Results 81 to 90 of about 311,180 (268)
Phacomatosis pigmentovascularis type IIa - case report [PDF]
Anais 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
Nevus of Ota with palatal involvement: a case report
Journal of Oral Medicine and Oral Surgery, 2023 Nevus of Ota is a macular discoloration of the face which is most commonly found in the Japanese and females are more commonly affected than males. It is first described by Ota and Tanino in 1939, involves the skin along the distribution of first and ...
Derache Anaïs +2 more
doaj +1 more source
Plaque‐Like Dermatofibroma: A Case Report and a Review of the Literature With a Focus on Dermoscopy
JEADV Clinical Practice, EarlyView.ABSTRACT Plaque‐like dermatofibroma (PLDF) is a rare clinical variant of dermatofibroma (DF), characterised by flat, infiltrative lesions, often larger than 50 mm in diameter and located on the trunk or lower extremities. A 44‐year‐old male presented to our clinic with a 20 cm brownish plaque with peripheral satellite lesions on the right antecubital ...
Francesco Cavallo +7 more
wiley +1 more source
Phakomatosis Pigmentovascularis [PDF]
, 1996 We report a patient with phakomatosis pigmentovascularis IIb and numerous iris hamartomas. Phakomatosis pigmentovascularis IIb is characterized by the simultaneous occurrence of a nevus flammeus, a mongolian spot, and sometimes a nevus anemicus in the ...
Gysel, D. (Dirk) van +3 more
core +2 more sources
Atypical Presentation of a Pigmented Oncocytoma of the Caruncle: A Case Report
Case Reports in Ophthalmology, 2013 We report an unusual case of a pigmented oncocytoma of the caruncle. The lesion presented the following atypical features: a well-circumscribed, partially pigmented, and lobulated mass that macroscopically resembled a caruncular nevus.
Maura Di Nicola +5 more
doaj +1 more source
Pigmented epithelioid melanocytoma: A clinico-histopathological enigma
Indian Journal of Dermatopathology and Diagnostic Dermatology, 2022 Blue nevi are a group of congenital or acquired benign dermal melanocytic tumors. Various clinical and histological variants have been described.Epithelioid blue nevus (EBN), an uncommon variant may present as blue gray nodule over trunk, extremities ...
Pooja Dilip Shah +3 more
doaj +1 more source
Acral pigmented spitz nevus that clinically mimicked acral lentiginous malignant melanoma.
Annals of Dermatology, 2011 Pigmented Spitz nevus is a benign melanocytic skin lesion with distinct clinical features and it is frequently found on the extremities. However, it rarely occurs on acral area of the body, and such a case has not yet been fully documented.
Y. Jang +4 more
semanticscholar +1 more source
CPT: Pharmacometrics &Systems Pharmacology, EarlyView.ABSTRACT Hemoporfin, a porphyrin derivative photosensitizer, has been approved for the treatment of port‐wine stain (PWS) in adults. However, its optimal dose for the pediatric population remains unclear. This study aimed to explore appropriate dosing for pediatric patients with PWS through population pharmacokinetics (PopPK) and exposure‐response (ER)
Rong Chen +6 more
wiley +1 more source
Gorlin syndrome in a patient with skin type VI [PDF]
, 2019 Gorlin syndrome, also known as nevoid basal cell carcinoma syndrome, is a rare autosomal dominant disorder that is characterized by multiple basal cell carcinomas developing at a young age, keratocystic odontogenic tumors of the jaw, palmar or plantar ...
Anderson, Kathryn L +3 more
core
Indian Journal of Ophthalmology, 2017 A 20-year-old girl presented with a large pigmented lesion over the temporal aspect of left lateral canthus involving the lateral one-third of both eyelids, since birth. A slow increase in its size had been noticed for the past 2 years. On examination, a
Manpreet Singh +3 more
doaj +1 more source