Results 31 to 40 of about 785 (157)

The case of a boy with nevus of Ota, extensive Mongolian spot, nevus flammeus, nevus anemicus and cutis marmorata telangiectatica congenita: a unique instance of phacomatosis pigmentovascularis [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2015
Phacomatosis pigmentovascularis is a rare, congenital condition characterized by a combination of cutaneous melanocytic lesions and vascular malformation.
Han MA   +5 more
doaj   +2 more sources

Efficacy and Safety of Fractional Q‐Switched Ruby Laser for Nevus of Ota in an Infant— Case Report [PDF]

open access: yesJ Cosmet Dermatol
Journal of Cosmetic Dermatology, Volume 24, Issue 8, August 2025.
Ahuja R, Huang P.
europepmc   +2 more sources

Phakomatosis Pigmentovascularis (Type IIb) With Bilateral Glaucoma and Urrets-Zavalia Syndrome Following MicroPulse TSCPC: A Case Report. [PDF]

open access: yesCase Rep Ophthalmol Med
Purpose We are aimed at describing the clinical course and management of a rare case of phakomatosis pigmentovascularis (PPV Type IIb) presenting with bilateral glaucoma, complicated by bilateral Urrets‐Zavalia syndrome (UZS) following MicroPulse transscleral cyclophotocoagulation (MP‐TSCPC).
Alshehri A, Thabet YB, Almutairi MN.
europepmc   +2 more sources

Bloom Syndrome Presenting With Early-Onset Myelodysplastic Syndrome and Triple Overlapping Vascular Neurocutaneous Phenotypes: A Case Report. [PDF]

open access: yesClin Case Rep
ABSTRACT Bloom syndrome is a rare autosomal recessive chromosomal instability disorder characterized by growth deficiency and early‐onset malignancies, and its coexistence with multiple vascular neurocutaneous syndromes is exceptionally uncommon. We report an 8‐year‐old girl who presented with severe growth failure and persistent pancytopenia.
Shahgholi E, Khosroshahi N, Sadeghi S.
europepmc   +2 more sources

Nevus of Ota with Rare Palatal Involvement: A Case Report with Emphasis on Differential Diagnosis

open access: yesCase Reports in Dentistry, 2011
Nevus of Ota, a dermal melanocytic nevus, is rare in the Indian subcontinent. It presents as a brown, blue, or gray patch on the face and is within the distribution of the ophthalmic and maxillary branches of the trigeminal nerve.
Gaurav Sharma, Archna Nagpal
doaj   +1 more source

Bilateral nevus of Ota

open access: yesPigment International, 2018
M. M. Aarif Syed   +2 more
doaj   +2 more sources

Role of Q-switched ND:YAG laser in nevus of Ota: A study of 25 cases

open access: yesIndian Journal of Dermatology, 2011
Background: Nevus of Ota is common condition in Indian patients. The condition is more common in females, with a male-female ratio of 1:4.8. Aim : To evaluate long-term efficacy safety and stability of Q-switched ND:YAG laser in treatment of Nevus of Ota.
Shivangi Sharma   +2 more
doaj   +1 more source

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

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

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