*These authors contributed equally to this study.
To assess whether the “testicular pool” could be used for histological analysis and whether it gave more accurate information than the standard testicular biopsy.
Between January 2017 and March 2018, this single-center prospective study included 60 azoospermic men undergoing conventional bilateral testicular sperm extraction. Six samples were excised from each testicle and transferred to an embryologist. One additional biopsy was randomly taken from each testis for a histological analysis. After processing, the testicular pool was also sent for a histological analysis, which showed normal spermatogenesis (NS), hypospermatogenesis (HYPO), maturation arrest (MA), Sertoli cell-only syndrome (SCOS), and tubular atrophy (TA).
Twenty of the 60 patients (33.3%) had obstructive azoospermia (OA), while the remaining 40 (66.6%) had nonobstructive azoospermia. Their mean age was 40.5 years. All patients with OA had previously undergone unsuccessful testicular fine-needle aspiration. Successful sperm retrieval (SSR) occurred in 93.3% of patients. Histological analysis of the testicular biopsy revealed NS in 12 patients (20%), HYPO and TA in 28 patients (46.6%), MA in eight patients (13.3%), and SCOS in 12 patients (20%). The testicular pool analysis showed NS in 12 patients (20%), HYPO and TA in 44 patients (73.3%), MA in four patients (6.6%), and SCOS in no patients. In four patients with MA (6.6% of the total sample) and 12 patients with SCOS (20% of the total sample) according to the standard testicular biopsy, the embryologist found SSR with cryopreservation. Overall, in 44 patients (73.3%), the testicular pool analysis confirmed the histological findings of the standard testicular biopsy. In the 16 cases (26.6%) with a discrepancy between the single-biopsy histological findings and SSR, the testicular pool analysis confirmed the embryological data on SSR.
The testicular pool proved to be easily analyzable, practical, manageable, and more accurate for predicting sperm retrieval than standard testicular biopsy.
Azoospermia, which affects around 1% of men in the Western world [
When recanalization surgery is not possible or indicated, in patients with OA, sperm can be usually easily retrieved with testicular fine needle aspiration (TEFNA), as normal spermatogenesis (NS) is expected to be diffusely present in the testicles. When attempting sperm retrieval in patients affected by NOA, in contrast, surgical TESE is necessary, with the hope of identifying focal areas of NS [
The main limitation of testis biopsy is that it is not representative of the whole anatomy, as usually only a single testicular sample harvested from each testis is sent for histopathological evaluation, although the seminiferous tubules of azoospermic patients are often heterogeneous throughout the testicle [
In order to study the histology of a larger sample, which would be more representative of the histopathology of the entire testis, in addition to the standard histological biopsy, it is possible to analyze the remnants of TESE specimens after spermatozoa have been extracted by the embryologist. This is because during processing of the TESE sample, only the supernatant with free spermatozoa is cryopreserved or utilized for ICSI, while the testicular solid tissue consisting of the residual seminiferous tubules after stretching, centrifugation, and extracting the spermatozoa, which in the current manuscript is defined as the “testicular pool,” is usually disposed. The main objective of the current study was to assess the feasibility of using the testicular pool for histological analysis in azoospermic patients undergoing conventional TESE in order to predict the likelihood of sperm retrieval.
Between January 2017 and March 2018, 60 azoospermic patients referred to the Assisted Reproductive Technology Centre of the University of Florence (Florence, Italy) were prospectively enrolled in the current study. Patients who presented for semen cryopreservation before undergoing oncologic treatment were excluded.
Azoospermic patients were referred to the Department of Urology for further assessment of the cause of azoospermia and for sperm retrieval after the couple had undergone a complete assessment, including a gynecological evaluation of the female partner. The diagnosis of NOA or OA was based on the patient's history, a physical and genital examination, semen analysis, the patient's endocrine profile, and genetic studies. The data analyzed included age; weight and height; smoking and drinking habits; and history of cryptorchidism, mumps orchitis, varicocele, environmental or radiation exposure, prescribed drug use, previous chemotherapy, and surgical procedures. All patients underwent a genital examination and a scrotal Doppler ultrasound scan to detect testicular volume and to exclude the presence of epididymis head or tail dilatation, unilateral or bilateral absence of the vas deferens, and varicocele. A transrectal ultrasound scan was performed to rule out the presence of prostate median cysts and of anomalies of the seminal vesicles suggestive of obstruction of the male genital tract [
All participants were adequately counseled, signed a detailed consent form prior to surgery, and agreed to have their data anonymously utilized. All procedures were performed in accordance with the ethical standards of the Institutional and National Research Committee and with the 1975 Helsinki Declaration.
