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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_3657_Библиотеки_им_академика_М_И_Перельмана.pdf
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- •Preface
- •Contents
- •Contributors
- •Endovascular Aneurysm Repair
- •Clinical Applications
- •Aortic Procedures Planning
- •Performance Assessment
- •Future Prospects
- •References
- •References
- •Introduction
- •Medical Error
- •Traditional Training
- •Animal Simulation Labs
- •Virtual Reality Simulation
- •3: Radiation Safety
- •Introduction
- •Basic Radiation Physics Units
- •Personnel Dose Limits
- •Pregnant Personnel
- •References
- •4: Tools of the Trade
- •Needles, Catheters, and Wires
- •Vascular Access
- •Double Wall
- •Single Wall
- •Advantages/Disadvantages
- •Nonvascular Needles (Table 4.1)
- •Guidewires
- •Curved
- •Straight/Angled
- •Stiffness
- •Flexibility
- •Coating
- •Torqueability
- •Opacity
- •Catheters
- •Flush Catheters
- •Visceral Catheters
- •Multipurpose Catheters
- •Cerebral Catheters
- •Guiding Catheters
- •Microcatheters
- •Vascular Sheaths
- •Vessel Dilators
- •Accessories
- •Embolic Agents
- •Temporary Agents
- •Permanent Agents
- •Pushable Coils
- •Detachable Coils
- •Coiling Techniques (Fig. 4.48)
- •Vascular Plugs
- •Particulates
- •Liquid Embolics
- •Fogarty Balloons
- •Angioplasty Balloons
- •Drug-Coated Balloons
- •Vascular Stents
- •Balloon Expandable Stents
- •Self-Expandable Stents
- •Specialty Stents
- •References
- •Consults
- •Pre-procedure Evaluation
- •Consent
- •Code Status
- •Laboratory Testing
- •Antibiotic Prophylaxis
- •Anticoagulation
- •Antihypertensives
- •Contrast Allergy Prophylaxis
- •Procedure Plan
- •Post-procedure Management
- •Hospital Admission
- •Discharge
- •Follow-up Visits
- •IR Clinic
- •Conclusion
- •References
- •6: The IR Road Map: Vascular Anatomy Overview
- •Introduction
- •Imaging Modalities
- •Ultrasound
- •Computed Tomography
- •Magnetic Resonance Imaging
- •Cross-Sectional Anatomy
- •Chest
- •Segmental Lung Anatomy
- •Mediastinum
- •Pulmonary Arteries
- •Pulmonary Veins
- •Bronchial Arteries
- •Liver
- •Arterial Access
- •Double-Wall Technique
- •Common Femoral Artery Access
- •Kidneys
- •Ureters
- •Bladder
- •Uterus
- •References
- •Alternative Arterial Access Sites
- •Venous Access
- •Manual Compression
- •Closure Devices
- •Compression Devices
- •Topical Agents
- •Invasive Devices
- •References
- •9: Central Venous Access
- •Pathophysiology
- •Non-tunneled Central Catheters (NTCCs)
- •Tunneled Central Catheters (TCCs)
- •Implantable Ports
- •Peripherally Inserted Central Catheters (PICCs)
- •Clinical Indication
- •Conventional Therapy
- •Non-tunneled Central Catheters
- •Tunneled Central Catheters
- •Ports
- •PICCs
- •Interventional Therapy
- •Ports
- •PICCs
- •Pre-procedural Prep
- •History
- •Physical Exam
- •Imaging
- •Complex Venous Access
- •Post-procedural Management
- •Complications
- •Acute Complications
- •Long-Term Complications
- •Device Removal
- •Tunneled Catheter Removal
- •Port Removal
- •References
- •Pathophysiology
- •Clinical Indication
- •Conventional Therapy
- •Interventional Therapy
- •References
- •11: IVC Filters
- •Pathophysiology
- •Clinical Indication
- •Conventional Therapy
- •Interventional Therapy
- •IVC Filter Placement
- •VTE Prevention
- •Preprocedural Preparation
- •Complication
- •Access Site
- •Device-Related
- •Postprocedural Management
- •IVC Filter Retrieval
- •Advanced IVC Filter Retrieval Techniques
- •Conclusion
- •References
- •Pathophysiology
- •Arteriovenous Fistula
- •Arteriovenous Graft
- •Clinical Indication
- •Conventional Therapy
- •Interventional Therapy
- •AVG Angioplasty
- •AVF Angioplasty
- •References
- •13: Pelvic Congestion Syndrome
- •Pathophysiology
- •Clinical Indication
- •Conventional Therapy
- •References
- •14: Varicocele
- •Pathophysiology
- •Conventional Therapy
- •Interventional Therapy
- •References
- •15: Varicose Veins
- •Pathophysiology
- •Clinical Indication
- •Conventional Therapy
- •Interventional Therapy
- •References
- •16: Vascular Malformations
- •Pathophysiology
- •Hemangiomas
- •Vascular Malformations
- •Arteriovenous Malformations (High Flow)
- •Venous Malformations (Low Flow)
- •Lymphatic Malformations
- •Clinical Indication
