2014, Number 5
<< Back Next >>
Medisur 2014; 12 (5)
Orbital rhabdomyosarcoma. A case report
Ferrer CD, Díaz ALR, Peralta DAS
Language: Spanish
References: 17
Page: 751-756
PDF size: 198.85 Kb.
ABSTRACT
Rhabdomyosarcoma is a malignant tumor arising
from normal skeletal muscle cells. Since these cells
are found in almost every part of the body, this type
of tumor may develop in any site, though it is not
very common. The case of a six-year-old Angolan
patient treated by Cuban collaborators serving in
this country is presented. The patient sought
medical attention due to inflammation and pain in
the right eye. His relative mentioned a history of
ocular trauma, resulting in the patient’s admission to
receive treatment a week before. On eye
examination, a whitish spot through the pupil and
slight proptosis were found. The patient had an
unsatisfactory recovery; consequently an
evisceration of the right eye was performed. Three
months later, he developed an enlarging mass
protruding in the orbital cavity. Several studies were
conducted and an orbital rhabdomyosarcoma was
diagnosed.
REFERENCES
Ferrari A, Dileo P, Casanova M, Bertulli R, Meazza C, Gandola L, et al. Rhabdomyosarcoma in adults: A retrospective analysis of 171 patients treated at a single institution. Cancer. 2003 ; 98 (3): 571-80.
Hawkins WG, Hoos A, Antonescu C, Urist MJ, Leung DH, Golds J, et al. Clinicopathologic analysis of patients with adult rhabdomyosarcoma. Cancer. 2001 ; 91 (4): 794-803.
Little DJ, Ballo MT, Zagars GK, Pisters P, Patel SR, El-Naggar AK, et al. Adult rhabdomyosarcoma: outcome following multimodality treatment. Cancer. 2002 ; 95 (2): 377-88.
Biblioteca Nacional de Medicina de Estados Unidos. Rabdomiosarcoma [Internet]. Bethesda: U.S National Library of Medicine; 2014. [ cited 23 Abr 2014 ] Available from: http://www.nlm.nih.gov/medlineplus/spanish/enc y/article/001429.htm.
Furlong MA, Mentzel T, Fanburg-Smith JC. Pleiomorphic rhabdomyosarcoma in adults: A clinicopathologic study of 38 cases with emphasis on morphologic variants and recent skeletal muscle-specific markers. Mod Pathol. 2001 ; 14 (6): 595-603.
Li FP, Fraumeni JF. Soft-tissue sarcoma, breast cancer, and other neoplasms: A familiar syndrome?. Ann Intern Med. 1969 ; 71 (4): 747-42.
Sung L, Anderson JR, Arndt C, Raney RB, Meyer WH, Pappo AS. Neurofibromatosis in children with rhabdomyosarcoma: a report from the Intergroup Rhabdomyosarcoma Study IV. J Pediatr. 2004 ; 144 (5): 666-8.
Steenman M, Westerveld A, Mannens M. Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways. Genes Chromosomes Cancer. 2000 ; 28 (1): 8-13.
Hartley AL, Birch JM, Blair V, Kelsey AM, Harris M, Jones PH. Patterns of cancer in the families of children with soft tissue sarcoma. Cancer. 1993 ; 72 (3): 923-30.
Demetri GD. Sarcomas de tecidos moles e osso, e outras neoplasias de tecidos. In: Goldman L, Schafer AI, editors. Internal Medicine. Philadelphia, PA: Saunders Elsevier; 2011. p. 231-6.
Trapatsas C, Sabina M. Tumores orbitarios en niños: la presentación inicial de dos casos orientó a un diagnóstico muy diferente al real. Revista Médico Científica. 2002 ; 15 (2): 103-7.
Instituto Nacional de Cáncer de los Institutos Nacionales de la Salud de Estados Unidos. Estadios del rabdiomiosarcoma infantil [Internet]. Bethseda: NCI; 2013. [ cited 23 Abr 2014 ] Available from: http://www.cancer.gov/espanol/pdq/tratamiento/r abdomiosarcomainfantil/Patient/page2.
Instituto Nacional de Cáncer de los Institutos Nacionales de la Salud de Estados Unidos. Información sobre los estadios del rabdomiosarcoma [Internet]. Bethseda: NCI; 2014. Available from: http://www.cancer.gov/espanol/pdq/tratamiento/r abdomiosarcomainfantil/HealthProfessional/page 3.
Abramson DH, Fass D, McCormick B, Servodidio CA, Piro JD, Anderson LL. Implante de braquiterapia: um novo tratamento para rabdomiossarcoma orbital recorrente. J AAPOS. 1997 ; 1: 154-7.
El-Badry OM, Minniti C, Kohn EC, Houghton PJ, Daughaday WH, Helman LJ. Insulin-like growth factor II acts as an autocrine growth and motility factor in human rhabdomyosarcoma tumors. Cell Growth Differ. 1990 ; 1 (7): 325-31.
Leaphart C, Rodeberg D. Pediatric surgical oncology: management of rhabdomyosarcoma. Surg Oncol. 2007 ; 16 (3): 173-85.
Instituto Nacional de Cáncer de los Institutos Nacionales de la Salud de Estados Unidos. Rabdomiosarcoma infantil sin tratamiento previo [Internet]. Bethseda: NCI; 2012. [ cited 23 Abr 2014 ] Available from: http://www.cancer.gov/espanol/pdq/tratamiento/r abdomiosarcomainfantil/HealthProfessional/page 5