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Pediatr Surg Int ; 21(7): 563-5, 2005 Jul.
Article in English | MEDLINE | ID: mdl-15776247

ABSTRACT

Aggressive angiomyxoma (AAM) is a rare and nonmetastasizing soft-tissue tumor predominantly found in the female pelvis and perineum. It has a high risk of local recurrence. We report the unusual case of a 15-year-old boy with an AAM presenting as a slowly enlarging scrotal mass. The patient had had chronic renal failure since 1997 and had needed hemodialysis for the previous 11 months. He presented with a 12-month history of a nontender soft mass in the right scrotum. Ultrasound examination revealed a solid mass in the scrotum. After surgical resection, pathological analysis disclosed spindle-shaped neoplastic cells widely separated by a myxoid stroma rich in collagen fibers and prominent irregularly shaped blood vessels; the histological examination confirmed an AAM.


Subject(s)
Genital Neoplasms, Male/complications , Kidney Failure, Chronic/complications , Myxoma/complications , Scrotum , Adolescent , Diagnosis, Differential , Genital Neoplasms, Male/diagnosis , Genital Neoplasms, Male/pathology , Humans , Male , Myxoma/diagnosis , Myxoma/pathology
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