Background/Aims: Seminal vesicle (SV) stones are a rare, and thus readily misdiagnosed condition in practice. Understanding the etiology, diagnosis, and management are crucial to guide a urologist's care, and are provided in this literature review. Methods: The inclusion criteria for the literature search, using the search engines MEDLINE® and PubMed was conducted using a combined query of “seminal vesicle stone” and the following keywords: calculi, hematospermia, calcification, and transrectal ultrasound (TRUS). Results: The etiology of SV stones is currently unknown where majority of the patients present with having painful ejaculation and hematospermia. However, clinicians have reported potential etiologies by categorization as an inflammatory or non-in-flammatory. A majority of the previous cases had shown multiple stones being present in the SV duct system that are typically diagnosed through radiological examination such as TRUS, MRI, or plain radiographs. Amongst the many imaging approaches, TRUS remains the primary imaging diagnoses of SV calculi. Transurethral seminal vesiculoscopy has shown to be used in an abundant of the case reports to be an ideal surgical approach for managing small SV stones. In regard to larger stones, a transperitoneal laparoscopic protocol is proper. Conclusion: The current imaging techniques have increased the case reports and diagnosis of SV calculi; however, more research is warranted for understanding the pathogenesis of the formation of SV stones. An optimal management of the extraction of SV stones depends on a number of factors such as size and location.

Seminal vesicles (SV) are paired secretory glands located posterior to the bladder in men that produce seminal fluid to maintain sperm. This seminal fluid contributes approximately up to 80% of the ejaculate volume [1]. Several benign and malignant conditions such as cysts, infections, abscess, neoplasms, and stones can afflict this organ. Presently, we focus on the latter - stones or calculi. White [2] had reported the first SV stone case in 1928, where a 48-year-old man complained of pain in the perineum and rectum along with urinary symptoms. However, SV stones are typically rare occurrences; limited cases have been reported mainly in adults older than 40 years of age, often associated with seminal vesiculitis, with some reports also in children. Since then, many of the cases have been related to urinary tract infections, anomalies, obstruction, and reflux into the ejaculatory duct [3]. Patients presenting with these stones may also be asymptomatic or symptomatic by expressing symptoms of peritoneal or testicular pain, painful ejaculation, low ejaculate volumes, hematospermia, or infertility. Transrectal ultrasound (TRUS) screening has been introduced in evaluating patients, detecting SV calculi in patients with hematospermia [4]. Due to the rarity of this condition, the etiopathogenesis of the stone formation is unclear to many clinicians leading to misdiagnosis and lack of awareness to various treatment protocols. The primary objective of this review is to facilitate the clinical importance by providing a comprehensive understanding of SV stones as well as compiling recent research to contribute the knowledge of the etiopathogenesis, clinical presentation, and available management options.

The SVs are part of the male genitourinary system, which is considered to be an accessory glandular structure of the male reproductive system [5]. The male genital organs consist of the penis, testes, excretory genital ducts, vas deferens, SVs, prostate, and bulbourethral glands. These organs work collectively together to generate and excrete semen, containing mature spermatozoa.

The SVs are bilateral glands approximately 5-7 cm in length. They are located dorsally to the bladder, and inferior and lateral to the vas deferens, posterior to the prostate, as well as superior to the rectum [6]. In addition, the SVs lie at the inferior end of the recto-vesicle space in the pelvic cavity. The ducts of the SV join with the ampulla of the vas deferens to form the ejaculatory duct. The ejaculatory ducts extend further inferiorly, which drain into the prostatic urethra through the verumonta-num. The primary function of SVs is to secrete a fluid that forms a majority of the ejaculate; however, SVs are not a reservoir of the semen [7]. The fluid that is secreted is composed of proteins, fructose, and various other enzymes that provide nutrition for the spermatozoa.

When evaluating through imaging, a normal SV appears to be elongated fluid-containing structures. The deviations in the appearance are secondary to age and hormonal changes in a patient. Normally, SVs shrink following the age of 70.

The nuclei of SV stones are composed of epithelial cells and a mucoid substance that is covered with lime salts [8]. Previous literature reports have shown SV stones to be composed of calcium phosphate, magnesium ammonium phosphate (e.g. struvite), or protein matrix. Menon et al. [9] found that most of the calculi are coated with calcium phosphate, phosphate, urate, carbonate, and struvite. However, Hepburn et al. [10] did not find any abnormality in the urinalysis of the calcium-coated calculi. In addition, Han et al. [11] reported the composition of the SV stone to be calcium fluorophosphate while Yun et al. [3] reported it as carbonate apatite along with urine reflux indicating it as an infectious stone.

