Testicular adrenal rest tumor in infertile man with congenital adrenal hyperplasia: case report and literature review

ABSTRACT CONTEXT: Synthesis of cortisol and aldosterone is impaired in patients with congenital adrenal hyperplasia (CAH) because of 21-hydroxylase deficiency. Men with CAH have low fertility rates compared with the normal population, and this is related to testicular adrenal rest tumors. Findings of azoospermia in combination with a testicular tumor on ultrasound are likely to have a mechanical cause, especially when in the testicular mediastinum. The preferred treatment method consists of intensive corticoid therapy. However, when the tumor is unresponsive to steroid therapy, surgical treatment should be considered. CASE REPORT: We present the case of a male patient with CAH due to 21-hydroxylase deficiency who presented a testicular tumor and azoospermia. Treatment with low daily corticoid doses had previously been started by an endocrinologist, but after 12 months, no significant change in sperm count was found. Although the adrenocorticotrophic hormone and 17-hydroxyprogesterone levels returned to normal values, the follicle-stimulating hormone (FSH), luteinizing hormone and testosterone levels remained unchanged. Ultrasound examination confirmed that the testicles were small and heterogenous bilaterally, and revealed a mosaic area at the projection of the testis network bilaterally. Magnetic resonance imaging confirmed the finding. Testicular biopsy revealed the presence of preserved spermatogenesis and spermiogenesis in 20% of the seminiferous tubules in the right testicle. The patient underwent testis-sparing tumor resection. After 12 months of follow-up, there was no tumor recurrence but the patient still presented azoospermia and joined an intracytoplasmic sperm injection program.


INTRODUCTION
Synthesis of cortisol and sometimes of aldosterone is impaired in patients with congenital adrenal hyperplasia (CAH) because of 21-hydroxylase deficiency.Men with CAH have low fertility rates compared with the normal population, and this is related to testicular adrenal rest tumors (TART). 1,2Development of the primitive adrenal cortex occurs close to the gonads and TART is considered to be an aberrant adrenal tissue that has descended with the testes. 3Pretumor development and growth of these cells is assumed to be adrenocorticotrophic hormone (ACTH) dependent, and undertreatment may play an important role in tumor development.][6][7][8][9][10] These tumors were first described by Wilkins et al. in 1940 and they are almost always present bilaterally. 113][14] CAH patients not only have anatomical lesions but also have impaired testicular function and hypogonadotropic hypogonadism due to chronic suppression of gonadotropin secretion caused by overproduction of adrenal androgens. 5We present the case of a male patient with congenital adrenal hyperplasia due to 21-hydroxylase deficiency who presented a testicular tumor and infertility.

