Endometrities: 1- pregnancy 2- PID 3-IUCD 4- Infarcted Polyps 5-Cancer Chronic specific endometrities: TB, Mycoplasma,Viral and Fungal
  • 12. Benign disease of the endometrium n Endomtrial hyperplasia Proliferation of a glands of irregular size and shape with increase in the gland/ stroma ratio compared with proliferative endometrium
  • 13. Classification Of Endometrial Hyperplasia WHO ( Kurman &Norris ) n  Simple ( Cystic ) Hyperplasia with and with out atypia n  Complex Hyperplasia with or with out atypia
  • 14.
  • 15.
  • 16. Benign disease of the endometrium ( Endometrial hyperplasia……..) n  Unopposed estrogen exposure n  PCO and unovulation n  Estrogen producing tumor n  Estrogen therapy n  Obesity .DM . HTN n  2% of pt. with out atypia progress to cancer n  23 % of pt. with atypia progress to
  • 17.
  • 18.
  • 19.
  • 20.
  • 21.
  • 22.
  • 23.
  • 24. Natural History of Endometrial Hyperplasia Type NO Mean age Regress (%) Progress to carcinoma no Mean ( years) Follow up ( years) Simple with out atypia 93 42 74(80) 1 11 1-26.7 10 preg. Complex with out atypia 29 39 23(79) 1 8.3 2-26 3 preg. Atypical hyperplasia 48 40 28(58) 11 4.1 1-25 3 preg. Atypical simple 13 9 1 Atypical complex 35 20 10 Kurman et al(170 patients )
  • 25. Young patients ( Endometrial Status) No Atypia Atypia simple complex Simple Mild atypia Complex Moderate Or severe No abnormal bleeding Abnormal Bleeding observe Intermittent Progestin therapy Intermittent Or continues Progestin therapy Consider 6-month sample Especially for Abnormal bleeding Continuous High dose Progestin therapy Sample 6 months
  • 26. Uterine preservation is not required ( Old Patients) Endometrial status NO CYTOLOGIC ATYPIA ATYPIA Intermittent or continuous therapy And sample in 6 months OR HYSTERECTOMY Pt. Is not surgical candida Fit for surgery Intermittent or continuous therapy And sample in 6 months Hysterectomy
  • 27. Medical Treatment n  With out atypia: 1- Provera 10 mg for 10 days for 3 mos 2- OCP n  Atypia pt: mild: I) 10 mg bid continuously followed by intermittent therapy 14 days per month Or OCP if contraception is required n  MOD OR SEVER ATYPIA: 10 MG TID continuous for 6 mos (SAMPLE IN 6 MONTHS)
  • 28. Medical Treatment n  PTS WANT TO CONCEIVE IS GIVEN GnRH agonist for 3 Months. Followed by Ovulation Induction n  LONG TERM PROGESTERONE : MEGACE 40-160 MG DAILY n  ALTERNATIVE: DEPOPROVERA 200 MG IM FOLLOWED BY 100 MG EVERY 2 WEEKS TWO TIMES AND THEN 100 MG MONTHLY FOR 6 MONTH
  • 29. Benign disease of the Uterus n Congenital anomalies
  • 30.
  • 31. Congenital Uterine Anomaly n  Precise incidence is unknown (range from 1-2 %) n  Clinical presentation: 1 Usually asymptomatic 2 Menstrual disorder 3 Dysmenorrhea 4 Recurrent abortion ( decrease intrauterine volume and vascularity, increase uterine irritability and cervical incompetance ) 5 Premature labor 6 Abnormal presentation 7 Primary infertility
  • 32. Congenital Uterine Anomaly n  Diagnosis: History Pelvic exam Hysterosalpingography U/S MRI Laproscopy Hysteroscopy IVP or U/S (Exclude Renal anomaly )
  • 33.
  • 34.
  • 35.
  • 36.
  • 37.
  • 38.
  • 39.
  • 40. Congenital Uterine Anomaly n  Treatment: 1- Double uterus (didelphic uterus): no need to treat. 2- Bicornate ut. --------- Strassmann procedure ( if indicated ) 3- Ut. Septum --------- (BCP for dysmenorrhea ), Tompkins metroplasty or Hysteroscopic resection of septum ) 4- Unicornate ut. -------- Surgery indicated if there is blind horn which cause symptom----- surgical resection of blind horn.
  • 41. Benign disease of the Myometrium n Leiomyoma n Adenomyosis
  • 42. Q5
  • 43.
  • 44. What Is Fibroids? Are benign clonal tumours that arise from the smooth-muscle cells of the human uterus. Most uterine leiomyomas are asymptomatic. Uterine leiomyoma locations; Incidance 25-50%
  • 45.
  • 46.
  • 47.
  • 48.
  • 49.
  • 50.
  • 51.
  • 52.
  • 53.
  • 54.
  • 55.
  • 56. Complication Of Fibroid n  Symptoms n  Infertility n  Degeneration
  • 57. Symptomatic Asymptomatic Want future pregnancy Exclude other. Med. Surg. myom. Ut.a. emb. Depened on size. <12 week F.U >12week myomectomy Not want future pregnancy Exclude other. Med. Surg.myom.,TAH. Ut.a.emb. Depened on size. <12week F.U >12 week Myom.,TAH. MANEGMENT
  • 60.
  • 61.
  • 62.
  • 63.
  • 64.
  • 65.
  • 66.
  • 67. Benign disease of the endometrium n DUB Abnormal uterine bleeding resulting from derangement in the magnitude or duration of estrogen and progestron on the endometrium. It is a clinical term used to describe bleeding not attributable to an underlying organic pathological condition
  • 68. Benign disease of the endometrium ( DUB……) n  Condition has to be excluded before making the diagnosis of DUB: 1-Systemic causes 2-Local Cause 3-Pregnancy related