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Ultrasonographic assessment of male anterior urethra. Description of the technique of examination and presentation of major pathologies.

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Received 25.01.2020 Accepted 16.03.2020 Med Ultrason

2020, Vol. 22, No 2, 236-242

Corresponding author: Jakub Krukowski, MD

Department of Urology, Medical University of Gdańsk, Gdańsk, Poland

Smoluchowskiego 17 St., 80-952, Gdańsk, Poland

E-mail: [email protected]

Introduction

For almost a hundred years, retrograde and voiding cystouretrography (R-CUG and V-CUG) have been the basic examination used in the imaging of the male ure- thra [1]. This test involves the urethra assessment using X-rays, after having previously filled it with contrast.

This currently used technique was described in the 1960s and still is used as the “gold standard” in the diagnosis of urethral disorders [2]. Despite many advantages, which are, among others, ease of execution and the ability to as- sess the entire urethra from the meatus to the bladder, this examination is not an ideal tool in the urethral pathology diagnosis. The lack of evaluation of the urethra in three dimensions, radiation or administration of a potentially sensitizing contrast agent are among the major disadvan- tages that prevent CUG from being awarded the title of an “ideal test”.

The next step in the development of urethral imag- ing techniques was the introduction of sonouretrography (SUG). The “milestone” was the presentation of the first results of the use of ultrasonography in the urethral stric- tures’ diagnosis by McAninch et al [3]. This study began the development of SUG as a diagnostic tool for urethral damage.

Over the past 30 years, numerous papers have ap- peared describing the role and usefulness of ultrasound examination of the urethra. The purpose of this article is to introduce the study technique itself and to describe the most common pathologies that can be encountered dur- ing examination.

Technique of examination

The technique of examination has not changed since its first description [3]. After decontaminating the mea- tus, a Foley catheter is inserted into distal segment of the urethra. To stabilize the catheter, at the level of fossa na- vicularis, the catheter’s balloon is filled to a volume of up to 2 mL (or the appearance of discomfort). An alternative to the catheter is the use of a penis clamp dedicated to this study [4]. In patients with meatal stenosis, when the catheter cannot be inserted into the urethra, a peripheral venous catheter can be used instead of the Foley catheter to deliver fluid into the urethra (fig 1) [5].

Abstract

During the last years the role of sonourethrography (SUG) in the assessment of anterior male urethra pathologies, has significantly increased. The investigation is easily performed, not time consuming and should be considered the imaging technique of choice for preliminary diagnosis, without exposing the patient to X-rays. In this paper we present the technique of examination and the most common pathologies in which SUG is indicated.

Keywords: male anterior urethra; sonourethrography; ultrasonography; urethral disease

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There are two techniques for delivering fluid to the urethra. In the most widely used, 20-100 mL of fluid, mainly 0.9% solution of Natrium Chloratum (NaCl), is injected with a syringe through the catheter [3]. In the second, a vial of fluid is placed up to 200 cm above the patient, to get the right fluid pressure and thus proper ure- thral extension [4]. Healthy urethra is presented as a uni- form, echo-free area, surrounded by the corpus spongio- sum, with a diameter between 8 to 10 mm (fig 2). Below the urethra an echogenic band can be presented produced by dorsal acoustic enhancement and reflection from the tunica albuginea.

Because of the risk of generating artifacts (air bub- bles) during installation and the weak extension of ure- thra, the use of gel is not recommended (fig 3).

Patients with a completely closed urethra are chal- lenging for the examiner. In these cases, examination preparation is divided into two steps. During the first part, through the suprapubic catheter, the bladder is filled up to 300-400 ml (or to the first strong sensation of mic- turition). In the second step, in the distal part of the penile urethra the Foley catheter is installed. After the filling of

the distal urethra, the patient is asked to push on the blad- der. During this manoeuvre the bladder neck opens and the urethra proximal to the stricture is stretched by the fluid (fig 4).

To facilitate the study, after positioning the penis on the midline of the hypogastric region, it can be immobi- lised by a strip of surgical tape. To assess the distal part of penile urethra (especially fossa navicularis and meatus), the examination can be performed during the voiding phase. This allows for the appropriate stretching of the urethra and thus enables a better assessment of possible pathologies within this part of the urethra.

The linear probe is the tool of choice. The transducer is placed lengthways on the ventral region of the penis and then moved transscrotally and transperineally to visualize the bulbar urethra. Due to the short distance between the urethra and the skin, the highest possible frequencies should be used to obtain the most accurate image. No strict rules are used concerning the frequen- cies Briefly, they depend on which urethral segment is

Fig 3. Urethral stricture (borders marked by pointers). In the urethral lumen the “snow storm” effect is visible after the use

of gel to the extension of the urethra Fig 4. Urethral stricture. The scar completely closed the ure- thral lumen.

