نتایج جستجو برای: desmoplastic small round cell tumor

تعداد نتایج: 2552004  

2016
Sarah Hackman Richard D Hammer Lester Layfield

Malignant mesotheliomas are generally classified into epithelioid, sarcomatoid, desmoplastic, and biphasic types with rare reports of a small cell form. These small cell variants display some morphologic overlap with desmoplastic small round cell tumors (DSRCTs) which generally occur within the abdominal cavity of young males and are defined by a characteristic t(11;22)(p13;q12) translocation. ...

A. Alibakhshi, A. Maddah Safaei, E. Esmati, F. Amouzegar Hashemi, F. Farhan, H. Nosrati , M. Babaei, M. Lashkari, M. Mirai Ashtiani , N. Khanjani,

Background: Due to limited clinical data in pediatric-type sarcomas (rhabdomyosarcoma, Ewing's sarcoma, PNET, and desmoplastic small round-cell tumor), the aim of this study was to evaluate the demographic characteristics and identifying prognostic factors for survival. Materials and Methods: We retrospectively reviewed 110 patients with pediatric-type sarcomas. Overall and disease free surviva...

Journal: :The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology 2014
Arzu Yaren Serkan Değirmencioğlu Neşe Callı Demirkan Atiye Gökçen Demiray Burcu Taşköylü Gamze Gököz Doğu

Primary mesenchymal tumors of the colon are extremely rare tumors among soft tissue sarcomas. These tumors are more aggressive and have poorer prognosis than adenocarcinoma of the colon. Here, we presented 3 cases of primary mesenchymal tumors of the colon. Their histopathological diagnoses are leiomyosarcoma, pleomorphic liposarcoma, and desmoplastic small round cell tumor, respectively. The r...

2002
Rogério Agenor de Araújo Breno Jeha Araújo

Here, we present 2 case reports of patients with desmoplastic small round cell tumor (DSRCT), a very rare and aggressive mesenchymal cancer, and we discuss 2therapeutic options for this sarcoma. This report focuses on men aged 22 and 37 years, respectively. The first patient presented with an abdominopelvic mass which was not suitable for surgery. He underwent chemotherapy (adriblastina and cis...

Journal: :iranian journal of medical sciences 0
zohreh yousefi cancer research center, ghaem hospital, school of medicine, mashhad university of medical sciences, mashhad, iran nourieh sharifhi department of pathology, ghaem hospital, school of medicine, mashhad university of medical sciences, mashhad, iran malihe hasanzadeh department of obstetrics and gynecology, ghaem hospital, school of medicine, mashhad university of medical sciences, mashhad, iran mansoureh mottaghi gynecologist, mashhad, iran somayeh bolandy department of obstetrics and gynecology, ghaem hospital, school of medicine, mashhad university of medical sciences, mashhad, iran

the primitive neuroectodermal tumor (pnet) belongs to a group of highly malignant tumors and is composed of small round cells of a neuroectodermal origin. categorized in the same tumor family as ewing sarcoma, the pnet is most likely to occur in bones and soft tissues. however, a small number of pnet cases arising in the pelvis have been reported as well. we present three cases of pelvic pnet: ...

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