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García Rojo, E.; Giannarini, G.; García Gómez, B.; Feltes Ochoa, J.A.; Guerrero Ramos, F.; Alonso Isa, M.; Brime Menendez, R.; Saenz Calzada, D.M.; Justo Quintas, J.; Fraile, A.; et al. Organ-Sparing Surgery for Testicular Germ Cell Tumors. Encyclopedia. Available online: https://encyclopedia.pub/entry/47514 (accessed on 08 August 2024).
García Rojo E, Giannarini G, García Gómez B, Feltes Ochoa JA, Guerrero Ramos F, Alonso Isa M, et al. Organ-Sparing Surgery for Testicular Germ Cell Tumors. Encyclopedia. Available at: https://encyclopedia.pub/entry/47514. Accessed August 08, 2024.
García Rojo, Esther, Gianluca Giannarini, Borja García Gómez, Javier Amalio Feltes Ochoa, Félix Guerrero Ramos, Manuel Alonso Isa, Ricardo Brime Menendez, David Manuel Saenz Calzada, Juan Justo Quintas, Agustín Fraile, et al. "Organ-Sparing Surgery for Testicular Germ Cell Tumors" Encyclopedia, https://encyclopedia.pub/entry/47514 (accessed August 08, 2024).
García Rojo, E., Giannarini, G., García Gómez, B., Feltes Ochoa, J.A., Guerrero Ramos, F., Alonso Isa, M., Brime Menendez, R., Saenz Calzada, D.M., Justo Quintas, J., Fraile, A., Manfredi, C., & Romero Otero, J. (2023, August 01). Organ-Sparing Surgery for Testicular Germ Cell Tumors. In Encyclopedia. https://encyclopedia.pub/entry/47514
García Rojo, Esther, et al. "Organ-Sparing Surgery for Testicular Germ Cell Tumors." Encyclopedia. Web. 01 August, 2023.
Organ-Sparing Surgery for Testicular Germ Cell Tumors
Edit

Organ-sparing surgery for testicular germ cell tumors offers a promising approach that balances oncological control and preservation of testicular function. Further research, including large-scale prospective studies and long-term follow-ups, is warranted to validate the effectiveness and durability of organ-sparing surgery and to identify optimal patient selection criteria.

testicular cancer testicular tumors organ sparing

1. Introduction

Testicular cancer is a rare form of cancer that accounts for less than 1% of all male cancers [1]. However, it is the most common cancer among young men aged 15 to 35 years old [2]. The incidence of testicular cancer has been increasing worldwide, with the highest rates observed in Northern Europe [3].
There have been numerous previous classifications of testicular tumors from a variety of panels and organizations. For many years, the British testicular tumor panel was widely used in many countries [4]. Currently, the most widely used classification is that of the World Health Organization (WHO), which was updated in 2022 [5].
The standard treatment for testicular cancer is radical orchiectomy, which involves removing the entire affected testicle [6]. This procedure is highly effective in curing the disease, but it also has significant drawbacks. Radical orchiectomy is associated with a high risk of psychological distress, sexual dysfunction, and infertility, which can have a significant impact on a young man’s quality of life [7][8][9][10].
Organ-sparing surgery, also known as testis-sparing surgery or partial orchiectomy, is a surgical approach that aims to remove the tumor while preserving the healthy tissue and the function of the testis. Organ-sparing surgery has gained increasing popularity in recent years as an alternative to radical orchiectomy for select cases of testicular tumors, with growing scientific evidence [9][11][12][13][14].
Testis-sparing surgery (TSS) is a guideline-recommended treatment option for patients with small non-palpable tumors, synchronous or metachronous bilateral testicular germ cell tumors (GCTs), or GCT in a solitary testicle [15]. The benefits of this surgery seem numerous: by preserving the healthy testicular tissue, organ-sparing surgery minimizes the risk of infertility, sexual dysfunction, and psychological distress associated with radical orchiectomy [16]. It also allows young men to maintain their endocrine function and testosterone production, which can have important implications for their overall health and well-being [14][15].

