“…These cells are considered uncommitted stromal cells and, as such, are endowed with plasticity [42,48,60,67] to undergo multilineage proliferation along different pathways leading to heterogeneous pathological conditions such as SFT and SCL of soft tissues [60], and fibroadenomas, phylloides tumors and pseudoangiomatous hyperplasia in the breast [48]. Another speculative observation suggesting the role of the mammary stroma in tumorigenesis of BSST as a whole is given by the evidence that both fibroblastic and myofibroblastic tumors may contain a variable admixture of two or three lines of differentiation within the same neoplasm such as fibroblastic plus adipocytic in SCL/SCL-like tumor [39,42,65], and SFT [24,44,50,61] or fibroblastic plus myofibroblastic (in most cases of MFBs), myofibroblastic plus adipocytic [43] and, as reported elsewhere, myofibroblastic plus smooth muscle [20,64] or cartilaginous [20,33,34,68] or osseous [33] in rare cases of MFB. This is in accordance with the well-known multidirectional differentiation ability of the mammary stromal cells that may undergo changes in their phenotype in several other breast benign pathological conditions, typical examples of which include fibroadenoma with leiomyomatous component [23,64], phylloides tumors with fat, bone, cartilage or even skeletal muscle metaplasia [54,63], hamartomas with adipocytic, smooth muscle, and chondroid stromal components [15,38,54], and some breast lesions labeled as "mesenchymoma" in which even three lines of differentiation (e.g., myo-chondro-lipoma) can be documented [4,32].…”