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Intraabdominal desmoplastic small round cell tumors : A diagnostic and therapeutic challenge

✍ Scribed by Imran Hassan; Roman Shyyan; John H. Donohue; John H. Edmonson; Leonard L. Gunderson; Christopher R. Moir; Carola A.S. Arndt; Antonio G. Nascimento; Florencia G. Que


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
78 KB
Volume
104
Category
Article
ISSN
0008-543X

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Desmoplastic small round cell tumor (DSRCT) is a rare neoplasm mainly affecting young males and typically located in the abdomen. Prognosis is generally very poor. We report a rare case of paratesticular DSRCT in a 17-year-old boy, presenting with an isolated left scrotal mass. The patient had an ex

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Background. The EWS gene, a transcription factor of unknown function, is involved in chromosomal translocations associated with a wide variety of tumors, particularly small round blue cell tumors such as Ewing sarcoma. It has previously been reported that desmoplastic small round blue cell tumor (DS

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## Abstract ## Background Desmoplastic small round cell tumor (DSRCT) is an aggressive and often misdiagnosed neoplasm of children and young adults. It is chemotherapy‐sensitive, yet patients often relapse off therapy because of residual microscopic disease at distant sites: peritoneum, liver, lym