2. Patient Eligibility

The use of TSS for testicular malignancies remains a matter of debate, particularly in cases where the other testis is normal. However, the urological community is showing an increasing interest in organ-preserving surgery as a viable substitute for radical orchiectomy in many instances.
As per the German Cancer Study Group’s indications, TSS could be a potential choice for select patients with malignant tumors in a solitary testis or bilateral tumors, provided that the lesion’s diameter is less than 2 cm, there is no invasion of the rete testis, and the preoperative serum luteinizing hormone (LH) levels are normal. In such scenarios, the removal of the mass should be accompanied by multiple biopsies of the surrounding tissue and adjuvant radiotherapy should be considered for seminomas [17].
On the other hand, TSS has been broadly utilized in the treatment of benign tumors, with testicular ultrasound (US) and intraoperative frozen-section examination enabling the surgeon to confirm the benign nature of the testicular mass with near certainty, effectively reducing the risk of recurrence to virtually zero [18][19][20][21].
The size of the mass appears to be a critical factor in considering elective TSS; various studies have suggested that for nonpalpable, asymptomatic masses with diameters of less than 2 cm, TSS could be the most suitable approach, given that the probability of benign histology is about 80% [22][23][24][25][26][27]. Until recently, the threshold for tumor volume was 30% of total testicular volume, but this could be increased to a maximum of 50% if serum testosterone and LH concentrations are within normal limits to exclude compensated Leydig cell failure [25][28].
Furthermore, TSS is increasingly accepted in pediatric surgery due to the higher incidence of benign tumors. This method is particularly beneficial in younger children, as it can minimize the risk of late-onset hypogonadism and provides significant physiological and cosmetic advantages [29][30][31].
According to the guidelines of the European Association of Urology (EAU), testicular-sparing surgery is considered a viable option for patients with suspected benign tumors or uncertain masses with negative tumor markers. However, they emphasize that radical orchidectomy is the preferred standard of care for patients with likely malignant testicular tumors. Nonetheless, in cases of synchronous bilateral tumors or tumors in a single testis, testicular sparing surgery can be considered, but only in conjunction with frozen section examination. These guidelines note that it is important for patients to understand that there is limited data on the oncological safety of testicular-sparing surgery, and local recurrence rates can be as high as 26.9%. Additionally, patients should be informed about the potential need for radiotherapy if the histology reveals evidence of germ cell neoplasia in situ (GCNIS). The guidelines also stress that testicular-sparing surgery should only be performed in experienced medical centers [32].
The American Urological Association (AUA) guidelines propose TSS as an alternative to radical orchiectomy in patients with tumors < 2 cm, having ambiguous US/physical exam results and negative tumor markers, a solitary testis, or bilateral synchronous tumors. However, patients must be advised on potential risks such as higher recurrence, the regular monitoring necessity, the role of adjuvant radiotherapy in reducing local recurrence, the effect of radiotherapy on sperm and testosterone production, and the possibility of testicular atrophy necessitating testosterone replacement therapy or potential subfertility/infertility. Biopsies of the normal testicle tissue are advised during TSS. A trans-scrotal approach is cautioned against due to higher recurrence rates [33].
Table 1 provides a summary of the criteria that patients must meet to be eligible for organ-sparing surgery for testicular tumors.
Table 1. Summary of patient eligibility criteria for organ-sparing surgery for testicular cancer.

3. Surgical Technique

The first detailed presentation of this surgical technique was given by Stoll et al. in 1986 [34]. They described how high-frequency ultrasound could be used as a guidance system for the enucleation of a non-palpable Leydig cell tumor. The methodology evolved over time, culminating in 2002 when Hopps and Goldstein standardized the procedure [35]. They introduced a magnification system to enhance the detection and thorough removal of small, non-palpable lesions.
Organ-sparing surgery for testicular tumors is not without its challenges. The main challenge is ensuring that the surgery removes all cancerous tissue while preserving the healthy tissue. This requires skilled surgeons and careful planning before and during the procedure. Another challenge is ensuring that the remaining healthy testicular tissue functions normally and does not develop complications such as atrophy or fibrosis [19].
It is generally recommended to use a conventional inguinal approach when performing a TSS to prevent any disturbance to the scrotum [36]. Some authors suggest that clamping the cord before bringing the testicle into the operative area can reduce the risk of tumor spread due to manipulation, but there is scant literature to support this traditional practice. The use of clamping, and whether it should be done under cold or warm ischemia conditions, remains a topic of debate. In a large study by Leonhartsberger et al., 65 patients underwent radical orchiectomy and TSS without early cord clamping and the authors reported that no patients showed signs of disease after a median follow-up period of 52.5 months [13].
If TSS is to be performed, a crosswise cut in the tunica albuginea is typically made after the testicle has been exposed, which allows for identification of an avascular plane [15]. Upon exposure, the tumor is typically surrounded by a pseudocapsule, enabling it to be easily distinguished from the normal parenchyma; however, a challenging extraction might suggest malignant infiltration. If the tumor is not physically detectable, tools such as an ultrasound or a microscope can be used to locate the lesion, followed by the removal of an excision margin of 2–5 mm [26][36]. The tumor that has been removed, along with any additional collected samples from the tumor site, are then put through a frozen section examination. This examination is used for histological identification of the tumor, detection of GCNIS, and confirmation of whether the surgical margins are positive [37].
A microsurgical approach, involving an operating microscope, can be employed if the necessary equipment is accessible and the surgeon possesses the required skills. The primary reason for utilizing a microsurgical technique is typically to address a nonpalpable tumor that has been detected via ultrasound [22][25]. Another situation where this approach might be used is in cases where a man with azoospermia is undergoing testicular sperm extraction (TESE) for assisted reproductive methods and incidental testicular abnormalities are discovered on ultrasound [38]. Proponents of microsurgical techniques assert that it can offer several advantages, such as enhanced preservation of healthy tissue and reduced risk of damaging the tunica albuginea’s vasculature. These benefits could theoretically decrease the risk of hypogonadism, testicular atrophy, and infertility.
De Stefani et al. conducted the most extensive study of testis-sparing surgeries using a microsurgical approach, involving 23 patients. Tumors were nonpalpable and showed no evidence of elevated tumor markers. One patient underwent a second operation five years after the initial surgery, as the initial pathology reported normal testicular tissue. The subsequent procedure revealed seminoma, necessitating a radical orchiectomy. None of the patients in this study experienced disease progression. All were free of disease and exhibited normal scrotal ultrasound results after an average follow-up period of 35 ± 25 months [25].
However, because each of these surgical techniques lacks concrete evidence supporting their functional or oncological benefits, researchers believe that the choice of surgical approach should be based on the surgeon’s individual preference [9].

