- •Contents
- •Contributors
- •1 Introduction
- •2.1 Posterior Compartment
- •2.2 Anterior Compartment
- •2.3 Middle Compartment
- •2.4 Perineal Body
- •3 Compartments
- •3.1 Posterior Compartment
- •3.1.1 Connective Tissue Structures
- •3.1.2 Muscles
- •3.1.3 Reinterpreted Anatomy and Clinical Relevance
- •3.2 Anterior Compartment
- •3.2.1 Connective Tissue Structures
- •3.2.2 Muscles
- •3.2.3 Reinterpreted Anatomy and Clinical Relevance
- •3.2.4 Important Vessels, Nerves, and Lymphatics of the Anterior Compartment
- •3.3 Middle Compartment
- •3.3.1 Connective Tissue Structures
- •3.3.2 Muscles
- •3.3.3 Reinterpreted Anatomy and Clinical Relevance
- •3.3.4 Important Vessels, Nerves, and Lymphatics of the Middle Compartment
- •4 Perineal Body
- •References
- •MR and CT Techniques
- •1 Introduction
- •2.1 Introduction
- •2.2.1 Spasmolytic Medication
- •2.3.2 Diffusion-Weighted Imaging
- •2.3.3 Dynamic Contrast Enhancement
- •3 CT Technique
- •3.1 Introduction
- •3.2 Technical Disadvantages
- •3.4 Oral and Rectal Contrast
- •References
- •Uterus: Normal Findings
- •1 Introduction
- •References
- •1 Clinical Background
- •1.1 Epidemiology
- •1.2 Clinical Presentation
- •1.3 Embryology
- •1.4 Pathology
- •2 Imaging
- •2.1 Technique
- •2.2.1 Class I Anomalies: Dysgenesis
- •2.2.2 Class II Anomalies: Unicornuate Uterus
- •2.2.3 Class III Anomalies: Uterus Didelphys
- •2.2.4 Class IV Anomalies: Bicornuate Uterus
- •2.2.5 Class V Anomalies: Septate Uterus
- •2.2.6 Class VI Anomalies: Arcuate Uterus
- •2.2.7 Class VII Anomalies
- •References
- •Benign Uterine Lesions
- •1 Background
- •1.1 Uterine Leiomyomas
- •1.1.1 Epidemiology
- •1.1.2 Pathogenesis
- •1.1.3 Histopathology
- •1.1.4 Clinical Presentation
- •1.1.5 Therapy
- •1.1.5.1 Indications
- •1.1.5.2 Medical Therapy and Ablation
- •1.1.5.3 Surgical Therapy
- •1.1.5.4 Uterine Artery Embolization (UAE)
- •1.1.5.5 Magnetic Resonance-Guided Focused Ultrasound
- •2 Adenomyosis of the Uterus
- •2.1 Epidemiology
- •2.2 Pathogenesis
- •2.3 Histopathology
- •2.4 Clinical Presentation
- •2.5 Therapy
- •3 Imaging
- •3.2 Magnetic Resonance Imaging
- •3.2.1 Magnetic Resonance Imaging: Technique
- •3.2.2 MR Appearance of Uterine Leiomyomas
- •3.2.3 Locations, Growth Patterns, and Imaging Characteristics
- •3.2.4 Histologic Subtypes and Forms of Degeneration
- •3.2.5 Differential Diagnosis
- •3.2.6 MR Appearance of Uterine Adenomyosis
- •3.2.7 Locations, Growth Patterns, and Imaging Characteristics
- •3.2.8 Differential Diagnosis
- •3.3 Computed Tomography
- •3.3.1 CT Technique
- •3.3.2 CT Appearance of Uterine Leiomyoma and Adenomyosis
- •3.3.3 Atypical Appearances on CT and Differential Diagnosis
- •4.1 Indications
- •4.2 Technique
- •Bibliography
- •Cervical Cancer
- •1 Background
- •1.1 Epidemiology
- •1.2 Pathogenesis
- •1.3 Screening
- •1.4 HPV Vaccination
- •1.5 Clinical Presentation
- •1.6 Histopathology
- •1.7 Staging
- •1.8 Growth Patterns
- •1.9 Treatment
- •1.9.1 Treatment of Microinvasive Cervical Cancer
- •1.9.2 Treatment of Grossly Invasive Cervical Carcinoma (FIGO IB-IVA)
- •1.9.3 Treatment of Recurrent Disease
- •1.9.4 Treatment of Cervical Cancer During Pregnancy
