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Hysteroscopic Management
https://t.me/med1917
ofUterine Synechiae
JudeEhiabhiOkohue, AngeloB.Hooker, andPreyeOwenFiebai
1 Introduction
Intrauterine adhesions (IUAs) or uterine syn­echiae describe situations where scar tissues develop within the uterine cavity. This eventu­ally leads to partial or complete agglutination between the uterine walls and can result in clini­cal manifestations. It was rst described and published by a German gynaecologist, named Henrich Fritsch in 1894 following postpartum dilatation and curettage (D&C) [1]. This condi­tion however was characterized by Joseph Asherman, who in 1948, identied the aetiology and frequency of this syndrome, since known as the Asherman syndrome. He described a series of 29 cases with intrauterine cavity involvement
J. E. Okohue (*) Assisted Reproduction Unit, Department of Obstetrics and Gynaecology, Gynescope Specialist Hospital and Madonna University, Port Harcourt, Rivers State, Nigeria e-mail: jude.okohue@npmcn.edu.ng
A. B. Hooker Department of Obstetrics and Gynaecology, Zaans Medical Centre, Zaandam, Netherlands
P. O. Fiebai Department of Obstetrics and Gynaecology, University of Port Harcourt Teaching Hospital, Port Harcourt, Rivers State, Nigeria e-mail: preye.abai@uniport.edu.ng
following hysterography and linked endometrial trauma and adhesions to menstrual irregularities and infertility [2].
The terms IUAs and Asherman syndrome are often used interchangeably, although the syn­drome, as described by Asherman, requires signs and symptoms: when IUAs become associated with menstrual irregularities or infertility. Sometimes the same symptoms are present, but the cause of the IUA is not pregnancy-related. While some authors believe the term Asherman syndrome can still be used in such situations, oth­ers suggest it should be restricted to cases of IUAs resulting from endometrial damage related to a gravid uterus [3].
2 Aetiology
Intrauterine adhesion formation is multifactorial with multiple predisposing and causal factors, while the pathogenetic mechanism is still poorly understood. The true prevalence of IUAs remains unknown; the condition is considered rare in the general population. Intrauterine adhesions are thought to develop following trauma to the uter­ine cavity. The damage to the basal layer of the endometrium results in the formation of granula­tion tissue on the opposing surfaces of the uterine cavity. Once these coalesce, adhesions form,
© The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Switzerland AG 2022 J. E. Okohue et al. (eds.), Gynaecological Endoscopic Surgery,
https://doi.org/10.1007/978-3-030-86768-3_29
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leading to a partial or total obliteration of the uterine cavity. Hooker and colleagues recently performed a systematic review of the literature and reported a prevalence of 19.1% among 912 women hysteroscopically evaluated within 12months following a spontaneous miscarriage or after medical or surgical management, 86% of the patients following D&C [4]. In a study of 1856 women with Asherman syndrome, Schenker and Margaloith found that 90.8% of the cases were pregnancy-related, following termination of pregnancy, miscarriage, vaginal birth, or caesar­ean section [5]. Dilatation and curettage of a pregnant or recently pregnant uterus, therefore, appear to be the most common predisposing fac­tor for uterine synechiae.
Other causes of uterine synechiae or IUAs include myomectomy, the use of the B-lynch com­pression sutures, the use of intrauterine devices, uterine artery embolization, infections such as tuberculosis of the genital tract, and following sur­geries for Mullerian abnormalities [68].
3 Classication
A variety of classication systems exist, but none have been validated or linked to reproduc­tive performance. To date, no comparative anal-
ysis of studies has been performed, making a comparison between different studies difcult to interpret. The internationally most used clas­sication systems are those of March etal., the American Fertility Society (AFS), and the European Society of Gynecological Endoscopy (ESGE).
In the classication system of March etal. (1978), the adhesions are categorized in mini­mal, moderate, and severe groups based on a combination of the type of adhesions and cavity involvement. The AFS classication (1988) is based on the extent of cavity involvement, type of adhesions, and menstrual pattern. Cumulative scores determine the severity ranging from stage I to III.The ESGE classication emerged from the European Society of Hysteroscopy; both classications are based on a combination of the type of adhesions, site, and extent of cav­ity involvement and the presence of amenor­rhea or pronounced hypomenorrhoea. The severity of the adhesion is classied into seven grades.
