منابع مشابه
Paratesticular Neuroblastoma Presenting as Bilateral Paratesticular Tumors
We describe a case of simultaneous bilateral paratesticular neuroblastoma presenting as spermatic cord tumors in a 6-month-old boy. He was diagnosed as having stage IV neuroblastoma originated from right adrenal gland with metastases to the paratesticular region, right femur, and right maxilla. The tumor showed favorable biological features according to Shimada’s classification and had no N-myc...
متن کاملParatesticular Spindle Cell Rhabdomyosarcoma
Spindle cell rhabdomyosarcoma is a rare variant of embryonal rhabdomyosarcoma that affects young males and most commonly involves the paratesticular region. We report a case of paratesticular spindle cell rhabdomyosarcoma in a 14-year-old boy, who presented with a painless scrotal mass. Left inguinal orchidectomy was performed. Histopathological and immunohistochemical examination of the mass r...
متن کاملRhabdomyosarcoma metastatic paratesticular.
OBJECTIVES To report one case of metastatic paratesticular rhabdomyosarcoma in a 14 years old patient, classified as stage IIb (IRSG). METHODS After treatment with radical surgery (orchiectomy and lymphadenectomy), polychemotherapy and radiotherapy, showed good evolution initially. RESULTS 12 months after surgery the patient is disease free. CONCLUSIONS Adjuvant treatment is very importan...
متن کاملMalignant paratesticular mesothelioma
Mesothelioma of the tunica vaginalis testis (MTVT) is a rare tumor that usually affects patients after the sixth decade of life. Exposure to asbestos is a known risk factor. Enlargement of the scrotal volume is the most common initial clinical manifestation, and about 15% of cases present metastasis at diagnosis. The treatment relies on surgical resection while the role of adjuvant chemotherapy...
متن کاملParatesticular Fibrous Pseudotumors
Paratesticular fibrous pseudotumors (PFPs) are rare pathologies with quite wide and variable topographic-morphological features. It is difficult to distinguish PFPs from malignant masses. Treatment can be done by resection of the mass. We reported a young patient's findings about this rare pathology.
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ژورنال
عنوان ژورنال: Archivos Españoles de Urología (Ed. impresa)
سال: 2009
ISSN: 0004-0614
DOI: 10.4321/s0004-06142009000700013