Guiding role of seminal tract anatomical study in transurethral seminal vesiculoscopy.

INTRODUCTION: There have been problems with low qualification operator-related complications and failures of transurethral seminal vesiculoscopy (TSV) in China. AIM: To study the guiding role of seminal tract anatomical study (STAS) in TSV.
MATERIAL AND METHODS: We performed STAS to study the structure, morphology, duct trajectory, and anatomical relationships between the seminal vesicles and the adjacent tissue in pelvic specimens from 12 adult cadavers. Then the surgical effects and complications of 82 cases of TSV performed by 3 doctors were retrospectively studied to compare the difference between the two groups of before and after the anatomical study.
RESULTS: The anatomical studies of the 12 adult cadaveric pelvis specimens identified the lengths and widths of the right- and left-side seminal vesicles and tracts. The TSV can treat lesions located in the distal seminal tract and vesicle, but proximal lesions cannot be reached, which is an anatomical limitation of this technique. There were significant differences in the surgical times and the surgical validity rates between the 2 groups.
CONCLUSIONS: Our anatomical study of the seminal tract and seminal vesicles is valuable for guiding TSV in clinical practice. Copyright:

Introduction

Ejaculatory duct and seminal vesicle diseases are common male urological disorders and include chronic seminal vesiculitis, spermatic calculus, seminal vesicle cyst, and ejaculatory duct stenosis or obstruction [1]. Seminal tract obstruction may lead to obstructive azoospermia, and affected patients may experience intractable hemospermia, perineal discomfort and pain, ejaculation pain, azoospermia, or infertility [2]. In the past, the outcome of conservative treatment was poor, and open surgery, laparoscopic or even flexible vesiculovasoscopy surgery has been performed for common seminal vesicle diseases [3-8]. For seminal tract and seminal vesicle diseases in certain locations, there is no appropriate and effective treatment method [7]. Transurethral seminal vesiculoscopy (TSV) is an endoscopic technique that has developed rapidly in recent years. Because it is a relatively simple procedure and does not change the normal anatomical structures of seminal vesicles, this technique is becoming an alternative for the diagnosis and treatment of seminal vesicle and seminal tract diseases [9, 10].

However, we have found that there have been issues with low qualification operator-related complications and failures in China recently. Our department used TSV to treat 48 patients from January 2013 to July 2016, performed by 3 surgeons. They were not able to locate the ejaculatory duct opening in some cases, which led to surgical failures; in addition, we have identified other complications, such as epididymitis, urinary tract infection (UTI), ejaculation abnormality (EA), continuous hematuria (CH) and clinical symptoms of rectal injury [11]. The main reason that the low qualification operator training system results in errors is an emphasis on surgical techniques while neglecting the anatomy and holistic view of the seminal tract. We performed a seminal tract anatomical study (STAS), which included the seminal tract and seminal vesicles, studying the structure, morphology, duct trajectory, and anatomical relationships between the seminal vesicles and the adjacent tissues, in pelvic specimens from 12 adult cadavers. Then, we compared the surgical effects and complications between after and before STAS performed by the same 3 surgeons.

Aim

The aim of this research is to study the guiding role of STAS in TSV.

Material and methods

Ethical standards

The present study was approved by the Ethics Committee of Xuzhou Central Hospital and the Medical Ethics Committee of Xuzhou Medical University.

Seminal tract anatomical study

Twelve pelvic specimens were selected from adult cadavers, and the local structure, morphology, duct trajectory, and anatomical relationships between the seminal vesicles and adjacent tissues were observed. All specimens were provided by the Department of Anatomy, Xuzhou Medical University. The mean age at death was 50.2 ±6.4 years (range: 45–56 years). In all cadavers, the causes of death were not related to prostatic or bladder diseases. No prostate cancer was found in any of the specimens, and the normal structures of the seminal vesicles were not changed.