4. Complications

Organ-sparing surgery for testicular tumors is associated with a low risk of complications, with rates ranging between 1% and 6% across different studies [26][28]. The most common complications include bleeding/hematoma, infection, and testicular atrophy.
In the systematic review conducted by Favilla et al., which incorporated data from a total of 725 patients from 26 studies that reported this outcome, the authors reported a complication rate of 2%. Specifically, hematoma was observed in seven patients (1.2%), necessitating surgical intervention for hemostasis in one case. Additionally, testicular atrophy was noted in four patients (0.7%), and a single case (0.2%) of inflammation was reported during the postoperative period [39].
Heidenreich et al., in their systematic review published in 2023, concluded that severe complications following TSS are rare and are observed in less than 1% of patients [28].

5. Oncological Outcomes

The first successful case of TSS was performed by Richie in 1984, who employed this approach for a patient with synchronous bilateral seminoma. Remarkably, the patient remained disease-free without requiring permanent androgen replacement even after a 2.5-year follow-up. However, the author referred to this treatment strategy as “unorthodox” [40].
Since then, several series and case reports have described TSS for selected patients with testicular GCTs (organ-confined tumors in patients with synchronous bilateral tumors or solitary testis with normal preoperative endocrine function).
The most comprehensive series on TSS for malignant tumors was published by The German Testicular Cancer Study Group. The successful application of TSS was noted in 101 patients across eight high-volume institutions with either bilateral GCTs or a solitary testis GCT. The average tumor diameter was reported as 15 mm (ranging between 5–30 mm). GCNIS was discovered in 84% of the cases, with 79% of these patients receiving adjuvant radiation with 18 Gy. After a median follow-up of 80 months, 100 patients remained disease-free. Local recurrence was observed in six patients, all of whom were successfully treated with inguinal orchiectomy [17][41].
Bojanic et al. reported on 24 patients who underwent TSS for bilateral GCTs or solitary testis tumors. All tumors were less than 2 cm in diameter. Of these, seven patients experienced local recurrence but were successfully treated with either radical orchiectomy or a second TSS. The overall survival rate of the study group was 100% at a median follow-up of 51 months [42].
In another study by Steiner et al., TSS was performed on 11 patients with GCTs. All tumors were less than 25 mm in diameter, and 10 of them were diagnosed concurrently with ipsilateral GCNIS. One local recurrence was observed and TSS was repeated with subsequent local radiation. All patients were disease-free at an average follow-up of 46.3 months [43].
The management of GCNIS is of critical importance as the majority of untreated GCNIS cases will develop into invasive disease. The presence of GCNIS in a testis carries an estimated risk of evolving into invasive disease of 50% within 5 years and 70% within 7 years [44]. Therefore, it is necessary to consider local radiotherapy for patients with GCNIS, particularly for those with a solitary testis [45][46][47]. In Avuzzi et al.’s study, radiotherapy following testicular-sparing surgery showed no local or distant relapses in a medium-term follow-up, with hormonal function preserved in about 54.5% of patients. Associations were noted between baseline testosterone levels, tumor size, and risk of exogenous androgen replacement [46]. Dieckmann et al. highlight that 18–20 Gy local radiotherapy eradicates the majority of GCNIS. However, their study also emphasizes the potential for treatment failure, evidenced by cases of relapse occurring over a decade post-treatment. The failure rate is estimated to be around 1% [45].

