A Rare Intraoral Manifestation of Nevus Ota - A Case Report

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Rare Case Report on Nevus of Ota

Nevus of Ota is a hamartoma of dermal melanocytes. Clinically, Nevus of Ota is manifested as blue or gray patch on the face; such condition is congenital or acquired and is within the distribution of branches of the trigeminal nerve. The nevus can be unilateral or bilateral. In addition to skin, it may involve ocular and oral mucosal surfaces. The case of an 18-year old female with unilateral b...

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Congenital Becker’s nevus: report of a rare case

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Report of a case of Klippel-Trenaunay syndrome associated with bilateral nevus of Ota

Port-wine stain is a vascular malformation characterized pathologically by ectasia of superficial dermal capillaris and clinically by persistent macular erythema. The association of a port-wine stain on a limb with soft tissue swelling, with or without bony overgrowth, is termed klippel-Trenaunay syndrome. Phakomatosis pigmento-vascularis is a combination of port-wine stain and cutaneous ...

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nevus of ota with buccal mucosal pigmentation: a rare case

nevus of ota is a condition wherein the typical pattern of the bluish black pigmentation is noticed along with the cutaneous distribution of the trigeminal nerve. this condition is most prevalent in japanese population but comparatively rare among indians. we report a case of 23-year-old female presented with unilateral pigmented areas over the skin of forehead, malar area, ear and periorbital ...

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Nevus of Ota with Buccal Mucosal Pigmentation: A Rare Case

Nevus of Ota is a condition wherein the typical pattern of the bluish black pigmentation is noticed along with the cutaneous distribution of the trigeminal nerve. This condition is most prevalent in Japanese population but comparatively rare among Indians. We report a case of 23-year-old female presented with unilateral pigmented areas over the skin of forehead, malar area, ear and periorbital ...

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ژورنال

عنوان ژورنال: Journal of Dentistry Indonesia

سال: 2016

ISSN: 2355-4800,1693-9697

DOI: 10.14693/jdi.v23i3.998