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Boletín médico del Hospital Infantil de México
versión impresa ISSN 1665-1146
Resumen
EGUIA-AGUILAR, Pilar; LOPEZ-MARTINEZ, Briceida; RETANA-CONTRERAS, Carmen y PEREZPENA-DIAZCONTI, Mario. Alveolar rhabdomyosarcoma: origin and prognostic implications of molecular findings. Bol. Med. Hosp. Infant. Mex. [online]. 2016, vol.73, n.6, pp.405-410. ISSN 1665-1146. https://doi.org/10.1016/j.bmhimx.2016.09.001.
We present the case of a 2-year-old male patient with a facial tumor partially treated with chemotherapy before his admission to our institution. The tumor involved from the frontal region to the maxillary floor, the orbit, and the maxillary and sphenoid sinuses. The histopathological diagnosis revealed a stage IV alveolar rhabdomyosarcoma with infiltration to bone marrow and cerebrospinal fluid. He was managed with four cycles of adriamycin, actinomycin, cyclophosphamide and vincristine; cisplatin and irinotecan were added to the last cycle. The tumor had a 50% size reduction, but the patient died after a neutropenia and fever episode.
The aggressive behavior of alveolar rhabdomyosarcoma has been associated with the expression of oncogenic fusion proteins resulting from chromosomal translocations, particularly t(2;13) (q35;q14) PAX3/FOXO1, and t(1;13) (p36;q14) PAX7/FOXO1 which were present in this patient.
Palabras llave : Rhabdomyosarcoma; Alveolar rhabdomyosarcoma; Childhood; Translocation; Prognostic significance.