- •Conventional Therapy
- •Interventional Therapy
- •High-Flow AVMs
- •Low-Flow Venous Malformations
- •Klippel-Trenaunay Syndrome
- •Lymphatic Malformations
- •References
- •Pathophysiology
- •Abdominal Aortic Aneurysm (AAA)
- •Thoracic Aortic Aneurysm (TAA)
- •Clinical Indication
- •Abdominal Aortic Aneurysm
- •Thoracic Aortic Aneurysm
- •Conventional Therapy
- •Abdominal Aortic Aneurysm
- •Thoracic Aortic Aneurysm
- •Interventional Therapy
- •Abdominal Aortic Aneurysm
- •Thoracic Aortic Aneurysm
- •Common Complications
- •Access
- •Contrast Nephropathy
- •Spinal Cord Ischemia
- •Postoperative Monitoring
- •References
- •18: Aortic Dissection
- •Pathophysiology
- •Clinical Indication
- •Conventional Therapy
- •Interventional Therapy
- •Preprocedure Work-Up
- •Post-procedural Management
- •References
- •19: Endoleak
- •Pathophysiology
- •Clinical Indication
- •Conventional Therapy
- •Interventional Therapy
- •Type II Endoleaks
- •Type III Endoleaks
- •Type IV Endoleaks
- •Type V Endoleaks
- •References
- •20: Traumatic Aortic Injury
- •Pathophysiology
- •Clinical Indication
- •Conventional Therapy
- •Interventional Therapy
- •Pre-procedural Prep
- •Pre-procedural Imaging
- •Post-procedural Management
- •Post-procedural Imaging
- •References
- •21: Bronchial Artery Embolization
- •Pathophysiology
- •Clinical Indication
- •Conventional Therapy
- •Interventional Therapy
- •Outcomes
- •References
- •Pathophysiology
- •Pulmonary Arteriovenous Malformation
- •Pulmonary Artery Pseudoaneurysm
- •Clinical Indication
- •Pulmonary Arteriovenous Malformation
- •Pulmonary Artery Pseudoaneurysm
- •Conventional Therapy
- •Pulmonary Arteriovenous Malformation
- •Pulmonary Artery Pseudoaneurysm
- •Interventional Therapy
- •Pulmonary Arteriovenous Malformation
- •Pulmonary Artery Pseudoaneurysm
- •References
- •23: Lymphatic Interventions
- •Pathophysiology
- •Clinical Indication
- •Conventional Therapy
- •Interventional Therapy
- •Pedal Lymphangiography (PL)
- •Intranodal Lymphangiography (IL)
- •Dynamic Contrast Enhanced MR Lymphangiography (DCMRL)
- •Thoracic Duct Embolization
- •Plastic Bronchitis
- •References
- •24: Mesenteric Ischemia
- •Pathophysiology
- •Acute Mesenteric Ischemia
- •Chronic Mesenteric Ischemia
- •Clinical Indication
- •Acute Mesenteric Ischemia
- •Arterial Occlusive Disease
- •Nonocclusive Mesenteric Ischemia (NOMI)
- •Portomesenteric Vein Thrombosis
- •Chronic Mesenteric Ischemia
- •Conventional Therapy
- •Acute Mesenteric Ischemia
- •Arterial Occlusive Disease
- •Nonocclusive Mesenteric Ischemia (NOMI)
- •Portomesenteric Vein Thrombosis
- •Chronic Mesenteric Ischemia
- •Interventional Therapy
- •Acute Mesenteric Ischemia
- •Chronic Mesenteric Ischemia
- •References
- •25: Visceral Aneurysms
- •Pathophysiology
- •Visceral Artery True Aneurysms (VATAs)
- •Visceral Artery Pseudoaneurysm (VAPA)
- •Clinical Indication
- •VATA
- •VAPA
- •Conventional Therapy
- •Interventional Therapy
- •Splenic Artery Aneurysms
- •Renal Artery Aneurysms
- •Hepatic Artery Aneurysms
- •Celiac Artery Aneurysms
- •Complications
- •Splenic Aneurysm
- •Renal Aneurysm
- •Hepatic Aneurysm
- •References
- •26: Renal Artery Stenosis
- •Pathophysiology
- •Clinical Indications
- •Conventional Therapy
- •Interventional Therapy
- •Post-procedural Care
- •Conclusion
- •References
- •27: GI Bleeding
- •Pathophysiology
- •Clinical Indication
- •Conventional Therapy
- •Interventional Therapy
- •Complications
- •References
- •28: Uterine Artery Embolization
- •Pathophysiology
- •Fibroids
- •Adenomyosis
- •Postpartum Hemorrhage
- •Clinical Indication
- •Conventional Therapy
- •Fibroids
- •Adenomyosis
- •Postpartum Hemorrhage
- •Interventional Therapy
- •Fibroids
- •Adenomyosis
- •Postpartum Hemorrhage
- •AV Fistula
- •References
- •29: Prostate Artery Embolization
- •Pathophysiology
- •Benign Prostatic Hyperplasia
- •Prostate Cancer/Hematuria
- •Clinical Indication
- •Conventional Therapy
- •Interventional Therapy
- •References
- •30: Aortoiliac Disease
- •Pathophysiology
- •Blue Toe Syndrome
- •Leriche Syndrome
- •Fibromuscular Dysplasia
- •Clinical Indication
- •Conventional Therapy
- •Interventional Therapy
- •Abdominal Aorta
- •Aortic Bifurcation
- •Common Iliac Artery
- •External Iliac Artery
- •Internal Iliac Artery
- •Blue Toe Syndrome
