41 Omar M. Aboumarzouk1,2, Bryan Jenkins3, and Piotr L. Chlosta4 1 Glasgow Urological Research Unit, Department of Urology, Queen Elizabeth University Hospital, Glasgow, UK 2 University of Glasgow, School of Medicine, Dentistry & Nursing, Glasgow, UK 3 Department of Urology, University Hospital of Wales, Cardiff, UK 4 Academic Urology Unit of Collegium Medicum, Jagiellonski University, Krakow, Poland The seminal vesicles are about 5 cm long and hold 1–10 ml of fluid. Their secretions comprise 80% of the seminal fluid and all of the fructose content. Joining the vas deferens at the ejaculatory duct, their muscular tubes contract during ejaculation to release the alkaline seminal fluid. Similar to the rest of the body, the seminal vesicles may be afflicted by congenital anomalies, infections, and cancers. Vasectomy is one of the most common procedures for urology. Thorough counselling is essential before each procedure to warn patients of its potential risks and irreversibility. Only when azoospermia is achieved can the procedure be deemed successful. Vasectomy reversals are possible; however, the chance of pregnancy might be low, necessitating sperm retrieval methods and in vitro fertilisation. Keywords seminal vesicles; semen analysis; vasectomy; infertility; scrotal pain; vasectomy reversal For many years, the seminal vesicles were something of an enigma to urologists. With the advent of transrectal ultrasound, we have come to appreciate that they may suffer all the disorders that affect all other hollow organs in the body. Hippocrates noted a paired structure resembling a honeycomb on either side of the base of the bladder. Bold early investigators like Fallopius, de Graaf, and John Hunter all found that their secretions tasted sweet. But their function remained a mystery. The seminal vesicle arises in the third month of foetal life as a diverticulum from the vas deferens (mesonephric ducts) just before it joins the ejaculatory duct. Surrounding mesenchyme clothes it with a muscular coat. It remains small until puberty, when it swells and becomes convoluted. Blood supply is via the inferior vesical artery and vein and can also receive branches from the superior vesical artery through its umbilical artery branch. Lymphatics follow the blood supply to the internal iliac nodes. The hypogastric nerve via the pelvic plexus supplies the seminal vesicles. The seminal vesicles lie in the groove between bladder and prostate, inferior to the ampullae of the vasa efferentia. The ureter passes inferior to the vas deferens en route to the bladder. In adult life, the vesicle holds from 1.5 to 10 ml of fluid. When unravelled, each vesicle consists of a sac about 15 cm long, with one or two side arms. After the age of 40, its mucosa becomes thinner and flatter, decreasing in size. The wall, has an external connective tissue layer, a middle bilayered alpha‐adrenergic smooth muscle layer (i.e. external longitudinal and internal circular), and an internal mucosal layer. Stimulation of the presacral nerve causes them to contract. This contraction is inhibited by testosterone. Sympathectomy (e.g. during bilateral retroperitoneal node dissection for testicular cancer) is followed by ejaculatory paralysis. If one chain can be preserved, ejaculation is normal, though with a reduced volume. Contrast medium injected into the seminal tract show that the ampullae of the vasa efferentia empty first, and then the seminal vesicles, which function like a syringe to flush out the first sperm‐rich aliquot of semen. From puberty onwards, the seminal vesicles normally contain live spermatozoa and were considered to be reservoirs, hence the name; but probably the main sperm reservoir is the ampulla of the vasa efferentia and the epididymis. Their secretion makes up about 80% of the ejaculate; it is rich in fructose, citric acid, magnesium, ammonium, ascorbic acid, prostaglandins, and other specific proteins in an alkaline, viscous yellowish fluid. The seminal vesicles may be absent on one or both sides, the ureter may enter the vesicle, and the vesicle may have cysts and diverticula (Figures 41.1 and 41.2) [1–3]. Seminal vesical cysts can be very large and may contain up to 5 l of fluid, which may become infected and form stones (Figures 41.3 and 41.4) [2, 4]. Cysts of the seminal vesicles must be distinguished from cysts arising from the midline müllerian duct. Seminal vesical agenesis is associated with a cystic fibrosis gene mutation and can be associated with renal and vas deferens anomalies or agenesis. Gonococcal infection of the seminal vesicles was common and serious; however, with antibiotics, this infection is now rarely seen. Rarely, abscesses are seen and are associated with diabetes, long‐term catheters, and potentially cystoscopy. All the causes of chronic infection of the urinary tract (e.g. Schistosoma, tuberculosis, amoeba and trichomonas) may involve the seminal vesicles. Patients can present with haematospermia, perineal pain, painful ejaculation, or infertility or a mixture of these. Diagnosis can be made by ultrasound and perineal needle aspiration and treated with appropriate antibiotics. With the increasing use of transrectal ultrasound, it has become possible to identify seminal vesicle obstruction, which can be complicated by infection or a calculus lodged in the ejaculatory duct [5, 6]. Benign and malignant tumours may arise in the seminal vesicles, differentiated