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Minimally Invasive Isolated Limb Perfusion (MI-ILP) for Locally Advanced Melanomas and Sarcomas of the Extremity
Published on: January 31, 2025
Unveiling the enigma of myxoid liposarcoma: Diagnostic challenges and multidisciplinary triumphs in limb-salvage
Ikhwan Nasir1, Boon Tat Yeap1,2, Thai Hau Koo3
1Department of Anaesthesiology and Intensive Care, Hospital Universiti Malaysia Sabah, Kota Kinabalu, Sabah, Malaysia.
Abstract:
Liposarcoma is a rare soft-tissue sarcoma accounting for about 5% of adult cases; myxoid liposarcoma is the second most common subtype and typically arises in the lower extremities (especially the thigh). We report the case of a 48-year-old woman who presented with a rapidly enlarging, painful mass in the left thigh over 1 year, which was confirmed to be a myxoid liposarcoma on histopathological examination. The patient underwent wide local excision of the tumor with clear margins; she had an uncomplicated postoperative course and remained disease-free at 6 months of follow-up. This case highlights the importance of thorough imaging evaluation and biopsy for accurate diagnosis of soft-tissue masses, as well as the need for complete surgical resection and diligent long-term surveillance in myxoid liposarcoma.

