“…Clinically, and similarly to connective tissue naevi, FCTN present as solitary, slow growing, painless, plaque-like or nodular lesions. 1,2 However, agminated variants 3,4 suggestive of sarcoma, lipoma and vascular malformation have also been reported. 5 Histologically, FCTN is characterized by a poorly defined proliferation of bland spindle cells with pale eosinophilic cytoplasm and tapering nuclei, arranged in randomly orientated short intersecting fascicles infiltrating the reticular dermis and the upper subcutis.…”