There are different systematic reviews published over the years (Table 2), with different criteria for inclusion. In the one published by Ory et al. in 2021, in which no meta-analysis is carried out due to the heterogeneity of the studies (retrospective noncontrolled studies), they conclude that TSS is a safe and efficacious technique with regards to oncological control and postoperative hormonal function and should be given serious consideration in cases of nonpalpable, small tumors under 2 cm and in men with bilateral tumors or with solitary testicles [9].

Table 2. Oncological outcomes: most relevant systematic reviews and meta-analyses over the past five years. TSS: testicular-sparing surgery. N/A: not applicable.

Author and Year Number of Studies Included Number of Patients Median Follow-Up Oncological Outcomes Conclusions
Ory et al., 2021 [9] 32 N/A 57.8 months N/A (No Meta-Analysis Conducted) TSS is a safe and efficacious technique with regard to oncological control based on retrospective, non-controlled studies. TSS avoids unnecessary removal of benign testicular tissue and should be given serious consideration in cases of nonpalpable, small tumors under 2 cm.
Favilla et al., 2021 [39] 26 603 Not Specified Local recurrence of 3.48%. Overall recurrence: 0% to 26.9% for malignancy and from 0% to 0.1% for benign lesions. TSS was shown to be safe and practicable if used according to the specific guidelines. Urologists can consider TSS as an important means against testicular tumors in selected and well-informed patients.
Miao et al., 2021 [48] 9 320. Only Children. Not Specified Local recurrence 5.8% (benign rate was 70.9%) Most of the testicular tumors in children were benign, and the most common histologic subtype was teratoma. TSS should be provided to children with benign lesions. Very low rates of tumor recurrence were observed in children with testicular tumors.
Grogg et al., 2022 [11] 32 285 38 months Local recurrence: 13% (median 12 months),
97% disease-free after treatment for recurrence.
2% distant recurrence (median 19 months). Disease-free post-systemic treatment during a median follow-up of 52 months.
TSS should only be offered to well-informed patients with a singular testicle, excellent compliance, a singular tumor less than 2 cm located at the lower pole of the testicle, and normal preoperative endocrine function. Radical orchiectomy remains the standard of care, but future studies may support the use of TSS in selected men.
Heidenreich et al., 2023 [28] 8 252 Not Specified Local recurrence 4–6% to 15.9%.
2–4% Distant recurrence.
Cancer-specific survival close to 100%.
Oncological outcomes are excellent, with no local relapses if patients undergo adjuvant radiation therapy. The local recurrence rate might increase to 4–6% if adjuvant radiation is omitted.

In the systematic review conducted by Favilla et al. in 2021, which incorporated data from 26 studies and 603 patients, it was noted that the local recurrence rate was reported at 3.48%. Furthermore, the overall recurrence rate varied, with figures ranging from 0% to 26.9% for malignant cases, and from 0% to 0.1% for benign lesions. It is important to note that a meta-analysis was not performed due to the diversity of the included studies. The authors concluded that TSS is a safe and feasible method when applied in accordance with specific guidelines. They suggested that TSS should be considered as a significant tool for managing testicular tumors in selected and well-informed patients.

In the recent study published by Grogg et al. in 2022, which encompasses 32 studies and offers data from 285 patients, it was reported that 87% of the patients who underwent TSS experienced no relapse after a median follow-up period of 38 months. Meanwhile, local recurrence was documented in 13% of patients after a median duration of 12 months. Distant recurrence post-TSS was observed in 2% of the patients following a median period of 19 months. The authors conclude that TSS should only be offered to well-informed patients with a singular testicle, a singular tumor less than 2 cm located at the lower pole of the testicle, and normal preoperative endocrine function. Unless patients plan to father a child within a short time frame, adjuvant testicular radiotherapy should be recommended [11].

Finally, in the most recent systematic review published by Heidenreich et al. in 2023, data from eight studies, comprising a total of 252 patients, were evaluated. The authors reported a local recurrence rate ranging from 4–6% to 15.9%. The distant recurrence rate fell within the 2–4% range. In terms of cancer-specific survival, figures approached a near-100% rate, reinforcing the effectiveness of the treatment strategies evaluated. This review further emphasized the significance of adjuvant radiation therapy in preventing local relapses. In fact, the authors reported that oncological outcomes were excellent when this treatment strategy was incorporated. It was also noted that the local recurrence rate might increase to 4–6% should adjuvant radiation therapy be omitted. The results of this review contribute to the accumulating evidence that supports the use of TSS in combination with adjuvant radiation therapy, further emphasizing the importance of rigorous patient management strategies in the treatment of testicular tumors [28].

The follow-up protocol after TSS is still undefined and has not been studied in any published literature. Therefore, careful patient selection and frequent follow-ups incorporating ultrasound are necessary until better protocols are established.

6. Functional Outcomes

One of the main objectives of TSS for GCT is to preserve endocrine function [28].