The European Society of Hysteroscopy classication of intrauterine adhesions is pre­sented in Table1, while the American Fertility Society classication system is presented in Table2.
Table 1 European Society of Hysteroscopy classication of intrauterine adhesions
Grade Extent of intrauterine adhesions I Thin or lmy adhesions easily ruptured by hysteroscope sheath alone, cornual areas
II Singular rm adhesions connecting separate parts of the uterine cavity, visualization of
IIA Occluding adhesions only in the region of the internal cervical os. Upper uterine cavity
III Multiple rm adhesions connecting separate parts of the uterine cavity, unilateral
IIIA Extensive scarring of the uterine cavity wall with amenorrhea or hypomenorrhoea IIIB Combination of III and IIIA IV Extensive rm adhesions with agglutination of the uterine walls. Both tubal ostial areas
normal
both tubal ostia possible, cannot be ruptured by hysteroscope sheath alone
normal
obliteration of ostial areas of the tubes
occluded
Hysteroscopic Management ofUterine Synechiae
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The American Fertility Society (AFS) classication of intrauterine adhesions
Table 2
Adhesion score
Extent of cavity involved
(Score)
Type of adhesions
(Score)
Menstrual pattern
(Score) Prognostic classication
Disease severity Stage I (mild) 1–4 Stage II (moderate) 5–8 Stage III (severe) 9–12
a
Disease severity is staged based on cumulative score
a
<1/3
(1)
Filmy
(1)
Normal
(0)
Scores
1/3–2/3
(2)
Filmy and dense
(2)
Hypomenorrhoea
(2)
4 Presentation
Patients with IUAs can be asymptomatic, and therefore the diagnosis can remain undetected. It is uncertain whether the reproductive perfor­mance of asymptomatic women is inuenced by the presence of IUAs.
Women with IUAs or Asherman syndrome
can present with the following symptoms:
309
>2/3
(4)
Dense
(4)
Amenorrhoea
(4)
• Hypomenorrhoea/amenorrhea
• Cyclical lower abdominal/pelvic pain
• Recurrent pregnancy loss
• Infertility
5 Diagnosis
The diagnosis of intrauterine adhesion is made based on the clinical presentations and assess­ment of the endometrial cavity. The following investigative modalities assist in establishing a diagnosis of intrauterine adhesions:
5.1 Hysteroscopy
Hysteroscopy is still considered the gold stan­dard for establishing and conrming the diagno­sis of uterine synechiae or IUAs (Figs.1, 2, 3, 4, and 5). Hysteroscopy enables visualization of the uterine cavity: the extent, localization, and
Fig. 1 Intrauterine adhesions
Fig. 2 Adhesions on the left uterine wall
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degree of IUAs can be accurately determined, while other intrauterine abnormalities can also be detected. Furthermore, there is the possibility to perform adhesiolysis in the same session. In case hysteroscopy is not available or cannot be performed, other diagnostic modalities can be considered. Because of the high frequency of false-positive and diagnostic errors, hysterosal­pingography, ultrasonography, and sonohys­terography are less suitable for accurate detection of IUAs.
Fig. 3 Column of adhesion just proximal to the internal os
Fig. 4 Another column of intrauterine adhesions
5.2 Hysterosalpingography
Hysterosalpingography can show lling defects within the endometrial cavity and in severe cases might show complete obliteration of the uterine cavity. It can be performed as an ofce procedure.
5.3 Saline Infusion Sonography
This is performed in an ofce setting using saline, instilled via a special intrauterine catheter.
5.4 Transvaginal Ultrasound Scan
Versatile sonologists might be able to establish a diagnosis of uterine synechiae with the help of a transvaginal scan. This should not be considered an accurate diagnostic modality.
5.5 Magnetic Resonance Imaging
Fig. 5 Severe intrauterine adhesions
It is less frequently used because of the exorbi­tant cost.
5.6 3D Ultrasonography
This may also be helpful in diagnosing intrauter­ine synechiae and seems a promising diagnostic modality. Further research is necessary.
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6 Treatment
Hysteroscopic adhesiolysis is considered the appropriate treatment method for IUAs. Since the availability of hysteroscopy which allows a proper visualization of IUAs within the cavity, blind adhesiolysis has been relegated [9].
