A 2-week-old neonate born with generalized dark blue to magenta, nonblanchable, indurated, round to oval, hemispheric purpuric papules and plaques ranging from 1 mm to 1 cm. The lesions favored the face, trunk and limbs. There was no identifiable underlying cause.

         The main etiologic factors include congenital infections (rubella, cytomegalovirus, and parvovirus B19), hemolytic disease of the newborn (Rh incompatibility, blood group incompatibility), hereditary spherocytosis, neuroblastoma, rhabdomyosarcoma, Langerhans cell histiocytosis, and congenital leukemia.

         A warty brown-black linear plaque involved the lower part of left ear was noted since birth. With the passage of time the lesion became darker in color and had acquired more triangular shape. There were no associated cutaneous or systemic abnormalities.

          A 22-year-old male presented with localised depigmentation involved part of the lower lip and surrounding area of three months duration.

A 40-year-old man suffered bilateral facial nevus flammeus involved the entire face and with passage of years many vascular papules and nodules have appeared within the affected area.

          Since birth a flesh-colored to yellowish oval plaque with verrucous papillated surfcae devoid of hair has been noted on the occipital scalp.

         A 6-month-old female infant presented with a dark-red asymptomatic vascular nodule involving the area above the inner canthus of the right eye since birth.

          A middle-aged woman presented with vascular swelling of the lower half of the face with marked involvement of the lower lip since birth. No other cutaneous or systemic findings.

           A 12-year-old boy presented with asymptomatic, thick-roofed blister-like lesions involved one side of the trunk in dermatomal distribution since first year of life. Some of the lesions were bloody and others filled with clear fluid. The scar in the upper portion was due to bad surgical treatment at age of 6 years.