نتایج جستجو برای: naevus

تعداد نتایج: 557  

Journal: :Acta dermato-venereologica 2011
Akiko Tara Asuka Sada Takuya Inoue Noriyuki Misago Yutaka Narisawa

© 2011 The Authors. doi: 10.2340/00015555-1133 Journal Compilation © 2011 Acta Dermato-Venereologica. ISSN 0001-5555 Epidermal naevus syndromes include different diseases that share a common feature of mosaicism (1, 2). The association of a speckled lentiginous naevus, an organoid naevus with sebaceous differentiation, with skeletal and neurological anomalies, constitutes a specific syndrome ca...

Journal: :مجله دانشگاه علوم پزشکی شهید صدوقی یزد 0
علی اکبر اکابری aa akaberi پریچهر کفائی p kafaie . [email protected] حسین حاج حسینی h hadji hosseini

becker's naevus shows itself as a pigmented area of skin which is aquired , persistant and asymmetrical and sometimes shows evidence of increased androgen sensitivity. colocalization with other developmental anomalies is reported rarely. we report a 20 year old woman who developed an extensive and bilateral becker naevus since the age of 12 year and had left breast hypoplasia, too.

Journal: :Albrecht von Græfe's Archiv für Ophthalmologie 1913

Journal: :Collegium antropologicum 2008
Leo Cabrijan Jasna Lipozencić Tanja Batinac Maja Lenković Franjo Gruber Zrinka Stanić Zgombić

In this study 103 patients with skin tumors were examined. Among them there were 43 (42%) male patients and 60 (58%) female patients. Working diagnosis was obtained by clinical examination using dermoscope. After excision of lesion, working diagnosis was compared to pathohistological diagnosis. In our study we used dermoscope Heine proper delta 10. The clinical-dermoscopic diagnosis included ve...

Journal: :The British journal of ophthalmology 2001
R P Müskens J A Van Best J C Bleeker J E Keunen

AIMS To investigate whether corneal autofluorescence is different in patients with choroidal melanoma or choroidal naevus. METHODS Corneal autofluorescence was determined by fluorophotometry in both eyes of 32 patients with a unilateral choroidal melanoma, 32 patients with a unilateral choroidal naevus, and 32 age matched healthy controls. The corneal autofluorescence ratio between affected a...

2011
G. Fabbrocini C. Mazzella F. Pastore A. Monfrecola M. C. Annunziata M. C. Mauriello V. D'Arco C. Marasca V. De Vita

Background. The incidence of cutaneous melanoma is rapidly increasing in Europe. Active research is directed toward the identification of naevi as a risk factor. Objective. The aim of our case-control study was to observe different numbers of moles and different mole typology associations in order to evaluate clinical predictivity and to establish a new classification for some naevus variants. ...

Journal: :Acta dermato-venereologica 2014
Yasuyuki Fujita Satoru Aoyagi Masumi Tsujiwaki Erina Homma Hideyuki Ujiie Hiromi Fujita Kanako C Hatanaka Hiroshi Shimizu

© 2014 The Authors. doi: 10.2340/00015555-1641 Journal Compilation © 2014 Acta Dermato-Venereologica. ISSN 0001-5555 Spitz naevus was first described by Sophie Spitz in 1948 (1). It is a variant of benign melanocytic naevus composed of spindled and epithelioid melanocytes, found predominantly in children and adolescents. A number of histopathological variants have been reported, such as desmopl...

Journal: :Acta dermato-venereologica 2010
Simon Jacobelli Stéphanie Leclerc-Mercier Rémi Salomon Olivier Hartmann Frances Brunelle Rudolf Happle Christine Bodemer Smail Hadj-Rabia

Phacomatosis pigmentokeratotica is characterized by the coexistence of an organoid epidermal naevus, follow-ing Blaschko's lines, and a large speckled lentiginous naevus, typically arranged in a chequerboard pattern. This entity has been isolated from the group of epidermal naevus syndromes and is frequently associated with extracutaneous anomalies. We report here the first observation of phaco...

Journal: :British medical journal 1984
S J Adams M H Rustin T W Robinson D D Munro

Members of two different families were found to have the dysplastic naevus syndrome and coexistent endocrine abnormalities. The dysplastic naevus syndrome is probably inherited as an autosomal dominant trait and has been associated with other primary malignancies. This is the first time that it has been described in association with endocrine abnormalities.

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