Hysteroscopic adhesiolysis aims at restoring the normal anatomy of the uterine cavity, while at the same time steps are taken towards preventing recurrence. Randomized controlled trials com­paring different treatment modalities are lacking, and treatment, therefore, is essentially based on the personal experience of the gynaecologist, case series, and case reports, channelled towards the individual needs of the patient.
The rigid hysteroscope is the most used treat­ment modality for the treatment of IUAs. Over the years, developments in hysteroscopic equip­ment have occurred: renement in optic and bre-optic technology with newer accessories, which have led to an improvement in both visual resolution and surgical techniques [10].
The rst hysteroscopes had diameters of about
5.5–6mm but were associated with a reduction in quality of vision. Much later, the 2.9–4 mm diameter hysteroscopes were manufactured. Hysteroscopes with diameters less than 2mm are now available, with good quality of vision.
The hysteroscopes are attached to inner and outer irrigation and suction sheaths, respectively, ensuring a continuous ow of uid. Also attached is a 5 F operating channel through which hystero­scopic handheld instruments such as scissors and graspers can be introduced. In case of cervical ste­nosis, intravaginal misoprostol can be administered, facilitating dilatation of the cervical canal [11, 12].
Mild adhesions can be separated either because of the pressure effect of the distension medium or with the use of the tip of the hysteroscope [13]. Hysteroscopic scissors introduced through the operating channel is usually used for adhesiolysis (Fig.6a–c). The scissors are preferred for this pur­pose as it is believed to be associated with less injury to the endometrium compared with the use of an energy source [14, 15]. In the vast majority of cases, the use of energy is not required.
In cases where energy is used, there is the choice between the monopolar and bipolar energy. While the monopolar energy uses hypo­tonic non-electrolyte-containing and therefore non- conductive uids like 1.5% glycine, the bipolar uses isotonic, conductive uids such as normal saline and lactated Ringer solution. It must be borne in mind that strict assessment and documentation of uid input and output are essential for patient safety.
While a uid decit of up to 2.5 L can be allowed when using normal saline, the procedure needs to be stopped following a decit of 1 L with 1.5% glycine and hence monopolar energy.
It is important to have a clear eld with the lowest intrauterine pressure possible. Manual pressure cuffs and automated pumps are readily available for delivering uids during hysteros­copy. Visualization is improved by the use of low­pressure and high-ow uid delivery system rather than a high-pressure, low-ow system [16].
Intrauterine adhesions, centrally located within the uterine cavity, are dealt with rst before treating those located at the periphery of the cavity [16]. Hysteroscopic adhesiolysis can be performed under ultrasound scan or simulta­neous laparoscopy guidance, especially in cases where the anatomy is unclear, to minimize perfo­ration. Fluoroscopy is another modality that can offer the needed guidance during hysteroscopic adhesiolysis. Fluoroscopy can identify unseen areas of the endometrial cavity inaccessible to the hysteroscope [17].
While all the above are meant to prevent uter­ine perforation, hysteroscopic adhesiolysis still remains the procedure with the greatest risk of perforation of the uterus [18]. If a perforation is suspected, the management should depend on the source of the perforation. Those caused by the introduction of the hysteroscope, scissors, or grasping forceps can be managed conservatively as severe intra-abdominal bleeding or bowel per­foration would rarely occur [16]. Perforation caused by an energy device requires an emer­gency laparoscopy. The site of the perforation should be inspected, and severe haemorrhage ruled out. The bowel should also be inspected for
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a
b
c
Fig. 6 (a–c) Hysteroscopic adhesiolysis with scissors
any sign of injury, although this might not be immediately apparent.
Other reported modes of management of IUAs include the use of NdYAG (neodymium-doped yttrium aluminium garnet) and KTP (potassium­titanyl- phosphate) LASER, which are said to cause damage to the endometrium as well as being exorbitant [19].
Mccomb and Wagner reported their manage­ment of six cases with severe IUAs [20]. The uterine wall was separated into two hemi-cavities by inserting a 13F Pratt cervical dilator. Under laparoscopic control, the brotic septum formed was cut up to the fundus with hysteroscopic scis-
sors. The technique is associated with high mor­bidity and is therefore largely abandoned.