- •References
- •31: Infrainguinal Disease
- •Pathophysiology
- •Claudication (Rutherford Categories 1–3)
- •Critical Limb Ischemia: Rest Pain (Rutherford Category 4)
- •Critical Limb Ischemia: Skin Lesions (Rutherford Categories 5–6)
- •Acute Limb Ischemia
- •Clinical Indication
- •Conventional Therapy
- •Interventional Therapy
- •Percutaneous Transluminal Angioplasty
- •Stents
- •Acute Limb Ischemia
- •References
- •Pathophysiology
- •Spleen
- •Liver
- •Kidney
- •Clinical Indication
- •Spleen
- •Liver
- •Kidney
- •Conventional Therapy
- •Spleen
- •Liver
- •Kidney
- •Interventional Therapy
- •Spleen
- •Pre-procedure
- •Post-procedure
- •Liver
- •Pre-procedure
- •Post-procedure
- •Kidney
- •Pre-procedure
- •Post-procedure
- •References
- •Pathophysiology
- •Pelvic Fractures
- •Extremity Fractures
- •Clinical Indication
- •Conventional Therapy
- •Interventional Therapy
- •References
- •34: Transarterial Chemoembolization
- •Pathophysiology
- •Clinical Indications
- •Conventional Therapy
- •Medical Management
- •Surgical Management
- •Interventional Therapy
- •Post-procedure
- •References
- •35: Transarterial Radioembolization (TARE)
- •Introduction
- •Pathophysiology
- •Clinical Indication
- •Conventional Therapy
- •Interventional Therapy
- •Primary Liver Cancers
- •Hepatic Metastatic Disease
- •References
- •36: Liver Ablation
- •Pathophysiology
- •Liver Cancer
- •Liver Metastases
- •Liver Cysts
- •Clinical Indication
- •Conventional Therapy
- •Liver Cancer
- •Liver Metastases
- •Liver Cysts
- •Interventional Therapy
- •References
- •Pathophysiology
- •Lung Cancer
- •Renal Cell Carcinoma
- •Bone Lesions
- •Clinical Indication
- •Lung Cancer
- •Kidney Cancer
- •Bone Lesions
- •Conventional Therapy
- •Lung Cancer
- •Kidney Cancer
- •Bone Lesions
- •Interventional Therapy
- •Radiofrequency Ablation (RFA)
- •Microwave Ablation (MWA)
- •Cryoablation
- •Irreversible Electroporation (IRE)
- •Lung Cancer
- •Kidney Cancer
- •Bone Lesions
- •References
- •Pathophysiology
- •Conventional Therapy
- •Ascites
- •Varices
- •Interventional Therapy
- •References
- •Pathophysiology
- •Etiology
- •Clinical Indication
- •Conventional Therapy
- •Medical Management
- •Surgical Management
- •Interventional Therapy
- •Post-procedural Management
- •Complications
- •References
- •40: Biliary Drainage
- •Pathophysiology
- •Clinical Indication
- •Conventional Therapy
- •Interventional Therapy
- •Conclusion
- •References
- •41: Biopsy Techniques
- •Introduction
- •Clinical Indication
- •Interventional Therapy
- •Needle Selection
- •Biopsy Techniques
- •References
- •Introduction
- •Pathophysiology
- •Ascites
- •Clinical Indication
- •Ascites
- •Conventional Therapy
- •Ascites
- •Interventional Therapy
- •Ascites
- •References
- •43: Obstructive Uropathy
- •Pathophysiology
- •Clinical Indication
- •Conventional Therapy
- •Urolithiasis
- •Infection
- •Urothelial Carcinoma
- •Neurogenic Bladder
- •Interventional Therapy
- •References
- •Pathophysiology
- •Clinical Indications
- •Percutaneous Radiologic Gastrojejunostomy (PRGJ) Tube
- •Percutaneous Jejunostomy (PJ) Tube
- •Conventional Therapy
- •Interventional Therapy
- •Percutaneous Radiologic Gastrostomy (PRG)
- •Post-procedural Management
- •Percutaneous Radiologic Gastrojejunostomy (PRGJ)
- •Percutaneous Jejunostomy (PJ)
- •References
- •45: Stroke
- •Pathophysiology
- •Clinical Indication
- •Conventional Therapy
- •Interventional Therapy
- •Complications
- •Post-procedure Management
- •References
- •46: Cerebral Angiography: Aneurysms
- •Pathophysiology
- •Clinical Indication
- •Conventional Therapy
- •Interventional Therapy
- •Pre-procedural Preparation
- •Post-procedural Management
- •Complications
- •References

13 Pelvic Congestion Syndrome
165
Fig. 13.1 33-year-old female with vulvar varicosities and pelvic
heaviness following pregnancy. (a) Transvaginal ultrasound demonstrates multiple tubular structures (thin arrows) consistent with
ovarian varices. The ovary demonstrates multiple simple cysts
Fig. 13.2 Consecutive venography pictures demonstrate (a) a sheath
within the left renal vein (arrow head) with a catheter advanced through
a collateral vessel off of the left ovarian vein. Extensive collateral vessels are noted (thin arrows). (b) Filling of the distal ovarian vein col-
