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Desmoplastic small round cell tumors of the abdomen

✍ Scribed by D. Frappaz; E. Bouffet; D. Dolbeau; R. Bouvier; C. Carrie; D. Louis; Cori Pondarre; E. Tabone; T. Philip; M. Brunat-Mentigny


Publisher
John Wiley and Sons
Year
1994
Tongue
English
Weight
443 KB
Volume
73
Category
Article
ISSN
0008-543X

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Paratesticular desmoplastic small round
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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: Desmoplastic small round cell tumour (dsrct) is a rare highly aggressive neoplasm, and clinical studies are scarce. ## Procedure: We report six cases of children and adolescents (median age 14 years, range 6.9-17.5) with dsrct (5 abdominal, 1 paratesticular) registered by the itali

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## Background: The identification of recently described nonrandom chromosomal defects specific for various small round-cell and spindle-cell sarcomas can eliminate diagnostic uncertainty arising from the clinical and histopathologic overlap of soft tissue neoplasms. ## Methods: A 26-year-old man

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## BACKGROUND. Desmoplastic small round-cell tumor has been identified as a neoplasm with multidirectional immunohistochemical differentiation. The combination of topographic, morphologic, immunohistochemical, and molecular features of this tumor sets it apart as a pathologic entity. The optimal t

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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