Another hysteroscopic technique was described by Protopapas and colleagues [21]. They described making 6–8 longitudinal inci­sions, 4mm long into the myometrium from the fundus to the isthmus using a resectoscope tted with a Collins knife electrode.
They aimed to enlarge the uterine cavity with the intention of uncovering functional endome­trium. They reported an increase in menstrual bleeding in all cases. Hysteroscopic morcellation is emerging as a possible treatment modality in cases of IUAs.
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In the management of IUAs, stem cell therapy is gaining popularity. Stem cells could proliferate and differentiate into matured specialized cells both in vivo and invitro [22]. The use of stem cells in a patient with severe Asherman syndrome led to the development of endometrial thickness up to 8 mm with a subsequent successful IVF treatment [23].
7 Prevention ofAdhesion
Reformation
Numerous modalities have been employed with the aim of reducing the recurrence of uterine syn­echiae which should be considered an important problem, occurring in approximately 27% fol­lowing adhesiolysis [3]. The available evidence on this subject remains limited.
7.1 Intrauterine Device (IUD)
This separates the walls of the endometrium fol­lowing the completion of hysteroscopic adhe­siolysis. Originally, the Lippes loop was used, but its manufacture was stopped for economic rea­sons [24]. The copper contained in the copper T IUD causes an unwanted endometrial inamma­tory reaction, while the small surface area consti­tutes another disadvantage.
7.2 Intrauterine Foley Catheter
This also prevents the walls of the endometrium from colliding together thereby reducing the adhesion recurrence rate. A non-randomized study comparing the use of Foley’s catheter for 10 days with IUD insertion for 3 months fol­lowing adhesiolysis found fewer infections and a lower recurrence rate in the Foley catheter group [25]. Wrapping the Foley catheter bal­loon with fresh amnion has been shown to improve healing [26].
7.3 Intrauterine Balloon Stent
This acts in the same manner as a Foley catheter. Because of its triangular shape, it conforms to the shape of the endometrial cavity. Its use was recently found to be associated with a reduction in adhesions recurrence rate, compared with an IUD or hyaluronic acid [27].
7.4 Re-absorbable Agents: Intrauterine Gel
There are several re-absorbable agents that can be applied into the uterine cavity for the prevention of IUAs. Hyaluronic acid, a naturally occurring component of peritoneal uid that aids in tissue lubrication and structural integrity, is an agent that is registered for the prevention of IUAs. It was found in a systematic review and meta-analysis to be effective in preventing adhesion formation, although the evidence is limited [28].
8 Endometrial Preparation
Various agents are used with the intention of stim­ulating residual growth of the endometrium fol­lowing hysteroscopic adhesiolysis. One of such agents is oestrogens. There are few comparative studies investigating estrogen dosage and route of administration. A recent comparative study did not nd any difference between using a daily oral dose of 2mg, compared to 6mg [29]. Other medi­cations that increase blood ow such as aspirin, nitroglyceride, and sildenal citrate have also been tried. Unfortunately, the number of women treated with these modalities to date remains small, while there are no large studies in which the modalities are examined.
The use of autologous platelet-rich plasma (PRP) has been shown to improve endometrial thickness in women with refractory thin endome­trium and may play a role in the healing process following adhesiolysis [30]. About 1mL of PRP
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is prepared and administered within the endome­trial cavity. A transvaginal ultrasound scan is per­formed after 48–72h, measuring the endometrial thickness. If found to be less than 7mm, the PRP is again administered.
9 Follow-Up
Patients are usually assessed in order to detect any recurrence. This can be done via ofce hys­teroscopy, saline infusion sonography, and hys­terosalpingography. The aim is to detect a recurrence and offer treatment.
Learning Points
• Uterine synechiae are rare in the general population.
• The most important risk factor is pregnancy.
• There are no comparative analyses of the dif­ferent classication systems.
• Hysteroscopy is the gold standard in the diag­nosis and treatment of uterine synechiae.
• Hysteroscopic adhesiolysis remains the proce­dure with the greatest risk of uterine perforation.
• Available evidence on the prevention of adhe­sion reformation is limited.
