التفاصيل البيبلوغرافية
العنوان: |
Malignant ectomesenchymoma in children: The European pediatric Soft tissue sarcoma Study Group experience |
المؤلفون: |
Milano, Giuseppe Maria, Orbach, Daniel, Casanova, Michela, Berlanga, Pablo, Schoot, Reineke A., Corradini, Nadege, Brennan, Bernadette, Ramirez-Villar, Gema L., Lyngsie Hjalgrim, Lisa, van Noesel, Max M., Alaggio, Rita, Ferrari, Andrea |
المساهمون: |
Arts-assistenten Kinderen, Onderzoek Beeld, Cancer |
سنة النشر: |
2023 |
مصطلحات موضوعية: |
children, EpSSG, malignant ectomesenchymoma, outcome, treatment, Sarcoma/therapy, Humans, European People, Child, Preschool, Muscle Neoplasms, Rhabdomyosarcoma/therapy, Soft Tissue Neoplasms/therapy, Hematology, Oncology, Pediatrics, Perinatology, and Child Health, Research Support, Non-U.S. Gov't, Journal Article |
الوصف: |
Malignant ectomesenchymoma (MEM) is an extremely rare soft tissue tumor typical of young children, currently included in the category of skeletal muscle malignancies and characterized by a neuroblastic component. This study describes a series of 10 patients prospectively registered in the European paediatric Soft tissue sarcoma Study Group (EpSSG) database Of the 10 cases, seven had an initial local diagnosis of rhabdomyosarcoma. All patients received chemotherapy according to rhabdomyosarcoma strategy, four had radiotherapy. Overall, six patients were alive in first remission, two in second remission and one after second tumor. Only the patient with initially metastatic tumor died of disease. |
نوع الوثيقة: |
article in journal/newspaper |
وصف الملف: |
application/pdf |
اللغة: |
English |
تدمد: |
1545-5009 |
العلاقة: |
https://dspace.library.uu.nl/handle/1874/448169Test |
الإتاحة: |
https://dspace.library.uu.nl/handle/1874/448169Test |
حقوق: |
info:eu-repo/semantics/OpenAccess |
رقم الانضمام: |
edsbas.27399758 |
قاعدة البيانات: |
BASE |