The exact etiology of SV stones remains unclear. Analyses of SV stones are conducted through imaging; however, no definite cause has been ascertained to SV stones. Table 1 presents potential etiologies that have been reported [12].

Table 1

Differential diagnosis for calcification of the SV

Differential diagnosis for calcification of the SV
Differential diagnosis for calcification of the SV

Calcification of SV

Calcification of the vas deferens and SV is a rare condition of unknown incidence. Calcification of the SVs was first discovered in the year of 1906 by reporting calcium deposition in the right SV as well as in the left vas deferens [13]. In regard to the etiology, calcification cases of SV have been divided into inflammatory and non-inflammatory. The latter type is prevalent in patients of old ages secondary to sclerosis and impaired nutrition of the musculature and connective tissue of the SV, including the ampulla and ejaculatory ducts [14].

In 1951, based on radiographs depicting calcifications of vas deferens, Wilson et al. [15] associated the calcifications with diabetes mellitus (DM) and atherosclerotic changes. In his study, 93% of the patients exhibited DM and 2 patients presented with chronic inflammation of the genital tract as a presumed risk factor towards the calcifications. The role of DM in calcification is suggested to be due to insulin therapy, where patients suffering from DM for many years will exhibit degenerative vascular disease [16]. In regard to the inflammatory type, the calcifications can be mucosal or submucosal and, as a result, there may be partial or complete obstruction of the vas deferens [17,18,19]. In 2006, the analysis of SV stones by infrared spectroscopy had revealed magnesium ammonium phosphate [19]. However, no present cause has been ascertained towards the pathogenesis of SV calcification. Stasinou et al. [18] reported that the pathogenesis of the calcification of the wall of the SVs should be differentiated from SV stones.


Hematospermia is the presence of blood in seminal fluid. It is a relatively frequent urologic condition, which causes severe anxiety to patients and may be caused by inflammation, obstructive cystic lesions, calculi, benign or malignant neoplasms, and stasis [4,20,21]. However, malignancies are rare instances in causing hematospermia. In many patients presenting with hematospermia, calculi of ejaculatory ducts have found to be the root cause [22].

Impaired Drainage and SV Cysts

SV cysts are a rare entity that may be congenital or acquired and generally associated with hematospermia. However, SV cysts have been reported in cases where SV calculi have been present [22,23]. Stones may form secondary to the obstruction caused by the cysts as well as to the drainage of the secretions during ejaculation. Such calculi can contribute to wall thickness in the ejaculatory duct leading to the impaired drainage [20]. This has been noted in 60% of the case reports of patients diagnosed with SV calculi [20]. In a study where pancreatic stones were shown to have similar composition as SV calculi, it suggested that the lack of proteases be linked to SV stone formation [23]. SV cysts appear as large, anechoic masses on TRUS [4].

In addition, a few cases have reported urine reflux into ejaculatory ducts on post-voiding cystography. A combination of impaired drainage of the ejaculatory duct, urine reflux, urinary tract infections, and seminal vesiculitis can lead to the formation of SV calculi [1]. Yun et al. [3] reported that the reflux from the urethra to the SVs was identified in the retrograde urethrogram.

Physical Examination and Symptoms

Common symptoms for SV calculi ranges from asymptomatic to patients exhibiting hematospermia, per-ineal or testicular pain, painful ejaculation, or low ejaculation volume [19]. Ejaculatory pain and hematospermia are the two most common symptoms that lead patients to seek medical care. SV stones can be distinguished from a condition such as posterior urethral hemangioma as it uniquely presents with dark red blood-semen mixture with ejaculation pain and no blood clots - symptoms which withdraw upon anti-infective treatment [24]. Table 2 displays the diverse profiles of some symptoms occurring in patients associated with SV calculi. The occurrences of each symptom were gathered from case report studies that are depicted in Table 3. SV stones that are large and hard masses can be palpable during a rectal examination.