References
1. Asherman JG. Amenorrhoea traumatic (atretica). J Obstet Gynaecol Br Emp. 1948;55:23.
2. Asherman JG. Traumatic intrauterine adhesions. J Obstet Gynaecol Br Emp. 1950;57:892–6.
3. Hanstede MM, Van der Meij E, Goedemans L, Emmanuel MH.Results of centralised Asherman sur­gery, 2003–2013. Fertil Steril. 2015;104(6):1561–8.
4. Hooker AB, Lemmers M, Thurkow AL, Heymans MW, Opmeer BC, Brolmann HA, et al. Systematic review and meta-analysis of intrauterine adhesions after miscarriage: prevalence, risk factors and long term reproductive outcome. Hum Reprod Update. 2014;20(2):262.
5. Schenker JG, Marghioth EJ.Intra-uterine adhesions: an updated appraisal. Fertil Steril. 1982;37:593–610.
6. March CM. Asherman’s syndrome. Semin Reprod Med. 2011;29(2):83–94.
7. Rasheed SM, Amin MM, Abo Ellah AH, Abo Elhassan AM, El Zahry MA, Wahab HA. Reproductive per­formance after conservative surgical treatment of postpartum haemorrhage. Int J Gynaecol Obstet. 2014;124(3):248–52.
8. Song D, Liu Y, Xiao Y, Li T-C, Zhou F, Xie E. A matched cohort study of intrauterine adhesiolysis for Asherman syndrome after uterine artery emboliza­tion or surgical trauma. J Minim Invasive Gynecol. 2014;21(6):1022–8.
9. Okohue JE. Adhesions and abortion. In: Tinelli A, Alonso Pacheco L, Haimovich S, editors. Hysteroscopy. Cham: Springer; 2018.
10. Emmanuel MH.New developments in hysteroscopy. Best Pract Res Clin Obstet Gynaecol. 2013;27:421–9.
11. Oppegaard KS, Wesheim BI, Istre O, Qvigstad E. Comparison of self administered misoprostol versus placebo for cervical ripening prior to opera­tive hysteroscopy using a sequential design. BJOG. 2008;115(5):663–e9.
12. Al-Fozan H, Firwana B, Alkadri H, Hassan S, Tulandi T.Preoperative ripening of the cervix before opera­tive hysteroscopy. Cochrane Database Syst Rev. 2015;23(4):CD005998.
13. Sugimoto O.Diagnostic and therapeutic hysteroscopy for traumatic intrauterine adhesions. Am J Obstet Gynecol. 1978;131:539–47.
14. Yu D, Wong YM, Cheong Y, Xia E, Li TC.Asherman syndrome – one century later. Fertil Steril. 2008;89:759–79.
15. Kodaman PH, Arici AA. Intrauterine adhesions and fertility outcome: how to optimize success? Curr Opin Obstet Gynecol. 2007;19(3):207–14.
16. Emmanuel MH, Hanstede M. Hysteroscopic treat­ment of Asherman syndrome. In: Tinelli A, Alonso Pacheco L, Haimovich S, editors. Hysteroscopy. Cham: Springer; 2018.
17. Broome JD, Vancaille TG. Fluoroscopically guided hysteroscopic division of adhesions in severe Asherman syndrome. Obstet Gynecol. 1999;93:1041–3.
18. Hulka JF, Peterson HA, Philips JM, Surrey MW.Operative hysteroscopy: American Association of Gynecologic Laparoscopist’s 1993. Membership survey. J Am Assoc Gynecol Laparosc. 1995;2(2):131.
19. Emmanuel MH. New development in hysteroscopy. Best Pract Res Clin Obstet Gynecol. 2013;27:421–9.
20. McComb PF, Wagner BL. Simplied therapy for Asherman’s syndrome. Fertil Steril. 1997;11:1047–50.
21. Protopapas A, Shushan A, Magos A. Myometrial scoring: a new technique for the management of Asherman’s syndrome. Fertil Steril. 1998;69:860–4.
22. Herberts CA, Kwa MS, Hermsen HP.Risk factors in the development of stem cell therapy. J Transl Med. 2011;9:29.
23. Nagori CB, Panchal SY, Patel H.Endometrial regen­eration using autologous adult stem cells followed by conception by invitro fertilization in a patient of
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severe Asherman’s syndrome. J Hum Reprod Sci. 2011;4(1):43–8.