with a biopsy. The difficulty with the seminal vesicle is that by the time the diagnosis is made, it is almost impossible to be sure that the origin of the cancer was in the vesicle. Any cavity lined with mucosa may give rise to adenocarcinoma. Sarcomas and choriocarcinomas arising from the connective tissue of the seminal vesicle have been reported (22). However, local spread from prostate cancer is more commonly seen than primary cancer. Serum carcinoembryonic antigen can be elevated. Their spread, like the prostate, is by the Batson’s veins to the pelvis and femora, eroding the bone rather than causing sclerosis on imaging, but it seems that these metastases may be hormone sensitive. Asymptomatic benign lesions can be conservatively managed Malignant tumours are surgical excised where feasible. The role of radiotherapy and androgen ablation is unclear due to the scarcity of seminal vesical cancers. Amyloid is seen in the seminal vesicle as a normal feature in old men, and it occurs at an earlier age in those who have diabetes [7]. Clinically the seminal vesicles are impalpable on digital rectal examination (DRE) unless involved in a pathological process. Transrectal ultrasound show the vesicles with great clarity, and when there is an obstructed seminal vesicle, it allows aspiration and biopsy to be performed under ultrasound control. Fluid (cysts) is hypoechoic and a solid mass (cancer) is hyperechoic. Plain radiographs may show calculi in seminal vesicles and calcification of the vesicles and vasa is commonly seen in bilharziasis and may occur in those with diabetes or hyperparathyroidism. Injection of contrast medium into the vas gives an outline of the vasa, the ampulla, and the seminal vesicle but the wide range of normal variations makes them difficult to interpret. Computed tomography (CT) and magnetic resonance imaging (MRI) are both useful in imaging of the seminal vesicle and have been particularly useful in showing invasion of the vesicles by cancer of the prostate. The majority of the volume of the semen is derived from the seminal vesicles, as is all the fructose; so semen of small volume with an absence of fructose generally signifies disease of the vesicles. This is common in those with diabetes, but also occurs as a result of inflammation, obstruction, or absence. The most simple and direct approach to the vesicles is through an abdominal incision (i.e. open, laparoscopic, or robotic), stripping the peritoneum off the posterior surface of the bladder, and following the vas deferens down on either side. Care must be taken to avoid injury to the ureter which passes under the seminal vesicle. Attempts at male contraceptive methods or male contribution to contraception has been time tested for many years; however there are high failure rates, periodic abstinence 20%, withdrawal 19%, and condoms 3–14% [6]. This led to look to surgery for a relatively more permanent method, vasectomy. It was first described by Sir Astley Cooper in 1827; today it is one of the most commonly performed procedures. It is in danger of being regarded with too little seriousness and yet it is fraught with medicolegal consequence. Consultation with is essential before embarking on vasectomy. The wife may be about to undergo a hysterectomy. One must be cautious of the husband who is being driven to submit to vasectomy to save a failing marriage. Both partners must understand that the procedure should be considered irreversible, associated with a low complication rate, low but existing failure rate, advice to continue with other effective contraception until clearance is confirmed, and that the procedure is not associated with any serious, long‐term, side effects [6]. Examine the patient carefully before deciding to proceed, it is difficult to do a vasectomy under local anaesthetic in a frightened man with a tight scrotum or when there has been previous scrotal or inguinal surgery, or if the vas is impalpable or absent. Let the patient shave his own scrotum before the procedure to minimise infection; it is much more comfortable for him if he does it in the bath at leisure. Local infiltration with a local anaesthetic provides excellent anaesthesia, which is usually sufficient in the relaxed cooperative patient. The operation may be done through a single transverse, vertical scrotal incision, or through two incisions, one over each vas (Figure 41.5). There are many techniques for performing vasectomy. However, the most effective is when the lumen is cauterised and fascia interpositioned between the two ends [6]. The essential steps are that the vas deferens is located by its characteristic feel, like a hard cord (Figure 41.6). The sheath of the vas is incised longitudinally taking care to avoid the artery and veins of the vas. The vas is lifted up out of the sheath. Care is taken not to pull on the vas because this can cause vagal stimulation, bradycardia, fainting, and even cardiac arrest. The vas is doubly clamped and divided and a small segment of vas from each side resected, carefully labelled in formalin as medico‐legal proof that the right organ was removed, should questions arise afterwards. Coagulate the lumen of the vas with diathermy and interpositioning tissue while closing is essential. Another way is to ligate the testicular end of the vas with fine (4–0) suture, curl the end back on itself into a loop, and tie it again (Figure 41.6). The other