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Background: Malignant subcutaneous soft tissue sarcomas, including myxofibrosarcoma, are often misdiagnosed as benign soft tissue tumors by non-specialists. This study investigated the clinical features of subcutaneous myxofibrosarcoma before referral to our department specializing in bone and soft tissue tumors.
Methods: A retrospective case series analysis was conducted on 26 patients with subcutaneous myxofibrosarcoma who were referred to our department between 2013 and 2024.
Results: Of the 26 cases of subcutaneous myxofibrosarcoma referred to our department, 15 cases (57.7%) had "diagnostic errors before referral," including seven cases of referral delay of ˃6 months, three cases of tumor puncture performed without suspicion of a tumor, four cases of unplanned biopsy, and seven cases of unplanned excision. The average time from the patient's first visit at a medical institution to the referral to our department was 22.7 ± 40.4 months (median 5.0 months, range 1-148 months). We performed initial wide resection in seven patients, additional wide resection in four patients, wide resection for recurrence in two patients, and amputation in two patients.
Conclusions: Subcutaneous myxofibrosarcomas are rare; however, physicians who treat subcutaneous tumors need to be knowledgeable about them. This case series suggest that poorly planned biopsies may miss malignant tumors, and that careless puncturing may lead to deep invasion of the tumor. It also suggests that if you suspect a benign tumor, you should follow up with imaging, otherwise there is a possibility that it will lead to a significant delay in diagnosis.
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http://dx.doi.org/10.1093/jjco/hyaf084 | DOI Listing |
Jpn J Clin Oncol
September 2025
Department of Orthopedic Surgery, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Background: Malignant subcutaneous soft tissue sarcomas, including myxofibrosarcoma, are often misdiagnosed as benign soft tissue tumors by non-specialists. This study investigated the clinical features of subcutaneous myxofibrosarcoma before referral to our department specializing in bone and soft tissue tumors.
Methods: A retrospective case series analysis was conducted on 26 patients with subcutaneous myxofibrosarcoma who were referred to our department between 2013 and 2024.
World J Clin Oncol
November 2023
Department of Orthopaedic Surgery, Graduate School of Medicine, Kyoto University, Kyoto 606-8507, Japan.
Background: Flap reconstruction after resection of a superficial malignant soft tissue tumor extends the surgical field and is an indicator for potential recurrence sites.
Aim: To describe a grading system for surgical field extension of soft tissue sarcomas.
Methods: Grading system: CD-grading is a description system consisting of C and D values in the surgical field extension, which are related to the compartmental position of the flap beyond the nearby large joint and deeper extension for the pedicle, respectively.
Int J Surg Pathol
May 2024
Department of Pathology, Robert J. Tomsich Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH, USA.
Myxofibrosarcomas (MFS) present as slowly enlarging superficial masses in elderly patients. Even though these tumors fail to exhibit a distinct immunophenotype, diagnosis is straightforward when they present in subcutaneous tissue. Intramuscular MFS, however, are more challenging to diagnose as the differential also includes dedifferentiated liposarcoma with myxoid features.
View Article and Find Full Text PDFIndian J Otolaryngol Head Neck Surg
April 2023
Shaheed Bhagat Singh Marg, New Delhi, 110001 India Department of Otorhinolaryngology-Head and Neck Surgery, Lady Hardinge Medical College and Associated Hospitals.
Myxofibrosarcoma (MFS) is a soft tissue sarcoma that commonly occurs in late adult life. It is mainly located in the subcutaneous soft tissues of extremities characterized by a high recurrence rate at the original site. MFS of the head and neck is rare, while it occurrence in the maxilla is extremely rare.
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