24. Ortho Stops Marketing Lippers Loop; cites eco­nomic factors. Contracept Technol Update. 1985;6(11):149–52.
25. Orhue AA, Aziken ME, Igbefoh JO.A comparison of two adjunctive treatments for intrauterine adhesions following lysis. Int J Gynaecol Obstet. 2003;82:49–56.
26. Peng X, Li T, Zhao Y, et al. Safety and efcacy of amnion graft in preventing reformation of intrauterine adhesions. J Minim Invasive Gynecol. 2017;24(7):1204–10.
27. Lin X, Wei M, Li TC, Huang Q, Huang D, Zhou F, Zhang S.A comparison of intrauterine balloon, intra­uterine contraceptive device and hyaluronic acid gel in the prevention of adhesion reformation follow­ing hysteroscopic surgery for Asherman syndrome:
a cohort study. Eur J Obstet Gynecol Reprod Biol. 2013;170:512–6.
28. Hearly MW, Schexnayder B, Connell MT, Terry N, Decherney AH, Csokmay JM, et al. Intrauterine adhesion prevention after hysteroscopy: a system­atic review and meta-analysis. Am J Obstet Gynecol. 2016;215(3):267.
29. Guo J, Li T, Liu Y, etal. A prospective, randomized, controlled trial comparing two doses of oestrogen therapy after hysteroscopic adhesiolysis to prevent intrauterine adhesion recurrence. Reprod Biomed Online. 2017;35(5):555–61.
30. Kim H, Shin JE, Koo HS, etal. Effect of autologous platelet-rich plasma treatment on refractory thin endometrium during the frozen embryo transfer cycle. A pilot study. Frontline Endocrinol. 2019; https://doi.
org/10.3389/fendo.
Hysteroscopic Myomectomy
https://t.me/med1917
SundayOmaleOnuh, PhilipsUcheEkpe, andRaisS.Ibraheem
1 Introduction
Uterine leiomyoma or broids are benign tumours of the uterine muscle which are of monoclonal origin and rank the commonest tumour of the female reproductive system [1]. Based on loca­tion, uterine broids could be subserosal, intra­mural or submucosal. While submucosal broids constitute only 5.5–16.6% of all broids, they cause the most severe symptoms [2]. Most of the symptoms of submucosal broids are related to anatomical distortion of the endometrial cavity, manifesting as heavy menstrual bleeding (HMB), infertility and pregnancy loss among others [3].
Hysteroscopic myomectomy has now become the mainstay in the management of submucosal broids. Hysteroscopic myomectomy was rst performed in 1976 by Neuwirth and Amin [4]. Over the last three decades, advances in instru­ment and techniques have continued to improve the possibility and ease of surgical removal of submucosal broid using the hysteroscope and
S. O. Onuh (*) Department of Obstetrics and Gynecology, Deda Hospital, Abuja, Nigeria
P. U. Ekpe Department of Obstetrics and Gynaecology, Asokoro District Hospital, Abuja, Nigeria
R. S. Ibraheem Department of Obstetrics and Gynaecology, IVF Center National Hospital, Abuja, Nigeria
thus joining the ranks of minimally invasive sur­gery (MAS) [5].
In current practice, hysteroscopic myomectomy could be achieved via mechanical means with cold scissors, graspers or morcellators, or by the use of energy like monopolar, bipolar, radio frequency and laser energy [6]. Most cases of hysteroscopic myomectomy are performed in the operating the­atre under anaesthesia; however, a few cases can be performed as ofce procedures [6].
2 Classication ofSubmucosal
Fibroids
There are varied classications of submucosal broids which help in appropriate surgical man­agement with resultant elimination or reduction in the attendant morbidities. The most popular classication is that by the European Society for Gynaecological Endoscopy (ESGE) [7]. This classies submucosal broids into three groups as shown in Table1 and Fig.1.
There exists other methods of classication, notable among them is the STEPW Lasmar clas­sication [8], which uses trans-vaginal ultra­sound scan (TVUS) or magnetic resonance imaging (MRI) to assess the following parame­ters: size, topography, extension of the myoma base, depth of myoma penetration and lateral wall involvement.
© The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature Switzerland AG 2022 J. E. Okohue et al. (eds.), Gynaecological Endoscopic Surgery,
https://doi.org/10.1007/978-3-030-86768-3_30
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