Morpheahttps://en.wikipedia.org/wiki/Morphea
Morphea is a form of scleroderma that hardens skin on the face, hands, and feet, or anywhere else on the body, with no internal organ involvement. Morphea is a thickening and hardening of the skin and subcutaneous tissues from excessive collagen deposition. Morphea discriminates from "systemic sclerosis" by the lack of internal organ involvement.

Morphea is a very rare disease. Due to the composition of the photo, the algorithm may have mistaken it for morphea.

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  • The lesion of Morphea usually appears as an atrophic pigmented patch.
  • Frontal linear scleroderma
  • Frontal linear scleroderma
  • The black and white lesion with thinning (or fading) is suspicious of Morphea.
References Localized scleroderma: clinical spectrum and therapeutic update 25672301 
NIH
Scleroderma is a rare connective tissue disease that is manifested by cutaneous sclerosis and variable systemic involvement. Two categories of scleroderma are known: systemic sclerosis, characterized by cutaneous sclerosis and visceral involvement, and localized scleroderma or morphea which classically presents benign and self-limited evolution and is confined to the skin and/or underlying tissues. Localized scleroderma is a rare disease of unknown etiology. Recent studies show that the localized form may affect internal organs and have variable morbidity. Treatment should be started very early, before complications occur due to the high morbidity of localized scleroderma.
 Upcoming treatments for morphea 34272836 
NIH
Morphea (localized scleroderma) is a rare autoimmune connective tissue disease with variable clinical presentations, with an annual incidence of 0.4-2.7 cases per 100,000. Morphea occurs most frequently in children aged 2-14 years, and the disease exhibits a female predominance.