The entire seminal vesicles and seminal tracts were obtained. Along the routine approach for TSV, the seminal colliculus, prostatic utricle, ejaculatory duct, ejaculatory duct opening, vas deferens ampulla, and seminal vesicles were observed individually, and the length, width, and thickness of the seminal vesicles were measured using a digital micrometer. The seminal colliculus area was observed, and the presence of the prostatic utricle and the length and depth of the prostatic utricle were observed. The observed structures also included the excretory duct of each seminal gland, the trajectory of the vas deferens, the location of the bilateral ejaculatory duct openings, and the trajectory of the ejaculatory duct and its relationship with the prostatic utricle opening. The length and inner diameter of the ejaculatory duct were measured. F3–F6 ureteral catheters were inserted into the bilateral ejaculatory ducts, and the retrograde operation was simulated to observe the morphology, structure, and trajectory of the seminal tract and seminal vesicles and their anatomical relationships with the adjacent tissue.

Surgical procedure of TSV

Before surgery, transrectal ultrasound and/or magnetic resonance imaging (MRI) were performed to study the prostate, seminal vesicles, and ejaculatory duct. After spinal anesthesia, the patient was placed in the lithotomy position. Then, 4.5–6.5 Fr Storz ureteroscopes were inserted gently and slowly into the posterior urethra through the external urethral orifice to locate the seminal colliculus. Surgeons searched the ejaculatory duct openings at the 5 and 7 o’clock points on the bilateral sides of the prostatic utricle. If necessary, transrectal seminal vesicle massage was performed, and the overflow of milky-white fluid helped to identify the ejaculatory duct opening. If the ejaculatory duct opening could not be found, an F3 ureteral catheter was inserted into the prostatic utricle to dilate it slightly, and then the surgeon guided the ureteroscope into the prostatic utricle. After the device entered the prostatic utricle cavity, the surgeon identified the bilateral ejaculatory openings and inserted the ureteroscope into the seminal vesicle through the ejaculatory duct opening under the guidance of the F3 ureteral catheter. If the ejaculatory duct opening was not found, a window was made at the 3–5 o’clock or 7–9 o’clock positions of the bilateral walls of the prostatic utricle to enter the ejaculatory duct. If the prostatic utricle could not be detected, the distal end of the ejaculatory duct was cut open using a plasma urethral resectoscope.

Transurethral resection of the ejaculatory duct was performed by resectoscope plasma electric vaporization. The endoscope was inserted under direct vision, the seminal colliculus, bladder neck, and urethral external sphincter were examined, and both sides of the seminal colliculus were removed carefully. The bilateral ejaculatory ducts were identified observing the overflow of milky-white or yellowish-brown fluid. The endoscope was removed, and TSV was performed. If the ejaculatory duct opening could not be found after these procedures, methylene blue was injected into the vas deferens to identify the ejaculatory duct. The bilateral ampulla of the vas deferens and the internal structure of the seminal vesicle were observed. The presence of congestion, edema, bleeding, seminal vesicle stones, blood clots, neoplasm, or other abnormalities was confirmed by TSV. All the 3 surgeons had performed over 30 cases of TSV respectively before we collected the data to exclude the impact of the learning curve.

Effects and complications study of TSV

A respectively study was performed to compare the effects and complications after and before the anatomical study. 48 cases of patients who were diagnosed with obstructive azoospermia and received TSV therapy from January 2013 to July 2016 were enrolled in group A. Then, the surgeons attended the anatomical study in August 2016. After that, other 34 cases of patients were enrolled in group B from September 2016 to May 2018.

Baseline information, including age, smoking history, drinking history and body mass index (BMI), was collected and determined preoperatively. Comparisons of the complications included epididymitis, UTI, EA, CH and rectal injury, and the surgical parameters included surgical time (min), catheter days and length of hospital stays (day) before and after the anatomical study.

A total of 82 cases, including 48 patients (group A) and 34 patients (group B) were enrolled in the retrospective study. There were no statistically significant differences in baseline data between groups A and B (p > 0.05, Tables I and II).

Table I

Patient characteristics and preoperative continuous data

Parameter	Group A, mean ± SD	Group B, mean ± SD	t value	P-value
Age [years]	28.0±3.6	27.9±4.4	0.15	0.8837
BMI [kg/m2]	26.3±2.6	26.1±2.7	0.32	0.7510

There were no statistically significant differences in baseline continuous data (all p > 0.05).