Fig 1. Technique of insertion of fluid to the urethra in a patient with meatal stenosis: installation of peripheral venous catheter

to the urethra. Fig 2. Healthy male anterior urethra

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examined and on the thickness of the fat tissue around the perineum. In some cases, especially to assess a junction between the bulbar and the membranous urethra, a better option is using a convex probe (fig 5). In our opinion the best frequencies are 15-18 MHz for the penile urethra (from meatus to the peno-scrotal angle) and 9-12 MHz for the bulbar urethra (up to the urethral external sphinc- ter). To avoid generating artefacts, especially false views of the stricture, the pressure of the probe on the urethra cannot be too high.

Urethral stricture

The main cause of the urethral stricture is the forma- tion of a concentric scar within the corpus spongiosum, as result of inflammation caused by injury or infection.

This creates a stiff, non-stretchable section of the urethra.

In the SUG, the damage is visible as a part of urethra that does not stretch during the filling of the urethra by fluid (fig 6). Assessment of the length of urethral scarring is performed by measuring a hyperechogenic line on the urethral mucosa. Depth of fibrotic corpus spongiosum can be measured by the assessment of the hyperecho- genic part of this tissue.

In comparison to CUG, SUG has a higher accuracy in determining a length of urethral stricture. The correla- tion coefficient between the length of stricture measured during SUG and operation is between 0.73 and 0.92, and the highest accuracy is presented for penile urethra [6,7].

Sonoelastography, in comparison to the grey-scale ultra- sound technique, improves the accuracy of the spongiofi- brosis assessment [8].

There are two classifications assessing the degree of urethral damage. The first is the three-stage scale pro- posed by McAninch et al [3]. It estimates the degree of narrowing of the urethral lumen at its narrowest point.

The scale indirectly determinates the degree of fibrosis of corpus spongiosum (Table I.). In comparison to his- topathological findings, the accuracy of this scale in the assessment of spongiofibrosis is about 56% [9]. The sec-

ond classification is the five-level grading proposed by Chiou et al [10]. In this case, the staging of the urethral stricture depends on the number and length of the stric- ture and the amount of spongiosal tissue involvement (Table II.).

Urethral diverticulum

Urethral diverticulum is a condition where the urethra or the periurethral glands push into the spongiosal tissue that surrounds it. The lesion usually occurs at the peno- scrotal junction or the bulbous urethra [11]. Up to 10% of patients with urethral diverticulum develop stone forma- tion [12]. Acquired urethral diverticula can be a result of stricture, infection or trauma. But the most common cause is the surgical treatment of urethral strictures [13];

especially substitution urethroplasty with oral mucosa graft. In this situation the diverticulum may have a con- siderable size [14].

Fig 6. Stricture in the bulbar part of urethra: 6a) longitudinal view; 6b) transverse view.

nous urethra. In the urethral lumen a urethral stent (UroLume®) is visible. (5a – linear probe, 5b – convex probe).

Table II. Chiou et al [10] classification of the urethral stricture.

Stricture grading Ultrasonographic finding

I Short stricture with minimal

spongiosal tissue involvement

II Short stricture with moderate

spongiosal tissue involvement

III Short stricture with extensive

spongiosal tissue involvement

IV Long or multiple strictures with

moderate spongiosal involvement

V Long or multiple strictures with

extensive spongiosal involvement Table I. McAninch et al [3] classification of the urethral stricture.

Urethral stricture

staging Degree of lumen occluded based on SUG

Mild <1/3

Moderate 1/3 – 1/2

Severe >1/2

SUG, sonourethrography

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US can demonstrate a relatively echo-free cavity ad- jacent to the urethra. The communication between the urethral diverticula and true urethral lumen may have a narrow or a wide neck (fig 7).

SUG presents 100% sensitivity and 98% specificity in the diagnosis of urethral diverticula [15].

False passage

False passage is usually presented in patients after traumatic catheterisation or a previous urethral operation.

Typically, it is localised in the urethral angle. In most cas- es the false passage goes back toward the posterior ure- thra. In this situation, during voiding, the urinary stream closes the mucosal flap. This fact results in most cases, that the false passage is invisible during V-CUG [16].

The anatomical variant that can be misdiagnosed as a false passage is a duplication of the urethra. Types of this accessory organ may vary from a blind closed channel to a completely developed second urethra [17].

Sensitivity and specificity for SUG and R-CUG in the diagnosis of false tract is 100% [15].