- •1.10 Prognosis
- •2 Imaging
- •2.1 Indications
- •2.1.1 Role of CT and MRI
- •2.2 Imaging Technique
- •2.2.2 Dynamic MRI
- •2.2.3 Coil Technique
- •2.2.4 Vaginal Opacification
- •2.3 Staging
- •2.3.1 General MR Appearance
- •2.3.2 Rare Histologic Types
- •2.3.3 Tumor Size
- •2.3.4 Local Staging
- •2.3.4.1 Stage IA
- •2.3.4.2 Stage IB
- •2.3.4.3 Stage IIA
- •2.3.4.4 Stage IIB
- •2.3.4.5 Stage IIIA
- •2.3.4.6 Stage IIIB
- •2.3.4.7 Stage IVA
- •2.3.4.8 Stage IVB
- •2.3.5 Lymph Node Staging
- •2.3.6 Distant Metastases
- •2.4 Specific Diagnostic Queries
- •2.4.1 Preoperative Imaging
- •2.4.2 Imaging Before Radiotherapy
- •2.5 Follow-Up
- •2.5.1 Findings After Surgery
- •2.5.2 Findings After Chemotherapy
- •2.5.3 Findings After Radiotherapy
- •2.5.4 Recurrent Cervical Cancer
- •2.6.1 Ultrasound
- •2.7.1 Metastasis
- •2.7.2 Malignant Melanoma
- •2.7.3 Lymphoma
- •2.8 Benign Lesions of the Cervix
- •2.8.1 Nabothian Cyst
- •2.8.2 Leiomyoma
- •2.8.3 Polyps
- •2.8.4 Rare Benign Tumors
- •2.8.5 Cervicitis
- •2.8.6 Endometriosis
- •2.8.7 Ectopic Cervical Pregnancy
- •References
- •Endometrial Cancer
- •1.1 Epidemiology
- •1.2 Pathology and Risk Factors
- •1.3 Symptoms and Diagnosis
- •2 Endometrial Cancer Staging
- •2.1 MR Protocol for Staging Endometrial Carcinoma
- •2.2.1 Stage I Disease
- •2.2.2 Stage II Disease
- •2.2.3 Stage III Disease
- •2.2.4 Stage IV Disease
- •4 Therapeutic Approaches
- •4.1 Surgery
- •4.2 Adjuvant Treatment
- •4.3 Fertility-Sparing Treatment
- •5.1 Treatment of Recurrence
- •6 Prognosis
- •References
- •Uterine Sarcomas
- •1 Epidemiology
- •2 Pathology
- •2.1 Smooth Muscle Tumours
- •2.2 Endometrial Stromal Tumours
- •3 Clinical Background
- •4 Staging
- •5 Imaging
- •5.1 Leiomyosarcoma
- •5.2.3 Undifferentiated Uterine Sarcoma
- •5.3 Adenosarcoma
- •6 Prognosis and Treatment
- •References
- •1.1 Anatomical Relationships
- •1.4 Pelvic Fluid
- •2 Developmental Anomalies
- •2.1 Congenital Abnormalities
- •2.2 Ovarian Maldescent
- •3 Ovarian Transposition
- •References
- •1 Introduction
- •4 Benign Adnexal Lesions
- •4.1.1 Physiological Ovarian Cysts: Follicular and Corpus Luteum Cysts
- •4.1.1.1 Imaging Findings in Physiological Ovarian Cysts
- •4.1.1.2 Differential Diagnosis
- •4.1.2 Paraovarian Cysts
- •4.1.2.1 Imaging Findings
- •4.1.2.2 Differential Diagnosis
- •4.1.3 Peritoneal Inclusion Cysts
- •4.1.3.1 Imaging Findings
- •4.1.3.2 Differential Diagnosis
- •4.1.4 Theca Lutein Cysts
- •4.1.4.1 Imaging Findings
- •4.1.4.2 Differential Diagnosis
- •4.1.5 Polycystic Ovary Syndrome
- •4.1.5.1 Imaging Findings
- •4.1.5.2 Differential Diagnosis
- •4.2.1 Cystadenoma
- •4.2.1.1 Imaging Findings
- •4.2.1.2 Differential Diagnosis
- •4.2.2 Cystadenofibroma
- •4.2.2.1 Imaging Features
- •4.2.3 Mature Teratoma
- •4.2.3.1 Mature Cystic Teratoma
- •Imaging Findings
- •Differential Diagnosis
- •4.2.3.2 Monodermal Teratoma
- •Imaging Findings
- •4.2.4 Benign Sex Cord-Stromal Tumors
- •4.2.4.1 Fibroma and Thecoma
- •Imaging Findings
- •4.2.4.2 Sclerosing Stromal Tumor
- •Imaging Findings
- •4.2.5 Brenner Tumors
- •4.2.5.1 Imaging Findings
- •4.2.5.2 Differential Diagnosis
- •5 Functioning Ovarian Tumors
