Archivos espanoles de urologia · 2009
[Giant dedifferenciated liposarcoma of the spermatic cord].
Аннотация на английскомСтатьяОбзорНазвание и аннотация: Перевод в очереди
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Fernández Fernando, García Herney A
Аннотация
SUMMARY OBJECTIVES: To describe a patient with dedifferentiated liposarcoma of the spermatic cord and to perform a bibliographic review.
METHODS: We describe the case of a patient with dedifferentiated liposarcoma of the spermatic cord, and conducted an extensive search of literature in different databases that support the discussion of the case.
RESULTS: A 65 years old male presented a right scrotal mass with progressive growth, and underwent excision of the mass (measured 34 x 22 x 17 cm and weighed 5786 grams). Pathology reported dedifferentiated liposarcoma of the spermatic cord. This patient draws attention to the reoccurrence of papillary thyroid cancer.
CONCLUSIONS: Paratesticular tumors are rare entities, derived from mesenchymal tissue. Most of them are benign, but up to 30% could be of sarcomatoid type. Their treatment is based on the extraction of the mass along with radical orchiectomy, but being a very rare disease is not clear whether the benefit of adjuvant chemotherapy and radiotherapy in these patients is beneficial.
METHODS: We describe the case of a patient with dedifferentiated liposarcoma of the spermatic cord, and conducted an extensive search of literature in different databases that support the discussion of the case.
RESULTS: A 65 years old male presented a right scrotal mass with progressive growth, and underwent excision of the mass (measured 34 x 22 x 17 cm and weighed 5786 grams). Pathology reported dedifferentiated liposarcoma of the spermatic cord. This patient draws attention to the reoccurrence of papillary thyroid cancer.
CONCLUSIONS: Paratesticular tumors are rare entities, derived from mesenchymal tissue. Most of them are benign, but up to 30% could be of sarcomatoid type. Their treatment is based on the extraction of the mass along with radical orchiectomy, but being a very rare disease is not clear whether the benefit of adjuvant chemotherapy and radiotherapy in these patients is beneficial.