(curved blackarrow). Axial (b) and coronal (c) views through the
pelvis with IV contrast demonstrate extensive pelvic varicosities
(thin arrow). The uterus (thick arrow) and rectum (arrowhead) are
also visualized
laterals (thin arrow) result in rapid shunting of contrast into the dilated
left internal iliac vein (thick arrow). (c) Extensive cross-pelvic collateral vessels (thin arrow) can be seen

166
NSAIDs
N. A. Keefe and A. Roberts
Fig. 13.3 Chronic pelvic
pain treatment algorithm
Pelvic Congestion
Syndrome
Other pelvic pathology
(endometriosis, etc)
MSK, GI, GU pathology
Chronic Pelvic Pain
can have ovarian varices, and therefore it is important to exclude
other pathologies as the cause of the patients’ pain (Fig.13.3)
[7]. Chronic unremitting undiagnosed pain such as that caused
by PCS can often lead to depression. Frequently, these patients
can experience incomplete relief of their symptoms if there are
several pathologic causes to their pain. When venous incompetence is the sole contributing factor of their symptoms however,
patients can do extremely well following treatment.
Key Point
Ovarian and internal iliac venography is the gold standard
for PCS diagnosis.
Medical
Management
Psychotherapy
Surgical Management
Interventional
Management
Medoxyprogesterone
Goserelin
Ovarian vein ligation
Hysterectomy and
bilateral oopherectomy
Endovascular
embolization
neal resection of the left gonadal vein which demonstrated
improvement or resolution of symptoms of 73% of patients
[19]. With advances in technology, laparoscopic transperitoneal ovarian vein ligation became the mainstay therapy in the
late 1990s. A study of 23 patients demonstrated complete
resolution of patients’ symptoms at 1-year follow-up [20].
Although potentially useful, the procedure is not without its
drawbacks. Serious complications include DVT, retroperitoneal hematoma, ileus, and bowel obstruction secondary to
adhesions. With the development of interventional transcatheter therapies, this surgical technique has largely been supplanted. In difcult-to-treat patients and patients with
recurrent disease, hysterectomy and bilateral oophorectomy
are still employed by some gynecologists, but they are less
common than previously [21].
Conventional Therapy
Historically, pelvic congestion syndrome was treated with
hysterectomy and commonly oophorectomy. However, there
are nonsurgical options which may be tried prior to performing an invasive procedure. The goal of medical therapy is to
suppress ovarian function or cause vasoconstriction of the
dilated veins. Medroxyprogesterone acetate and the GnRH
analogue goserelin have both been used for the treatment of
PCS.Both of these drugs demonstrated mild relief of symptoms with short- term results. When combined with psychotherapy, the effects seemed to last longer [18]. This further
demonstrates the link between psychological and somatic
symptoms of PCS.Side effects of progestins include weight
gain and bloating, while side effects of GnRH analogues
include depression, night sweats, and vaginal dryness. Given
the limited efcaciousness and side effect prole, medical
therapy is not indicated for long-term use.
Surgical treatment for PCS directly addressing the
gonadal veins was rst described in 1984 with extraperito-
Interventional Therapy
Transcatheter embolotherapy of incompetent ovarian veins
was rst performed in 1993 by Edwards on a single patient
who experienced prolonged symptomatic relief of symptoms
[22]. Since that time, the technique has become widely available and now is the mainstay for treatment for pelvic congestion syndrome. Numerous studies have demonstrated varying
success rates for the reduction of pelvic pain ranging from
47% to 98% [11, 23–25]. Of note, patients with isolated
ovarian vein reux had improved outcomes compared to
patients with isolated iliac vein reux or combined disease
[11]. No large studies have been performed to date on outcomes of patients with vulvar and lower extremity varicosities after pelvic embolotherapy. Several small studies
reported a more than 80% reduction in vulvar varicosities
with limited improvement of lower extremity varicosities
after treatment [5]. Ovarian vein embolization is a relatively
straightforward outpatient procedure.

