Trismus Masquerading Embryonal Rhabdomyosarcoma- an extremely rare case report and literature review

Authors

  • Dr. Antony George Peediackel Associate Professor, Dept. of Oral and Maxillofacial Surgery, Government Dental College, Kottayam, Kerala University of Health Science, India.

Abstract

Rhabdomyosarcoma was first described by Weber1 in 1854. It is the most common soft tissue sarcoma and malignant orbital neoplasm in infants and children1, 2. It is a rare malignant tumour with extremely aggressive and infiltrative nature3, histologically; embryonal or botryoid type is the most common variant occurring in the head and neck region4. The alveolar type of rhabdomyosarcoma is mostly seen in extremities and trunk in children and young adults2. Here we present an extremely rare case of an embryonal rhabdomyosarcoma located in the maxillary sinus which extends into the orbital cavity with absolutely no ocular symptoms.

Key words: Rhabdomyosarcoma; embryonal rhabdomyosarcoma; orbital, rhabdomyosarcoma.

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Published

2018-10-28

How to Cite

Dr. Antony George Peediackel. (2018). Trismus Masquerading Embryonal Rhabdomyosarcoma- an extremely rare case report and literature review. International Journal of Medical Science And Diagnosis Research, 2(5). Retrieved from https://ijmsdr.com/index.php/ijmsdr/article/view/91

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Articles