Results 41 to 50 of about 149,105,965 (176)

Phacomatosis pigmentovascularis type IIa - case report [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2013
Phacomatosis Pigmentovascularis is a rare syndrome characterized by capillary malformation and pigmentary nevus. A case of a 2-year-old patient is reported, who presented extensive nevus flammeus and an aberrant Mongolian spot, without systemic disease ...
Majoriê Mergen Segatto   +4 more
doaj   +1 more source

Ipsilateral Nevi of Ota and Ito with multiple blue nevi: A case report

open access: yesPifu-xingbing zhenliaoxue zazhi, 2023
A 36-year-old female presented with brown patches on the left face, shoulder and chest for over 10 years. Dermatological examination showed a bluish-grey patch sized 11×5 cm around the left eye and brown patch on the sclera of the left eye.
Qiufeng HUANG   +3 more
doaj   +1 more source

Blue Nevus Hidden within the Nevus of Ota

open access: yesChinese Medical Sciences Journal, 2023
A 3-year-old boy presented with bluish patch and scattered blue spots on the left side of his face. After several sessions of laser treatment, the azury patch in the periorbital area became even darker. Histopathology showed many bipolar, pigment-laden dendritic cells scattered in the papillary and upper reticular dermis.
Xing, Liu   +7 more
openaire   +2 more sources

Melanoma in the setting of nevus of Ota: a review for dermatologists

open access: yes, 2021
Nevus of Ota, also known as oculodermal melanocytosis or nevus fuscoceruleus ophthalmomaxillaris, is a benign dermal melanocytic nevus that most commonly affects Asian women. While the lesion is largely a cosmetic concern, it has the potential to undergo
Gurnani, Pooja   +9 more
core   +1 more source

Double whammy: Congenital glaucoma in phakomatosis pigmentovascularis with Sturge–Weber syndrome and nevus of Ota

open access: yesTNOA Journal of Ophthalmic Science and Research, 2020
Phakomatosis pigmentovascularis (PPV) is a rare congenital condition characterized by a combination of cutaneous capillary hemangiomas and dermal melanocytosis.
S Podury, Bipasha Mukherjee
doaj   +1 more source

Nevus of ota associated with nevus of Ito [PDF]

open access: yes, 2004
Nevus of Ota is a dermal melanocytic nevus seen predominantly in females. It is uncommon in India. Its association with nevus of Ito, another dermal melanocytic nevus, is extremely rare. We report this rare association in a male patient, which is another
Amiya Kumar Mukhopadhyay
core   +2 more sources

‐mutated CNS melanoma in an adolescent with nevus of Ota

open access: yes, 2021
Nevus of Ota is an uncommon benign mesodermal melanosis that involves the first and second divisions of the trigeminal nerve. Primary non-cutaneous melanoma often involves distinct genetic mutations compared to cutaneous melanoma.
Elena B. Hawryluk   +7 more
core   +1 more source

Bilateral nevus of Ota

open access: yes, 2016
Nevus of Ota is a dermal melanocytosis seen in the distribution of ophthalmic, maxillary and mandibular divisions of the trigeminal nerve. Most of the cases reported are in females with a typical unilateral distribution.
C. Balachandran, Vandana Mehta
core   +1 more source

Bilateral nevus of Ota

open access: yesPigment International, 2021
Nevus of Ota (NOO) is a dermal melanocytoses characterized by bluish-brown macules along the distribution of trigeminal nerve. Ocular involvement is observed in most of the patients in the form of scleral pigmentation. Also reported associations in this condition are iris/ciliary body pigmentation/glaucoma, ocular melanoma ...
Pallavi Hegde, Rashmi Sarkar
openaire   +2 more sources

Bilateral Nevus of Ota with unilateral Nevus of Ito in a child – A case report and review of literature

open access: yesIndian Journal of Ophthalmology. Case Reports
Nevus of Ota, also known as oculodermal melanosis, is a rare dermal melanosis characterized by pigmentation of the sclera and facial skin in the distribution of ophthalmic and maxillary divisions of trigeminal nerve.
Saranya Settu   +3 more
doaj   +1 more source

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