tessa winterton, md, pgy3 11/9/2016 of... · partial to complete lack of resorption of the midline...
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Tessa Winterton, MD, PGY3
11/9/2016
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Müllerian duct abnormalities occur in 2-3%
of general population
Major anomalies are 3x more common in
women with recurrent miscarriages.• Recurrent first trimester loss: 5-10%
• Recurrent second trimester loss: 25%
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Many patients asymptomatic
Symptoms: amenorrhea, dysmenorrhea,
pelvic pain, dyspareunia, infertility
Pregnancy complications include: first &
second trimester losses, preterm labor,
breech presentation, need for cerclage
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WNT• Necessary for müllerian duct initiation and
suppresses Leydig cell development in the ovary.
• Implicated in müllerian agenesis
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Failure of müllerian ducts to • Fuse in the midline
• Connect with the urogenital sinus
• Create the appropriate lumen in the upper vagina and uterus by resorption of the central vaginal cells
• Resorb the septum between the fused ducts
Fusion begins in midline and extends caudally and cephalad; therefore, abnormal results can exist at either end.
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Hypoplasia/agenesis
Unicornuate
Didelphys
Bicornuate
Septate
Arcuate
DES related
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Distribution of Specific Anomalies
Septate Uterus 35%
Bicornuate Uterus 26%
Arcuate Uterus 18%
Unicornuate Uterus 10%
Uterus didelphys 8%
Other 3%
Fritz & Speroff, p 146.
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Transverse vaginal septum
Cervical agenesis
Complete müllerian agenesis (Mayer-
Rokitansky-Kuster-Hauser syndrome)• 1/4000-10,000 females
• Complete vaginal agenesis
• 90% have cervical and/or uterine agenesis
• 10% have rudimentary müllerian structure
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Clinical presentation: primary amenorrhea, normal breast & pubic hair development, no visible vagina
Evaluation• Karyotype, renal sono, spinal X-rays, pelvic sono or
MRI (if suspect function uterine remnant)
Urologic anomalies are common (15-50%)Skeletal malformations involving vertebrae
(scoliosis), ribs, or pelvis in 10-15% of patients
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Treatment:• Goal is for normal ovarian function
• Functional vagina can be created by progressive
vaginal dilation (>90% success)
• Vaginoplasty (Vecchietti or McIndoe)
• If functional müllerian remnant remains,
recommend laparoscopic removal
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Müllerian AgenesisAndrogen Insensitivity
Syndrome
Menses Primary amenorrhea Primary amenorrhea
Breast Present Present
Pubic & axillary
hairPresent Absent
Uterus, Vagina Absent Absent or short
Testosterone Female range Male range
Karyotype 46,XX 46, XY
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Failure of development of one müllerian duct
Increased risk of
• Endometriosis, early SAB, ectopic pregnancy,
abnormal fetal presentation, IUGR, preterm labor
Urinary tract anomaly in 40% of patients
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Rudimentary horn• Can cause chronic pain
• Increase risk of ectopic pregnancy
• Functional vs. Non-functional endometrium
Non-functional: do not require surgical intervention
Functional: resection is recommended
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Lack of fusion of two müllerian ducts leads
to duplication of corpus and cervix
Approximately 75% have midline
longitudinal vaginal septum
Increased risk of SAB and preterm labor
Occasionally one side is obstructed • Surgically corrected
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Incomplete fusion of the two müllerian
ducts produces single cervix w/ varying
degree of separation in the two uterine
horns
Increased risk of SAB and preterm labor
No surgical intervention is recommended.
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Partial to complete lack of resorption of the midline septum between the two müllerian ducts
Not an established cause of infertility, but improved pregnancy rates once removed
The greater the septum, the increased risk of SAB, preterm labor, IUGR, breech presentation.
Complete septum SAB rates: 90%• Decreases to 10% after hysteroscopic resection
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Slight midline septum, heart-shaped cavity
No adverse impact on reproductive outcome
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Women exposed to diethylstilbestrol from
1938 to early 1970s
DES alters HOX gene expression
Many anomalies: • Hypoplastic T-shaped uterus
• Irregular cavities with adhesions
• Increased risk of ectopic pregnancy, SAB, preterm
labor, cervical incompetence
• Vaginal clear cell carcinoma
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Class Description
I Transverse vaginal septum (obstructing or non-
obstructing)
II Longitudinal vaginal septum (obstructing or non-
obstructing)
III Stenosis or iatrogenic
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Vertical fusion defect
Rarely associated with uterine anomalies
Symptoms: primary amenorrhea and/or
cyclic pelvic pain
Need pre-op imaging to identify cervix
Surgical repair: resection with end-to-end
anastomosis
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Lateral fusion failure or incomplete
resorption
Associated with complete septate uterus,
uterus didelphys, bicornuate uterus
20% have associated renal anomalies
Symptoms: difficult tampon insertion or
dyspareunia
Surgical resection if symptomatic
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Pelvic ultrasound
(including 3D TVUS)
MRI*
Limitations of HSG• Failure to perfuse both
uterine horns
• Cannot reliably distinguish
bicornuate and septate uteri
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30% of patients with müllerian anomaliesAnomalies include
• Horseshoe kidney
• Ectopic kidney
• Duplicated collecting system
• Ipsilateral renal agenesis
Imaging• IV pyelogram
• Renal sono
• CT
• MRI
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Remember: embryologic origin of the
ovaries is separate & distinct from
müllerian structures.• Patients typically have normal ovaries and ovarian
function.
Use clinical presentation as clue to the
type of anomaly (obstruction vs. cavitary)
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ASRM.org. Developmental Disorders of the
Urogenital Tract. Resident Module. 2015.
Clinical Gynecologic Endocrinology and
Infertility. Fritz & Speroff. 8th Edition. 2011.
Müllerian Agenesis: Diagnosis, Management,
and Treatment. ACOG Committee Opinion.
2015.
PROLOG. Reproductive Endocrinology and
Infertility. 7th Edition. 2015.
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