Table 2

Symptoms presenting with SV stones

Symptoms presenting with SV stones
Symptoms presenting with SV stones
Table 3

Profiles of reported cases of SV stones

Profiles of reported cases of SV stones
Profiles of reported cases of SV stones


Imaging is the conventional way of diagnosing stones present in the SVs. Noninvasive imaging is recommended for essential diagnostic evidence of stones. Modalities for diagnosis include vasoseminal vesiculography, MRI, CT, and TRUS. Vasoseminal vesiculography is an invasive procedure; the lesion of the puncture site may be too narrow which can induce secondary seminal ductal obstruction [25]. The diagnosis of SV calculi can be done through an MRI, which is able to visualize the distal duct system. Nevertheless, its high expense detracts from its preference [20]. Clinicians advise that the combination of an endorectal coil and MRI will provide a more viable diagnosis. However, it has been noted that these examinations yield a false-positive rate as well as diagnostic limitations secondary to the false-negative cases [25]. Thus, clinical applications through the diagnosis of an MRI are limited. It was also previously reported that CT scans are not viable due to the poor visualization of the distal duct system.

TRUS is a noninvasive examination frequently used for diagnosing stones, cysts, increases in SV volume, Mullerian duct remnants, prostatic varices, and inflammatory changes [25,26]. It has shown to be the most accurate form of visualization of the distal duct system along with assorted abnormalities, which can provide clinicians with a comprehensive visual examination to administer the appropriate treatment protocols [20]. In a single case-control study using TRUS, calculi within the SVs appeared as well-circumscribed, hyperechoic, foci separate from the typical septal architecture of the prostate gland, with or without acoustic shadowing [22]. In children, a retrograde urethrogram or voiding cys-tourethrogram may be used to distinguish between SV and posterior urethral calculi [19].

Non-Surgical Treatment Protocols

Pre-Operative Sperm Banking. Patients who receive fertility preservation consultation often proceed to sperm banking, which provides a sense of security and reassurance in the future. Sperm banking is a noninvasive procedure that involves the collection and freezing of sperms for potential use in the future [27].

Surgical Intervention

SV calculi must be corrected through surgical treatment in a timely fashion, as they may progress to worsened pain and potentially obstruct the SVs leading to the need for an emergency surgery. Upon diagnosis through the various noninvasive diagnostic methods, including high-resolution TRUS, MRI, CT, or plain radiographs, the patient is recommended to undergo surgery for the removal of the stones present in the SV. However, the choice of surgical protocol depends on the location and size of the stone.

Endoscopic Removal. The SV organ is difficult to access. Most open surgical approaches used for treating primary or secondary lesions of the SVs have inherent shortcomings and require a significant incision for access [8]. However, open operation requires extensive dissection which might cause morbidities associated with an exposed operative field, long operative time, and intraperitoneal rupture [11]. Laparoscopic and endoscopic approaches are substitutes to the standard surgical treatments in order to overcome these complications. The first large sample study of transurethral endoscopy technique was conducted in 2002 by Yang et al. [28] where patients were suffering from SV disease, concluding that the method was feasible and safe.

Transurethral Seminal Vesiculoscopy. The standard recommended therapy includes laparoscopic/open seminal vesiculectomy or transurethral resection of ejacula-tory duct (TURED). Previous studies have reported that status post TURED has improved semen parameters by 50-60% in patients, despite being associated with a high risk of complications such as the impairment of semen parameters, retrograde ejaculation, urine reflux into the seminal duct, urinary incontinence, and rectal injury causing urethral fistula [25,29]. Postoperative complications of TURED are rare but often severe; for this, the procedure requires highly technical skills.

In recent years, transurethral seminal vesiculoscopy (TRU-SVS) has shown to be a safe, minimally invasive surgical procedure for the management of both SV and ejaculatory duct calculi. In comparison to TRUS, TRU-SVS requires surgical skills, anesthesia, and antibiotic cover. A retrospective study of TRU-SVS utilized a 6F vesiculoscope inserted through the orifice of the veru-montanum in a retrograde manner. Following insertion, the calculi were removed using grasping forceps or by disrupting the calculi with a holmium laser. Clinicians should be cautious regarding the insertion of the ve-siculoscope to avoid secondary injury to the urethra or rectum. Xu et al. [30] had used a 9F rigid ureteroscope in which gaining entry into the SV became challenging where applying excessive force could cause damage to the tissue. Thus, a 6F vesiculoscope is likely safer and more effective than using a 9F ureteroscope. TRU-SVS has shown to be a more attractive option than TURED due to lower complications and having significant improvement in sperm counts and ejaculation volume, thus improving fertility [29]. The avoidance of urine reflux was also postoperatively observed. Furthermore, seminal vesiculography can be performed transrectally in patients who do not want to undergo a transurethral procedure [31]. Many case reports have proven that TRU-SVS can lead to the solution of treating seminal vesiculitis, hema-tospermia, ejaculatory duct obstruction, and infertility.

