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Case Report

Intramuscular Myxomas: A Potential Diagnostic Dilemma

Amit Parasnis , Aditya Ghatnekar1 , Amit Parasnis2 , Saurabh Thakkar3 , Shweta Achuthan Kutty4

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New Indian Journal of Surgery 10(6):p 623-626, November-December 2019. | DOI: DOI: https://dx.doi.org/10.21088/nijs.0976.4747.10619.12

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Aditya Ghatnekar, Amit Parasnis, Saurabh Thakkar et al. Intramuscular Myxomas: A Potential Diagnostic Dilemma. New Indian J Surg. 2019;10(5):623-626.


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Abstract

Intramuscular myxomas are rare benign soft tissue tumors of mesenchymal origin. They show areas of increased cellularity and vascularity that can lead to a mistaken diagnosis of sarcoma, especially myxofibrosarcoma, low-grade fibromyxoid sarcoma, and myxoid liposarcoma. FNAC of such a tumor is inconclusive as it may show just myxoid stroma or hypercellularity depending on whether the hypercellular portion or myxoid portion is sampled which further impedes diagnosis. Hence, total surgical exision followed by histopathological examination of the tumor is the gold standard. Their recognition is important to avoid an erroneous diagnosis of sarcoma.2 Surgery is always curative and recurrence is rare. This is a case report of 55 years old male presenting with such a tumor.

Keywords: Intramuscular myxoma; Myxomas.


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Cite this article

Aditya Ghatnekar, Amit Parasnis, Saurabh Thakkar et al. Intramuscular Myxomas: A Potential Diagnostic Dilemma. New Indian J Surg. 2019;10(5):623-626.


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DOI: DOI: https://dx.doi.org/10.21088/nijs.0976.4747.10619.12

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