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1.
Clin. transl. oncol. (Print) ; 23(12): 2460-2473, dec. 2021.
Article in English | IBECS | ID: ibc-224103

ABSTRACT

Rhabdomyosarcoma (RMS) is the most frequent soft tissue sarcoma (STS) in children and adolescents. In Spain the annual incidence is 4.4 cases per million children < 14 years. It is an uncommon neoplasm in adults, but 40% of RMS are diagnosed in patients over 20 years of age, representing 1% of all STS in this age group. RMS can appear anywhere in the body, with some sites more frequently affected including head and neck, genitourinary system and limbs. Assessment of a patient with suspicion of RMS includes imaging studies (MRI, CT, PET-CT) and biopsy. All patients with RMS should receive chemotherapy, either at diagnosis in advanced or metastatic stages, or after initial resection in early local stages. Local control includes surgery and/or radiotherapy depending on site, stage, histology and response to chemotherapy. This guide provides recommendations for diagnosis, staging and treatment of this neoplasm (AU)


Subject(s)
Humans , Positron Emission Tomography Computed Tomography/methods , Rhabdomyosarcoma/therapy , Rhabdomyosarcoma/epidemiology , Rhabdomyosarcoma/pathology , Combined Modality Therapy , Incidence , Spain/epidemiology
2.
Clin Transl Oncol ; 23(12): 2460-2473, 2021 Dec.
Article in English | MEDLINE | ID: mdl-34212338

ABSTRACT

Rhabdomyosarcoma (RMS) is the most frequent soft tissue sarcoma (STS) in children and adolescents. In Spain the annual incidence is 4.4 cases per million children < 14 years. It is an uncommon neoplasm in adults, but 40% of RMS are diagnosed in patients over 20 years of age, representing 1% of all STS in this age group. RMS can appear anywhere in the body, with some sites more frequently affected including head and neck, genitourinary system and limbs. Assessment of a patient with suspicion of RMS includes imaging studies (MRI, CT, PET-CT) and biopsy. All patients with RMS should receive chemotherapy, either at diagnosis in advanced or metastatic stages, or after initial resection in early local stages. Local control includes surgery and/or radiotherapy depending on site, stage, histology and response to chemotherapy. This guide provides recommendations for diagnosis, staging and treatment of this neoplasm.


Subject(s)
Positron Emission Tomography Computed Tomography/methods , Practice Guidelines as Topic/standards , Rhabdomyosarcoma/therapy , Child , Combined Modality Therapy , Humans , Incidence , Rhabdomyosarcoma/diagnostic imaging , Rhabdomyosarcoma/epidemiology , Rhabdomyosarcoma/pathology , Spain/epidemiology
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