- •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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J. Lopes Dias and T.M. Cunha |
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The risk of an acute reaction to a gadolinium-based contrast agent is low when compared to iodine-based contrast agents. However, similar cautions should be taken. Risk patients are those with a history of previous acute reaction to gadolinium-based contrast agent, asthma, and allergy requiring medical treatment. Unlike iodine-based contrast agents, the risk of reaction to gadoliniumbased contrast agents is not related to osmolality (Beckett et al. 2015).
Nephrogenic systemic fibrosis (NSF) is recognized as a very late reaction to gadoliniumbased contrast media since 2006. It usually starts with pain, pruritus, swelling, and erythema in the legs, and progresses to thickening of the skin and subcutaneous tissues, as well as to fibrosis of internal organs and respiratory muscles, which may lead to variable consequences ranging from contractures to cachexia and death. The severity of the disease implies the prompt recognition of high-risk patients, which are those with chronic kidney disease (CKD) 4 and 5 (GFR <30 mL/ min), including patients on dialysis, and those with acute kidney insufficiency. Gadoliniumbased contrast agents with higher risk of NSF are gadodiamide (DTPA-BMA), gadopentetate dimeglumine (DTPA), and gadoversetamide (DTPA-BMEA). These high-risk agents should never be given in higher doses than 0.1 mmol/kg and are contraindicated in patients with stage 4 and 5 CKDM, including those on dialysis, in patients with acute renal insufficiency, in pregnant women, and in neonates (Beckett et al. 2015; Thomsen et al. 2013, 2016; Mathur and Weinreb 2016).
Low-risk gadolinium contrast agents may be used in pregnancy when there is a strong need and no neonatal tests are necessary. Lactating women are frequently object of concern. If the above-mentioned high-risk agents are used, breastfeeding should be stopped for 24 h (Beckett et al. 2015; Thomsen et al. 2013, 2016; Mathur and Weinreb 2016).
3\ CT Technique
3.1\ Introduction
The advent of helical scanning movement and multislice data collection gave rise to a new era of fast and high-resolution acquisitions.
Modern CT scans show substantial improvement on volume coverage, scan speed, as well as a more efficient use of X-ray tubes. Helical CT scans allow near-isotropic acquisitions, thus enabling high-resolution multiplanar reconstructions (MPR) and volume rendering. Moreover, the detector size decreased and multiple arrays were incorporated inside. Therefore, several slices can be recorded simultaneously, shortening the exposure time; thus thinner slices can be obtained and partial volume artifacts can be decreased.
The high speed of current CT scanners allows a complete thoracic, abdominal, and pelvic examination in only one breath-hold. A CT pelvic acquisition is rarely performed alone. The scan is usually extended to the upper abdomen not only for staging and for the follow-up of malignant diseases but also when characterization of vascular, inflammatory, or infectious entities is needed.
By shortening the scan time, motion artifacts are also reduced and distinct phases of enhancement may be accurately obtained after intravenous contrast administration. Overall, multidetector CT (MDCT) scans yield high spatial, temporal, and contrast resolution, thus increasing diagnostic accuracy. MDCT has rapidly evolved from 4-detector row systems to 256-slice and 320-detec- tor row CT systems. Currently, most centers use scanners with at least 8- to 16-detector rows. Submillimeter or millimeter volumetric acquisitions with subsequent reconstruction into 2–5 mm thick axial, sagittal, and coronal images is a suitable protocol for routine CT scans (Thomsen et al. 2016; Rydberg et al. 2000; Goldman 2007; Yitta et al. 2009) (Fig. 2). Table 2 resumes a suitable general protocol for gynecological CT scans.
MR and CT Techniques |
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a |
b |
c
Fig. 2 Examples of different orientations on CT in three distinct patients. Axial image, after oral and intravenous contrast administration, depicting anterior peritoneal carcinomatosis (arrow) in a patient with endometrial carcinoma (a). Sagittal image, after oral contrast administration (intra-
venous contrast was contraindicated), showing ascites and huge solid peritoneal implants (arrow) in a patient with ovarian carcinoma (b). Coronal image, after intravenous contrast administration, identifying an acute appendicitis (arrow) in a young patient during early puerperium (c)
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J. Lopes Dias and T.M. Cunha |
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Table 2 Suitable general protocol for gynecological CT at a 64-detector scanner
• 4–6 h of fasting
• Administration of a fast-acting laxative enema to clean the bowel, one on the day before the exam and another during the morning of the exam (optional)
• Water or iodine-based oral contrast: 1000–
1500 mL of contrast medium administered in separate doses 45 to 60 min prior to the examination
• Water or iodine-based rectal contrast: catheter and enema bag; 200 mL to the rectosigmoid and 900–1200 mL to the entire colon
• Supine and “foot-first” positions
• Range from diaphragm to pubic bone
• Inspiration
• Scout image: 120 kV, 10–50 mA
• Final acquisition: (20 kV, 100–200 mAs)
• Sub-mm or mm volumetric acquisitions with subsequent reconstruction into 2 to 5 mm thick axial, sagittal and coronal images
• Correction of hip prosthesis artifacts if need: filtered back projection, adaptive filtering or iterative algorithms
• Intravenous iodine-based contrast: 100–150 mL at 3–4 mL/s
• Scan delay
– 70–100 s (covering all range)
– 3–5 min (if pelvic vein thrombosis is suspected)
– 5–10 min (if bladder and ureteral opacification is needed)
3.2\ Technical Disadvantages
Among the main disadvantages of CT, there are two with great relevance in daily practice: ionizing radiation exposure and metallic artifacts. Despite the kind of CT scan, radiation reduction and protection should always be considered. Both technicians and radiologists should be familiarized with some technical features including the tube current, X-ray beam collimation, and pitch, and cautiously select both the number and length of scan sequences. Dose quantification parameters like volume CT dose index (CTDlvol) and dose-length product (DLP) are usually displayed in current CT scans and should be routinely checked. Hip prosthesis causes substantial artifacts due to photon starvation and beam hardening, consequently hampering not only the joint and the surrounding muscles, but also pelvic organs. Methods may be used to reduce these
artifacts: filtered back projection (FBP), which uses information from areas adjacent to regions affected by metal artifacts and replaces the metal- corrupted raw data by the interpolated values; adaptive filtering, which corrects the excessive noise produced by the photon starvation effect; or iterative algorithms, which use a combination of different metal artifact reduction algorithms and algebraic reconstruction techniques (Morsbach et al. 2013). Iterative reconstruction techniques also enable performing reduced-dose CT examinations (due to either tube current or tube potential lowering) without altering image quality (Padole et al. 2014).
