“…RP has been classified clinically into two types: primary RP, which is mostly benign; and secondary RP, which in 10–20% of cases is associated with an underlying systemic disease [such as Sjören’s syndrome, systemic sclerosis, CREST syndrome (calcinosis, RP, esophageal dysmotility, sclerodactyly, and telangiectasia), systemic lupus erythematosus, or dermatomyositis], or with drugs or extrinsic vascular obstruction [7]. Primary RP is characterized by symmetrical attacks on the digits in the absence of peripheral vascular disease, tissues necrosis, ulceration, or gangrene [2, 8]. Meanwhile, the attacks of secondary RP are associated with more severe asymmetric affection with tissue necrosis, ulceration, and gangrene [2, 8].…”