Einleitung Das Rhabdomyosarkom (RMS) ist eines der häufigsten Weichteilsarkome im Kindesalter. Im Gegensatz ist das adulte Rhabdomyosarkom (aRMS; Patienten Alter > 18 Jahre) ein sehr seltenes Sarkom und wenig klinische Daten veröffentlicht wurden. Im Rahmen dieser Studie wurden alle Patientenmit aRMS die an einer muskuloskelettalen Tumor-Abteilung behandelt wurden analysiert. Material und Methoden 29 aRMS (5 Frauen und 24 Männer) Patientin mit einem medianen Alter von 61 Jahren (Spanne 20 78) und einem medianen Nachuntersuchungszeitraum von 26 Monaten (1 161) wurden eingeschlossen. Zehn Patienten (34%) hatten Metastasen zum Zeitpunkt der Erstvorstellung h und sechs Patienten entwickelten Metastasen im median neun Monate (6 41) nach Operat...
Our present study is a retrospective analysis of the treatment results of new rhabdomyosarcoma pedia...
Objectives: The study goal was to retrospectively review the treatment results of childhood rhabdomy...
Le rhabdomyosarcome de l'adulte est une tumeur rare au pronostic. Le présent travail propose d'étudi...
Rabdomiosarkom (RMS) je najčešći od svih sarkoma mekih tkiva, a zauzima oko 6% svih malignih neoplaz...
INTRODUÇÃO: Rabdomiossarcoma (RMS) representa o sarcoma de partes moles mais freqüente da infância, ...
BACKGROUND Pleomorphic rhabdomyosarcoma (RMS) is a rare sub-type of RMS. Optimal treatment remain...
Background: The prognosis of rhabdomyosarcoma (RMS) in children and adolescents has improved since t...
IF 3.202International audienceFive-year overall survival (OS) of localized RMS exceeds 70% in childr...
BACKGROUND: Rhabdomyosarcoma (RMS) diagnosed during the first year of life is reported to have poor ...
OBJECTIVE Although rhabdomyosarcoma (RMS) is the most frequent soft tissue sarcoma diagnosed in chil...
Introduction: Rhabdomyosarcoma is the most common soft tissue sarcoma in children. This paper aimed ...
OBJECTIVE Although rhabdomyosarcoma (RMS) is the most frequent soft tissue sarcoma diagnosed in chil...
BACKGROUND: The prognosis of rhabdomyosarcoma (RMS) in children and adolescents has improved since t...
Background: The prognosis of rhabdomyosarcoma (RMS) in children and adolescents has improved since t...
Our present study is a retrospective analysis of the treatment results of new rhabdomyosarcoma pedia...
Objectives: The study goal was to retrospectively review the treatment results of childhood rhabdomy...
Le rhabdomyosarcome de l'adulte est une tumeur rare au pronostic. Le présent travail propose d'étudi...
Rabdomiosarkom (RMS) je najčešći od svih sarkoma mekih tkiva, a zauzima oko 6% svih malignih neoplaz...
INTRODUÇÃO: Rabdomiossarcoma (RMS) representa o sarcoma de partes moles mais freqüente da infância, ...
BACKGROUND Pleomorphic rhabdomyosarcoma (RMS) is a rare sub-type of RMS. Optimal treatment remain...
Background: The prognosis of rhabdomyosarcoma (RMS) in children and adolescents has improved since t...
IF 3.202International audienceFive-year overall survival (OS) of localized RMS exceeds 70% in childr...
BACKGROUND: Rhabdomyosarcoma (RMS) diagnosed during the first year of life is reported to have poor ...
OBJECTIVE Although rhabdomyosarcoma (RMS) is the most frequent soft tissue sarcoma diagnosed in chil...
Introduction: Rhabdomyosarcoma is the most common soft tissue sarcoma in children. This paper aimed ...
OBJECTIVE Although rhabdomyosarcoma (RMS) is the most frequent soft tissue sarcoma diagnosed in chil...
BACKGROUND: The prognosis of rhabdomyosarcoma (RMS) in children and adolescents has improved since t...
Background: The prognosis of rhabdomyosarcoma (RMS) in children and adolescents has improved since t...
Our present study is a retrospective analysis of the treatment results of new rhabdomyosarcoma pedia...
Objectives: The study goal was to retrospectively review the treatment results of childhood rhabdomy...
Le rhabdomyosarcome de l'adulte est une tumeur rare au pronostic. Le présent travail propose d'étudi...