Article Data

  • Views 1224
  • Dowloads 141

Original Research

Open Access

Alveolar rhabdomyosarcoma originating from the uterine cervix

  • B. Cakar1,*,
  • U. Muslu1
  • B. Karaca1
  • B. Junushova2
  • R. Uslu1
  • E. Goker1

1Division of Medical Oncology, Tulay Aktas Oncology Hospital, School of Medicine, Ege University, Bornova, Izmir, Turkey

2Division of Internal Medicine, School of Medicine, Ege University, Bornova, Izmir, Turkey

DOI: 10.12892/ejgo201102196 Vol.32,Issue 2,March 2011 pp.196-198

Published: 10 March 2011

*Corresponding Author(s): B. Cakar E-mail: burcu.cakar@gmail.com

Abstract

Cervical alveolar rhabdomyosarcoma is a rare condition associated with poor prognosis. An 18-year-old patient presented with vaginal bleeding and a protruding mass from the vagina. Biopsy of the mass revealed alveoler rhabdomyosarcoma (ARMS), and radiological evaluation demonstrated that it originated from the uterine cervix. First, Wertheim's operation was carried out followed by four cycles of vincristine, actinomycine-D, ifosfamide (VAI) chemotherapy. However, the disease relapsed within three months, and the patient died of disease progression. Despite combination treatment, we could not achieve a desirable survival advantage in ARMS. Future studies may unveil the genomic profile of this rare condition, leading to invention of targeted therapies, which is the emerging trend in the treatment of sarcomas.

Keywords

Alveolar rhabdomyosarcoma; Cervix; Treatment

Cite and Share

B. Cakar,U. Muslu,B. Karaca,B. Junushova,R. Uslu,E. Goker. Alveolar rhabdomyosarcoma originating from the uterine cervix. European Journal of Gynaecological Oncology. 2011. 32(2);196-198.

References

[1] Emerich J.,Senkus E., Konefka T.: “Alveolar rhabdomyosarcoma of the uterine cervix”. Gynecol. Oncol., 1996, 3, 398.

[2] Ng T.Y., Loo K.T., Leung T.W., Lo S.H., Yuen K.K.: “Alveolar rhab-domyosarcoma of the cervix”. Gynecol. Oncol., 2003, 91, 623.

[3] Case A.S., Kirby T.O., Conner M.G., Huh W.K.: “A case report of rhabdomyosarcoma of the uterus with uterin inversion”. Gynecol. Oncol., 2005, 96, 850.

[4] Pappo A.S., Lyden E., Breneman J., Wiener E., Teot E., Meza J. et al.: “Up front window trial of Topotecan in previously untreated chidren and adolescents with metastatic rhabdomyosarcoma: An Intergroup Rhabdomyosarcoma Study”. J. Clin. Oncol., 2001, 19, 213.

[5] Baker K.S., Anderson J.R., Link M.P., Grier H.E., Qualman S.J., Maurer H.M. et al.: “Benefit of intensified therapy for patients with local or regional embryonal rhabdomyosarcoma: Results from the Intergroup Rhabdomyosarcoma Study IV”. J. Clin. Oncol., 2000, 18, 2427.

[6] Parham D., Ellison D.: “Rhabdomyosarcomas in adults and children: an update”. Arch. Pathol. Lab. Med., 2006, 130, 1454.

[7] Crist W.M., Anderson J.R., Meza J.L., Fryer C., Raney R.B., Ruymann F.B. et al.: “Intergroup rhabdomyosarcoma study IV: results for patients with nonmetastatic disease”. J. Clin. Oncol., 2001, 19, 3091.

[8] Raney R.B., Maurer H.M., Anderson J.R., Andrassy J.R., Donaldson S.S., Qualman S.J. et al.: “The Intergroup Rhabdomyosarcoma Study Group (IRSG): major lessons from the IRS-I through IRS-IV studies as background for the current IRS-V treatment protocol”. Sarcoma, 2001, 5, 9.

Submission Turnaround Time

Top