Table II

Patient baseline data

Parameter	Total, n (%)	Group A, n (%)	Group B, n (%)	P-value
Patient number	82 (100.0)	48 (58.5)	34 (41.5)
Smoking history:	–	–	–	0.3915
Yes	31 (37.8)	20 (24.4)	11 (13.4)	–
No	51 (62.2)	28 (34.2)	23 (28.1)	–
Drinking history:	–	–	–	0.6569
Yes	22 (26.8)	12 (14.6)	10 (12.2)	–
No	60 (73.2)	36 (43.9)	24 (29.3)	–
Seminal blood:	–	–	–	0.9736
Yes	36 (43.9)	21 (25.6)	15 (18.3)	–
No	46 (56.1)	27 (32.9)	19 (23.2)	–

There were no statistically significant differences in smoking history, drinking history and seminal blood between the 2 groups (all p > 0.05).

Statistical analysis

Statistical analyses were performed using SAS v8.02 software (SAS Institute Inc., Cary, NC, USA). Continuous data are presented as the mean ± SD, and categorical data are presented as a percentage. Continuous data between the two groups were compared using Student’s t test. Categorical data were compared using the χ2 test. If 50% of the cells have expected counts less than 5, continuity adjustment χ2 test will be performed. A p < 0.05 was considered significant.

Results

Results of the anatomical observation

After the anatomical observation of the seminal tracts and seminal vesicles of 12 adult pelvic specimens, we found the following:

The length of the seminal vesicle was 32.6 ±6.3 mm on the left side and 33.1 ±5.2 mm on the right side; the width was 15.7 ±3.3 mm on the left side and 15.2 ±4.5 mm on the right side; and the thickness was 7.4 ±2.1 mm on the left side and 7.5 ±2.8 mm on the right side.

The seminal colliculus was identified in most specimens. The prostatic utricle was observed in 7 of 12 cadavers (58.3%), while only a tiny depression was observed and the prostatic utricle was not found in the 5 other cases. The mean size of the prostatic utricle opening was 4.8 ±1.4 mm in the 12 cadavers, and the opening was cave-shaped (Photo 1 A). The prostatic utricle was located between the bilateral ejaculatory ducts. In addition, the interval tissue between two bilateral ejaculatory ducts was thin.

Photo 1

Results of local anatomical study of the specimens. A – The prostatic utricle opening is located at the seminal colliculus of the urethra (black arrow). B – The ejaculatory duct enters the prostate gland (black arrow) and exits from the seminal colliculus. C – The length of the ejaculatory duct is approximately 1.5–3 cm, and it extends in cases with ejaculatory duct dilation or seminal vesicle dilation. D – Bilateral seminal vesicles and the ampulla of the ductus deferens merge into the ejaculatory duct (black arrow) at the dorsal side of the prostate. E – After dissection, the seminal vesicle is exposed clearly, joins the ampulla of the ductus deferens (black arrow), merges into the ejaculatory duct, and has its opening in the seminal colliculus of the prostatic urethra. F – The seminal vesicle is honeycomb-shaped, with obvious segmentation in the cross-section

The angle between the ejaculatory duct and the midline was 10–15° at the point where the ejaculatory duct entered the prostate gland (Photo 1 B). The needle-like opening of the ejaculatory duct was found on the seminal colliculus, the size was 0.1 mm, and it was not observed in some specimens. The length of the ejaculatory duct was 14.3 ±2.3 mm on the left side and 14.1 ±3.7 mm on the right side; the inner diameter was 1.3 ±0.4 mm on the left side and 1.2 ±0.3 mm on the right side. The ejaculatory duct openings were located at the 5 and 7 o’clock positions on both sides of the prostatic utricle. Following the dilatation of the ejaculatory duct or the seminal vesicle, the ejaculatory duct was extended accordingly (Photo 1 C).

F4–F5 ureteral stents were used in patients with narrow ejaculatory duct openings and for distorted or thin seminal tracts.

The lower end of the vas deferens became thin and joined with the duct of the seminal vesicle to form the ejaculatory duct (Photo 1 D).