Endoscope Laser Lithotripsy. Seminal vesiculoscopy with endoscopic laser lithotripsy is an efficient and safe minimally invasive surgical approach, where patients are able to recover fully 1 day after.

Laparoscopic Removal. The transurethral endoscopy approach had been used in cases where patients had stone sizes of less than 3.5 cm and did not undergo the correction of the dilated SV [3]. A 20-year-old male had presented with a stone size of 6.0 × 3.5 × 3.5 cm which consequently dilated the SV wall. However, the transurethral endoscopic removal was too narrow to reach the stone as well as impossible to remove the dilated SV. Yet, the transperitoneal laparoscopic approach allowed for stone removal as well as the anatomical correction of the SV, with respect to larger stones. Laparoscopic surgery may be conducted where the patient must be placed under general anesthesia. The total operative time ranges 80-120 minutes [11].

In the transperitoneal laparoscopic approach, with the camera placed at the umbilicus, 4 auxiliary ports were utilized: 11 mm at the lateral border of the rectus muscle and a 5 mm port on the iliac fossa [3]. Under the direct vision of Cul-de-sac, the left SV, bladder, and rectum were visualized. Further, the retrovesical peritoneum was incised transversely, in which the SV was easily identified. The stone was then extracted upon incision of the SV by dissecting medially to the ampulla, through the extended 11 mm trocar site incision. The dilated wall was dissected and excised at one-third of proximal SV. The remained vesicle is secured with sutures.

Since the first report of SV calculi in 1928, only a few cases have been reported as shown in Table 3. Because SV calculi are considered to be rare, the etiology and pathogenesis of the formation of the stone is unclear. It is often associated with hematospermia, ejaculatory pain, and low ejaculation volume. The diagnoses of SV stones have been easily identified due to upcoming diagnostic modalities. Majority of the case reports had identified the stones through TRUS, where clinicians have proven to be an ideal detection of SV calculi. Several surgical approaches have been described to manage SV calculi. Each surgical protocol is specific for the location and size of the stone due to SV to be a difficult organ to access, requiring significant incisions to access. TRU-SVS is considered a safe and effective method in the management of SV calculi, more specifically when small stones are present in the SV. In regard to larger stones, a laparoscopic approach is advised due to the endoscopic approach is unable to extract the stone. The surgical protocols have been proven to have no recurrence postopera-tively. Evaluation through modern imaging is ongoing in understanding the pathogenesis of SV stones.

The authors are thankful to Drs. Kelly Warren, Inefta Reid, Todd Miller, and Peter Brink for departmental support, as well as Mrs. Wendy Isser and Ms. Grace Garey for literature retrieval.