13 Pelvic Congestion Syndrome
167
Key Point
Contraindication to embolization
• Active infection
• Contrast allergy
• Severe coagulopathy
Once a patient has decided to seek treatment for PCS, preoperative imaging with a venous phased MRI or CT (MRV or
CTV, respectively) may be performed. This can both determine the extent of varicosities as well as assist with procedural
planning. If the patient’s symptoms are very consistent with
pelvic congestion syndrome, and she has not had previous
cross-sectional images, then some interventional radiologists
will proceed directly to venography and embolization. If there
is a question as to the diagnosis, then cross-sectional imaging
may be helpful, although it is important to recognize that less
severe reux could be missed since the patient will be supine.
The How To
1. Venous access is gained through the femoral,
jugular, or arm vein approach.
2. An optional venogram of the IVC can be per-
keep the sclerosing agent from crossing the crosspelvic collaterals and moving into systemic circulation through the contralateral ovarian vein.
6. In order to perform the balloon occlusion technique,
a balloon is advanced into the distal ovarian vein.
A microcatheter is advanced distal to the balloon.
up around the ipsilateral ovarian or iliac vein.
7. Sclerosing agent is injected into the pelvic veins
until near occlusion. Completion of embolization
can be demonstrated by increased resistance to
further injection of contrast which can be seen as
8. Embolization coils or plugs are used to embolize
The microcatheter and balloon are then retracted
halfway in the ovarian vein, and the procedure is
repeated with both deployment of SDS and coils.
This is typically repeated three times in one ovarian vein before moving to the contralateral side
13.4c).
9. Alternatively, one can advance a catheter into the
distal ovarian vein, and inject contrast, measuring
internal iliac, and then use an amount of sclerosant
venography should be performed with the patient
in a reverse Trendelenburg position. A cavogram
and usually demonstrate the position of the renal
3. Catheterization of the left renal vein with an
injection near the renal hilum to seek spontaneous
catheter is then advanced into the left ovarian
vein. Injection of contrast will demonstrate a
vasculature.
4. The catheter is advanced down the ovarian vein
terminating just above the pelvic brim. Injection of
rial into the pelvic veins, cross-pelvic collaterals,
and any varices
13.4a ).
5. Embolotherapy varies based on user preferences
including glue, coils, sclerosing agents and
Gelfoam, or a combination of various embolics
[26]; frequently, a sclerosing agent such as sodium
tetradecyl sulfate (Sotradecol, SDS) is used, fol-
13.4b). In order to use a scle-
rosing agent, the accessed vein may be occluded
using a balloon occlusion technique. This can help
collaterals. Another method is to mix the Sotradecol
with Gelfoam and air to make a foam slurry and
inject this mixture. The Gelfoam helps to hold the
Sotradecol into the veins perhaps increasing the
contact with the vein wall. Then coil embolization
can be performed through the catheter, which
allows the use of larger .035 inch coils.
10. There remains debate as to the optimal technique
for ovarian vein embolization; however a combination of coils and sclerosis has been demonstrated as
studies. The decision to treat one or both ovarian
-
-
-
eral embolization, whereas a patient with unilateral
dilatation and only moderate varicosities may only
need unilateral embolization.
11. If the internal iliac veins demonstrate evidence of
coils, or a combination. Some interventionalists
treated at the same session as the ovarian vein(s)
treatment, and other interventionalists feel that the
then perform another procedure with embolization
if the patient continues to have symptoms.

168
N. A. Keefe and A. Roberts
Fig. 13.4 (a) Due to the rapid internal iliac vein shunting and exten-
sive cross-pelvic collaterals, the decision was made to obtain bilateral
femoral vein access and inate a balloon in bilateral internal iliac veins.
Contrast injection demonstrates decreased shunting (thin arrow)compared to Fig13.1 without balloon occlusion. A Foley catheter (curved
arrow) can be seen with a small volume of contrast within the bladder.
Complications of embolotherapy are thankfully rare but do
occur. The major complication is migration of coils into the
pulmonary arteries, reported in 2% of patients following internal iliac vein embolization [27]. Migration can also occur from
coils deployed in the gonadal vein. This risk is increased in
vessels >12mm. Some people advocate for the use of detachable coils to mitigate this risk. Detachable coils are coils that
can be deployed but remain attached to the deployment device.
