Intramuscular Myxoma – A Rare Tumor

 

What to Learn from this Article?

Presentation and Differential Diagnosis of Intramuscular Myxoma.


Case Report |  Volume 3 | Issue 4 | JOCR Oct-Dec 2013 | Page 38-41 | Yaligod V, Ajoy S M

DOI: 10.13107/jocr.2250-0685.130


Authors: Yaligod V[1], Ajoy S M[1]

[1]Dept of Orthopadics, Sapthagiri Institute of Medical Sciences and Research Centre, Chikkasandra, Bangalore 560090. India.

Address of Correspondence:

Dr Vishwanath Yaligod, MS (Ortho), No 117, 5th Main, 5th Cross, NGEF Layout, Sanjaynagar, Bangalore 560094. India. Email: vvyaligod@gmail.com


Abstract

Introduction: Intramuscular myxoma is a rare benign soft tissue tumor involving the musculoskeletal system. The incidence is reported as varying from 0.1 to 0.13 per 100,000 population. Most patients present between the fifth and sixth decade of life. The swelling commonly occurs in the large muscles of the thigh, shoulder, buttocks and arms. The tumor can be diagnosed with certainty only with histopathological examination. Local recurrence is rare after excision.

Case Report: A 73 year old male patient presented to us with a swelling of the anterior aspect of the middle third of the right thigh measuring about 8 x 4 centimeters. He was thoroughly investigated and the swelling excised in toto. The soft cystic swelling excised was found on histopathology to be an intramuscular myxoma.

Conclusion: This case report is being presented since the tumor is rare and also an important consideration in the differential diagnosis of sarcomas, intramuscular lipoma, hemangioma, hematoma, and desmoid tumor. Another important feature is that it can be diagnosed with certainty only after excision. 

Keywords: Intramuscular myxoma, soft tissue swelling, benign.


 

How to Cite This Article: Yaligod V, Ajoy S M. Intramuscular Myxoma – A Rare Tumor. Journal of Orthopaedic Case Reports 2013 Oct-Dec ;3(4): 38-41. Available from: http://www.jocr.co.in/wp/2013/04/13/2250-0685-098-fulltext/


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