Comparative experimental re-evaluation of the two implanting methods of silicone gel testicular prostheses in beagle dogs
© Hao et al; licensee BioMed Central Ltd. 2011
Received: 4 October 2010
Accepted: 2 April 2011
Published: 2 April 2011
Testicular prosthesis has been applied clinically for decades, and implantation of testis prosthesis under the tunica albuginea has been considered to be the standard method in the most of the reports. However, postoperative scrotal appearance, the mobilization and the palpitation of the prosthesis are not always satisfactory to all the patients. Modifications in surgical techniques might be necessary to bring improvements to the clinical outcomes in testicular prosthesis implantation.
In a group of 9 beagle dogs in this study, an orchiectomy succeeded with a testicular prosthesis implantation under the tunica vaginalis, and a complete mechanical denudation of the testicular parenchyma succeeded with an implantation under the tunica albuginea were performed, respectively. Histopathological evaluations of the scrotal tissues and the implants, which were made at the end of the follow-up, showed that all the tested animals lived uneventful lives during the follow-up period, and no rejections or infections were found. Prostheses implanted under the tunica vaginalis showed a more satisfying mobilization and palpation than those implanted under the tunica albuginea. Chronic inflammation in the para-prosthesis tissues with vascular proliferation and fibrinogenesis were more common in the "under tunica albuginea" group than that in the "under tunica vaginalis" group, although differences in fibrinogenesis between the two groups were found to be statistically insignificant.
In this comparative study, we have re-evaluated the two most popular implantation methods of testicular prosthesis, the "under the tunica albuginea" and the "under the tunica vaginalis" pathways, in animal models. We found that the testicular prosthesis were all well tolerated, but the prosthesis implanted under the tunica vaginalis showed a more satisfying result concerning appearance, palpability, and histopathological findings than that of the "under the tunica albuginea" group. The "under the tunica vaginalis" method might become a more practical method for future testicular prosthesis implantation.
The psychological effect of castration secondary to the loss of testes as a result of testicular trauma, cancer or spermatic cord torsion often results in negative impacts to the lives of the patients. In the past, prostate cancer was once considered to be rare in the Chinese population. Nowadays, the incidence of prostate cancer in the Chinese population is increasing rapidly. As an alternative to surgical treatment of prostate cancer, orchiectomy is often performed. In China, during the past several decades, fewer demand for reconstruction of the "vacant" scrotum was actively requested by these patients. With the social and economic changes in China, the demand for testicular prosthesis is increasing rapidly now. However, postoperative pain still remains a relatively common problem for the testicular prosthesis recipients. The relationship between the surgical technique and the location of the prosthesis remains unclear. In the present study, comparative observations concerning the effects of silicone gel testicular prostheses implanted in different locations, "under the tunica albuginea" or "under the tunica vaginalis", in Beagle dogs are reported.
The testicular prostheses used in the present study were a product of the Weining Rubber Product Company (Shanghai, China). The prostheses consisted of two components, silica gel as the filler, and silicon rubber as the shell. According to pre-operative measurements of the testicles, the prostheses were manufactured in the range of 4.0 to 6.0 ml, and sterilized with ethylene oxide prior to use. The safety and biocompatibility of the prosthesis has been tested in accordance with the institutional review board.
Overall, nine healthy adult male Beagle dogs were enrolled in the present study. The study protocol was approved by the Institutional Ethical Committee.
Levels of serum testosterone, kidney function, and liver function of all the dogs were tested before and after the implantation of testicular prosthesis.
Following intravenous administration of a mixture of Sumianxin II (Institute of Animal Science, Changchun University of Agriculture and Animal Sciences) and ketamine (Shanghai No.1 Biochemical Pharmaceutical Co., Ltd.) in a 1:1 ratio, a midline scrotal incision was made in each side of the scrotum. For the left, a longitudinal incision in the tunica albuginea was made, and the testicular parenchyma was carefully denuded bluntly with a stainless steel scalpel holder. For homeostasis, the inner surface of the tunica albuginea was gently pressed with gauze. For the right, a routine orchiectomy was performed with the spermatic stump transfixed using silk suture.
