Update on pediatric rhabdomyosarcoma: A report from the APSA Cancer Committee

DS Rhee, DA Rodeberg, RM Baertschiger… - Journal of pediatric …, 2020 - Elsevier
Abstract Background/Purpose Rhabdomyosarcoma is the most common soft tissue sarcoma
in children and young adults and requires multimodality treatment. The purpose of this …

Treatment of pediatric adrenocortical carcinoma with surgery, retroperitoneal lymph node dissection, and chemotherapy: the Children's Oncology Group ARAR0332 …

C Rodriguez-Galindo, MD Krailo, EM Pinto… - Journal of Clinical …, 2021 - ascopubs.org
PURPOSE Adrenocortical carcinoma (ACC) is a rare aggressive pediatric malignancy with
distinct biology. Its treatment follows the principles developed for adults; pediatric-specific …

Pediatric rhabdomyosarcomas of the genitourinary tract

JT Castle, BE Levy, DB Allison, DA Rodeberg… - Cancers, 2023 - mdpi.com
Simple Summary Rhabdomyosarcomas are soft tissue tumors more commonly found in
children than adults. The diagnosis and management of these tumors continues to change …

European guideline for imaging in paediatric and adolescent rhabdomyosarcoma—joint statement by the European Paediatric Soft Tissue Sarcoma Study Group, the …

R van Ewijk, RA Schoot, M Sparber-Sauer… - Pediatric …, 2021 - Springer
Appropriate imaging is essential in the treatment of children and adolescents with
rhabdomyosarcoma. For adequate stratification and optimal individualised local treatment …

Surgical management of paratesticular rhabdomyosarcoma: A consensus opinion from the Children's Oncology Group, European paediatric Soft tissue sarcoma Study …

TN Rogers, G Seitz, J Fuchs, H Martelli… - Pediatric blood & …, 2021 - Wiley Online Library
The treatment of paratesticular rhabdomyosarcoma (PT‐RMS) has varied over time and by
cooperative group. The International Soft Tissue Sarcoma Database Consortium …

Adrenocortical carcinoma in childhood: A systematic review

M Riedmeier, B Decarolis, I Haubitz, S Müller… - Cancers, 2021 - mdpi.com
Simple Summary Pediatric adrenocortical tumors are rare. Little information is available on
the incidence, risk factors, prognostic factors, treatment, and overall survival. In this …

Paratesticular rhabdomyosarcoma—Impact of locoregional approach on patient outcome: A report from the European paediatric Soft tissue sarcoma Study Group …

TN Rogers, F De Corti, GG Burrieza… - Pediatric Blood & …, 2020 - Wiley Online Library
Abstract Background Paratesticular rhabdomyosarcoma (PT RMS) is rare compared to
benign scrotal pathology. Inappropriate first surgery (InFS) required supplementary …

[HTML][HTML] Genito-urinary rhabdomyosarcoma—challenges and controversies for the urologist

E Bortnick, J Stock, F Ferrer - Translational Andrology and Urology, 2020 - ncbi.nlm.nih.gov
Furthermore, among 173 patients> 10 years old, RPLND improved five-year overall survival
rate from 64% to 86%(P< 0.01)(4). In a review of 25 patients 10 years or older from the …

Importance of Adequate Surgical Local Control in Fusion-Negative Para-Testicular Rhabdomyosarcoma: Data From the Cooperative Weichteilsarkom Studiengruppe …

I Martynov, M Sparber-Sauer, A Heinz… - Annals of Surgical …, 2024 - Springer
Background This study aimed to assess the impact that the quality of primary and
subsequent surgeries has on the survival of patients with para-testicular rhabdomyosarcoma …

Robotic retroperitoneal lymph node dissection for paratesticular rhabdomyosarcoma in adolescents: a case series

CN Clark, J Smith, ME Fuchs, CB Ching… - Journal of Robotic …, 2023 - Springer
Robotic assisted (RA) retroperitoneal lymph node dissection (RPLND) has grown in
popularity as it offers decreased morbidity and faster recovery compared to the open …