If the coil is felt not to be in satisfactory positioning, it can be
retracted and redeployed; once it is in appropriate positioning,
it can be detached from the deployment device. To prevent coil
migration, the diameter of the coil used should be 30–50%
larger than the diameter of the internal iliac vein or the gonadal
vein [27]. Another complication includes perforation of the
ovarian vein; this is not a serious problem since the vein is
being embolized and perforation does not cause signicant
extravasation. Some patients can experience ank pain, thrombophlebitis, postprocedural fevers, and puncture site hematomas also [25]. Recurrence is rare but has been reported in the
literature [28]. When nutcracker syndrome is presentconcurrently, it may be necessary to relieve compression of the left
renal vein as well to assure durable relief of PCS symptoms.
Key Point
Complications of ovarian vein embolization
• Nontarget embolization
• Coil migration
• Vessel perforation
(b) Gelfoam embolization followed by coiling was performed in the
distal left ovarian vein. This was then performed subsequently in a retrograde fashion up the ovarian vein. The same procedure was performed on the contralateral side. (c) Following completion of
embolization, venography with the balloons deated demonstrates no
contrast lling the ovarian veins
Chronic pelvic pain can be a diagnostic challenge for
practitioner and patient alike. In those patients with signs and
symptoms of pelvic congestion syndrome, embolization can
provide a minimally invasive means of relieving pain and
improving quality of life.
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Varicocele
SiobhanE.Alexander andAndreUacker
Pathophysiology
Male varicocele is dened as dilation of the pampiniform
plexus, a network of normally tiny veins within the spermatic cord. Increased venous pressure is caused by incompetent gonadal venous valves or obstruction of venous return
within the gonadal vein more centrally [1]. Varicoceles are
relatively common, occurring in approximately 15% of
young, healthy males, and have a natural predilection for the
left side in 75–90% of patients [2–4]. The left gonadal vein
is longer and inserts into the left renal vein, unlike the right
gonadal vein, which inserts directly into the IVC.The resulting increased hydrostatic pressure in the left gonadal vein
creates a favorable environment for formation of varicoceles
[5]. Varicoceles occur bilaterally in up to 30–80% of cases
[6]. Isolated right-sided varicoceles warrant further work-up
as they may be the only sign of retroperitoneal pathology.
Evaluation with cross-sectional imaging should be performed to exclude a potential neoplasm [7].
Key Point
The left gonadal vein inserts into the left renal vein.
The right gonadal vein inserts directly into the IVC.
Key Point
Varicoceles are most common unilaterally on the left
or bilaterally. An isolated right-sided varicocele warrants further work-up for retroperitoneal pathology.
S. E. Alexander · A. Uacker (*)
University of Virginia Health System, Department of Radiology
and Medical Imaging, Charlottesville, VA, USA
e-mail: sea9w@hscmail.mcc.virginia.edu; au2b@virginia.edu
14
Varicoceles are present in 35% of primary infertility cases
and in 80% of secondary infertility cases. Fortunately, they
are the most common correctable cause of male infertility [4].
It is hypothesized that the pooling of blood within the pampiniform plexus raises scrotal temperature and negatively
affects spermatogenesis resulting in decreased sperm counts,
sperm deformity, and decreased motility [8].Varicoceles are
associated with ipsilateral testicular atrophy, and early intervention can arrest that atrophy [8]. Nonsurgical and surgical
treatment of varicoceles has been proven to arrest the decline
of testicular function and improve the serum testosterone,
sperm concentration, and sperm quality [4, 9].
Most varicoceles are asymptomatic; however, orchialgia,
or testicular pain, is present in up to 10% of males with varicoceles [10]. Orchialgia is most often described as a dull,
throbbing pain worsened by straining or prolonged standing
[2]. Chronic orchialgia, dened as testicular pain for at least
3months, is a rare presentation of varicoceles and is present
in only 2–10% of males with varicocele [11, 12].
Varicocele is diagnosed clinically on physical exam and
classically presents as a painless “bag of worms” upon palpation of the scrotum (Fig.14.1). The Valsalva maneuver is
performed with the patient in the upright position to increase
distal venous pressure and accentuate the size of the varicocele. The size of the varicocele decreases in the supine position due to a decrease in the venous system hydrostatic
pressure [5]. Grading of a varicocele is done on physical
exam using the Dubin-Amelar grading system (Table14.1).
Evaluation of testicular atrophy is an essential part of the
physical examination. In some scenarios, such as pediatric
varicocele, clinically occult varicocele, or male infertility,
scrotal ultrasonography is the imaging modality of choice
for varicocele diagnosis and further evaluation of the testes.
Color-ow or Doppler imaging enables the clinician to conrm the diagnosis by visualizing venous dilation and reux
of blood into the pampiniform plexus, assess the size of the
varicocele, and evaluate testicular blood ow [13].
Ultrasound ndings to support a diagnosis of varicocele
include visualizing the pampiniform plexus as multiple
© Springer International Publishing AG, part of Springer Nature 2018
N. A. Keefe et al. (eds.), IR Playbook, https://doi.org/10.1007/978-3-319-71300-7_14
171

172
Epididymis
look and feel like a “bag of worms”.
obstruction.
