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Diagnostic ultrasound ( PDFDrive )

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CHAPTER 10 The Prostate and Transrectal Ultrasound 393

SV

SV

V

RSV

A

B

C

C

LSV

FIG. 10.10 Infertility. (A) Bilateral dilated seminal

vesicles (SV) (>1.5 cm). This is presumptive evidence

of mechanical obstruction to the ejaculatory ducts, which

may be the cause of the infertility. The inding is not

speciic because this degree of enlargement can also

be seen in normal, fertile men. (B) Unilateral agenesis

of left seminal vesicle and vas deferens (V). Only the

right side is intact. (C) Unilateral right seminal vesicle

cyst (C); transvesical scan. This patient also had absence

of the ipsilateral right kidney. LSV, Left seminal vesicle;

RSV, right seminal vesicle.

4. Detection of genetic abnormalities (e.g., cystic ibrosis) that

may afect the health of children if afected sperm are harvested

or used for assisted reproductive techniques.

Male factors can be categorized as pretesticular, testicular, and

posttesticular. Pretesticular factors include conditions such as

faulty reproductive behavior and genetic abnormalities (e.g., CFTR

gene of cystic ibrosis, Y chromosome microdeletions). Testicular

factors include congenital and acquired intrinsic disorders of

spermatogenesis (e.g., infections, trauma, and treated cryptorchidism)

that, except for varicocele, are generally irreversible.

Also tumors and testicular microlithiasis are more common in

infertile men. Posttesticular causes of azoospermia (no sperm

in ejaculate) and oligospermia (low numbers of sperm in ejaculate)

generally relate to obstructive issues and are found in about 40%

of infertile men, although only 1% to 5% have ejaculatory duct

obstructions that are amenable to surgical therapies such as

prostate cyst unrooing or transurethral resection of ejaculatory

ducts. 50 his excludes vasectomy reversal, which is successful in

70% to 95% of patients and results in achievement of pregnancy

in 30% to 70% of couples. In 100 consecutive azoospermic men,

the causes of azoospermia were genetic abnormalities, 27%; diseases

or external inluence (orchitis, radiotherapy, infections, surgery,

trauma), 22%; corrected cryptorchidism, 27%; and unexplained,

22%. 51 his illustrates the broad spectrum of disorders apart from

ejaculatory duct obstructions that relate to azoospermia and that

are part of the investigation of infertile men. 48,49

Imaging investigations—ultrasound and MRI—are used to

evaluate for abnormalities and focus on the scrotum and testes,

prostate, and seminal ducts and occasionally the developmentally

related urinary tract. 50,52,53

he role of TRUS and increasingly MRI is to identify anatomically

correctable ejaculatory duct obstructions and anomalies in

men who are azoospermic or oligospermic and who have VD on

palpation. Obstructions can result from calculi in the vas, müllerian

or wolian duct cysts, postsurgical or inlammatory scars, calculi,

or atresia of the ejaculatory ducts (see Fig. 10.10). Note that the

presence or absence of the VD is diagnosed clinically by palpation

of the spermatic cord and not through imaging. Vasography has

been used to demonstrate obstruction, but this generally has been

discontinued because of the risk of injury to the VD. On occasion,

TRUS can be used to inject SVs with ultrasound or x-ray contrast

agents to demonstrate patency of the ejaculatory ducts or to retrieve

sperm from the SVs for assisted reproduction. 50,52,53

here are no speciic symptoms associated with ejaculatory

duct obstruction. he diagnosis is suggested in infertile males

with azoospermia or oligospermia who have low ejaculate volume,

normal secondary sex characteristics and testes, pain during or

ater ejaculation or orgasm, or history of prostatitis. he relative

frequencies of TRUS indings in infertile men with low-volume

azoospermia are as follows: normal appearance (25%); bilateral

absence of VD (34%); bilateral occlusion of the VD, SVs, and

ejaculatory ducts by calciication or ibrosis (16%); unilateral

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