NSAIDS (Indomethacin Suppositories, 25 mg) was given to the dogs every 12 hours in the first 7 postoperative days. The animals were followed up for a period of 3 months, and the testis together with the whole scrotum was removed en bloc at the end of the observation. All the samples were preserved in 4% formaldehyde solution for later histopathological evaluations.
Qualitative and quantitative evaluation under a standard light microscope for levels of chronic inflammation and fibrosis were made according to the criteria below referring to the Karademir's Method with appropriate modifications :
The presence of plasmocytes, hystiocytes, lymphocytes as well as vascular proliferation in the tissues around the prosthesis or testicle was graded from 0 to 3.
0 = No inflammation.
1 = Focal inflammation areas with little vascular proliferation.
2 = Medium level inflammation, where sparse inflammation exists in all microscope fields.
3 = Significant inflammation with dense infiltration and vascular proliferation.
The fibrohyalinization in the surrounding tissue was evaluated. All the parameters were measured in 10 separate microscopic fields from different sites.
Grade I: Focal and mild fibroblastic activation.
Grade II: Diffuse mild fibroblastic activation.
Grade III: Significant fibroblastic activation.
For statistical evaluation, SPSS 16.0 software was used. Variables are presented as mean ± SD. A Mann-Whitney U-test was utilized for data analysis and a level of p < 0.05 was considered to be statistically significant.
During the follow-up of 3 months, all the nine research subjects survived uneventfully with no apparent weight loss. Postoperative slight scrotal edema was found in both side of the scrotum and lasted for 3 days and 7 days for the right and the left, respectively. Rejection and infection were not found in any of the prosthesis-implanted dogs. In all the dogs, the scrotal wounds healed within a week after surgery, and proliferative scar or keloid tissue were not present. The testicular prostheses were mobile and palpated at normal localizations in the right scrotum. However, in 7 out of the 9 dogs, prostheses in the left scrotum were found to be slightly asymmetric to and hanged higher than that in the right. As for the palpation, the prosthesis in the left scrotum seemed to be more rigid than that in the right.
The prostheses were removed en bloc together with the scrotal wall at the end of the follow- up. All the prostheses were well enclosed by surrounding tissues, and no apparent interspace was found between the tunica vaginalis and the tunica albuginea in the left scrotum. No macroscopic leakage of the contents from the testicular prostheses was identified. The prostheses could be easily detached from the tunica albuginea or the tunica vaginalis.
Comparison of chronic inflammation between the two groups
Left (n = 9)
Right (n = 9)
Comparison of fibrosis between the two groups
Left (n = 9)
Right (n = 9)
Liver and kidney function before and after implantation of testicular prosthesis ( ± s, n = 9)
36.2 ± 5.3
39.2 ± 4.3
37.5 ± 5.1
32.3 ± 6.6
30.8 ± 5.4
51.1 ± 6.3
49.6 ± 5.1
48.8 ± 6.1
50.5 ± 4.7
46.3 ± 3.8
40.5 ± 3.6
38.1 ± 2.7
40.2 ± 3.8
39.7 ± 5.5
37.2 ± 4.6
3.5 ± 0.6
3.6 ± 0.3
2.5 ± 0.3
4.0 ± 0.5
3.1 ± 0.2
37.0 ± 8.1
38.5 ± 7.6
32.8 ± 6.1
35.5 ± 5.3
30.1 ± 4.9
66.5 ± 3.9
65.4 ± 4.2
57.5 ± 3.0
60.6 ± 4.2
58.3 ± 6.1
2.3 ± 0.1
2.6 ± 0.3
3.1 ± 0.2
2.9 ± 0.3
2.4 ± 0.3
27.6 ± 3.1
29.1 ± 2.8
30.2 ± 2.2
27.9 ± 1.8
30.5 ± 2.2
Testicular prosthetic devices have been developed to restore the normal appearance of the scrotum and hopefully to restore quality of life. The first testicular prosthetic device was introduced in 1939 by Bowers using the metal alloy vitalium . The practicality and safety of testicular prostheses has been tested clinically for several decades, especially following the immergence of the silicone gel prosthesis in the 1970s . Despite the concerns over the relationship of silicone implants to connective tissue disease [4–6], multispecialty expert panels in the United States (Institute of Medicine and the National Science Panel) and the United Kingdom failed to find evidence which could indicate any causal linkage between them. Silicone gel filled implants are currently still widely used all over the world, especially in China .