CASE REPORT
A 39-year-old male patient was referred to our Andrology Division because of primary infertility.He had a past medical history of CAH due to 21-hydroxylase deficiency.
At four years of age, the patient was diagnosed as having the simple virilizing non-salt wasting form of CAH.Treatment with low-dose glucocorticoid (0.5 mg of dexamethasone) was started and he did not need any mineralocorticoid replacement.The patient evolved normally until 22 years of age, when he abandoned his treatment and was lost from follow-up consultations.
He sought medical counseling fifteen years later because of infertility.He was healthy and not taking any medications at that time.He and his wife failed to achieve pregnancy for two years.She did not have any previous offspring, and all possible causes of female infertility were ruled out.
At physical examination, he was seen to have small stature (height: 1.68 m; weight: 78 kg; body mass index: 27.6 kg/m 2 ) and small topically softened testicles compatible with testicular atrophy.Semen analyses revealed azoospermia.Serum hormonal screening showed increased levels of follicle-stimulating hormone (FSH) and luteinizing hormone (LH) and low levels of testosterone, albeit within the normal range, thus suggesting testicular failure.The ACTH and 17-hydroxyprogesterone (17-OHP) levels were high, while the levels of other hormones were within the normal range.Treatment with low-dose daily glucocorticoid therapy (0.5 mg of dexamethasone) had been started by an endocrinologist before our first visit, but after twelve months no significant change in sperm count was found.
Although the ACTH and 17-OHP levels returned to normal values, the FSH, LH and testosterone levels showed no great improvement (Table 1).
Testicular ultrasound examination confirmed that the testicles were small and heterogenous bilaterally (right: 9.1 ml; left: 9.3 ml).It also revealed the presence of a hyperechogenic hypervascularized tumor mosaic area of 1.5 x 1.5 centimeters at the projection of the testis network, in both testicles, thereby suggesting the presence of duct occlusion at this point.Further evaluation using magnetic resonance image (MRI) revealed T2-weighted low-sign bilateral solid elongated serpiginous lesions in the testicular mediastinum, for which adrenal rest tumor was a differential diagnosis (Figures 1 and 2).In order to distinguish testicular failure from obstructive azoospermia, the patient underwent bilateral testicular biopsy.This revealed preserved spermatogenesis and spermiogenesis in 20% of the seminiferous tubules in the right testicle.It also revealed left testicular atrophy characterized by germ cell hypoplasia and basal membrane thickening.[40][41][42][43] Depending on the detection method (palpation or ultrasound), the reported prevalence of TART among CAH patients may range The patient underwent testis-sparing tumor resection (Fig- ure 3).Bilateral inguinal incisions were made to access the testis and the tumor masses were microdissected using ultrasound guidance (Figure 4).The patient's hospital stay was uneventful.
After twelve months of follow-up, ultrasound showed that there was no evidence of tumor recurrence, but the patient still presented azoospermia.He and his wife agreed to join an intracytoplasmic sperm injection (ICSI) program.
from 0 to 95%. 5,27,43Absence of palpable tumors does not rule out the existence of TART, and ultrasound is the preferred method for evaluating TART because it is as sensitive as MRI but more accessible. 2In our case, MRI was necessary to confirm the ultrasound findings.Histologically, electron microscopy shows that TART resembles Leydig cell tumors, with features that are consistent with steroid-secreting cells.However, unlike Leydig cell tumors, they never contain Reinke crystalloids, are often bilateral and may diminish with corticosteroid therapy. 44fferent mechanisms have been proposed to explain infertility in males with CAH. 21,22Stikkelbroeck et al. demonstrated the presence of testicular dysfunction due to decreased plasma testosterone levels in 35% of the CAH patients that they evaluated, with poor semen quality in 63% of them.This could be caused mechanically by TART, or by local steroid production. 30,456][47][48] In one study, sperm production was found to be impaired in seven of the eleven patients tested, and three (40%) even showed azoospermia.In two of the azoospermic patients, the serum FSH levels were increased, thereby indicating primary testicular dysfunction.In the third azoospermic patient, the serum levels of both LH and FSH were undetectably low, thus suggesting the presence of testicular dysfunction due to hypogonadotropism.With these findings, the authors proposed that routine semen analysis should be performed for such patients.When azoospermia is found in combination with a large testicular tumor on ultrasound, it is likely to have a mechanical cause, especially when in the mediastinum.At this location, large tumors can easily compress the testis network and cause obstructive azoospermia, 49 as found in our patient.The preferred treatment method for testicular adrenal rest tumors and/or impaired spermatogenesis in patients with CAH is intensive glucocorticoid therapy.1][52] Clomiphene citrate may also be administered, and successful cases have been reported. 46,53However, when the tumor is unresponsive to steroid therapy, surgical treatment should be considered, preferably using a testis-sparing procedure. 5Recently, Fernandes et al reported a case of a 16-year-old boy who underwent bilateral orchiectomy because of TART that could not be differentiated from a malignant tumor, thus expressing this diagnostic dilemma. 54cause of the rarity of TART and its management, we carried out a systematic analysis of the indexed articles published since 1966, in order to provide the best treatment for our patient.
We searched using the terms "adrenal rest tumor" and/or "infertility" in the Lilacs (Literatura Latino-Americana e do Caribe em

Figure 3 .
Figure 3. Tumor marking (A) for intraoperative ultrasound examination and needle driving (B).

Table 2 )
. Most were descriptive series or case reports.The prevalence of testicular tumors in male CAH patients is high, despite adequate treatment.Semen production and testosterone secretion may be impaired, especially when large testicular tumors are present.The diagnosis can be achieved using ultrasound or MRI, and early treatment for TART by means of glucocorticoid should be of primary concern.Testis-sparing surgery is Lilacs = Literatura Latino-Americana e do Caribe em Ciências da Saúde; Medline = Medical Literature Analysis and Retrieval System Online; MeSH = Medical Subject Headings.
50ar function.Cryopreservation of the semen or testicular sperm extraction (TESE) with intrauterine injection (IUI) or intracytoplasmic sperm injection (ICSI) can be offered for these patients, as we did in our case, because the fertility prognosis is uncertain.50CONCLUSION

Table 2 .
Complete literature database search using the terms "adrenal rest tumor" and "infertility" as medical subject headings (MeSH)