Penis
Spermatic cord
a. pampiniform plexus
b. arteries
c. nerves
d. lymphatics
e. vas deferens
f. tunica vaginalis
Scrotum
S. E. Alexander and A. Uacker
Varicocele
Testes
On physcial exam, a varicocele can
Fig. 14.1 Varicocele
Table 14.1 The Dubin-Amelar grading system for varicocele
Grade Physical exam nding
0 Non-palpable
1 Palpable with Valsalva only
2 Palpable at rest
3 Visible and palpable at rest
anechoic dilated tubular structures superolateral to the testis
measuring greater than 2mm in diameter [13] (Fig.14.2).
Varicoceles that are non-palpable on physical exam and
show no evidence of reduced testicular function or abnormal
sperm parameters can be treated conservatively and should be
offered regular clinical follow-up [14]. In adult males with
clinically palpable varicoceles but otherwise asymptomatic,
semen parameters can be obtained. If normal counts and
motility, then 1- to 2-year follow-up is recommended to monitor for the development of symptoms, testicular atrophy, or
semen dysfunction [14, 15]. In males with unilateral or bilateral varicoceles without evidence of decreased testicular size,
annual clinical evaluation of semen analysis or testicular size
should be performed to assess for early dysfunctional spermatogenesis. Invasive varicocele treatment can be considered
in males with clinical varicocele and reduced testicular size or
evidence of semen dysfunction (Table14.2) [14].
Key Point
Varicocele treatment is indicated for males with clinical
symptoms + testicular atrophy or semen dysfunction.
A varicocele is a dilation of the
pampiniform plexus due to
incompetent valves or venous
Conventional Therapy
There is no effective pharmacologic treatment; all available
treatment options are surgical or image-guided [16].
Varicocele treatment was rst described in the 1900s via an
open surgical approach with removal of the pampiniform
plexus. This approach has fallen out of favor due to the high
risk of injury to the testicular artery [3]. The most common
surgical approaches include open or laparoscopic spermatic
vein ligation (the Palomo technique), inguinal varicocele
ligation (the Ivanissevich technique), or microscopic inguinal or subinguinal varicocele ligation [7].
The Palomo technique involves high ligation of the testicular vein (and possibly the artery and lymphatics) above
the internal inguinal ring. Some benets to this technique
include technical ease and reduced risk of injury to important vascular structures. However, this approach has high
recurrence rates due to the formation of distal collateral
vessels [7]. The Ivanissevich technique, or inguinal
approach, ligates the cremasteric and gonadal veins within
the inguinal canal. This approach allows for better access
for collateral vessel ligation but has increased risk of arterial
and lymphatic injury without the use of a microscope.
Introduction of an operating microscope for dissection of
the inguinal canal signicantly reduces the risk of varicocele recurrence and the development of a hydrocele [17].
The subinguinal approach has been shown to reduce postoperative pain as it avoids incision of the external oblique
aponeurosis.

14 Var ic oc ele
173
Fig. 14.2 Left-sided varicocele in a 31year-old male. (a) Grayscale
ultrasound image of the right scrotum showing a normal testis (white
arrow) and normal size of a pampiniform plexus vein (cursors) in the
transverse view. (b) Transverse view of the left scrotum shows multiple
dilated veins of the pampiniform plexus, all measuring greater than
Table 14.2 Clinical indications for varicocele embolization according
to the 2014 committee of the American society for reproductive medicine and society for male reproduction and urology
Patient population Symptoms
Male partner of an
infertile couple
Adult male Palpable varicocele
Adolescent male Unilateral or bilateral varicocele
Palpable varicocele on exam
Abnormal semen parameters
Female partner has normal fertility or a
treatable cause of infertility
Abnormal semen analysis
Desire for future fertility
Associated testicular pain
Reduced testicular size
2 mm in diameter (cursors), surrounding the normal testis (white
arrow). The normal epididymis is also seen in this image (black arrow).
(c) Doppler ow conrms that the dilated veins are patent and increase
in size with Valsalva (image right)
Surgical varicocele ligation is currently more common but
not superior to percutaneous treatment in many clinical scenarios (i.e., painful varicocele without infertility or testicular
atrophy) [18, 19]. Research has shown similar rates of success when comparing surgical and percutaneous techniques
in clinical outcome for men with infertility [20, 21]. A retrospective study performed by Shlansky-Goldberg showed a
similar increase in semen parameters after surgical intervention (34%) versus percutaneous intervention (39%) [22].
Some of the benets of minimally invasive percutaneous
interventions include the elimination of large surgical incisions resulting in less pain for the patient, moderate conscious
sedation anesthesia instead of general anesthesia, shortened

174
hospitalization, and decreased risk of unintentional injury to
the testicular artery or lymphatic system that would be possible during traditional surgical approaches [17].
