2017, Number 1
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Rev Mex Urol 2017; 77 (1)
Rhabdomyosarcoma and yolk sac tumor of the testis
Pineda-Murillo J, Sánchez-Bermeo AF, Martínez-Carrillo G, Torres-Aguilar J, Viveros-Contreras C, González-Medina WE
Language: Spanish
References: 13
Page: 50-55
PDF size: 388.21 Kb.
ABSTRACT
Background: Testicular neoplasias make up a group of tumors
with diverse morphologic characteristics and clinical manifestations.
They represent approximately 1 to 2% of the malignant cancers in
men and up to 10% of all malignant diseases of the male genitourinary
system.
Objective: To demonstrate the incidence, diagnosis, treatment, and
prognosis of testicular rhabdomyosarcoma and yolk sac tumor.
Clinical Case: A 43-year-old man presented with symptoms of
8-month progression that included an enlarged left testis with moderate
pain irradiating to the lower ipsilateral limb with periods of remission
and exacerbation and accompanied by difficulty in breathing.
He underwent left radical orchiectomy and the histopathology study
reported a mixed germ cell tumor composed of a sarcomatoid yolk
sac tumor (50%) and rhabdomyosarcoma (30%).
Conclusions: Intratesticular rhabdomyosarcomas are aggressive
and rare and it is common for them to present with lymph node
involvement or metastasis at the time of diagnosis. Clinical stage,
histologic type, and treatment adherence influence the natural history
of the cancer.
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https://www.nccn.org/professionals/physician_gls/pdf/ testicular.pdf. Consultado el 16 de julio de 2016.
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