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Canadian Urological Association Journal logoLink to Canadian Urological Association Journal
. 2019 Sep 27;14(3):E101–E103. doi: 10.5489/cuaj.6083

Case – Confirmed testicular mass on ultrasound with no evidence on histology in two teenagers

Sarah Emilie Lebel 1, Stéphane Bolduc 1, Katherine Moore 1,
PMCID: PMC7053368  PMID: 31599712

Introduction

The estimated incidence of testicular masses in pediatrics is 0.5–2 in every 100 000 children.1 The first peak of incidence is found at around two years of age, and a second peak occurs around puberty.1 Patients generally present with painless palpable mass, but it may also be an incidental finding on scrotal ultrasound performed for another testicular complaint, most commonly pain.2 Among the possible diagnoses of intratesticular mass, benign teratoma is the most frequently encountered in pediatrics prior to puberty.1 Despite abundant literature on this subject, we present, to our knowledge, the first two cases of peripubertal testicular masses demonstrated on ultrasound whose tumor markers, surgical exploration, and histological analyses showed no significant abnormality. Ultrasonographic followups showed no recurrence for more than two years after surgical exploration.

Case reports

Case 1

A healthy, 11-year-old, Caucasian boy initially presented to his community hospital for left testicular pain with edema and palpable mass after minor scrotal trauma. Ultrasound showed a hyperechoic left intratesticular mass (10 × 4.4 mm) with no vascular flow. A second ultrasound performed at our pediatric center one month later confirmed the persistence of the non-vascularized hyperechoic homogeneous nodular image (9 mm × 6 mm) (Fig. 1). On physical exam, both testicles were symmetrical, with no persistent edema or palpable mass in this Tanner 1 boy. Preoperative alphafetoprotein (AFP) and human chorionic gonadotropin (hCG) were negative, and lactate dehydrogenases (LDH) were slightly above normal at 204 (normal <200). During surgical exploration, an inguinal partial orchiectomy was performed two days after the ultrasound, but no mass was palpated or visualized. An intraoperative testicular ultrasound did not show the previously described hyperechoic lesion and the right testis remained within the normal range. We performed several large testicular biopsies and they revealed normal testicular parenchyma without significant lesion. Two control ultrasounds, at six and 18 months postoperative, showed no pathology other than the changes associated with surgical exploration. Four years out of his scrotal exploration, the patient has not been seen back in the urology department.

Fig. 1.

Fig. 1

Patient 1: Preoperative testicular ultrasound.

Case 2

A healthy, 13-year-old, Caucasian man with no relevant history presented for acute left testicular pain without other symptoms. No mass was palpated. On ultrasound, homogeneous and hyperechoic intratesticular mass with well-defined contours of 6.8 × 5.6 × 4.2 mm was visualized in the left testicle, with few microlithiasis and signs of epididymitis. One month later, the ultrasound was repeated, and the mass had slightly decreased on size (3.4 × 5.6 × 6) with no vascular flow. At referral, two months after his initial presentation, a third ultrasound was performed and still demonstrated the presence of the stable left testicular mass in this Tanner 1 teenager (Fig. 2). AFP and hCG were negative, and LDHs were slightly elevated at 207 (normal <200). An ultrasoundguided inguinal partial orchiectomy was performed one month after the latest ultrasound. However, the appearance of the two testicles appeared quite normal on palpation and ultrasound. As with the first case, the fresh frozen sections analysis showed no abnormality and the definitive histological aspect of the several large, random biopsies was negative for malignancy. Ultrasonographic followups were regularly performed and were still normal at two years post-exploration. We can extrapolate that 2.5 years later, the patient has not had testicular problem, as he was not referred back to our center — the closest (300 km) pediatric urological center — and no further scrotal ultrasound was seen on the provincial imaging database.

Fig. 2.

Fig. 2

Patient 2: Preoperative testicular ultrasound.

Discussion

As in adults, the assessment of pediatric testicular masses is mainly based on the clinical exam, tumor markers, and Doppler ultrasound (the imaging study of choice).2 While ultrasound alone cannot exclude malignant tumor, it can be used to guide surgical exploration of non-palpable testicular mass.3 In the peripubertal period, physiological changes are observed on testicular echogenicity, mainly related to the increasing in size of seminiferous tubules. At age nine, there is gradual increase in testicular echogenicity on ultrasound, which is more marked between 12 and 15 years of age. According to the available literature, however, these changes on imaging studies occur homogeneously throughout the testis, regardless of the stage of maturation.4 A recent Brazilian study by Camela et al conducted with Dorper rams demonstrated significant difference in testicular heterogeneity during puberty, which was more pronounced in the peripubertal than in the post-pubertal period.5 By extrapolation, this study supports our main hypothesis regarding the two previously reported cases, namely that the hyperechoic masses discovered on ultrasound could represent a normal but inhomogeneous maturation of the testis.

Despite the fact that the majority of pediatric testicular tumors are hypoechoic, they can also be hyperechoic or mixed.2 Although less likely, several cases of germinal tumors with spontaneous regression (burned-out) have been reported in the literature.68 To our knowledge, no pediatric cases of this phenomenon have been described and all patients had retroperitoneal metastases and/or positive tumor markers, both absent from our two patients. On ultrasound, these tumors usually appear as hypoechoic or heterogeneous mass, and all burned-out testicular tumors have a well-circumscribed fibrous scar with generalized testicular atrophy.6 These findings have not been demonstrated in the two pediatric cases we are reporting. Therefore, we did not retain this hypothesis, as the interval between imaging and surgery was short. Frequent tumors of the prepubertal period (teratoma, Yolk sac tumor, and stromal tumors) were part of the differential diagnosis, but they do not tend to regress spontaneously.6,7

Active surveillance can be considered for small testicular lesions, especially in the prepubertal population with negative markers, benign masses being more frequent. This practice seems to have also been adopted in the adult population for small masses incidentally found during infertility screening.9 If surgical exploration is considered, we reiterate that it remains essential to opt for a conservative approach for small intratesticular masses, namely the inguinal partial orchiectomy in the pediatric and peripubertal population.

Conclusions

We present the first two cases of intratesticular masses seen on several ultrasounds in peripubertal males, in whom paraclinical assessment, surgical exploration, and histopathological analysis, as well as ultrasound followup were all negative. Knowing that most pediatric testicular lesions with negative markers are benign, active surveillance should be discussed as a legitimate option. Given the significant consequences of total orchiectomy for an ultimately histologically normal testis, we conclude that a partial approach should be prioritized in prepuberty, but also during the peripubertal period if surgical management is chosen.

Footnotes

Competing interests: Dr. Bolduc has been a principle investigator in clinical tails supported by Astellas and Pfizer. Dr. Moore has been an advisory board member for Pfizer; a speaker for Duchesnay and Hollister; and an investigator in clinical trials supported by Astellas and Pfizer. Ms. Lebel reports no competing personal or financial interests related to this work.

This paper has been peer-reviewed.

References

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