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Case report: A challenging case of mixed-variant myofibroblastoma with complex imaging and pathological diagnosis.

Authors :
Kawasaki T
Ichikawa J
Kanno S
Onohara K
Wako M
Tatsuno R
Ochiai S
Watanabe T
Torigoe T
Source :
Frontiers in oncology [Front Oncol] 2024 Oct 18; Vol. 14, pp. 1438162. Date of Electronic Publication: 2024 Oct 18 (Print Publication: 2024).
Publication Year :
2024

Abstract

Myofibroblastomas are benign mesenchymal tumors that frequently occur in the groin. They show variable morphology, and the differential histopathological diagnoses are broad, including lipomatous to myxoid tumors. In addition, both pathological and imaging findings may be complex, which makes diagnosis challenging. We herein present a case of a mixed-variant myofibroblastoma of the wrist in a 73-year-old woman. Considering the long clinical course of more than 20 years and the imaging findings, a benign myxoid tumor including a schwannoma was suspected; however, the histopathological findings from resected specimens suggested a diagnosis of myxofibrosarcoma. Additional histopathological findings led to a diagnosis of mixed-variant myofibroblastoma. The differential diagnosis of myofibroblastoma extends beyond imaging to pathological findings because of the number of possible variants. This case reinforces the notion that the gold standard treatment for soft tissue tumors is to perform surgery only after determining the correct diagnosis by biopsy.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2024 Kawasaki, Ichikawa, Kanno, Onohara, Wako, Tatsuno, Ochiai, Watanabe and Torigoe.)

Details

Language :
English
ISSN :
2234-943X
Volume :
14
Database :
MEDLINE
Journal :
Frontiers in oncology
Publication Type :
Academic Journal
Accession number :
39493459
Full Text :
https://doi.org/10.3389/fonc.2024.1438162