|  Boudahna L, Benbrahim Z, Amaadour L, Mazouz A, Benhayoune K, Tahiri Y, Farih MH, Amarti A, Arifi S, Mellas N. Pan Afr Med J. Analysis was performed on all nonmetastatic PT RMS patients enrolled in the European paediatric Soft tissue sarcoma Study Group (EpSSG) RMS 2005 protocol. Further advance in genomic testing would lead us to tailor treatment based on individual risk factors and minimize long-term side effects. Multimodal treatment; Paratesticular; Rhabdomyosarcoma. eCollection 2014. Learn about our remote access options, Department of Paediatric Surgery, University Hospitals Bristol NHS Foundation Trust, Bristol, UK. Case Discussion During … PARATESTICULAR MYXOMA: CASE REPORT AND REVIEW STEPHEN F. SCHIFF,* MARY F. LACHMAN AND LYNWOOD HAMMERS From the Departments of Surgery, Section of Urology, Pathology … The young patient with a rapidly growing tumour usually has a rhabdomyosarcoma, many of which have already metastasised at the time of presentation. Lei WH, Wu WF, Zhen JY, Li YH, Li J, Xin J. The aim of this study was to determine to what extent the quality of locoregional approach impacted on patient morbidity and survival. 1. Would you like email updates of new search results? OS and EFS did not highlight a significant difference in patients undergoing appropriate versus InFS (P = .8479, P = .2780, respectively). Surgical staging of the retroperitoneal lymph nodes should be performed in patients ≥10 years old. Though most (60%-80%) … Rhabdomyosarcomas are the most common soft tissue tumor in children and account for 5-8% of childhood cancers6-7, and 19% of all pediatric soft tissue sarcomas 7. InFS required intensified chemotherapy (10) and local therapy. Locally recurrent paratesticular rhabdomyosarcoma treated with surgery and radiotherapy. Rhabdomyosarcomas are the most common soft tissue sarcomas during childhood (15% of all the pediatric neoplasias), but only 7% of them are presented in a paratesticular location. In both cases a retroperitoneal disease was present … Of the other malignant paratesticular tumours … Embryonal rhabdomyosarcoma is a common tumor of children, rarely appearing in the scrotum from tunica vaginalis or paratesticular tissues. We report a 16-year-old male patient diagnosed with paratesticular rhabdomyosarcoma and mediastinal tuberculous lymphadenitis. This study and literature review … Copyright © 2016 Elsevier Inc. All rights reserved. [Paratesticular embryonal rhabdomyosarcoma-- a case report]. Paratesticular rhabdomyosarcoma: Importance of initial therapy. Graiouid EM, Chakir Y, Gallouo M, Dakir M, Debbagh A, Aboutaieb R. Pan Afr Med J. [Article in Chinese] Li L(1), Wang Y. 2004 Jun;33(3):259. Paratesticular rhabdomyosarcoma (PT RMS) is rare compared to benign scrotal pathology. Results: Children (Basel). Pathology The masses can be … Kilciler M(1), Kadihasanoglu M(2), Atahan O(3). Surgical Pathology Criteria Diagnostic Criteria General Embryonal Rhabdomyosarcoma Alveolar Rhabdomyosarcoma Mixed Alveolar - Embryonal Sclerosing Rhabdomyosarcoma Pleomorphic Rhabdomyosarcoma … Inappropriate first surgery (InFS) required supplementary treatment to maintain excellent outcomes. [Paratesticular rhabdomyosarcoma]. We give insight into the evolution of treatment, present the oncologic outcomes of seminal studies, and summarize the current recommendations for the management of these patients. Keywords: Case reports were excluded, clinical trials from all the oncologic society were reviewed and relevant articles are included in the review. Reporting 2 cases of paratesticular embryonal rhabdomyosarcoma with different locations, one epididymal and one in the testicle tunic vaginalis. Paratesticular tumors are the only genitourinary tract rhabdomyosarcomas that tend to occur in older children, typically adolescents. J Clin Oncol. One was a 53-year-old male, who was admitted … Cancer 61: 209-220, 1988 The Intergroup Rhabdomyosarcoma Study II Saint … Any queries (other than missing content) should be directed to the corresponding author for the article. Uropathology : high-yield pathology [edited by] Ming Zhou, George Netto, Jonathan Epstein Elsevier/Saunders, c2012 Pediatric Surgery Unit, Department of Woman's and Child's Health, University Hospital of Padova, Padova, Italy, Department of Paediatric Surgery, Vall d'Hebron University Hospital, Barcelona, Spain, Department of Paediatric Surgery, Bicêtre Hospital, Hôpitaux Universitaires Paris‐Sud, Le Kremlin‐Bicetre, France, Department of Paediatric Surgery, Prinses Máxima Centrum voor Kinderoncologie, Utrecht, The Netherlands, Department of Urology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK, Department of Paediatric Surgery, Royal Manchester Children's Hospital, Manchester, UK, Department of Pediatric Oncology, Children's Hospital for Wales Heath Park, Cardiff, UK, Department of Pediatric Histopathology, Royal Manchester Children's Hospital, Manchester, UK, Hematology Oncology Division, Department of Women's and Children's Health, University of Padova, Padova, Italy, Clinical Trials and Biostatistics Unit, IRCCS Istituto Oncologico Veneto, Padova, Italy. 2013 Jul;82(1):220-3. doi: 10.1016/j.urology.2012.11.051. 2014 Nov 14;19:279. doi: 10.11604/pamj.2014.19.279.4784. 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