Nevus is a group of melanocytes that grow together to form benign growth on the skin. It often black lesion may protrude from Becker's nevus hyperpigmented presents congenitally or acquired. The pigmentation and unusually high hair might darker with time. nevus, which can interchangeably be called melanosis, rare disease usually presented by men. following case 21-year-old male who his right ar...

We report a case of basal cell carcinoma that appeared from an epidermal verrucous nevus in a 61-year-old patient. The onset of basal cell carcinoma in sebaceous nevi, basal cell nevi and dysplastic nevi is relatively common, but it is rarely associated with epidermal verrucous nevi. There is no consensus on whether the two lesions have a common cellular origin or whether they merely represent ...

1 of 2 DESCRIPTION Gorlin syndrome (basal cell nevus syndrome or nevoid basal cell carcinoma syndrome) is an uncommon but, well known, autosomal dominant cancer syndrome. 1 This condition affects the hands commonly. 2 However the hand is not the common presenting clinical feature. 2 We wish to present an unusual presentation of Gorlin’s syndrome which has not been noted in the literature previo...

BACKGROUND Gorlin syndrome, also known as the basal cell nevus syndrome (OMIM #109400), is a rare autosomal-dominant genetic disease. The disease, which shows mutation of the patched receptor gene (PTCH1) of the sonic hedgehog pathway, is characterized by developing multiple basal cell carcinomas (BCCs) in adolescent patients. Other clinical features include mandibular keratocysts, palmar and p...

A 19-year old female with blue rubber bleb nevus syndrome. Endoscopic laser photocoagulation and surgical resection of gastrointestinal angiomata. cerebellum: a case report and review of the literature. 39. Hofhuis WJD, Orange AP, Bouquet J, et al. Blue rubber blue nevus syndrome: report of a case with consumption coagulopathy complicated by manifest thromboses. A case report: pregnancy complic...

beckwith and wiedemann for the first time described a syndrome characterised by macroglossia,macrosomia and omphalocele.nowadays inaddition to the above symptoms,visceromegaly,mild microcephaly,facial nevus flammeus,earlobe cerase,persistent neonatal hypoglycemia,and polycythemia are also considered various manifestations of Beckwith-Wiedemann syndrome. This study report a female neonate with ...