Dermoscopic Findings of Nevus of Ota [PDF]
Balkan Medical Journal, 2020 To the Editor, Nevus of Ota, also known as oculodermal melanocytosis, is characterized by a macular pigmentation usually localized on the forehead and periocular region.
Ömer Faruk Elmas, Asuman Kilitçi
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Indian Journal of Ophthalmology, 2015 Nevus of Ota is a hamartoma of dermal melanocytes presenting as blue hyperpigmented patches on the face usually within the distribution of ophthalmic and maxillary branches of the trigeminal nerve.[1] A case of giant nevus of Ota involving all three branches of the trigeminal nerve is presented.
Pukhraj Rishi +2 more
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Nevus of Ota with excellent response to Q-switched Nd:YAG (1064 nm) pigmented laser: a case report [PDF]
Dermatology ReportsNevus of Ota is a benign pigmentation disorder that commonly affects areas of the skin and eye supplied by the ophthalmic and maxillary branches of the trigeminal nerve.
Lulwa Alogayell +3 more
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Utility of anterior segment optical coherence tomography in the surgical planning of superficial sclerectomy in oculodermal melanocytosis (nevus of Ota): A case report and review of literature [PDF]
American Journal of Ophthalmology Case Reports, 2021 Purpose: to report the utility of Anterior Segment Optical Coherence Tomography (AS OCT) for planning superficial sclerectomy in a patient with nevus of Ota.
Alessandro Mularoni +4 more
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Nevus of Ota – an intraoral presentation: a case report [PDF]
Journal of Medical Case Reports, 2019 Background Nevus of Ota or “oculodermal melanocytosis” is a rare congenital hamartoma of dermal melanocytes causing a blue-gray hyperpigmentation of the eye and surrounding structures. The condition, originally described by Ota and Tanino in 1939, mainly
Jennifer Maguire, Deborah Holt
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Bilateral nevus of Ota in association with nevus flammeus: a case report [PDF]
Dermatology ReportsNevus of Ota and nevus flammeus are distinct congenital pigmentary and vascular anomalies, respectively, with different etiologies and clinical implications. While both conditions can present unilaterally, their bilateral coexistence is rare.
Lulwa Alogayel +4 more
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Wilson’s Disease and Nevus of Ota in a Child: A Case Report [PDF]
Case Reports in OphthalmologyIntroduction: Wilson’s disease is a rare autosomal recessive disorder that disrupts copper metabolism. It presents with distinctive ocular manifestations.
Achia Nemet +5 more
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Bilateral Nevus of Ota Treated with Combination of CO2 Fractional Laser and 1064 nm Nd:YAG Laser [PDF]
Berkala Ilmu Kesehatan Kulit dan Kelamin (Periodical of Dermatology and Venerology), 2017 Background: Ota’s nevus (nevus fuscocaeruleus ophthalmomaxillaris) was first described by Ota in 1939. It is characterized by blue–black or gray–brown dermal melanocytic pigmentation and typically occurs in areas innervated by the first and second ...
Dewi Nurasrifah, Iskandar Zulkarnain
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Nevus of Ota”- A Rare Pigmentation Disorder with Intraoral Findings [PDF]
Journal of Clinical and Diagnostic Research, 2014 Nevus of Ota is a dermal melanocytosis seen along the distribution of ophthalmic and maxillary divisions of the trigeminal nerve. Only 12 cases so far have been reported in English literature & it is rare in Indian subcontinent.
Jitender Solanki +4 more
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Neurofibromatosis type 1 with Becker's nevus and nevus of ota
Indian Journal of Dermatology, 2020 Hai-En Wu +3 more
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