There is an elevated risk of early-onset hypogonadism in patients with testicular GCTs. This condition might be further exacerbated by supplementary local radiation therapy [7][8].

In the study by The German Testicular Cancer Study Group with a total of 101 patients, 84 (over 83%) maintained normal testosterone serum levels after an average follow-up of 84 months. Of the remaining patients, six already had low serum testosterone preoperatively and the rest exhibited new-onset hypogonadism requiring testosterone supplementation postoperatively [16]. Factors like tumor size exceeding 2 cm, increased serum LH, and TSS with warm ischemia were associated with postoperative hypogonadism. Therefore, meticulous patient selection and proficient surgical technique are crucial.

In the work published by Steiner et al., only one out of 12 patients displayed hypogonadism after an average follow-up of 60 months [43].

The meta-analysis of Patel et al. revealed a 9.7% risk of hypogonadism development. They inferred that significant tumor volume and poor preoperative hormonal status are the main risk factors for postoperative hypogonadism [16].

On the other hand, Grogg et al.’s review revealed a 27% incidence of hypogonadism. However, it lacked information on preoperative endocrine function and the size of the removed lesion. Thus, no conclusions about hypogonadism prevention could be derived [11].

Although it is well established that most men with GCT and GCNIS suffer from subfertility or infertility because of azoospermia or significantly diminished spermatogenesis, another goal of TSS is fertility preservation [49][50][51]. In cases of synchronous tumors or a tumor in a single testis, TSS remains the only viable option for men aiming for natural conception in the future [9].
The data regarding fertility following TSS are limited, but sperm parameters do not seem to exhibit significant changes. The most comprehensive study of TSS investigating sperm parameters in men undergoing surgery for benign lesions observed that most men were preoperatively oligospermic and asthenospermic, with no noteworthy decline postoperatively [52]. This differs from radical orchiectomy, where semen parameters invariably deteriorate, even without adjuvant therapies [49].
Previous research has indicated that GCNIS can evolve in just a few testicular lobules, leaving the remaining parenchyma with functioning spermatogenesis. If biopsies of the parenchyma surrounding the tumor indicate intact spermatogenesis and semen analysis reveals normozoospermia or oligozoospermia, around 50% of cases might result in successful paternity [16]. For such men, adjuvant radiation therapy should be deferred and replaced by routine testicular ultrasound. The latest systematic reviews seem to establish similar paternity rates in cases where TSS has been performed, with rates around 50–52% [9][28].

7. Conclusions

Testis-sparing surgery stands as a promising surgical approach for managing testicular tumors, providing a balance between effective oncological control and the preservation of testicular function. Particularly beneficial in cases of small, nonpalpable tumors and individuals with either bilateral tumors or solitary testicles, TSS has demonstrated low recurrence rates and nearly perfect cancer-specific survival rates.

However, these positive outcomes underline the importance of careful patient selection, taking into account individual and tumor characteristics, as well as the utility of adjuvant radiation therapy. Future large-scale and long-term studies are necessary to solidify these findings and further optimize patient selection and management strategies for TSS in testicular tumors.