Christodoulidou M, Parnham A, Nigam R: Diagnosis and management of symptomatic seminal vesicle calculi. Scand J Urol 2017; 51:237-244.
Uchijima Y, Hiraga S, Akutsu M, Yoshida K, Hobo M, Okada K: stones of the seminal vesicles and ejaculatory duct in infant: Report of a case. Hinyokika Kiyo 1984;30:1843-1849.
Yun S, Kim T, Kwon W, Kim YJ; Lee SC, Kim WJ: A largestone in the dilated left seminal vesicle: Laparoscopic removal andpartial seminal vesiculectomy. Korean J Urol 2008; 49:656-658.
Yagci C, Kupeli S, Tok C, Fitoz S, Baltaci S, Gogus O: Efficacy of transrectal ultrasonography in the evaluation of hematospermia. Clin Imaging 2004;28:286-290.
Dagur G, Warren K, Suh Y, Singh N, Khan SA: Detecting diseases of neglected seminal vesicles using imaging modalities: a review of current literature. Int J Reprod Biomed (Yazd) 2016;14:293-302.
McKay AC, Sharma S: Anatomy, seminal vesicle. Statpearls. Treasure Island (FL)2018.
Reddy MN, Verma S: Lesions of the seminal vesicles and their MRI characteristics. J Clin Imaging Sci 2014;4:61.
Ozgok Y, Kilciler M, Aydur E, Saglam M, Irkilata HC, Erduran D: Endoscopic seminal vesicle stone removal. Urology 2005;65:591.
Menon M, Resnick MI: Urinary lithiasis: etiology, diagnosis and medical management; in Walsh PC, Retik AB, Vaughan ED Jr, Wein AJ (eds): Campell Urology, ed 7. Philadelphia, WB Saunders, 1998.
Hepburn JS, Yount PE: Chemical composition of seminal vesicle calculi. J Franklin Inst 1947;243:487.
Han P, Yang YR, Zhang XY, Wei Q: Laparoscopic treatment of a calcium fluorophosphate stone within a seminal vesicle cyst. Asian J Androl 2008;10:337-340.
Schned AR, Cozzolino DJ: Idiopathic dense calcification of the seminal vesicles. J Urol 1997;157:2263.
George S: Calcification of the vas deferens and the seminal vesicles. JAMA 1906;47:103.
Bacic J, Kuzmic M: Spermolithiasis. Int Urol Nephrol 1975;7:235-239.
Wilson JL, Marks JH: Calcification of the vas deferens; its relation to diabetes mellitus and arteriosclerosis. N Engl J Med 1951; 245:321-325.
Andersen PE: Calcification of the vasa deferentia. Acta Radiol 1950;34:89-95.
Herts BR: Calcification of the seminal vesicles. J Urol 2015;194:209-211.
Stasinou T, Bourdoumis A, Owegie P, Kachrilas S, Buchholz N, Masood J: Calcification of the vas deferens and seminal vesicles: a review. Can J Urol 2015;22:7594-7598.
Iqbal S, Ansari MS: Idiopathic bilateral giant seminal vesicle calculi and calcification of the male ejaculatory system: current review of diagnosis and management. Indian J Surg 2006;68:38-40.
Razek AA, Elhanbly S, Eldeak A: Transrectal ultrasound in patients with hematospermia. J Ultrasound 2010;13:28-33.
Raviv G, Laufer M, Miki H: Hematospermia - the added value of transrectal ultrasound to clinical evaluation: Is transrectal ultrasound necessary for evaluation of hematospermia? Clin Imaging 2013;37:913-916.
Littrup PJ, Lee F, McLeary RD, Wu D, Lee A, Kumasaka GH: Transrectal US of the seminal vesicles and ejaculatory ducts: clinical correlation. Radiology 1988;168:625-628.
Corriere JN Jr: Painful ejaculation due to seminal vesicle calculi. J Urol 1997;157:626.
Tian L, Han H, Lei HE, Zhang XD: Clinical features of haematospermia associated with seminal vesicle calculi versus posterior urethral haemangioma. Andrologia 2018;58: e13072.
Han CH, Liang Q, Dong BZ, Hao L, Fan T, Zhang JJ, Zhang WD, Chen B, Qiu XZ, Zhou XJ, Pei CS: The transurethral seminal vesiculoscopy in the diagnosis and treatment of the seminal vesicle disease. Cell Biochem Biophys 2013;66:851-853.
Kumar P, Kapoor S, Nargund V: Haematospermia - a systematic review. Ann R Coll Surg Engl 2006;88:339-342.
Frankel Kelvin J: Sperm banking: fertility preservation for male patients with cancer. Clin J Oncol Nurs 2015;19:108-110.
Yang SC, Rha KH, Byon SK, Kim JH: Transutricular seminal vesiculoscopy. J Endourol 2002;16:343-345.
Wang H, Ye H, Xu C, Liu Z, Gao X, Hou J, Wang L, Piao S, Sun Y: Transurethral seminal vesiculoscopy using a 6F vesiculoscope for ejaculatory duct obstruction: initial experience. J Androl 2012;33:637-643.
