نتایج جستجو برای: epidermal nevus syndrome

تعداد نتایج: 679851  

Journal: :Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.] 2003
Akira Momosawa Kotaro Yoshimura Gentaro Uchida Katsujiro Sato Emiko Aiba Daisuke Matsumoto Hisayo Yamaoka Saori Mihara Katsuhiko Tsukamoto Kiyonori Harii Takao Aoyama Tatsuji Iga

BACKGROUND AND OBJECTIVE Acquired dermal melanocytosis (ADM; acquired bilateral nevus of Ota-like macules) is known for its recalcitrance compared with Nevus of Ota, and we assume that one of the reasons is a higher rate and degree of postinflammatory hyperpigmentation (PIH) seen after laser treatments. METHODS Topical bleaching treatment with 0.1% tretinoin aqueous gel and 5% hydroquinone oi...

Journal: :Indian Journal of Dermatopathology and Diagnostic Dermatology 2015

Journal: :Indian Journal of Paediatric Dermatology 2015

2015
Pravesh Yadav Vibhu Mendiratta Shiwangi Rana Ram Chander

A case of nevus comedonicus syndrome with atypical cutaneous presentation (widespread involvement without any particular pattern, midline lesions involving lower abdomen and involvement of bilateral pinna), and some unusual skeletal (adduction deformity involving bilateral metatarsal along with medial deviation at the level of tarsometatarsal joint), central nervous system (agenesis of corpus c...

Journal: :Journal of Investigative Dermatology 2022

Introduction: Nevus sebaceous (NS) is a hamartoma composed of epidermal, dermal, follicular, and apocrine appendages found in the pediatric population. The current standard treatment full-thickness excision, but this controversial as much still unknown about malignant potential benign neoplasm. Secondary lesions associated with nevus include poromas, trichoblastomas, syringocystadenomas. purpos...

2014
André Laureano Rodrigo Carvalho Cristina Amaro Isabel Freitas Jorge Cardoso

Phacomatosis pigmentovascularis is a rare syndrome characterized by the coexistence of a pigmented nevus and a cutaneous vascular malformation. We report a 5-year-old boy with all the typical findings of phacomatosis pigmentovascularis type Ia. Although its existence according to the traditional classification has been questioned, this case represents a very rare association of a capillary vasc...

Journal: :gastroenterology and hepatology from bed to bench 0
mohammad taghi safari gastroenterology and liver disease research center, shahid beheshti university of medical sciences, tehran, iran shabnam shahrokh gastroenterology and liver disease research center, shahid beheshti university of medical sciences, tehran, iran shahram ebadi gastroenterology and liver disease research center, shahid beheshti university of medical sciences, tehran, iran amir sadeghi gastroenterology and liver disease research center, shahid beheshti university of medical sciences, tehran, iran

cronkhite- canada syndrome (ccs) considered as a rare and non-hereditary disorder. gastrointestinal polyposis and diarrhea along with some extra signs and symptoms such as hypoproteinemia, and epidermal manifestations are recognized in this syndrome. the pathophysiology of this syndrome is not completely understood and it seems that inflammatory processes may be involved. we present a 50 year-o...

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