end is ligated and dropped back into the sheath of the vas, which is then closed with a stitch. The looped‐back end is left outside the sheath. It is the intention that the fascia of the sheath will prevent the ends coming together again. Many urologists now advocate a ‘no‐scalpel’ vasectomy where a sharp haemostat is used to puncture the scrotal skin. The incision usually does not require a suture and may decrease the incidence of haematoma and infection rates. Every large series of vasectomies records complications, few are severe, but all of them are notoriously apt to generate resentment and litigation [8–15]: When reactionary haemorrhage occurs and leads to a haematoma, it is usual to return the patient to the operating theatre and evacuate the clot under anaesthesia. In practice, it is rare that a single bleeding vessel can be identified, and the blood is usually found between the tissues of the scrotum. After evacuation of the haematoma, the swelling may take several weeks to resolve completely. It is common for the patient to complain of pain in the scrotum for some time afterwards. The mechanism of spontaneous recanalization seems to be that sprouts of the epithelium lining the vas burrow into the granulation tissue filling the gap between the divided ends of the vasa. If the sprouts meet each other, continuity is re‐established. It is believed that this recanalization took place in the first few months after vasectomy, when the granuloma was new before scar tissue had contracted to form an impenetrable barrier. Very occasional cases were reported where the vasa would reunite years later; they were regarded as an extreme rarity. However, whenever spontaneous reunion of the vas results in an unwanted pregnancy, the surgeon is likely to be accused of negligence; hence, the intense medico‐legal interest in the issue of ‘late’ recanalization (i.e. after the semen had been shown to be entirely free from spermatozoa in at least two consecutive specimens). Few surgeons would think it necessary to warn of complications so rare, but vasectomy is an exception because of the suspicions and ill feeling that are aroused by an unexpected pregnancy years after vasectomy. It is therefore a wise precaution to warn the patient and his wife that this, however rare, can happen. Increased risk of prostate cancer or systemic illnesses, like atherosclerosis or cardiovascular disease has not been proven after vasectomy [6]. After vasectomy, two consecutive semen samples (12 and 16 weeks) must show no sperm to be considered a success. Azoospermia is achieved in 80% of patients after 12 weeks and 20 ejaculations; however it is recommended that only after 16 weeks and 24 ejaculations that initial assessment for sperm motility be carried out and when examination of a well‐mixed, uncentrifuged, fresh postvasectomy sample shows azoospermia or only rare nonmotile sperm (<100 000 nonmotile sperm/ml) can other contraceptive precautions be stopped [15–17]. Clearance to stop contraception can be given to some patients who have very few nonmotile sperm (<10 000 nonmotile sperm/ml) found in a fresh specimen examined at least seven months after vasectomy [6, 12]. However, be cautious; paternity has been proven when not a single sperm can be found [18]. Nearly 6% of patients that undergo vasectomy, undergo a reversal [19]. Vasovasostomy and vasoepidiymostomy are vasectomy reversal techniques used. Both require patience, time, and adequate anaesthesia. Surgeons should use loupes or the operating microscope and smaller suture material [20]. The divided ends of the vasa are exposed and sectioned until the lumen is revealed (Figure 41.8). The ends are anastomosed, either an end‐to‐end method, or end‐to‐side method can be used (Figure 41.9). The results of reversal of vasectomy are disappointing. Although sperms reappear in the ejaculate in 90%, the pregnancy rate decreases with the increase in the interval from the vasectomy to reversal (Table 41.1) [6, 21]. There are several explanations. First the couples are older and biologically less likely to conceive. Second, while the sperms are retained in the epididymis, they may leak into the tissues and provoke an immunological reaction which will result in death or immobilisation of the sperms. Table 41.1 Patency and pregnancy rate with time. Ten year post‐vasectomy, 25% of men develop epididymal blockages that will require tubulovasostomy during reversal to give patency [6, 22]. If the vasectomy reversal fails, then sperm retrieval methods (i.e. microsurgical epididymal sperm aspiration and testicular sperm extraction) and in vitro fertilisation (i.e. intracytoplasmic sperm injection) can be used however are quite costly [6].
Vasectomy and Seminal Vesicle Disorders
Abstract
41.1 Seminal Vesicles
41.1.1 Anatomy and Physiology
41.1.2 Topographical Anatomy
41.1.3 Congenital Anomalies
41.1.4 Infection
41.1.5 Neoplasms
41.1.6 Degenerative Diseases
41.1.7 Investigations
41.1.8 Imaging
41.1.9 Semen Analysis
41.1.10 Surgical Approach to the Seminal Vesicles
41.2 Vasectomy
41.2.1 Counselling
41.2.2 Examination
41.2.3 Shaving
41.2.4 Anaesthesia
41.2.5 Choice of Incision
41.2.6 Operative Technique
41.2.7 Complications
41.2.7.1 Early Complications
41.2.7.2 Later Complications
41.2.8 Postoperative Semen Analysis
41.2.9 Vasectomy Reversal
Time from vasectomy to reversal (years)
Patency rate (%)
Pregnancy rate (%)
3
97
76
3–8
88
53
9–14
79
44
>15
71
30