Helmi, Masdar and Rani Himayani, Rani and Diki, Prawira Adifa (2021) Gambaran Klinis dan Prognosis Rabdomiosarkoma pada Anak. Medula, 10 (4). ISSN 2615-479X

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Rhabdomyosarcoma is a soft tissue malignancy with prevalences about 5% of all malignancies in children and 20% of soft tissue malignancies that occur in children. The most common primary tumor sites include the head and neck area followed by the genitourinary and extremities. Meanwhile, the most common subtypes are embryonic in children and alveolar in adolescents. Although the specific etiology for RMS is largely unknown, there are increased risk factors for environmental factors such as radiation and drugs, syndromes, and chromosomal abnormalities. The clinical symptoms vary and are related to the location of the mass and the blockage it caused. Histopathological and immunohistochemical examinations are gold standard tests for diagnosing RMS and determining subtypes that serve as prognosis and therapy. Various therapeutic approaches can be surgery, chemotherapy, radiotherapy, or in a combination.

Item Type: Article
Subjects: R Medicine > R Medicine (General)
Divisions: Fakultas Kedokteran (FK) > Prodi Pendidikan Dokter
Date Deposited: 21 May 2021 09:31
Last Modified: 21 May 2021 09:31
URI: http://repository.lppm.unila.ac.id/id/eprint/30413

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