نتایج جستجو برای: ewings sarcoma skull

تعداد نتایج: 90436  

2015
Yunseon Choi Do Hoon Lim Soo Hyun Lee Chuhl Joo Lyu Jung Ho Im Yun-Han Lee Chang-Ok Suh

PURPOSE The aim of this study was to evaluate the role of radiotherapy (RT) in the management of Ewing sarcoma family tumors (ESFT). MATERIALS AND METHODS Retrospective analysiswas performed on 91 patientswith localized ESFT treated from 1988 to 2012. Primary tumor size was ≥ 8 cm in 33 patients. Surgery, RT, and combined surgery with RT were applied in 37, 15, and 33 patients, respectively. ...

2015
José Luis Ordóñez Ana Teresa Amaral Angel M. Carcaboso David Herrero-Martín María del Carmen García-Macías Vicky Sevillano Diego Alonso Guillem Pascual-Pasto Laura San-Segundo Monica Vila-Ubach Telmo Rodrigues Susana Fraile Cristina Teodosio Agustín Mayo-Iscar Miguel Aracil Carlos María Galmarini Oscar M. Tirado Jaume Mora Enrique de Álava

Supplementary Figure S1: (A) IC50 of proliferation after treatment with Olaparib: 72 hours versus 6 days. (B) Grafic representation of IC50 of ES cell lines after treatment with Olaparib with regard to ES cell lines1q status. (C) Grafic representation of IC50 of ES cell lines with regard to their p53 status.

2013
KB Bimal Krishna Valsa Thomas Jayasree Kattoor P Kusumakumari

Ewing's sarcoma (ES) is an uncommon round cell tumor with an aggressive course affecting mainly children and young adults. Only 1% of cases is reported with jaw involvement and have mandibular predilection. Radiographic finding in ES reflect many destructive nature of the lesion, like osteolysis, cortical erosion, periostitis and soft tissue mass. A case of ES of the mandible is reported with s...

2014
Monsef Boufettal

Ewing’s sarcoma (ES) is the second most common malignant bone tumor in children and young adults. Most cases are reported in the bone, and extraosseous Ewing’s sarcoma (ESS) is an extremely rare disease. We present a case of 36 year old female with extraosseous Ewing’s sarcoma developing at the soft tissue in the leg. Their diagnosis was radiological and essentially histological. The Treatment ...

2015
Giuseppe Loverro Leonardo Resta Edoardo Di Naro Anna Maria Caringella Salvatore Andrea Mastrolia Mario Vicino Massimo Tartagni Luca Maria Schonauer

Ewing sarcoma-primitive neuroectodermal tumors (ES/PNETs) constitute a family of neoplasms characterized by a continuum of neuroectodermal differentiations. ES/PNET of the uterus is rare. There are 48 cases of ES/PNET of the uterus published in the literature as far as we know. We describe a case of Ewing sarcoma of the uterus occurring in a 17-year-old woman presenting with a two-month history...

2014
Su Kyung Hwang Dong Kwan Kim Seung-Il Park Yong-Hee Kim Hyeong Ryul Kim

Most cases of Ewing's sarcoma are reported in the bone, and extraosseous Ewing's sarcoma is an extremely rare disease. Here, we report a rare case of primary pulmonary Ewing's sarcoma in a patient with hemoptysis. The patient underwent right upper lung lobe lobectomy with adjuvant chemotherapy and radiation therapy and has been free of recurrent disease for 4 years.

Journal: :Journal of neurology, neurosurgery, and psychiatry 1991
G T Plant J J Donald A Jackowski S J Vinnicombe B E Kendall

Two cases are described in which raised intracranial pressure occurred as a result of superior sagittal sinus (SSS) occlusion by an occipital skull tumour. One was a plasmacytoma, the other a metastatic deposit from a Ewing's sarcoma. The difficulties in diagnosis of this syndrome are illustrated together with the importance and success of appropriate treatment. From the literature it appears p...

Journal: :Neurologia medico-chirurgica 1994
Anil Garg Faiz Uddin Ahmad Ashish Suri Ashok Kumar Mahapatra Veer Singh Mehta Surender Atri Mehar Chand Sharma Ajay Garg

A 12-year-old boy presented with primary Ewing's sarcoma of the occipital bone manifesting as intermittent high fever and local pain in the occipital region. Plain skull x-ray films disclosed an unclear lytic lesion in the occipital bone. Computed tomography and magnetic resonance imaging demonstrated the irregularly enhanced mass. The tumor was removed totally. He received intensive chemothera...

2017
Badredine Hassam

Neurofibromatosis type 1 is the most frequent phacomytosis. Patients with neurofibromatosis type 1 (NF1) have a high risk to develop benign or malignant tumors of neurogenic or non-neurogenic origin. The association of (NF1) to low-grade fibromyxoid sarcoma (LGFMS) is very rare. These tumors rarely develop at the skull and have a high incidence of local recurrence and distant metastasis. We rep...

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