Page 155 - Remedial Andrology
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10.6.1.1   Classification of obstructive azoospermia
            10.6.1.1.1  Intratesticular obstruction
            Intratesticular obstruction occurs in 15% of men with OA  [1832]. Congenital forms are less common than
            acquired forms (post-inflammatory or post-traumatic) (Table 42).

            10.6.1.1.2  Epididymal obstruction
            Epididymal obstruction is the most common cause of OA, affecting 30-67% of azoospermic men [1832-1835].
            Congenital epididymal obstruction usually manifests as CBAVD, which is associated with at least one mutation
            of the CF gene in 82% of cases [1835]. Other congenital forms of epididymal obstruction include chronic sinu-
            pulmonary infections (Young’s syndrome)  [1836]. Acquired forms secondary to acute (e.g., gonococcal) and
            subclinical (e.g., Chlamydial) epididymitis are most commonly due to infections [1837, 1838]. Other causes may
            be trauma or surgical intervention [1839, 1840] (Table 42).

            10.6.1.1.3  Vas deferens obstruction
            Vas deferens obstruction is the most common cause of acquired obstruction following vasectomy  [1837]
            (Table 42). Approximately 2-6 % of these men request vasectomy reversal (see 2019 EAU Guidelines on Male
            Infertility). Vasal obstruction may also occur after hernia repair  [1841, 1842]. The most common congenital
            vasal obstruction is CBAVD, often accompanied by CF. Unilateral agenesis or a partial defect is associated with
            contralateral seminal duct anomalies or renal agenesis in 80% and 26% of cases, respectively [1524].

            10.6.1.1.4  Ejaculatory duct obstruction
            Ejaculatory duct obstruction is found in 1-5% of cases of OA and is classified as cystic or post-inflammatory
            or calculi of one or both ejaculatory ducts [1664, 1843] (Table 42). Cystic obstructions are usually congenital
            (i.e., Mullerian  duct  cyst  or  urogenital  sinus/ejaculatory  duct  cysts)  and  are  typically  midline.  In  urogenital
            sinus abnormalities, one or both ejaculatory ducts empty into the cyst  [1844], while in Mullerian duct
            anomalies, the ejaculatory ducts are laterally displaced and compressed by the cyst  [1845]. Paramedian or
            lateral intraprostatic cysts are rare [1846]. Post-inflammatory obstructions of the ejaculatory duct are usually
            secondary to urethra-prostatitis [1847]. Congenital or acquired complete obstructions of the ejaculatory ducts
            are commonly associated with low seminal volume, decreased or absent seminal fructose, and acidic pH. The
            seminal vesicles (anterior-posterior diameter > 15 mm) and ejaculatory duct (> 2.3 mm in width) are usually
            dilated [1843, 1847-1849].

            10.6.1.1.4.1   Functional obstruction of the distal seminal ducts
            Functional obstruction of the distal seminal ducts might be attributed to local neurogenic dysfunction [1850].
            This abnormality is often associated with urodynamic dysfunction. Impaired sperm transport can be observed
            as idiopathic or due to spinal cord injury, multiple sclerosis, retroperitoneal lymph node dissection, pelvic
            surgery, SSRIs, α-blockers and typical antipsychotic medications [1851].

            Table 42: Causes of obstruction of the genitourinary system

             Epydidimis
             Infection (acute/chronic epididymitis)
             Trauma
             Post-surgical iatrogenic obstruction (i.e., MESA; hydrocelectomy or other scrotal surgery)
             Congenital epididymal obstruction (usually manifests as congenital bilateral absence of the vas deferens
             [CBAVD])
             Other congenital forms of epididymal obstruction (Young’s syndrome)
             Vas deferens
             Vasectomy
             Vasotomy/vasography (with improper technique)
             Post-surgical iatrogenic obstruction (i.e., scrotal surgery or herniorraphy)
             Congenital unilateral (CUAVD) or bilateral absence of the vas deferens (CBAVD)
             Ejaculatory ducts
             Cysts (Mullerian utricular, prostatic or seminal vesicular)
             Infection (acute/chronic epididymitis)
             Traumatic
             Post-surgical iatrogenic obstruction
             Functional obstruction
             Idiopathic/acquired local neurogenic dysfunction



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