Rhabdomyosarcoma with TFCP2 rearrangement in a young adult: a rare case with unique clinical and pathological features DOI
Hannah Chaudhury,

Nicole Hancock,

Jorge Rodriguez Vazquez

et al.

Baylor University Medical Center Proceedings, Journal Year: 2025, Volume and Issue: unknown, P. 1 - 5

Published: April 28, 2025

Language: Английский

EUROPEAN STANDARD CLINICAL PRACTICE RECOMMENDATIONS FOR CHILDREN AND ADOLESCENTS WITH RHABDOMYOSARCOMA A joint EpSSG, CWS and ERN PaedCan Project DOI Creative Commons
Johannes H. M. Merks, Eva Brack, Martin Ebinger

et al.

EJC Paediatric Oncology, Journal Year: 2025, Volume and Issue: unknown, P. 100229 - 100229

Published: April 1, 2025

Language: Английский

Citations

0
Role and regulatory mechanism of DLX5 in rhabdomyosarcoma tumorigenesis DOI
Yuhan Zhao, Xinpei Liu,

Zining Wu

et al.

Biochimica et Biophysica Acta (BBA) - Molecular Cell Research, Journal Year: 2025, Volume and Issue: 1872(5), P. 119959 - 119959

Published: April 19, 2025

Language: Английский

Citations

0
Genitourinary Rhabdomyosarcoma in a Child with Urinary Incontinence as the Initial Symptom: A Case Report and Literature Review DOI Creative Commons
Jinyuan Wu, Rong Ma, Qing‐Wei Zhang

et al.

Urology Case Reports, Journal Year: 2025, Volume and Issue: 61, P. 103051 - 103051

Published: April 23, 2025

Rhabdomyosarcoma (RMS) is a morphologically heterogeneous high-grade malignancy that occurs uncommonly in the pediatric genitourinary (GU) system, and most typical clinical symptoms are urinary frequency, urgency, hematuria, associated with infection. The boys this case, persistent incontinence was relatively rare, it easily misdiagnosed as diagnosis. Incontinence disease lower tract were identified by imaging examination, final pathological biopsy confirmed diagnosis of GU embryonal rhabdomyosarcoma (ERMS). Learning through case report literature can help clinicians to better understand manifestations accurate diagnostic treatment disease.

Language: Английский

Citations

0
Rabdomiossarcoma do Subtipo Alveolar em Região Tenar com Invasão Linfonodal Axilar em Adulto: Relato de Caso DOI Creative Commons

Aline Graciele Henriques Campos,

Estela Cesar Oyama, Maria Eduarda Pardal Simonato

et al.

Revista Brasileira de Cancerologia, Journal Year: 2025, Volume and Issue: 71(2)

Published: April 24, 2025

Introdução: O rabdomiossarcoma é um subtipo raro de neoplasia maligna tecidos moles cujas células são semelhantes a mioblastos. Representa 1% das neoplasias em adultos, com mau prognóstico e alta taxa recidiva. Neste trabalho, objetiva-se relatar caso ultrarraro alveolar que acometeu mão uma paciente adulta, além realizar revisão integrativa casos semelhantes, haja vista cânceres primários na têm incidência inferior 1%. Relato do caso: Mulher, 33 anos, procurou atendimento clínico por presença lesão arroxeada não ulcerada região tenar da esquerda, linfadenomegalia axila esquerda. Inicialmente, ressonância revelou formação expansiva tenar, qual biópsia incisional o exame-histoquímico sugeriram alto grau. Realizou-se amputação primeiro metacarpo esquerda dissecção axilar dos linfonodos comprometidos, quimioterapia SAIME intercalada SAVAC cada três semanas, radioterapia intervalo, seis meses. Tratamento sem complicações atualmente recidivas. Conclusão: relatado apresentação anatômica faixa etária pouco comum para rabdomiossarcoma, os principais aspectos bom seguimento diagnóstico precoce terapia multimodal.

Citations

0
Rhabdomyosarcoma with TFCP2 rearrangement in a young adult: a rare case with unique clinical and pathological features DOI
Hannah Chaudhury,

Nicole Hancock,

Jorge Rodriguez Vazquez

et al.

Baylor University Medical Center Proceedings, Journal Year: 2025, Volume and Issue: unknown, P. 1 - 5

Published: April 28, 2025

Language: Английский

Citations

0