Low-grade fibromyxoid sarcoma (LGFMS) is a rare type of low-grade sarcoma first described by H. L. Evans in 1987.[1] LGFMS are soft tissue tumors of the mesenchyme-derived connective tissues; on microscopic examination, they are found to be composed of spindle-shaped cells that resemble fibroblasts.[2] These fibroblastic, spindle-shaped cells are neoplastic cells that in most cases of LGFMS express fusion genes, i.e. genes composed of parts of two different genes that form as a result of mutations.[2] The World Health Organization (2020) classified LGFMS as a specific type of tumor in the category of malignant fibroblastic and myofibroblastic tumors.[3]
LGFMS tumors occur in individuals of almost any age but up to 20% are less than 18 years/old. The tumors typically involve the proximal extremities but can occur virtually anywhere in the body.[4] The progression of these tumors commonly takes an indolent, prolonged course involving many years or decades. Over this time, however, the tumors often recur at the site of their surgical removal and/or metastasize usually to the lung or pleural tissues surrounding the lungs.[5] These metastasis can develop decades after the tumor's initial presentation and diagnosis.[6]
LGFMS can be difficult to distinguish from other mesenchymal tumors,[7] particularly from sclerosing epithelioid fibrosarcoma (SEF).[8] LGFMS tumors present with many clinical and pathological features that are similar to those in SEF. Indeed, current studies suggest that LGFMS may be an early form of SEF. For example, a tumor may present with features typical of LGFMS but over time progress to features typical of sclerosing epithelioid fibrosarcomas. This progression may be particularly evident in recurrent or metastatic "LGFMS" tumors.[8][9] Since the World Health Organization has classified LGFMS as one of the malignant fibroblastic and myofibroblastic tumors that is distinctly different than SEF,[3] SEF and LGFMS are here regarded as separate tumor forms.
^Evans HL (November 1987). "Low-grade fibromyxoid sarcoma. A report of two metastasizing neoplasms having a deceptively benign appearance". American Journal of Clinical Pathology. 88 (5): 615–9. doi:10.1093/ajcp/88.5.615. PMID3673943.
^Porrino J, Al-Dasuqi K, Irshaid L, Wang A, Kani K, Haims A, Maloney E (June 2021). "Update of pediatric soft tissue tumors with review of conventional MRI appearance-part 1: tumor-like lesions, adipocytic tumors, fibroblastic and myofibroblastic tumors, and perivascular tumors". Skeletal Radiology. 51 (3): 477–504. doi:10.1007/s00256-021-03836-2. PMID34191084. S2CID235678096.
^Martínez-Trufero J, Cruz Jurado J, Gómez-Mateo MC, Bernabeu D, Floría LJ, Lavernia J, Sebio A, García Del Muro X, Álvarez R, Correa R, Hernández-León CN, Marquina G, Hindi N, Redondo A, Martínez V, Asencio JM, Mata C, Valverde Morales CM, Martin-Broto J (September 2021). "Uncommon and peculiar soft tissue sarcomas: Multidisciplinary review and practical recommendations for diagnosis and treatment. Spanish group for Sarcoma research (GEIS - GROUP). Part I". Cancer Treatment Reviews. 99: 102259. doi:10.1016/j.ctrv.2021.102259. PMID34311246.
^Evans, Harry L (2011). "Low-Grade Fibromyxoid Sarcoma: A Clinicopathologic Study of 33 Cases With Long-Term Follow-Up". The American Journal of Surgical Pathology. 35 (10): 1450–1462. doi:10.1097/PAS.0b013e31822b3687. PMID21921785. S2CID21592343.
^ abMustafa S, VandenBussche CJ, Ali SZ, Siddiqui MT, Wakely PE (2020). "Cytomorphologic findings of low-grade fibromyxoid sarcoma". Journal of the American Society of Cytopathology. 9 (3): 191–201. doi:10.1016/j.jasc.2020.01.006. PMID32197967. S2CID212810533.