All patients underwent conventional multiple bilateral TESE, under local anesthesia and sedation. The testicles were delivered through a small scrotal incision on the median raphe. Testis samples were harvested through three separate transverse tunical incisions in the upper pole, in lower pole, and at the equator of the testis, respectively. Depending on the size of the testis, two samples measuring at least 3×2×1 mm (6 mm3) up to 8×5×3 mm (120 mm3) were sharply excised from each tunical incision. Once harvested, the fragments were immediately delivered to the embryologist. In addition to the biopsies for TESE, one representative sample was randomly taken from each testis and sent to histopathology. The tunica albuginea was subsequently closed with a running Vicryl 4-0 suture.
The samples of seminiferous tubules were instantaneously examined. Each testicular tissue sample was placed in a sterile Petri dish with a medium solution and then stretched between two sterile glass slides under stereomicroscope. Subsequently, the suspension was directly observed under inverted microscope at ×200 for the first evaluation of the presence of spermatozoa.
Finally, the entire suspension was transferred to tubes and, after sedimentation of the solid tissue, the supernatant containing free sperm cells was processed by centrifugation at 1,800 rpm for 8 minutes. The pellet was then resuspended in about 300 µL of flushing medium. Only the supernatant with free spermatozoa was utilized for assisted reproductive technology purposes.
If retrieved, spermatozoa were either used fresh for an ICSI cycle or alternatively cryopreserved for later use. If the embryologist observed more than 1–2 sperm cells per field (corresponding to an estimated concentration of 0.001 ×106 spermatozoa/mL), sperm retrieval was considered to be successful for use. Usually, if the sperm concentration was sufficient for future utilization, the residual solid tissue was not utilized for cryopreservation. This remnant, defined as the “testicular pool” and consisting of the residual seminiferous tubules, was fixed in 40% formaldehyde solution and sent for analysis to the histopathology laboratory (
A histopathological analysis of the standard biopsy and testicular pool samples was performed by a single dedicated uropathologist. Tissue sections were stained with hematoxylin and eosin. The pathological analysis involved examining at least 100 different sections of seminiferous tubules. The sperm count was carried out under ×10 magnification, exposing several tubules in a single field of vision. In cases of doubt, the presence of spermatozoa was checked with ×25 magnification. Based on the main morphological pattern, the testicular histological findings were categorized as follows (
Patient characteristics were described using means and standard deviations for continuous variables and numbers and percentages for dichotomous variables. The Student
Data from 60 azoospermic men who underwent sperm retrieval attempts with TESE for fertility treatment at the Assisted Reproductive Technology Centre, University of Florence (Florence, Italy) and whose remnants were sent for histopathological assessment were prospectively collected. Overall, 20 of the 60 participants (33.3%) had OA and 40 (66.6%) had a clinical presentation of NOA. The baseline characteristics of the study cohort are shown in
All patients had a normal urine analysis with a negative urine culture, as well as a negative semen culture test. Screening for sexually transmitted diseases was negative in all patients. Scrotal and transrectal ultrasonography documented a median testicular right volume of 13.32±5.48 mL (range, 4–25 mL) and a median left testicular volume of 13.18±6.16 mL (range, 4.3–25 mL).
At baseline, the mean serum level of FSH was 11.56±5.32 IU/L (range, 2.8–42.7 IU/L), the mean serum level of LH was 4.89±2.0 IU/L (range, 2.7–9.6 IU/L), and the mean TT level was 4.70±1.67 ng/mL (range, 1.44–9.5 ng/mL). Prolactin and TSH levels were in the normal range in all patients. The overall SSR rate was 93.3% (56 of 60 patients). Thirty-six of the 40 NOA patients (90%) had positive sperm retrieval, while SSR occurred in all 20 of the OA patients (100%). The mean sperm concentration was 0.12±0.25 ×106/mL (range, 0.001–1 ×106/mL). The mean total sperm motility was 2.13%±0.58% (range, 0%–20%). A mean number of 6.8±3.28 (range, 1–15). Bio System straws were cryopreserved. The histopathological findings of the testicular pool were compared to those of the standard testicular biopsies.