- •References
- •1 Introduction
- •2.1 Context
- •2.2.2 Indications According to Simple Rules
- •References
- •CT and MRI in Ovarian Carcinoma
- •1 Introduction
- •2.1 Familial or Hereditary Ovarian Cancers
- •3 Screening for Ovarian Cancer
- •5 Tumor Markers
- •6 Clinical Presentation
- •7 Imaging of Ovarian Cancer
- •7.1.2 Peritoneal Carcinomatosis
- •7.1.3 Ascites
- •7.3 Staging of Ovarian Cancer
- •7.3.1 Staging by CT and MRI
- •Imaging Findings According to Tumor Stages
- •Value of Imaging
- •7.3.2 Prediction of Resectability
- •7.4 Tumor Types
- •7.4.1 Epithelial Ovarian Cancer
- •High-Grade Serous Ovarian Cancer
- •Low-Grade Serous Ovarian Cancer
- •Mucinous Epithelial Ovarian Cancer
- •Endometrioid Ovarian Carcinomas
- •Clear Cell Carcinomas
- •Imaging Findings of Epithelial Ovarian Cancers
- •Differential Diagnosis
- •Borderline Tumors
- •Imaging Findings
- •Differential Diagnosis
- •Recurrent Ovarian Cancer
- •Imaging Findings
- •Differential Diagnosis
- •Value of Imaging
- •Malignant Germ Cell Tumors
- •Dysgerminomas
- •Imaging Findings
- •Differential Diagnosis
- •Immature Teratomas
- •Imaging Findings
- •Malignant Transformation in Benign Teratoma
- •Imaging Findings
- •Differential Diagnosis
- •Sex-Cord Stromal Tumors
- •Granulosa Cell Tumors
- •Imaging Findings
- •Sertoli-Leydig Cell Tumor
- •Imaging Findings
- •Ovarian Lymphoma
- •Imaging Findings
- •Differential Diagnosis
- •7.4.3 Ovarian Metastases
- •Imaging Findings
- •Differential Diagnosis
- •7.5 Fallopian Tube Cancer
- •7.5.1 Imaging Findings
- •Differential Diagnosis
- •References
- •Endometriosis
- •1 Introduction
- •2.1 Sonography
- •3 MR Imaging Findings
- •References
- •Vagina and Vulva
- •1 Introduction
- •3.1 CT Appearance
- •3.2 MRI Protocol
- •3.3 MRI Appearance
- •4.1 Imperforate Hymen
- •4.2 Congenital Vaginal Septa
- •4.3 Vaginal Agenesis
- •5.1 Vaginal Cysts
- •5.1.1 Gardner Duct Cyst (Mesonephric Cyst)
- •5.1.2 Bartholin Gland Cyst
- •5.2.1 Vaginal Infections
- •5.2.1.1 Vulvar Infections
- •5.2.1.2 Vulvar Thrombophlebitis
- •5.3 Vulvar Trauma
- •5.4 Vaginal Fistula
- •5.5 Post-Radiation Changes
- •5.6 Benign Tumors
- •6.1 Vaginal Malignancies
- •6.1.1 Primary Vaginal Carcinoma
- •6.1.1.1 MRI Findings
- •6.1.1.2 Lymph Node Drainage
- •6.1.1.3 Recurrence and Complications
- •6.1.2 Non-squamous Cell Carcinomas of the Vagina
- •6.1.2.1 Adenocarcinoma
- •6.1.2.2 Melanoma
- •6.1.2.3 Sarcomas
- •6.1.2.4 Lymphoma
- •6.2 Vulvar Malignancies
- •6.2.1 Vulvar Carcinoma
- •6.2.2 Melanoma
- •6.2.3 Lymphoma
- •6.2.4 Aggressive Angiomyxoma of the Vulva
- •7 Vaginal Cuff Disease
- •7.1 MRI Findings
- •8 Foreign Bodies
- •References
- •Imaging of Lymph Nodes
- •1 Background
- •3 Technique
- •3.1.1 Intravenous Unspecific Contrast Agents
- •3.1.2 Intravenous Tissue-Specific Contrast Agents
- •References
- •1 Introduction
- •2.1.1 Imaging Findings
- •2.1.2 Differential Diagnosis
- •2.1.3 Value of Imaging
- •2.2 Pelvic Inflammatory
- •2.2.1 Imaging Findings
- •2.3 Hydropyosalpinx
- •2.3.1 Imaging Findings
- •2.3.2 Differential Diagnosis
- •2.4 Tubo-ovarian Abscess
- •2.4.1 Imaging Findings
- •2.4.2 Differential Diagnosis
- •2.4.3 Value of Imaging