Interventional Therapy
One of the rst successful attempts at percutaneous therapeutic intervention for varicocele occurred in 1978 with the
injection of hypertonic glucose and a sclerosant into the left
gonadal vein via the transfemoral approach [23, 24]. Since
then, embolization techniques have evolved considerably
with the introduction of the microcatheter, improved sclerosing agents, micro-coils, and vascular plugs. The most
commonly used embolic agents in treatment of varicoceles
include coils and sclerosants, although Gelfoam and cyanoacrylate are used as well [25]. The mechanism of gonadal
vein thrombosis with coils is a mechanical reduction in
ow, with platelet aggregation on the coils, which often
contain thrombogenic bers [26]. Liquid sclerosant embolic
agents cause vessel occlusion by inducing a thrombogenic
and inammatory reaction and endothelial damage.
Cyanoacrylate glue precipitates into a solid when in contact
with ionic solutions and thus lls the vessel lumen inducing
thrombosis. In general, coils are easier to control than liquid
embolics, which require more operator experience to administer safely and effectively.
The How To
Laboratory work-up is not necessary in the young,
healthy adult male. When appropriate, typical labs
obtained include a CBC, PT, PTT, and creatinine. After
appropriate pre-procedural assessment, the three key
components of interventional management of varicoceles are obtaining venous access, renal, and then
gonadal catheterization, venography, and embolization.
S. E. Alexander and A. Uacker
is then carried out from the inguinal ring proximally, typically with coils and sclerosants, with
14.5).
4.
the gonadal vein with the renal vein, to prevent
14.6).
5. Occlusion of collateral veins should also be performed. Embolization technique for right-sided
varicocele is the same as for left varicocele up to the
15].
6.
room prior to discharge home. Patients should not
the procedure.
A small percentage (~10%) of patients may have back
pain or testicular swelling and pain after the procedure. This
may be a sign of pampiniform plexus thrombophlebitis. This
is usually self-limiting and can be treated with nonsteroidal
anti-inammatory drugs (NSAIDs) and limited activity until
symptoms resolve. Patients should have a 3-month follow-up
ultrasound to evaluate for treatment response and evidence
of recanalization.
The risks associated with the use of coils include vessel
perforation, coil migration to the heart or pulmonary arteries,
and gonadal vein recanalization. The risks associated with liquid embolics include too distal occlusion causing testicular
venous infarcts, nontarget embolization through reux, and
vessel rupture due to pressurization during injection.
1. Access is usually obtained through the right internal jugular or common femoral veins using the
Seldinger technique.
2. The venogram is performed through a 4F or 5F
catheter, positioned in the left renal vein, during
Valsalva, with a hand injection of contrast. Reverse
Trendelenburg positioning is also helpful to demon-
14.3).
3. The gonadal vein is then catheterized and another
14.4). This venogram
varicocele at risk for recanalization. Embolization
Fig. 14.3 Venogram shows an endovascular sheath within the left
renal vein. Contrast material is injected through the sheath into the renal
vein and is seen reuxing into the left gonadal vein (black arrow) and
antegrade ow to the IVC (thick white arrow)

14 Var ic oc ele
175
Fig. 14.4 Contrast injection in the left gonadal vein (white arrows)
shows a dilated pampiniform plexus within the scrotum (black arrow).
In most cases, direct uoroscopy over the testes can be avoided
Fig. 14.5 Embolization treatment of varicocele. Embolization coils
extend from internal ring(white line) of the inguinal canal up near the
left renal vein
Fig. 14.6 Venogram taken after gonadal vein coil embolization with
the sheath still in the origin of the gonadal vein demonstrates no lling
of the gonadal vein (black arrow) and reux into the renal vein. No
further collateral vessels are identied
Key Point
Procedural complications:
• Vessel perforation
• Coil migration
• Nontarget embolization
• Gonadal vein recanalization
• Pampiniform plexus thrombophlebitis
References
1. Iaccarino V, Venetucci P.Interventional radiology of male varicocele:
current status. Cardiovasc Intervent Radiol. 2012;35(6):1263–80.
2. Muthuveloe DW, During V, Ashdown D, Rukin NJ, Jones RG, Patel
P.The effectiveness of varicocele embolisation for the treatment of
varicocele related orchalgia. Spring. 2015;4:392.
3. Choi WS, Kim SW. Current issues in varicocele management: a
review. World JMens Health. 2013;31(1):12–20.
4. Halpern J, Mittal S, Pereira K, Bhatia S, Ramasamy R.Percutaneous
embolization of varicocele: technique, indications, relative contraindications, and complications. Asian JAndrol. 2016;18(2):234–8.
5. Kwak N, Siegel D.Imaging and interventional therapy for varicoceles. Curr Urol Rep. 2014;15(4):399.
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