References

  1. Testicular Cancer Statistics. Cancer Research UK. Available online: https://www.cancerresearchuk.org/health-professional/cancer-statistics/statistics-by-cancer-type/testicular-cancer (accessed on 2 May 2023).
  2. Smith, Z.L.; Werntz, R.P.; Eggener, S.E. Testicular Cancer. Med. Clin. N. Am. 2018, 102, 251–264.
  3. Gurney, J.K.; Florio, A.A.; Znaor, A.; Ferlay, J.; Laversanne, M.; Sarfati, D.; Bray, F.; McGlynn, K.A. International Trends in the Incidence of Testicular Cancer: Lessons from 35 Years and 41 Countries. Eur. Urol. 2019, 76, 615–623.
  4. Berney, D.M.; Cree, I.; Rao, V.; Moch, H.; Srigley, J.R.; Tsuzuki, T.; Amin, M.B.; Comperat, E.M.; Hartmann, A.; Menon, S.; et al. An introduction to the WHO 5th edition 2022 classification of testicular tumours. Histopathology 2022, 81, 459–466.
  5. Moch, H.; Amin, M.B.; Berney, D.M.; Compérat, E.M.; Gill, A.J.; Hartmann, A.; Menon, S.; Raspollini, M.R.; Rubin, M.A.; Srigley, J.R.; et al. The 2022 World Health Organization Classification of Tumours of the Urinary System and Male Genital Organs—Part A: Renal, Penile, and Testicular Tumours. Eur. Urol. 2022, 82, 458–468.
  6. Dotzauer, R.; Salamat, A.; Nabar, N.D.; Thomas, A.; Böhm, K.; Brandt, M.P.; Mager, R.; Borgmann, H.; Kurosch, M.; Hoefner, T.; et al. The timing of initial imaging in testicular cancer: Impact on radiological findings and clinical decision making. Minerva Urol. Nephrol. 2022, 74, 72–76.
  7. Nord, C.; Bjøro, T.; Ellingsen, D.; Mykletun, A.; Dahl, O.; Klepp, O.; Bremnes, R.M.; Wist, E.; Fosså, S.D. Gonadal Hormones in Long-Term Survivors 10 Years after Treatment for Unilateral Testicular Cancer. Eur. Urol. 2003, 44, 322–328.
  8. Petersen, P.M.; Skakkebæk, N.E.; Vistisen, K.; Rørth, M.; Giwercman, A. Semen Quality and Reproductive Hormones before Orchiectomy in Men with Testicular Cancer. J. Clin. Oncol. Off J. Am. Soc. Clin. Oncol. 1999, 17, 941–947.
  9. Ory, J.; Blankstein, U.; Gonzalez, D.C.; Sathe, A.A.; White, J.T.; Delgado, C.; Reynolds, J.; Jarvi, K.; Ramasamy, R. Outcomes of organ-sparing surgery for adult testicular tumors: A systematic review of the literature. BJUI Compass 2021, 2, 306–321.
  10. Ramos, S.A.; Pinheiro, A.M.; Barcelos, A.P.; Cardoso, A.P.; Varregoso, J. Satisfaction with testicular prosthesis: A Portuguese questionnaire-based study in testicular cancer survivors. Rev. Int. Androl. 2022, 20, 110–115.
  11. Grogg, J.B.; Dursun, Z.H.; Beyer, J.; Eberli, D.; Poyet, C.; Hermanns, T.; Fankhauser, C.D. Oncological and functional outcomes after testis-sparing surgery in patients with germ cell tumors: A systematic review of 285 cases. World J. Urol. 2022, 40, 2293–2303.
  12. La Rocca, R.; Capece, M.; Spirito, L.; Cumberbatch, M.K.; Creta, M.; Altieri, V.; Franco, G.; Albisinni, S.; Mirone, V.; Esperto, F.; et al. Testis-sparing surgery for testicular masses: Current perspectives. Minerva Urol. Nefrol. Ital. J. Urol. Nephrol. 2019, 71, 359–364.
  13. Leonhartsberger, N.; Pichler, R.; Stoehr, B.; Horninger, W.; Steiner, H. Organ-sparing surgery is the treatment of choice in benign testicular tumors. World J. Urol. 2014, 32, 1087–1091.
  14. Borghesi, M.; Brunocilla, E.; Schiavina, R.; Gentile, G.; Dababneh, H.; Della Mora, L.; del Prete, C.; Franceschelli, A.; Colombo, F.; Martorana, G. Role of testis sparing surgery in the conservative management of small testicular masses: Oncological and functional perspectives. Actas Urol. Esp. 2014, 39, 57–62.
  15. EAU Guidelines on Testicular Cancer-Introduction-Uroweb. Uroweb-European Association of Urology. Available online: https://uroweb.org/guidelines/testicular-cancer (accessed on 4 June 2023).
  16. Patel, H.D.; Gupta, M.; Cheaib, J.G.; Sharma, R.; Zhang, A.; Bass, E.B.; Pierorazio, P.M. Testis-sparing surgery and scrotal violation for testicular masses suspicious for malignancy: A systematic review and meta-analysis. Urol. Oncol. Semin. Orig. Investig. 2020, 38, 344–353.