Xu B, Niu X, Wang Z, Li P, Qin C, Li J, Liu B, Wang P, Jia Y, Wu H, Zhang W: Novel methods for the diagnosis and treatment of ejaculatory duct obstruction. BJU Int 2011; 108:263-266.
Meyer JJ, Hartig PR, Koos GW, McKinley CR: Transrectal seminal vesiculography. J Urol 1979;121:129-130.
Font MD, Pastuszak AW, Case JR, Lipshultz LI: An infertile male with dilated seminal vesicles due to functional obstruction. Asian J Androl 2017;19:256-257.
Lee TH, Juan YS, Jang MY, Wang SH, Shen JT: Successful seminal vesiculoscopic lithotripsy of seminal vesicle stone: a case report and literature review. Urol Sci 2014;25:134- 136.
Wesson L, Steinhardt G: Case profile: seminal vesicle stones. Urology 1983;22:204- 205.
Etherington RJ, Clements R, Griffiths GJ, Peeling WB: Transrectal ultrasound in the investigation of haemospermia. Clin Radiol 1990;41:175-177.
Li YK: Diagnosis and management of large seminal vesicle stones. Br J Urol 1991;68: 322-323.
Wilkinson AG: Case report: calculus in the seminal vesicle. Pediatr Radiol 1993;23:327.
Amano T, Kunimi K, Ohkawa M: Transrectal ultrasonography of the prostate and seminal vesicles with hemospermia. Urol Int 1994;53:139-142.
Worischeck JH, Parra RO: Chronic hematospermia: assessment by transrectal ultrasound. Urology 1994;43:515-520.
Cho IR, Lee MS, Rha KH, Hong SJ, Park SS, Kim MJ: Magnetic resonance imaging in hemospermia. J Urol 1997;157:258-262.
Carachi R, Gobara D: Recurrent epididymo-orchitis in a child secondary to a stone in the seminal vesicle. Br J Urol Int 1997; 79:997.
Lencioni R, Ortori S, Cioni D, Morelli G, Ceretti E, Cosottini M, Menchi I, Bartolozzi C: Endorectal coil MR imaging findings in hemospermia. MAGMA 1999;8:91-97.
Gordon Z, Monga M: Endoscopic extraction of an ejaculatory duct calculus to treat obstructive azoospermia. J Endourol 2001;15: 949-950.
Kilciler M, Saglam M, Ozgok Y, Somuncu I, Erduran D, Harmankaya C: Giant seminal vesicle stones. Report of two cases. Urol Int 2002;69:250-251.
Namjoshi SP: Large bilateral star-shaped calculi in the seminal vesicles. J Postgrad Med 2002;48:122-123.
Cuda SP, Brand TC, Thibault GP, Stack RS: Case report: endoscopic laser lithotripsy of seminal-vesicle stones. J Endourol 2006;20: 916-918.
Modi PR: Case report: endoscopic management of seminal vesicle stones with cutaneous fistula. J Endourol 2006;20:432-435.
Vellayappan BA, Tiong HY, Chua WJ, Consigliere DT: Seminal vesicle calculus after transurethral resection of ejaculatory duct. Can J Urol 2007;14:3595-3597.
Prando A: Endorectal magnetic resonance imaging in persistent hemospermia. Int Braz J Urol 2008;34:171-177.
Han WK, Lee SR, Rha KH, Kim JH, Yang SC: Transutricular seminal vesiculoscopy in hematospermia: Technical considerations and outcomes. Urology 2009;73:1377-1382.
Hadidi M, Hadidy A, Alrabadi AF, Ahdul-Wahab AD, Murshidi MM: Bilateral very large calcium oxalate stones in the seminal vesicles: case report and literature review. Urol Res 2011;39:509-513.
Song T, Zhang X, Zhang L, Fu WJ: Transurethral seminal vesiculoscopy in the diagnosis and treatment of seminal vesicle stones. Chin Med J (Engl) 2012;125:1475-1478.
Xing C, Zhou X, Xin L, Hu H, Li L, Fang J, Liu Z: Prospective trial comparing transrectal ultrasonography and transurethral seminal vesiculoscopy for persistent hematospermia. Int J Urol 2012;19:437-442.
Liu B, Li J, Li P, Zhang J, Song N, Wang Z, Yin C: Transurethral seminal vesiculoscopy in the diagnosis and treatment of intractable seminal vesiculitis. J Int Med Res 2014;42:236-242.
Xiao HJ, Pang J, Liu XP: The aetiology and efficacy of endoscopic interventions for the treatment of persistent and recurrent hemospermia (abstract). J Endourol 2014;28:A256.
Williams SA, Christodoulidou M, Nigam R: Large bilateral seminal vesicle calculi presenting with spermolithiasis. BMJ Case Rep 2017;2017.
Open Access License / Drug Dosage / Disclaimer
This article is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND). Usage and distribution for commercial purposes as well as any distribution of modified material requires written permission. Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug. Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.