ALVEOLAR RHABDOMYOSARCOMA: PRESENTATION OF A CASE AND REVIEW OF THE LITERATURE

Author:

Muñoz Murillo Jessica Alejandra1,Jaime Aguirre Andrea Carolina2,González Pinilla Andres Mauricio3,Ramirez Munõz Daniel Santiago4,Cardenas Casallas Jonathan Gerardo1,Martos Narváe Marly Yonency5,Chamorro Garcia Yesid6

Affiliation:

1. MD. Universidad Pedagógica y Tecnológica de Colombia.

2. MD. Universidad Pedagógica y Tecnológica de Colombia

3. MD. Fundación Juan N. Corpas.

4. MD Universidad Pedagógica y Tecnológica de Colombia.

5. MD. Universidad Surcolombiana.

6. MD. Fundacioń Universitaria San Martiń .

Abstract

Rhabdomyosarcoma (RMS) is a rare type of soft tissue malignant neoplasm that currently represents about 7% of cancers in children, it is found in a much smaller proportion in adults, which represents about 1% of cancers, the global incidence of RMS is 4.5/million people under 20 years of age. Alveolar rhabdomyosarcoma (ARMS) is a widely studied subtype in minors and very rarely in adults. The most common presentation in extremities is of the alveolar subtype, most frequently affecting the lower extremities. We present a narrative review based on a case report of a patient with alveolar rhabdomyosarcoma in a lower extremity

Publisher

World Wide Journals

Reference14 articles.

1. Skapek Stephen FA,AG,JLP,EB,SJ,BFG,SH. Rhabdomyosarcoma. NATURE REVIEWS. 2019;: p. 1-3.

2. SEER. J Surg Res PE. Rabdomiosarcoma en niños: un estudio basado en la población. (2011);: p. e243–251.

3. Arnold C PMMFM. Rhabdomyosarcoma. Curr Probl Cancer. 2008.

4. Ferrari A DPCMBRMCGLNPCPGAOPFBFCP. Rhabdomyosarcoma in adults. A retrospective analysis of 171 patients treated at a single institution. 2003;: p. 2-4.

5. Laquaglia MP. Extremity Rhabdomyosarcoma Biological Principles, Staging, and Treatment. Seminars in Surgical Oncology. 1993.

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