- •2.5 Ovarian Torsion
- •2.5.1 Imaging Findings
- •2.5.2 Differential Diagnosis
- •2.5.3 Diagnostic Value
- •2.6 Ectopic Pregnancy
- •2.6.1 Imaging Findings
- •2.6.2 Differential Diagnosis
- •2.6.3 Value of Imaging
- •3.1 Pelvic Congestion Syndrome
- •3.1.1 Imaging Findings
- •3.1.2 Differential Diagnosis
- •3.1.3 Value of Imaging
- •3.2 Ovarian Vein Thrombosis
- •3.2.1 Imaging Findings
- •3.2.2 Differential Diagnosis
- •3.2.3 Value of Imaging
- •3.3 Appendicitis
- •3.3.1 Imaging Findings
- •3.3.2 Value of Imaging
- •3.4 Diverticulitis
- •3.4.1 Imaging Findings
- •3.4.2 Differential Diagnosis
- •3.4.3 Value of Imaging
- •3.5 Epiploic Appendagitis
- •3.5.1 Imaging Findings
- •3.5.2 Differential Diagnosis
- •3.5.3 Value of Imaging
- •3.6 Crohn’s Disease
- •3.6.1 Imaging Findings
- •3.6.2 Differential Diagnosis
- •3.6.3 Value of Imaging
- •3.7 Rectus Sheath Hematoma
- •3.7.1 Imaging Findings
- •3.7.2 Differential Diagnosis
- •3.7.3 Value of Imaging
- •References
- •MRI of the Pelvic Floor
- •1 Introduction
- •2 Imaging Techniques
- •3.1 Indications
- •3.2 Patient Preparation
- •3.3 Patient Instruction
- •3.4 Patient Positioning
- •3.5 Organ Opacification
- •3.6 Sequence Protocols
- •4 MR Image Analysis
- •4.1 Bony Pelvis
- •5 Typical Findings
- •5.1 Anterior Compartment
- •5.2 Middle Compartment
- •5.3 Posterior Compartment
- •5.4 Levator Ani Muscle
- •References
- •Evaluation of Infertility
- •1 Introduction
- •2 Imaging Techniques
- •2.1 Hysterosalpingography
- •2.1.1 Cycle Considerations
- •2.1.2 Technical Considerations
- •2.1.3 Side Effects and Complications
- •2.1.5 Pathological Findings
- •2.1.6 Limitations of HSG
- •2.2.1 Cycle Considerations
- •2.2.2 Technical Considerations
- •2.2.2.1 Normal and Abnormal Anatomy
- •2.2.3 Accuracy
- •2.2.4 Side Effects and Complications
- •2.2.5 Limitations of Sono-HSG
- •2.3 Magnetic Resonance Imaging
- •2.3.1 Indications
- •2.3.2 Technical Considerations
- •2.3.3 Limitations
- •3 Ovulatory Dysfunction
- •4 Pituitary Adenoma
- •5 Polycystic Ovarian Syndrome
- •7 Uterine Disorders
- •7.1 Müllerian Duct Anomalies
- •7.1.1 Class I: Hypoplasia or Agenesis
- •7.1.2 Class II: Unicornuate
- •7.1.3 Class III: Didelphys
- •7.1.4 Class IV: Bicornuate
- •7.1.5 Class V: Septate
- •7.1.6 Class VI: Arcuate
- •7.1.7 Class VII: Diethylstilbestrol Related
- •7.2 Adenomyosis
- •7.3 Leiomyoma
- •7.4 Endometriosis
- •References
- •MR Pelvimetry
- •1 Clinical Background
- •1.3.1 Diagnosis
- •1.3.2.1 Cephalopelvic Disproportion
- •1.3.4 Inadequate Progression of Labor due to Inefficient Contraction (“the Powers”)
- •2.2 Palpation of the Pelvis
- •3 MR Pelvimetry
- •3.2 MR Imaging Protocol
- •3.3 Image Analysis
- •3.4 Reference Values for MR Pelvimetry
- •5 Indications for Pelvimetry
- •References
- •MR Imaging of the Placenta
- •2 Imaging of the Placenta
- •3 MRI Protocol
- •4 Normal Appearance
- •4.1 Placenta Variants
- •5 Placenta Adhesive Disorders
- •6 Placenta Abruption
- •7 Solid Placental Masses
- •9 Future Directions
- •References
- •Erratum to: Endometrial Cancer
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menstrual bleeding (Stewart and Nowak 1996; deSouza and Williams 2002).