For successful testicular prosthesis implantation, the key to the surgical procedure is the correct positioning of the prosthesis in right location within the scrotum. Surgically, the traditional inguinal procedure for testicular prosthesis implantation has been applied for a long time, and has proven to be minimally successful in maintaining the mobility and sensibility of the "testis". For this traditional method, there is a possibility of inguinal migration of the prosthesis, spontaneous exit of the implant, infection, hemorrhage, breakage of the implant, or persistent pains. With developments in surgical techniques, testicular prosthesis implantation techniques have improved greatly, and scrotal procedures with the testicular prosthesis implanted under the tunica albuginea after denudation of the testicular parenchyma has been practiced for many years. According to the literature, this technique has proven to be successful, especially with regard to cosmetic appearance (mobility and sensibility, etc.) . Despite these benefits, clinical observations have indicated that a postoperative pain rate in 1% to 5%, or even to 9% can be found in the prosthesis recipients [9–11]. In the past, the majority of the recipients of testicular prosthesis in China were those with unilateral or bilateral testicle loss from scrotum injuries, testicular cancers, or testicular torsions. Nowadays, with the increasing incidence of prostate cancer, the demand for testicular prosthesis implantation has also increased rapidly. In our clinical practices, scrotal (under the tunica vaginalis) or subalbugenous (under the tunica albuginea) implantation of the testicular prosthesis are the two most popular surgical methods performed in this field. Despite a relative higher general satisfaction rate to these procedures in most of the recipients, discomforts, especially postoperative pains, have become a common problem. This phenomenon exposed the need for a comparative re-evaluation between these two methods on a basis of scientific study. For a successful testis prosthesis implantation, the recipient's satisfaction is a very important issue. However, it is a subjective problem, and we could only get it from human recipients. As for an intensive investigation, especially the histopathological study, we have to use animal models. In fact, human recipients' satisfaction with their testis prosthesis had been reported in a lot of literatures in the past. Because the focus of this study is on those objective issues, such as the reasons for pains, asymmetric appearances, and palpations, etc., so we decided to take an animal model.
In this perspective controlled animal study, a popular testicular prosthesis material, silicone gel, is used to obviate the interference from prosthesis materials. In order to maintain a relatively reasonable comparability, testicular prosthesis are implanted in each side of the scrotum but at different locations, with one inside the scrotal cavity (under the tunica vaginalis) after regular orchiectomy and another under the tunica albuginea following denudation of the testicular parenchyma. During a follow-up of 3 months, we found no incidence of infection, rejection or rupture of the implants, and all the 9 dogs survived uneventfully. These results indicate the safety of the silicone gel prosthesis utilized. Apparently, this is not a indicative of the superiority of this testicular prosthesis to the materials used in other studies .
In animal experiments, one can not objectively quantify the subjective feelings of recipient animals. However, postoperative scrotal appearances and histopathological findings might provide useful information. In the present study, we found that in 7 out of the 9 animals, the bilateral scrotum were not symmetric, with the left "testicle" in a relative higher position. On the one hand, we attribute this to the equal gravity but unequal support to the prosthesis in the bilateral scrotum, where there is the spermatic cord acts as a support for the left "testicle", but not for the right. On the other hand, we speculate that the spontaneous contraction of smooth muscle in the spermatic cord in the left might also play an important role. All these facts naturally lead us to contemplate some deep initiative factors in behind. Histopathological findings in our study revealed that slight to moderate inflammation and vascular proliferation in the left scrotum are more common than that in the right throughout the entire follow-up period of 3 months. According to these findings, we could naturally speculate that chronic inflammation might act as a very important stimulating factor for the contraction of the spermatic smooth muscles and thus the subsequent elevation of the left "testicle". It could also be speculated that this might be a result of the denudation of the testicular parenchyma, which could lead to edema and subsequent adhesion of the tunica albuginea to the surrounding tissues.
