Abstract:【Abstract】 Objective To investigate the pathologic feathers, diagnosis, differential diagnosis and prognosis of dendritic fibromyxolipoma ( DFML). Methods We collected three cases of dendritic fibromyxolipoma diagnosed from 2013 to 2015 at the Xin Qiao Hospital of Third Military Medical University. The three cases of dendritic fibromyxolipoma were studied by hematoxylineosin and EliVision immunohistochemical staining. The clinicaland pathological feathers were analyzed with review of the literatures. Results Two of three cases were male, one case was female, with mean age 50 years. The shape of tumor was round or ovoid, and the size of these tumors ranged from 40 cm to 55cm in diameter. They were well circumscribed and encapsulated,with a grayyellow in color and solidgelatinous, soft, myxoid appearance on cut surface. Microscopically, the tumor is mainly consisted of a proliferation of stellate to spindle fibroblasts ,ropelike collagen fibers and varying amount of uneven density mature lipocytes embedded in myxoid stroma. There was a transitional between stellate cells and spindle cells, and with a longthin cytoplasmic dendritic processes. These nucleus chromatin evenly, no obviously cytological atypia or mitotic activity can be identified. Immunohistochemical stain showed that spindle cells and stellate cells were positive for vimentin, CD34 and BCL2 and less than 1% positive rate for Ki67. Conclusion DFML is a rare special variant of lipoma. Its biological behavior is benign, and seems to be misdiagnosed for sarcoma. The pathological histomorphology and immunohistochemistry phenotype are helpful to the diagnosis and differential diagnosis.