The histological results of the standard testicular biopsies revealed NS in 12 of 60 patients (20%), while 28 of 60 patients (46.6%) had HYPO and TA, eight of 60 patients (13.3%) had MA, and 12 of 60 patients (20%) had SCOS. No cases of germ cell neoplasia
No testicular pool samples were damaged, and they were therefore adequate for histological assessment. The majority of the testicular pool samples consisted of ample amounts of seminiferous tubules with minimal crushing artifacts from the sperm extraction procedure. In 44 of 60 cases (73.3%), the analysis of the testicular pool confirmed the histopathological features found through the standard testicular biopsy, as verified by the presence or absence of spermatozoa in embryological processing. In the 16 cases (26.7%) where there was a conflict between the histological results of the standard biopsy and sperm retrieval, the testicular pool analysis proved to be more accurate than the standard histological biopsy as verified by the embryological data. Indeed, in four cases in which the analysis of standard histological biopsy revealed MA and in 12 cases where the standard analysis showed SCOS, the testicular pool demonstrated a histological pattern of HYPO associated with severe TA (
The results of the present study show that it is possible to analyze a waste material, such as testicular pool, as a means of predicting SSR. Patients suffering from OA who had previously undergone failed TEFNA were enrolled in the current study, as well as patients with NOA. It should be noted that patients with OA may also have some damage in spermatogenesis, as a result of the long-lasting obstruction causing damage to the spermatogenic tubules [
Testicular histology has previously been suggested to play a role as a predictor of SSR [
In the current series, in four patients (6.7%) with negative sperm retrieval, the results of the standard histological biopsy and the testicular pool analysis showed the same pattern, equivalent to severe MA of spermatogenesis, and these findings explain the complete absence of mature spermatozoa found by the embryologist. Thus, considering the histological findings, both patients were discouraged from undergoing a further sperm retrieval attempt. Moreover, a single testicular biopsy specimen may not reflect the characteristics of the entire testicular tissue because testicular tubules are usually heterogeneous; therefore, to a certain extent, a single failed attempt at sperm collection cannot exclude the possibility of existing foci of spermatogenesis in the testes [
The objective of the present study was to identify a way of providing the histopathologist with as much tissue as possible without depleting the testicles of an excessive amount of parenchyma. However, the dimension of the samples chosen was dependent on the baseline characteristics of each patient. Traditionally, only one small sample is used for histology, while the remaining samples are exclusively used for sperm recovery. Depending on the size or number of spermatogenic foci, this may neither be representative of the tissue extracted nor of the whole testis. As the sample for histology is usually obtained simultaneously with the biopsy for sperm retrieval, its usefulness in terms of predicting SSR is limited [
One of the strengths of the current study is that the histological analysis of all testicular samples was performed by the same highly-experienced pathologist. This is the first study of this new method of histological analysis, in which the remnants of a larger biopsy taken for fertility treatment are analysed in their totality. The principal advantage of this approach is that all available testicular tissue can be used both for sperm retrieval and histopathological evaluation, improving the assessment of spermatogenesis. The main limitations of the current study are the small number of the study cohort and by the fact that the hormone levels were not checked after TESE.
Even if the clinical implementation of the testicular pool analysis may seem unlikely, this technique could prove to be useful, especially in cases where sperm retrieval has failed and the histopathological assessment of the standard testicular biopsy confirms the absence of spermatozoa, but the testicular pool shows the presence of mature spermatozoa (i.e., HYPO). In such cases, the histological evaluation of the testicular pool, as it is more representative of the testis, could guide the clinician to perform the surgical procedure a second time. In our case study, there was no case in which this discrepancy occurred, but we believe that it is an important possibility to highlight. Therefore, although the concept of using remnants for histology represents a very interesting and promising option, its accuracy must be proven in a larger comparative study before it can be implemented in clinical practice. The testicular pool proved to be easily analyzable, practical, manageable, and more accurate than the standard testicular biopsy for predicting sperm retrieval, as it was more representative of the whole testicular parenchyma.
Values are presented as number (%) or mean±standard deviation.
OA, obstructive azoospermia; NOA, nonobstructive azoospermia; BMI, body mass index; TV, testicular volume; FSH, follicle-stimulating hormone; LH, luteinizing hormone; TT, total testosterone; PRL, prolactin; TSH, thyroid-stimulating hormone; SSR, successful sperm retrieval.
Values are presented as number (%).
NS, normal spermatogenesis; HYPO, hypospermatogenesis; TA, tubular atrophy; MA, maturation arrest; SCOS, Sertoli cell-only syndrome.