The seminal vesicle was honeycomb-shaped, with obvious segmentation in the cross-section, and there was often a liquid residue inside the seminal vesicle (Photo 1 F); thus, a full view was never obtained with TSV.

Retrospective study of TSV

There were no significant differences in the complications between the two groups (all p > 0.05, Tables III and IV), but the differences in surgical times and surgical validity rates between the two groups were statistically significant (p < 0.05, Tables III and IV).

Table III

Surgical parameters

Parameter	Group C, mean ± SD	Group D, mean ± SD	t value	P-value
Catheter days	1.8 ±0.7	1.7 ±0.7	0.50	0.6183
Hospital stays [days]	4.5 ±0.8	4.3 ±0.8	1.20	0.2325
Surgical time [min]	24.6 ±5.4	21.9 ±5.8	2.19	0.0311*

There were no significant differences in the catheter days and hospital stays between the two groups (both p > 0.05), but the differences in surgical time between the two groups were statistically significant (*p < 0.05).

Table IV

Surgical validity rates and complications

Parameter	Total, n (%)	Group A, n (%)	Group B, n (%)	P-value
Patient number	82 (100.0)	48 (58.5)	34 (41.5)
Valid:	–	–	–	0.0236*
Yes	59 (72.0)	30 (36.6)	29 (35.4)	–
No	23 (28.0)	18 (22.0)	5 (6.1)	–
Epididymitis:	–	–	–	0.9877
Yes	12 (14.6)	7 (8.5)	5 (6.1)	–
No	70 (85.4)	41 (50.0)	29 (35.4)	–
UTI:	–	–	–	1.0000#
Yes	8 (8.8)	5 (6.1)	3 (3.7)	–
No	74 (91.2)	43 (52.4)	31 (37.8)	–
EA:	–	–	–	0.6509
Yes	15 (18.3)	8 (9.8)	7 (8.5)
No	67 (81.7)	40 (48.8)	27 (32.9)
CH:	–	–	–	0.5989
Yes	17 (20.7)	9 (11.0)	8 (9.8)
No	65 (79.3)	39 (47.6)	26 (31.7)
Rectal injury:	–	–	–	1.0000#
Yes	3 (3.7)	2 (2.4)	1 (1.2)	–
No	79 (96.3)	46 (56.1)	33 (40.2)	–
Complications:	–	–	–	0.7069
Yes	26 (31.7)	16 (19.5)	10 (12.2)
No	56 (68.3)	32 (39.0)	24 (29.3)

There were no significant differences in the complications between the two groups (all p > 0.05), but the differences in surgical validity rates between the two groups were statistically significant (*p < 0.05). Fifty percentof the cells have expected counts less than 5, so the continuity adjustment χ2 test was performed (#).

Discussion

The seminal tract and seminal vesicles are located deep in the body and are hidden. Therefore, traditional surgical treatments for seminal tract and seminal vesicle diseases are relatively complicated, and often the outcomes are not ideal. Jarzemski et al. [5] emphasize that the laparoscopic or robotic technique is an excellent choice for treating seminal vesicle diseases. TSV is a newly developed technique for the diagnosis and treatment of the distal seminal tract and seminal vesicle diseases [12-14]. During the diagnosis and treatment of obstructive azoospermia using TSV, local lesions in the seminal tract and seminal vesicles can be observed, and cysts, stones, and neoplasms in the seminal vesicle cavity can be treated [15]; therefore, this technique may achieve better outcomes compared with traditional treatments [16]. However, many patients still cannot obtain satisfactory outcomes. Because the seminal tract and seminal vesicle are hidden, thin, and narrow and because no special instruments are available for TSV, the surgery is difficult, as is achieving excellent clinical outcomes. The best method for entering the seminal vesicle safely, accurately, and rapidly during TSV is the most critical issue.