  17. Heidenreich, A.; Albers, P.; Krege, S. Management of bilateral testicular germ cell tumors--experience of the German Testicular Cancer Study Group (GTCSG). Eur. Urol. Suppl. 2006, 5, 97.
  18. Heidenreich, A.; Engelmann, U.H.; Vietsch, H.V.; Derschum, W. Organ preserving surgery in testicular epidermoid cysts. J. Urol. 1995, 153, 1147–1150.
  19. Giannarini, G.; Mogorovich, A.; Bardelli, I.; Manassero, F.; Selli, C. Testis-sparing surgery for benign and malignant tumors: A critical analysis of the literature. Indian J. Urol. 2008, 24, 467–474.
  20. Paffenholz, P.; Held, L.; Loosen, S.H.; Pfister, D.; Heidenreich, A. Testis Sparing Surgery for Benign Testicular Masses: Diagnostics and Therapeutic Approaches. J. Urol. 2018, 200, 353–360.
  21. Sheynkin, Y.R.; Sukkarieh, T.; Lipke, M.; Cohen, H.L.; Schulsinger, D.A. Management of nonpalpable testicular tumors. Urology 2004, 63, 1163–1167.
  22. Rolle, L.; Tamagnone, A.; Destefanis, P.; Bosio, A.; Timpano, M.; Fiori, C.; Ceruti, C.; Burlo, P.; Fauciglietti, P.; Fontana, D. Microsurgical “testis-sparing” surgery for nonpalpable hypoechoic testicular lesions. Urology 2006, 68, 381–385.
  23. Brunocilla, E.; Gentile, G.; Schiavina, R.; Borghesi, M.; Franceschelli, A.; Pultrone, C.V.; Chessa, F.; Romagnoli, D.; Ghanem, S.M.; Gacci, M.; et al. Testis-sparing surgery for the conservative management of small testicular masses: An update. Anticancer. Res. 2013, 33, 5205–5210.
  24. Shilo, Y.; Zisman, A.; Raz, O.; Lang, E.; Strauss, S.; Sandbank, J.; Segal, M.; Siegel, Y.I.; Leibovici, D. Testicular sparing surgery for small masses. Urol. Oncol. Semin. Orig. Investig. 2012, 30, 188–191.
  25. De Stefani, S.; Isgrò, G.; Varca, V.; Pecchi, A.; Bianchi, G.; Carmignani, G.; Derchi, L.E.; Micali, S.; Maccio, L.; Simonato, A. Microsurgical Testis-sparing Surgery in Small Testicular Masses: Seven Years Retrospective Management and Results. Urology 2012, 79, 858–862.
  26. Giannarini, G.; Dieckmann, K.-P.; Albers, P.; Heidenreich, A.; Pizzocaro, G. Organ-Sparing Surgery for Adult Testicular Tumours: A Systematic Review of the Literature. Eur. Urol. 2010, 57, 780–790.
  27. Staudacher, N.; Tulchiner, G.; Bates, K.; Ladurner, M.; Kafka, M.; Aigner, F.; Pichler, R.; Horninger, W. Organ-Sparing Surgery in Testicular Tumor: Is This the Right Approach for Lesions ≤ 20 mm? J. Clin. Med. 2020, 9, 2911.
  28. Heidenreich, A.; Seelemeyer, F.; Altay, B.; Laguna, M.P. Testis-sparing Surgery in Adult Patients with Germ Cell Tumors: Systematic Search of the Literature and Focused Review. Eur. Urol. Focus 2023, 9, 244–247.
  29. Muñoz, M.I.R.; Cerezo, V.N.; Reyes, M.D.; Sánchez, A.V.; González-Peramato, P.; Pereira, P.L.; Urrutia, M.J.M. Testicular tumours in children: Indications for testis-sparing surgery. An. Pediatría 2018, 88, 253–258.
  30. Woo, L.L.; Ross, J.H. The role of testis-sparing surgery in children and adolescents with testicular tumors. Urol. Oncol. Semin. Orig. Investig. 2016, 34, 76–83.
  31. Valla, J.S.; the Group D’Etude en Urologie Pédiatrique. Testis-sparing surgery for benign testicular tumors in children. J. Urol. 2001, 165 Pt 2, 2280–2283.
  32. Jungwirth, A.; Giwercman, A.; Tournaye, H.; Diemer, T.; Kopa, Z.; Dohle, G.; Krausz, C.; EAU Working Group on Male Infertility. European Association of Urology Guidelines on Male Infertility: The 2012 Update. Eur. Urol. 2012, 62, 324–332.
  33. Stephenson, A.; Eggener, S.E.; Bass, E.B.; Chelnick, D.M.; Daneshmand, S.; Feldman, D.; Gilligan, T.; Karam, J.A.; Leibovich, B.; Liauw, S.L.; et al. Diagnosis and Treatment of Early Stage Testicular Cancer: AUA Guideline. J. Urol. 2019, 202, 272–281.
  34. Stoll, S.; Goldfinger, M.; Rothberg, R.; Buckspan, M.; Fernandes, B.; Bain, J. Incidental detection of impalpable testicular neoplasm by sonography. Am. J. Roentgenol. 1986, 146, 349–350.
  35. Hopps, C.V.; Goldstein, M. Ultrasound Guided Needle Localization and Microsurgical Exploration for Incidental Nonpalpable Testicular Tumors. J. Urol. 2002, 168, 1084–1087.
  36. Zuniga, A.; Lawrentschuk, N.; Jewett, M.A.S. Organ-sparing approaches for testicular masses. Nat. Rev. Urol. 2010, 7, 454–464.