The impairment of quality of life caused by leiomyoma-related problems and the measurable loss of economic productivity due to absence from work are considerable.
In a national survey study conducted in the USA it was reported that women waited an average of 3.6 years before seeking treatment for leiomyomas and 28% of employed respondents reported missing work due to leiomyoma symptoms (Borah et al. 2013).
For the USA it has been estimated that at least 5 million workdays are lost per year due to leiomyomas and that the annual treatment cost amounts to US$ 3 billion (Greenberg and Kazamel 1995). The high incidence of leiomyomas and its socioeconomic implications as well as individual loss of quality of life are in sharp contrast to our still limited understanding of the pathogenesis of uterine leiomyomas and inadequate therapeutic options. A lack of research into the epidemiology, pathogenesis, and pathophysiology of leiomyomas of the uterus as well as their “benign nature” are the most important factors that have so far inhibited the search for alternative therapeutic options to replace the radical surgical approach of hysterectomy (Myers et al. 2002). Surgical removal of the uterus continues to be the most widely used therapeutic approach in patients with symptomatic leiomyomas. In Western industrialized countries, uterine leiomyomas are the most frequent indication for removal of the uterus, accounting for 175,000 hysterectomies per year in the USA alone (Wright et al. 2013). Women are increasingly asking for alternative nonsurgical, uterus-sparing therapies and research and scientific evaluation of alternative therapeutic options such as uterine artery embolization have markedly increased over the last two decades (Borah et al. 2013; ACOG 2001).
1.1.5\ Therapy
1.1.5.1\ Indications
Treatment of uterine leiomyomas is indicated when they cause symptoms (American College of Obstetricians and Gynecologists 2008) while a
wait-and-see approach is in order in women without symptoms. Whether treatment is indicated or not does not depend on the size of the uterus or that of individual leiomyoma tumors since there is no evidence that marked enlargement of the uterus is associated with an increased surgical morbidity. Traditionally, rapid growth of a leiomyoma has been interpreted as a sign of malignancy (leiomyosarcoma) while the results of larger studies do not confirm this assumption (Leibsohn et al. 1990; Parker et al. 1994). A relative indication for treating asymptomatic leiomyomas exists in women who want to conceive and have a history of miscarriage and proven leiomyoma-related deformity of the uterine cavity. In these cases treatment may be indicated because the leiomyomas can interfere with placentation and pregnancy is associated with additional risks (Hasan et al. 1991; Phelan 1995; Pritts 2001; Rice et al. 1989). A systematic review, however, concluded that there is no conclusive evidence that intramural or subserosal leiomyomas adversely affect fecundity and good maternal and neonatal outcomes are expected in pregnancies with uterine leiomyomas (Klatsky et al. 2008).