In SUG, during retrograde fluid insertion, false pas- sage is presented as a channel running along the true ure- thral lumen (fig 8). The border between the channels is urethral mucosa. Careful evaluation of periurethral struc- tures and proper transverse scanning is needed.

Urethral fistulas

Urethroperineal fistulas and urethrocutaneous fistulas may result from surgical treatment of urethral strictures, repair of hypospadias, prostate surgery, chronic untreated periurethral abscesses and trauma [18].

In US a fistula is visible as an echo-free canal that goes from the urethral lumen, through the corpus spon- giosum, to the skin (fig 9). In comparison to CUG, SUG can easier identify an origin of fistula and delineate the periurethral extent [10].

Urethral calculi

Most urethral calculi consist of small stones expelled from the bladder into the urethra during voiding; these are referred to as migrant calculi. Occasionally, however, a stone may be large enough to become lodged at a point

Fig 9. Urethral fistula in a patient with a urethral stricture

(transverse view of the bulbar part of urethra). Fig 10. Urethral calculus in the bulbar urethra.

Fig 7. Urethral diverticulum. Diverticulum developed in the place previously operated because of the urethral stricture (aug-

mented by buccal mucosal graft). Fig 8. Urethral stricture. False passage in the penile part of ure- thra.

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of urethral narrowing such as the membranous urethra.

Rarely, primary (native) formation of a stone occurs in the urethra when the stricture is present, or it may be as- sociated with a urethral diverticulum [19,20].

In USG, the picture of calculus is similar to stones in other parts of the urinary tract. It is presented as a hyper- echogenic structure with acoustic shadowing, sometimes mobile, localised in the urethral lumen (fig 10). In colour Doppler the “twinkling artifact” can be presented. One of the main problems during SUG are the air bubbles de- veloped during fluid intake. Because they can look like small stones, they may be accidentally taken for calculi.

Condyloma acuminata

Genital warts are skin papules that are formed as a re- sult of epidermal hyperplasia. They belong to a group of conditions resulting from Human Papillomavirus (HPV) infection. Urethral involvement affects 0.5-5% of cases.

Due to the risk of spreading the virus, retrograde fluid ad- ministration is not recommended. Voiding SUG becomes the test of choice. In the ultrasound image, 3 forms of le- sions corresponding to condyloma can be distinguished:

polyp, papilloma and, the most common, cauliflower mass [21].

Primary urethral cancer

Primary urethral cancer is one of the rarest cancers of the urinary tract. Bulbar urethra is the part most com- monly affected by the tumor, followed by the penile and prostatic urethra. Due to non-specific symptoms, this can- cer is most often detected at the locally advanced stage.

SUG is not the imaging tool of choice, thus not much information about ultrasonographic morphology of this tumor is provided in the literature. The appearance of a tumor closely depends on the stage. Less advanced can- cer resembles a polypous structure on the urethral mu- cosa. In more advanced stages, urethral cancer is seen as a well-delimited, heterogeneous, well vascularized, ir-

regular structure closing of the urethral lumen (fig 11). In locally advanced cancer, infiltration of the corpus spon- giosum and cavernosal bodies can be presented [22].

Foreign body

The urethra is the main and the most vulnerable or- gan to be damaged if a foreign body is inserted into the urinary tract. The reasons for foreign body insertion into the urethra vary from curiosity, autoerotic stimulation or medical procedures. The material of the foreign bodies is varied.

In most cases US can be the first step in preoperative examination. It can help to detect the size, depth and dis- tance from the meatus of the object to guide the approach to extraction of the foreign object. In contrast to other urethral pathologies, in these cases the fluid insertion is not mandatory [23,24].

Some forms of foreign bodies are hairs in the urethral lumen. One of the forms of treatment of anterior urethral strictures, in particular in the penile part, is the using of skin flap [25]. The principle is to use the skin with no hairs, but in some cases it is impossible. In this situation hairs growing inside the urethral lumen can be a source of infection or urethral stones. In SUG these structures are visible as linear, hyperechogenic, mobile structures (fig 12) [5].

Periurethral abscess

A periurethral abscess is a life-threatening infection of the male urethra and periurethral tissue and frequently a sequela of gonococcal infection or urethral stricture disease. Rarest causes are urethral perforation after trau- matic catherisation or necrosis in the place of the cuff of artificial urethral sphincter installation. A periurethral abscess arises initially when a Littré gland becomes ob- structed by inspissated pus or fibrosis. The most common infecting organisms are gram-negative rods, enterococci, and anaerobes. Pseudodiverticulum formation results Fig 11. Primary urethral cancer. Fig 12. Neourethra in a patient after female-to-male conver-

sion. Hairs in the urethral lumen.

