Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy (SHML), is a rare and nonneoplastic histiocytic proliferative disorder. Found worldwide and affecting individuals predominantly with mean onset age of 20.6 years, RDD is slightly more common in men (1.4:1) and is significantly more common among whites and blacks than Asians. Clinically, it is characterised by massive bilateral painless lymphadenopathy of the head and neck region, with affected patients often presenting with fever, leukocytosis, an elevated erythrocyte sedimentation rate and polyclonal hypergammaglobulinaemia. Lymphatic involvement is the most characteristic finding, but 43% of cases show extranodal involvement such as skin and soft tissue, eyelids, orbits, upper respiratory tract, salivary glands, bone, testes, lungs, kidneys, thyroid, and gastrointestinal tract. However, simple soft tissue manifestation of RDD (without lymphadenopathy or other systemic symptoms) is rarely seen, which occurs in <3% of patients. Nodal based RDD usually regresses spontaneously, whereas isolated soft tissue RDD is indolent in nature and may recur years or even decades later. We here in, describe two case of isolated soft tissue RDD which presented initially as a painless nodular nose mass.