  37. Whitehurst, L.; Chetwood, A. Organ Sparing Surgery in Testicular Cancer. In Urologic Cancers; Barber, N., Ali, A., Eds.; Exon Publications: Brisbane, Australia, 2022. Available online: http://www.ncbi.nlm.nih.gov/books/NBK585984/ (accessed on 21 May 2023).
  38. Hallak, J.; Cocuzza, M.; Sarkis, A.S.; Athayde, K.S.; Cerri, G.G.; Srougi, M. Organ-Sparing Microsurgical Resection of Incidental Testicular Tumors Plus Microdissection for Sperm Extraction and Cryopreservation in Azoospermic Patients: Surgical Aspects and Technical Refinements. Urology 2009, 73, 887–891.
  39. Favilla, V.; Cannarella, R.; Tumminaro, A.; DI Mauro, D.; Condorelli, R.A.; LA Vignera, S.; Ficarra, V.; Cimino, S.; Calogero, A.E. Oncological and functional outcomes of testis sparing surgery in small testicular mass: A systematic review. Minerva Urol. Nephrol. 2021, 73, 431–441.
  40. Simultaneous Bilateral Tumors with Unorthodox Management|CiNii Research. Available online: https://cir.nii.ac.jp/crid/1570854174607762048 (accessed on 21 May 2023).
  41. Heidenreich, A.; Weißbach, L.; Höltl, W.; Albers, P.; Kliesch, S.; Köhrmann, K.U.; Klaus, P.; Dieckmann For The German Testicular Cancer Study Group. Organ sparing surgery for malignant germ cell tumor of the testis. J. Urol. 2001, 166, 2161–2165.
  42. Bojanic, N.; Bumbasirevic, U.; Vukovic, I.; Bojanic, G.; Milojevic, B.; Nale, D.; Durutovic, O.; Djordjevic, D.; Nikic, P.; Vuksanovic, A.; et al. Testis sparing surgery in the treatment of bilateral testicular germ cell tumors and solitary testicle tumors: A single institution experience. J. Surg. Oncol. 2015, 111, 226–230.
  43. Steiner, H.; Höltl, L.; Maneschg, C.; Berger, A.P.; Rogatsch, H.; Bartsch, G.; Hobisch, A. Frozen section analysis-guided organ-sparing approach in testicular tumors: Technique, feasibility, and long-term results. Urology 2003, 62, 508–513.
  44. von der Maase, H.; Rorth, M.; Walbom-Jorgensen, S.; Sorensen, B.L.; Christophersen, I.S.; Hald, T.; Jacobsen, G.K.; Berthelsen, J.G.; Skakkebaek, N.E. Carcinoma in situ of contralateral testis in patients with testicular germ cell cancer: Study of 27 cases in 500 patients. BMJ 1986, 293, 1398–1401.
  45. Dieckmann, K.-P.; Tribius, S.; Angerer, M.; Salzbrunn, A.; von Kopylow, K.; Mollenhauer, M.; Wülfing, C. Testicular germ cell tumour arising 15 years after radiotherapy with 18 Gy for germ cell neoplasia in situ. Strahlenther. Und Onkol. 2023, 199, 322–326.
  46. Avuzzi, B.; Tittarelli, A.; Andreani, S.; Chiorda, B.N.; Seregni, E.; Villa, S.; Tana, S.; Valdagni, R.; Salvioni, R.; Biasoni, D.; et al. Radiotherapy after testis-sparing surgery for seminoma in monorchid patients: Safety and efficacy. Tumori J. 2022, 108, 165–171.
  47. Paffenholz, P.; Pfister, D.; Heidenreich, A. Testis-preserving strategies in testicular germ cell tumors and germ cell neoplasia in situ. Transl. Androl. Urol. 2020, 9 (Suppl. 1), S24–S30.
  48. Miao, X.; Li, Y.; Zhou, T.; Lv, M. Testis-sparing surgery in children with testicular tumors: A systematic review and meta-analysis. Asian J. Surg. 2021, 44, 1503–1509.
  49. Parekh, N.V.; Lundy, S.D.; Vij, S.C. Fertility considerations in men with testicular cancer. Transl. Androl. Urol. 2020, 9 (Suppl. 1), S14–S23.
  50. Lee, S.H.; Shin, C.H. Reduced male fertility in childhood cancer survivors. Ann. Pediatr. Endocrinol. Metab. 2013, 18, 168–172.
  51. Ku, J.Y.; Park, N.C.; Jeon, T.G.; Park, H.J. Semen Analysis in Cancer Patients Referred for Sperm Cryopreservation before Chemotherapy over a 15-Year Period in Korea. World J. Men’s Heal. 2015, 33, 8–13.
  52. Pozza, C.; Pofi, R.; Tenuta, M.; Tarsitano, M.G.; Sbardella, E.; Fattorini, G.; Cantisani, V.; Lenzi, A.; Isidori, A.M.; Gianfrilli, D.; et al. Clinical presentation, management and follow-up of 83 patients with Leydig cell tumors of the testis: A prospective case-cohort study. Hum. Reprod. 2019, 34, 1389–1403.
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