3.3\ Patient Preparation
and Positioning
Before a CT scan, an inquiry about the patient medical history, routine medication, and potential contraindications is mandatory. Pregnancy is not a formal contraindication to CT; however, it should be avoided mainly during the first trimester. Patient preparation for CT scans is mainly related to contrast material administration (see next sections). Due to the need of intravenous contrast, patients are optimally asked to fast at least for 4 h. Administrating a fast-acting laxative enema to clean the bowel may also be recommended.
Patients are usually scanned in supine and “foot-first” positions, with their arms raised above their heads. Claustrophobic patients tolerate lying with the head outside the gantry better. Moreover, these positions allow for a face- to-face communication with the patient and facilitate the access to the patient whenever the examination has to be interrupted. “Foot-first” positioning also eases the connection of contrast medium tubes, which can be done immediately after inserting the venous access.
3.4\ Oral and Rectal Contrast
Oral and rectal contrast media are frequently used in abdominal and pelvic CT imaging. Classically, it is given in cases of suspected bowel perforation or of anastomosis leakage. However, opacification
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of the digestive tract is also helpful for distinguishing collapsed loops from lymph nodes, peritoneal implants, pelvic masses, and fluid collections.
Water as negative or positive iodinated solutions may be used for bowel opacification. In female pelvis imaging, positive contrast is particularly useful for staging and follow-up of ovarian and endometrial cancer. Iodinated solutions are preferable over barium suspensions due to its moderate effect on peristalsis and easier distribution along the digestive tract. Contrarily, barium suspensions are more prone to flocculate and may give rise to streak artifacts that hamper wall evaluation. Both types of contrast are usually safe, with only rare cases of mild diarrhea being reported. However, if bowel perforation is suspected, only iodinated solution should be administered due to the higher peritoneal toxicity of barium-based contrast media. As 1–2% of oral contrast is absorbed through the gut patients who had previous moderate to severe IV contrast allergy should be managed carefully.
Protocols for oral contrast vary according to the center. Typically, 1000–1500 mL of contrast medium is ingested in separate doses 45–60 min prior to the examination. Some authors advocate the administration of 20 mg metoclopramide at the beginning of the ingestion, in order to shorten patient preparation.
Rectal contrast is administered when the patient lies on the scanning table by using a catheter and an enema bag. 200 mL of contrast usually opacifies the rectum and the sigmoid colon adequately, whereas the entire colon may require 900– 1200 mL of contrast. Sometimes, anal diseases like hemorrhoids and fissures hamper the introduction of the rectal tube due to pain. Special care should also be taken in patients with anal and lower third rectal carcinoma due to the risk of ulceration or perforation (Beckett et al. 2015).
3.5\ Intravenous Iodine-Based
Contrast Media
Intravenous iodine-based contrast media are usually given as a rapid bolus via an IV cannula, by using a pump injector. A suitable protocol for abdominal and pelvic CT scan is to administer 100–150 mL of 350 mg iodine contrast media at
3–4 mL/s. As the time to contrast material arrival and peak enhancement are affected by the choice of intravenous access sites, particularly when forearm or hand veins are used, lower flow rates are desirable (Bae 2010).
A suitable routine gynecological CT scan includes the upper abdomen and is acquired 70–100 s after contrast injection. Liver metastases from gynecological malignancies are typically hypovascular, so an arterial phase is usually unnecessary. Delayed images are recommended whenever pelvic vein thrombosis is suspected (3–5 min) or bladder and ureteral opacification is needed (5–10 min).
In order to reduce the risk of an acute reaction to iodine-based contrast media, some procedures should be taken according to the European Society of Urogenital Radiology (ESUR) guidelines: a nonionic contrast medium should be used; the patient should be kept in the Radiology Department for 30 min after the injection; and drugs and equipment for resuscitation have to be readily available. For patients at increased risk of reaction (history of previous moderate or severe acute reaction to an iodine-based contrast agent, asthma, and allergy requiring medical treatment), an alternative imaging tool not requiring an iodine-based contrast agent should be considered. The use of premedication for allergy prevention is widely accepted, despite its underlying limited clinical evidence. The ESUR guidelines recommend oral administration of prednisolone 30 mg (or methylprednisolone 32 mg), 12 and 2 h before contrast medium administration (Thomsen et al. 2016).
There is usually some concern regarding thyrotoxicosis, a potential very late reaction to iodine-based contrast media that usually occurs more than 1 week after injection. As a general rule, iodinated contrast media should not be given to patients with manifest hyperthyroidism. Patients at risk—those with untreated Graves’ disease, or multinodular goiter and thyroid autonomy, especially if they are elderly and/or live in areas of dietary iodine deficiency—should be strictly monitored by endocrinologists after injection (Van der Molen et al. 2004).
Pregnancy and lactation are also usual sources of concern for both clinicians and radiologists.