Currently, identifying the location of the ejaculatory duct opening and making an approach for TSV is controversial. Some scholars assert that the ejaculatory duct openings are located at the 5 o’clock and 7 o’clock positions of the seminal colliculus cavity (prostatic utricle) [8, 17, 18]. Wang et al. [19] performed transurethral procedures for 86 patients with benign prostatic hyperplasia or urethral stricture and simultaneously performed transrectal seminal vesicle massage and observed the ejaculatory duct openings. They found that two ejaculatory duct openings were located 2 mm away from the prostatic utricle opening and that these three points formed a triangle or a straight line. Four approaches are recommended for TSV [1]: (1) via the natural opening of the ejaculatory tract; (2) via the prostatic utricle; (3) via the windows made at the 5 or 7 o’clock directions from the prostatic utricle bottom; and (4) via the pathway established by the transurethral resection of the ejaculatory duct opening. However, there are significant differences in validity rates [9, 17–19], which greatly limits the application of this technology. To further improve the success rates and postoperative outcomes of TSV, we selected 12 adult pelvic specimens and studied the structure, morphology, duct trajectory, and anatomical relationships between the seminal vesicles and adjacent tissues.

We identified thin, film-like substances at the 5 and 7 o’clock directions from the prostatic utricle bottom, and entered the seminal vesicle after making a window. Later, we found bilateral ejaculatory openings near the prostatic utricle opening of the seminal colliculus. There were mucosal folds at the opening, which proved to be the ejaculatory duct openings. The seminal colliculus is an eminence at the lower end of the prostatic urethra, and three depressions or orifices can be observed under TSV. The upper depression is the prostatic utricle opening, and the lower two depressions are ejaculatory duct openings. The ejaculatory duct openings are located 2 mm away from the prostatic utricle opening. In rare pathological situations, the ejaculatory duct opening may be located in the small sac [20].

Through the anatomical observation of the seminal tract, we have improved the validity rate of TSV and shortened the operation time. During surgery, the ejaculatory duct openings can be dilated by Storz F4.5–F6.5 ureteroscopes. After the locations of the ejaculatory ducts are confirmed by semen expulsion from the ejaculatory duct opening, using transrectal massage of the seminal vesicle, the ureteroscope can be inserted via the natural pathway into the seminal vesicle under the guidance of a guidewire. The ureteroscope should be inserted into the seminal vesicle after the dilation of the natural pathway via the ejaculatory duct opening to better protect the surrounding tissue and to avoid seminal tract injury. In addition, these procedures can better protect the peripheral vital tissues and organs, reduce postoperative scar formation, and decrease the recurrence rate. At present, this approach is preferred during TSV in our department.

During the anatomical study of the seminal vesicles and seminal tract in the anatomical observation experiment, we found that the seminal colliculus could be identified clearly in formalin-fixed specimens. The prostatic utricle was observed clearly in 7 of 12 specimens (58.3%). Morgan et al. [21] reported that the prostatic utricle was observed in 12 out of 13 cases in their series. The prostatic utricle is a dead space between the bilateral ejaculatory ducts and is approximately 6 mm in length. For quite some time, physicians and anatomical experts have not paid sufficient attention to its structure and function. In our anatomical study, we found that the prostatic utricle was located between the bilateral ejaculatory ducts. There was a thin membrane between the two ejaculatory ducts. We hypothesize that it bulges because of the tension at the time of ejaculatory duct occlusion because it is near the prostatic utricle, and it is the anatomical basis for establishing the ejaculatory duct bypass in the prostatic utricle. Therefore, a window can be made via this area when the natural opening of the ejaculatory duct is not found. However, this is not the preferred approach. When the ejaculatory duct opening is not found, a window should be made at the 5 or 7 o’clock point from the bottom of the prostatic utricle, and this approach is preferred by most surgeons [22, 23]. However, when we make a hole to enter the ejaculatory duct, it is in theory a false channel; if the size of the hole is too large, it may result in reflux, and if the hole size is too small, it may induce recurrent stenosis or even occlusion after surgery [15].

