Rhabdomyosarcoma (RMS) is a malignant tumor that represents the most common form of pediatric soft tissue sarcoma. It arises from mesenchymal origin and forms part of the group …
CM Salgado, CK Gestrich… - Surgical Pathology …, 2024 - surgpath.theclinics.com
Pediatric cancer is relatively rare compared to cancer in adults. Most pediatric neoplasms affect the hemopoietic and central nervous systems. Of the solid extracranial tumors, renal …
WJ Hammond, BA Farber, AP Price, SL Wolden… - Journal of pediatric …, 2017 - Elsevier
Purpose To evaluate factors associated with progression-free and disease-specific survival in patients with paratesticular rhabdomyosarcoma, we performed a cohort study. Also, since …
H Goldberg, LM Wong, B Dickson, C Catton… - BJU …, 2019 - Wiley Online Library
Objectives To present long‐term oncological outcomes of patients with paratesticular sarcoma treated by a multidisciplinary team. Patients and methods Patients managed at the …
Y Zhu, Z Zhu, Y Xiao, Z Zhu - Frontiers in Oncology, 2021 - frontiersin.org
Paratesticular rhabdomyosarcoma (RMS) accounts for only 7% of all the RMS cases. Due to the limited available data, there is no consensus on the diagnosis and management of the …
A Sabbagh, A Hamza, MW Sukkari… - Annals of Medicine …, 2023 - journals.lww.com
Discussion: Paratesticular RMS mainly presented as a painless mass in the scrotum. It was a very metastatic lesion that required an immediate management. However, a lot of cases of …
L Improta, R Passa, C Pagnoni, M Angelucci… - Annals of Surgical …, 2024 - Springer
Spermatic cord sarcomas (SCS) are a group of mesenchymal tumors whose rarity and anatomical location often lead to clinical misdiagnosis such as inguinal hernia, testicular …
Z Oruc, S Ebinç, MA Kaplan - Prague Medical Report, 2020 - karolinum.cz
Rare tumours of the testis includes a wide variety of tumours. We aim to present clinical and histological characteristics of our patients with rare tumours of the testis. The medical …