1.1.5.2\ Medical Therapy and Ablation
Medical therapy is usually symptomatic and aims to relieve leiomyoma-related abnormal menstrual bleeding (hypermenorrhea, menorrhagia), dysmenorrhea,andbulksymptoms.Oralcontraceptives of different hormonal composition and nonsteroidal anti-inflammatory drugs with analgesic and antifibrinolytic effects are used although evidence for their long-term effectiveness in treating uterine leiomyomas is not available (Myers et al. 2002; Stewart 2001). Moreover, there is no data demonstrating a growth-reducing effect of oral contraceptives. These therapeutic options are used in the routine clinical setting to bridge the time until definitive therapy is performed. Treatment with GnRH analogues improves leiomyoma-related symptoms and leads to a transient reduction of leiomyoma size. Maximum size reduction is seen after about 3 months of treatment. Once GnRH analogues are discontinued, however, leiomyomas will again increase in size. This is why GnRH analogues
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are given only to reduce leiomyoma size prior to surgery (Ylikorkala et al. 1995). GnRH administration is also beneficial to minimize blood loss in case of larger leiomyomas or for the transient treatment of anemia resulting from heavy menstrual bleeding. However, GnRH treatment causes softening of leiomyomas, which is a disadvantage for surgical enucleation. Progesterone receptor modulators (PRMs) have recently demonstrated effectiveness for intermittent treatment of symptomatic uterine leiomyomas (Donnez et al. 2012, 2014, 2015).
The severity of menstrual bleeding can be reduced by insertion of a levonorgestrel- releasing intrauterine device (IUD) (Mercorio et al. 2003; Wildemeersch and Schacht 2002). The effect of such IUDs is based on the local activity of continuously released progesterone, which effectively suppresses the endometrium. A recent systematic review concluded that levonorgestrel-releasing intrauterine systems could decrease uterine volume and endometrial thickness and reduce menstrual blood loss and increase blood hemoglobin, ferritin, and hematocrit levels significantly. However, no evidence for decreasing uterine leiomyoma volume was found (Jiang et al. 2014). It is known that an IUD for the treatment of hypermenorrhea has a higher failure rate in the presence of submucosal leiomyomas (Wildemeersch and Schacht 2002).
Endometrial ablation is a permanent and invasive therapeutic option which relieves excessive menstrual bleeding in 62–79% of cases (Soysal et al. 2001). Thermoablation of the endometrium is performed using a balloon or roller ball technique and a hysteroscopic access. The success of endometrial ablation in the presence of leiomyomas is small because not the entire endometrium is accessible in women with multiple leiomyomas because of enlargement and deformity of the uterine cavity.
1.1.5.3\ Surgical Therapy
Hysterectomy is a definitive cure in patients with a symptomatic multileiomyoma uterus. Both abdominal and vaginal hysterectomy is associated with a low mortality and morbidity. However,
given that uterine leiomyomas are benign lesions, the large number of hysterectomies performed worldwide to treat this condition appears to be disproportionate (Broder et al. 2000; Stewart et al. 2012). As an alternative to hysterectomy, uterus-sparing operative, ablative, and interventional radiological procedures are available, depending on location and size of leiomyomas present, the patient’s age, desire to have children, and personal preferences.
Depending on their location, leiomyomas can be resected or enucleated using a hysteroscopic or laparoscopic access or open laparotomy. Hysteroscopic resection is suitable to remove submucosal leiomyomas. Hysteroscopic resection is generally considered unsuitable for submucosal leiomyomas larger than 5 cm in size, if more than three leiomyomas are present, or if the uterine cavity is very large (length of uterine probe >12 cm). Moreover, the size of the intramural component is a risk factor of the hysteroscopic resection because the risk of perforation increases when the residual myometrium is thin (Wamsteker et al. 1993). A laparoscopic access is used to remove visible subserosal and intramural leiomyomas in combination with reconstruction of the uterus. This approach is unsuitable in the presence of very large leiomyomas or a markedly enlarged uterus because these factors limit the use of the laparoscope and visibility. Using the laparoscopic approach, multiple leiomyomas can be enucleated in one session. Only visible leiomyomas can be removed while intramural tumors are not easily accessible to laparoscopic removal. Incision of the uterine cavity necessary for the removal of transmural leiomyomas is considered a disadvantage because it is associated with the risk of synechia. Adhesions are observed in 33–54% of patients following laparoscopic interventions (Hasson et al. 1992; Dubuisson et al. 1998; Malzoni et al. 2003). The risk of recurrence after laparoscopic leiomyoma removal is between 21 and 50% in women followed up for up to 5 years (Doridot et al. 2001; Radosa et al. 2014). (Mini-) Laparotomy is primarily used in patients with one or more large leiomyomas, which are
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removed using an adjusted abdominal incision. The perioperative risks of laparotomy are comparable to those of hysterectomy while the rate of adhesions may be as high as 90% (Sawin et al. 2000; Tulandi et al. 1993). The reported recurrence rate after abdominal myomectomy is 10% within 5 years and up to 27% after 10 years. One-third of the patients with recurrent leiomyomas will ultimately undergo hysterectomy (Candiani et al. 1991; Fauconnier et al. 2000).