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from urethral communication with a periurethral abscess.

Because the tunica albuginea of the penis prevents the dorsal spread of infection, the abscess tends to track ven- trally along the corpus spongiosum, where it is confined by the Buck fascia. However, when the Buck fascia is perforated, there can be extensive necrosis of the subcu- taneous tissue and fascia [26].

In sonography, the presentation of the abscess varies from the degree of infection. In an early stage, the pic- ture is similar to urethral diverticulum. In more advanced stages, the fluid is surrounding the corpus spongiosum and penetrates to subcutaneous tissues of the penis, the scrotum or perineum (fig 13).

Conclusion

SUG is a fast and easy method for performing an ex- amination which allows an assessment of the male ante- rior urethra. It is mainly used in the diagnosis of urethral strictures but it may be useful in investigating of other patholgies of male urethra. The main limitation of this study is the experience of the examiner. Despite this, SUG can be a “first step” in the evaluation of the male urethra.

After a review of the literature and after some per- sonal practical experience with urethral ultrasound, we believe that this technique can be recommended for the wider use in the diagnosis of any urethral pathology.

Conflict of interest: none References

1. Cunnigham JH. The diagnosis of stricture of the ure- thra by Roentgen rays. Trans Am Assoc Genitourin Surg 1910;5:369-371.

raphy be useful in the diagnosis of urethral disorders of female-to-male transsexuals? Med Ultrason 2019;21:359- 6. Krukowski J, Kałużny A, Kłącz J, Matuszewski M. Com-361.

parison between cystourethrography and sonourethrogra- phy in preoperative diagnostic management of patients with anterior urethral strictures. Med Ultrason 2018;20:436-440.

7. Mitterberger M, Christian G, Pinggera GM, et al. Gray scale and color Doppler sonography with extended field of view technique for the diagnostic evaluation of anterior urethral strictures. J Urol 2007;177:992-996.

8. Talreja SM, Tomar V, Yadav SS, et al. Comparison of so- noelastography with sonourethrography and retrograde urethrography in evaluation of male anterior urethral stric- tures. Turk J Urol 2016;42:84-91.

9. Gupta N, Dubey D, Mandhani A, Srivastava A, Kapoor R, Kumar A. Urethral stricture assessment: a prospective study evaluating urethral ultrasonography and conventional radiological studies. BJU Int 2006;98:149-153.

10. Chiou RK, Anderson JC, Tran T, Petterson RH, Wobig R, Taylor RJ. Evaluation of urethral strictures and associated Abnormalities using high-resolution and color Doppler ul- trasound. Urology 1996;47:102-107.

11. Allen D, Mishra V, Pepper W, Shah S, Motiwala H. A sin- gle-center experience of symptomatic male urethral diver- ticula. Urology 2007;70:650–653.

12. Shalev M, Mistry S, Kernen K, Miles BJ. Squamous cell carcinoma in a female urethral diverticulum. Urology 2002;59:773.

13. Cinman NM, McAninch JW, Glass AS, Zaid UB, Breyer BN. Acquired Male Urethral Diverticula: Presentation, Di- agnosis and Management. J Urol 2012;188:1204–1208.

14. Miller J, Hauck EW, Rohde V, Weidner W. Giant ureethral diverticulum – unusual complication following ventral buc- cal mucosa onlay graft urethroplasty. Urol Int 2006;77:368- 15. 370.Hatgaongar A. A Comparative Study of Sonourethrography

and Retrograde Urethrography in Evaluation of Anterior Male Urethral Strictures. Int J Sci Stud 2014;2:5-12.

16. Friedland GW, Nino-Murcia M, Gill HS, Perkash I. Ac- quired Nontraumatic Lesions of Urethra. In: Jafri SZH, Amendola MA, Diokno AC (eds). Lower Genitourinary Radiology: Imaging and Intervention. 1st edition, Springer, 1998:352-389.

17. Treviño-Rangel RdJ, Bodden-Mendoza BA, Cantú-Salinas N, García-Rodríguez MA. Decision-making in the manage- Fig 13. Periurethral abscess. The fluid is surrounding an artifi-

cial urethral sphincter’s cuff.

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tum in men. Zhonghua Yi Xue Za Zhi 2005;85:773-776.

22. Krukowski J, Czajkowski M, Kłącz J, Wawrzaszek O, Gołębiewska M, Matuszewski M. Primary urethral carcino-

King BF Jr, Goldman SM. Imaging of urethral disease:

a pictorial review. Radiographics 2004;24 Suppl 1:S195- S216.

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