The outer layer of the ejaculatory duct is longitudinal smooth muscle. At the proximal end, it becomes thin rapidly, and the inner smooth muscle disappears [8, 24]. Therefore, the ejaculatory duct has no sphincter functions, such as peristalsis or contraction, and urinary reflux is prevented only by the presence of the sharp angle between the ejaculatory duct and the prostatic urethra [23]. An experiment in animals found that the relationship between the seminal vesicle and the ejaculatory duct was similar to that between the bladder and the urethra [25]. When transurethral resection of the ejaculatory duct opening must be performed to enter the ejaculatory duct and the ejaculatory duct is not removed sufficiently, symptoms may still be present after surgery, or recurrent stenosis and obstruction may occur; if the ejaculatory duct is removed too extensively, the anti-reflux mechanism may be injured.

According to our anatomical study, the mean length of the ejaculatory duct was 12.2 ±3.4 mm, which is consistent with the findings of Nguye et al. [26]. The human ejaculatory duct is 1–2 cm and gradually becomes thinner from the seminal vesicle to the urethra. The diameters of the proximal, middle, and distal ends of the duct were 0.3–1.74 mm, 0.1–0.64 mm, and only 0.1–0.34 mm, respectively. The ejaculatory duct is generally divided into three segments, the seminal vesicle segment, the prostatic segment, and the seminal colliculus segment. If ejaculatory duct dilation or seminal vesicle dilation occurs, the ejaculatory duct will be extended accordingly. Sometimes, the ejaculatory duct opening is dilated, the ejaculatory duct is extended and enlarged, and a cyst can be formed. At the time of surgery, the ejaculatory duct may be mistaken for the seminal vesicle, which results in misdiagnosis. In the present study, the dilated ejaculatory duct was 1.5 cm in diameter in one patient, and small yellow granules were present. The dilated ejaculatory duct was initially considered to be the seminal vesicle, and the real seminal vesicle was reached only after repeated manipulations [27, 28].

F3 or F4 ureteral stents can be used for patients with small ejaculatory duct openings or twisted or narrow seminal tracts. Our anatomical study showed that the narrow end of the vas deferens may be located at the junction of the vas deferens and the seminal vesicle, to which sufficient attention has not been paid in the past. The opening we identified was ring-shaped and 1–2 mm in size. The opening of the vas deferens ampulla is often located on the medial side, and the endoscope may not enter the vas deferens ampulla during TSV. Because the thinnest endoscope at present is still relatively thick for the opening of the vas deferens ampulla, we recommend not entering the proximal end of the vas deferens ampulla to avoid iatrogenic injury and the subsequent obstruction of the vas deferens.

Complication rates in TSV and laparoscopic or robotic techniques were comparable. The incidence of complications of fenestration under seminal vesiculoscopy was 40.0% (8/20), while the complication rate of transperitoneal laparoscopic unroofing was 36.3% (12/33) [29]. The complication rate was comparable with the data in our research (31.7%, 26/82).

Before the operation, the surgeon should fully communicate with the patient, inform the patient of possible surgical outcomes, and allow the patient to consider having his sperm frozen, if necessary, for intracytoplasmic sperm injection. Therefore, we believe that TSV should be performed strictly based on the following surgical indications: (1) the history of intermittent hemospermia should be > 6 months or > 3 months, if conservative treatment is ineffective; (2) the imaging examination should suggest anatomic abnormalities, recurrent inflammation, or secondary stone formation in the seminal tract, e.g., an associated ejaculatory duct or seminal vesicle cyst or Mullerian cyst, and the auxiliary examination should suggest ejaculatory duct obstruction or there should be a suspected neoplasm that requires biopsy; and (3) hemospermia caused by prostate cancer or tuberculosis should be excluded.

Conclusions

According to our experiences with TSV and following our local anatomical study of the seminal tract and seminal vesicles, we believe that minimally invasive transurethral TSV is feasible for the treatment of seminal tract and seminal vesicle diseases. However, as a new surgical procedure, TSV still has some limitations, and better outcomes can be achieved only by combining it with other treatment methods. Our anatomical study of the seminal tract and seminal vesicles has value in guiding TSV in clinical practice. However, our study is still insufficient, due to the limited number of cases and research methods, and thus requires further in-depth clinical and scientific studies. We believe that TSV will have a better future with the development of new minimally invasive endoscopic instruments.