Ota nevushttps://en.wikipedia.org/wiki/Nevus_of_Ota
Ota nevus is a hyperpigmentation that occurs on the face, most often appearing on the white of the eye. It also occurs on the forehead, nose, cheek, periorbital region, and temple. Women are nearly five times more likely to be affected than men, and it is rare among white population. Ota nevus may not be congenital, and may appear after puberty.
The use of a Q-switched 1064 nm laser has been reported to be successful in treating nevus of Ota.

Treatment
#QS-1064 laser
☆ In the 2022 Stiftung Warentest results from Germany, consumer satisfaction with ModelDerm was only slightly lower than with paid telemedicine consultations.
  • It can can affect the conjunctival area.
  • QS1064 laser treatment can usually yield good results.
References Nevus of Ota and Ito 32809409 
NIH
Nevus of Ota is a benign melanosis that primarily involves the region of the trigeminal nerve distribution. The first and second divisions of the trigeminal nerve, namely the ophthalmic V1 and the maxillary V2 are most commonly involved. There is associated hyperpigmentation of the eye. Nevus of Ota is also known as ocular dermal melanosis. The characteristic gray-blue hyperpigmentation occurs due to entrapped melanocytes. Unilateral presentation is more common. The melanocytes are entrapped leading to gray-blue hyperpigmentation of the conjunctiva and sclera along with ipsilateral facial skin. There is an increased risk of uveal melanoma and glaucoma in these cases. Palatal involvement may also occur. Nevus of Ito is very similar to nevus of Ota except it differs in the territory of distribution. It was described by Minor Ota in 1954. It involves the distribution territory of lateral cutaneous brachial nerves of the shoulder and posterior supraclavicular nerves. Both of these diseases share similar pathophysiology.
 Dermal Melanocytosis 32491340 
NIH
Congenital dermal melanocytosis, also known as Mongolian spot or slate gray nevus, is one of many frequently encountered newborn pigmented lesions. It is a type of dermal melanocytosis, which presents as gray-blue areas of discoloration from birth or shortly thereafter. Congenital dermal melanocytosis is most commonly located in the lumbar and sacral-gluteal region, followed by shoulders in frequency. They most commonly occur in Asian and Black patients, affect both genders equally, and commonly fade by age 1 to 6 years old. Congenital dermal melanocytoses are usually benign and do not require treatment.