In contrast to the left scrotum, chronic inflammation and fibrosis are relatively slight in the right. Except for the lack of the denudation procedure of the testicular parenchyma, the good elasticity and abundant blood supplies of the scrotal tissues might help to alleviate the inflammation and provide a suitable accommodative environment for the testicular prosthesis. All these findings imply that the presence of chronic inflammation might even be the very cause of postoperative pains in the prosthesis recipients. Recently, some researchers have reported that silicone could be used as inducing materials in peritoneal cavity to produce a kind of mesothelium-lined fibroblast-rich tissue for tissue-engineering purposes. These findings are indicative of a better compatibility of silicone materials in peritoneal or scrotal tissues. In this study, we have also found a thinner layer of mesothelium-lined fibroblast-rich tissues in the inner surface of the false capsule in the right side .
In this comparative study, we have re-evaluated the two most popular implantation methods of testicular prosthesis, the "under the tunica albuginea" and the "under the tunica vaginalis" pathways, in animal models. From this study, we found that the testicular prosthesis were all well tolerated, but the prosthesis implanted under the tunica vaginalis showed a more satisfying result concerning with appearance, palpability, and histopathological findings than that of the under the tunica albuginea group. The "under the tunica vaginalis" method might be a more practical method for future testicular prosthesis implantation.
- Karademir K, Senkul T, Demir S, Erden D, Iseri C, Baykal K: A new testis prosthesis material: polymethylmethacrylate. Urol Int. 2004, 72: 71-75. 10.1159/000075277.PubMedView ArticleGoogle Scholar
- Girdansky J, Newman HF: Use of a vitallium testicular implant. Am J Surg. 1941, 53: 514-10.1016/S0002-9610(41)90676-1.View ArticleGoogle Scholar
- Lattimer JK, Vakili BF, Smith AM, Morishima A: A natural-feeling testicular prosthesis. J Urol. 1973, 110: 81-83.PubMedGoogle Scholar
- Van Nunen SA, Gatenby PA, Basten A: Post-mammoplasty connective tissue disease. Arthritis Rheum. 1982, 25: 694-697. 10.1002/art.1780250613.PubMedView ArticleGoogle Scholar
- Henderson J, Culkin D, Mata J, Wilson M, Venable D: Analysis of immunological alterations associated with testicular prostheses. J Urol. 1995, 154: 1748-1751. 10.1016/S0022-5347(01)66775-2.PubMedView ArticleGoogle Scholar
- Pidutti R, Morales A: Silicone gel-filled testicular prosthesis and systemic disease. Urology. 1993, 42: 155-157. 10.1016/0090-4295(93)90639-R.PubMedView ArticleGoogle Scholar
- Adshead J, Khoubehi B, Wood J, Rustin G: Testicular implants and patient satisfaction: a questionnaire-based study of men after orchidectomy for testicular cancer. BJU Int. 2001, 88: 559-562. 10.1046/j.1464-4096.2001.02392.x.PubMedView ArticleGoogle Scholar
- Aguilera RG, López JP, Aldosa RR, Rius-Espina G: Intralbugineous testicular prosthesis, a new technique. Summary of 30 implants. Int Urol Nephrol. 1990, 22: 367-371. 10.1007/BF02549798.PubMedView ArticleGoogle Scholar
- Lynch MJ, Pryor JP: Testicular prostheses: the patient's perception. Br J Urol. 1992, 70: 420-422. 10.1111/j.1464-410X.1992.tb15801.x.PubMedView ArticleGoogle Scholar
- Marshall S: Potential problems with testicular prostheses. Urology. 1986, 28: 388-390. 10.1016/0090-4295(86)90068-3.PubMedView ArticleGoogle Scholar
- Turek PJ, Master VA: Safety and effectiveness of a new saline filled testicular prosthesis. J Urol. 2004, 172 (4 Pt 1): 1427-1430. 10.1097/01.ju.0000139718.09510.a4.PubMedView ArticleGoogle Scholar
- Herrinton LJ, Brox T, Greenland S, Finkle WD, Cattolica E, Shoor S: Regarding: a cohort study of systemic and local complications following implantation of testicular prostheses. Ann Epidemiol. 2003, 13: 73-77. 10.1016/S1047-2797(02)00270-3.PubMedView ArticleGoogle Scholar
- Campbell GR, Turnbull G, Xiang L, Haines M, Armstrong S, Rolfe BE, Campbell JH: The peritoneal cavity as a bioreactor for tissue engineering visceral organs: bladder, uterus and vas deferens. J Tissue Eng Regen Med. 2008, 2: 50-60. 10.1002/term.66.PubMedView ArticleGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.