©
2007 THE AUTHORS
JOURNAL COMPILATION
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2 0 0 7 B J U I N T E R N A T I O N A L | 9 9 , 11 2 3 – 11 2 6 | doi:10.1111/j.1464-410X.2007.06796.x 1123
Original Article
TESTICULAR TUMOURS IN CHILDREN
OOTTAMASATHIEN
et al.
Testicular tumours in children:
a single-institutional experience
Siam Oottamasathien, John C. Thomas, Mark C. Adams,
Romano T. DeMarco, John W. Brock III, and
John C. Pope IV
Department of Urologic Surgery, Vanderbilt University Medical Center, and
Division of Paediatric Urology, Vanderbilt Children’s Hospital, Nashville, TN,
USA
Accepted for publication 24 November 2006
OBJECTIVE
To report our experience of testicular and
paratesticular tumours in children, as such
tumours are rare, and historically yolk sac
tumour has been described as the most
common lesion in children, but recent reports
suggest that benign testicular lesions might
be more common.
PATIENTS AND METHODS
We reviewed retrospectively the records
of children treated for testicular tumours
from 1998 to 2005. The patients’ age,
clinical presentation, diagnostic procedures,
treatment methods, histopathological
findings, and outcome were recorded.
Patients aged > 144 months and those
with non-primary metastatic lesions were
excluded.
RESULTS
In all, 11 patients met our criteria, with a
mean age of 37 months (range 9 days to
144 months). Pathological analysis revealed
teratoma in four patients, yolk sac tumour in
two, epidermoid cysts in two, extrarenal
nephroblastomatosis in one, and
paratesticular rhabdomyosarcomas in two.
The most common clinical presentation was a
painless testicular mass. Depending on the
clinical presentation and pathology, scrotal
ultrasonography, tumour markers ( α -
fetoprotein and β -human chorionic
gonadotrophin), and/or staging computed
tomography (CT) were obtained in eight
patients. All patients had a radical
orchidectomy. Three patients had elevated
tumour markers that normalized after
orchidectomy. CT revealed extensive
mediastinal adenopathy in one patient with
rhabdomyosarcoma. Chemotherapy was
administered to both patients with
rhabdomyosarcoma.
CONCLUSION
Although there were few patients, most of the
lesions were benign tumours, with the most
common histological subtype being teratoma.
As both malignant and paratesticular lesions
occurred at a significant frequency, we would
continue to advocate an initial radical
inguinal approach at which time testis-
sparing could be considered if the
preoperative evaluation was favourable, and
frozen-section analysis at the time of surgery
confirms a benign lesion.
KEYWORDS
prepubertal testis tumour, testis sparing
surgery, benign testis tumour, teratoma
Authors from the USA present a
retrospective review of children in
their institution who were treated
for testicular cancer. They found
that most of the lesions were
benign, the commonest being
testicular. They also found several
malignant and paratesticular
lesions, and make
recommendations as to the
surgical approach.