1.1.5.4\ Uterine Artery Embolization (UAE)
Uterine artery embolization (UAE) is an established technique that has been used to stop life- threatening vaginal hemorrhage in women with malignancy, postpartum uterine atony, or traumatic injury since the mid-1970s (Margolies et al. 1972; Goldstein et al. 1975; Athanasoulis et al. 1976; Higgins et al. 1977; Brown et al. 1979). The first successful treatment of symptomatic leiomyomas of the uterus by UAE was reported by Ravina et al. in 1994 (Ravina et al. 1994).
Embolization of the uterine artery induces infarction of leiomyomas while uterine perfusion is maintained (Katsumori et al. 2001; McCluggage et al. 2000). Infarction leads to coagulation necrosis and subsequent complete hyalinization of the leiomyomas (Weichert et al. 2005; McCluggage et al. 2000; Colgan et al. 2003). Further transformations cause softening and shrinkage of the tumors. Follow-up for 3–24 months has shown that there is an average size reduction of the uterus of 23–60% while the dominant leiomyoma decreases by 42–78% on average. Progressive shrinkage of the leiomyomas has been documented for a period of 12 months (Kroncke et al. 2005; Brunereau et al. 2000; Hutchins et al. 1999; McLucas et al. 2001a; Prollius et al. 2004; Pron et al. 2003; Spies et al. 2001a; Walker and Pelage 2002). Several studies provide evidence for a relief of bleeding-related symptoms in 80–100% of patients and a regression of bulk symptoms in 60–100% of patients followed up for 3–60 months (Kroncke et al. 2005; Brunereau et al. 2000; Hutchins et al. 1999; McLucas et al. 2001a; Prollius et al. 2004;
Pron et al. 2003; Spies et al. 2001a; Walker and Pelage 2002; Andersen et al. 2001; Katsumori et al. 2002). Studies comparing UAE with hysterectomy and myomectomy in the treatment of symptomatic uterine leiomyomas suggest that UAE has a similar success rate in terms of symptom relief and patient satisfaction while it has a lower complication rate and shorter recovery period as compared with the surgical procedures (Razavi et al. 2003; Broder et al. 2002; Spies et al. 2004a; Mara et al. 2005). These results are confirmed by two randomized studies (Pinto et al. 2003; Hehenkamp et al. 2005). Long-term results after UAE are limited but the available data suggests that permanent improvement of symptoms can be expected in two-thirds of women (Broder et al. 2002; Spies et al. 2005a; Scheurig-Muenkler et al. 2011). Complications during the intervention are extremely rare (Spies et al. 2002a; Kroncke et al. 2004). Following UAE, 5–10% of the patients report vaginal discharge with or without tissue passage and expulsion of infarcted leiomyomas may occur (Kroencke et al. 2003; Park et al. 2005; Berkowitz et al. 1999; Abbara et al. 1999). Leiomyoma expulsion occurs weeks to months after the intervention and may necessitate administration of antibiotics and pain medication if complicated by superinfection and in rare cases surgically assisted removal or hysteroscopic resection (Hutchins et al. 1999; McLucas et al. 2001a; Spies et al. 2001a). Transient amenorrhea persisting for up to three cycles is not unusual while permanent amenorrhea is rare and occurs more commonly in patients above 45 years old than in younger ones (Walker and Pelage 2002; Chrisman et al. 2000; Tropeano et al. 2004). UAE can be performed in patients with single or multiple leiomyomas but, based on current knowledge, patients who wish to preserve their fertility should be treated by UAE only if alternative, uterus-sparing therapeutic approaches have been attempted or are not an option. All uterus-sparing therapeutic approaches share the risk of newly occurring leiomyomas and may require repeat interventions or hysterectomy due to complications of surgical or interventional treatment.