نتایج جستجو برای: basal cell nevus syndrome

تعداد نتایج: 2291746  

Journal: :Brain & development 2012
Akihisa Okumura Tsubasa Lee Mitsuru Ikeno Keiko Shimojima Kazunori Kajino Yuka Inoue Naomi Yoshikawa Hiroki Suganuma Mitsuyoshi Suzuki Ken Hisata Hiromichi Shoji Jun-ichi Takanashi A James Barkovich Toshiaki Shimizu Toshiyuki Yamamoto Masaharu Hayashi

Here we report a boy with epidermal nevus syndrome associated with brainstem and cerebellar malformations and neonatal medulloblastoma. The patient had epidermal nevi and complicated brain malformations including macrocephaly with polymicrogyria, dysmorphic and enlarged midbrain tectum, enlarged cerebellar hemispheres with small and maloriented folia. The patient died after surgical resection o...

Journal: :Nepalese journal of ophthalmology : a biannual peer-reviewed academic journal of the Nepal Ophthalmic Society : NEPJOPH 2009
P Lavaju S K Arya A Sinha S Pandey S Adhikari B G Shrestha S Chetan T L Agarwal

BACKGROUND ocular tumors are commonly encountered in ophthalmic practice. OBJECTIVE to study the clinical pattern of ocular tumors in the eastern region of Nepal. MATERIALS AND METHODS the hospital records of patients with ocular tumors treated at B P Koirala Institute of Health Sciences in the eastern region of Nepal over a period of 5 years (April 2003 - March 2008) were studied retrospec...

Journal: :Acta dermato-venereologica 2012
Erika Kis Eszter Baltás Agnes Kinyó Erika Varga Nikoletta Nagy Rolland Gyulai Lajos Kemény Judit Oláh

Gorlin-Goltz syndrome is a rare multisystemic disease, characterized by numerous basal cell carcinomas. The ideal approach for patients with the syndrome would be a treatment with a high cure rate, minimal scarring, short healing time and mild side-effects. Electrochemo-therapy is a novel therapeutic option that ablates tumours with electrical current and simultaneously administered anticancer ...

Journal: :Anais brasileiros de dermatologia 2011
Cristiani Banhos Ferreira Lucia Martins Diniz João Basilio de Souza Filho

Basal cell carcinoma is the most common type of malignant cutaneous neoplasm in humans, being more frequently located in exposed areas and in fair-skinned individuals. It is reported the case of a 62-yearold female patient, brown-skinned ,with multiple lesions with edges slightly raised, reddish-brown in the pubic region, whose clinical diagnosis was pigmented basal cell carcinoma, confirmed by...

Journal: :Environmental Health Perspectives 1997
L Grossman

The following conclusions are derived from an epidemiological study. Reduced repair of ultraviolet (UV)-induced DNA damage contributes directly to basal cell carcinoma (BCC) in individuals with prior sunlight overexposure. A family history of BCC is a predictor of low DNA repair. Repair of UV-damaged DNA declines at a fixed rate of approximately 1% per annum in noncancerous controls. The DNA re...

2015
Catarina Moreira Paulo Morais Paulo Santos Miguel Castro Filomena Azevedo

Gorlin's syndrome is an autosomal dominant disorder, mainly characterized by the presence of multiple and early-onset basal cell carcinomas, odontogenic keratocysts and palmoplantar pits. We describe the case of a patient with clinical and imaging features of Gorlin syndrome, and highlight the role of dermoscopy in the early detection of basal cell carcinomas. In addition, we discuss the dermos...

2015
Dinesh Chhillar

Epidermal nevi are congenital hamartomas of embryonal ectodermal origin classified on the basis of their main component. The compone keratinocytic. An estimated 1/3 of individuals with epidermal nevi have involvement of other organ systems; hence this condition is considered to be epidermal nevus syndrome. Solomon defined epidermal nevus syndrome as a sporadic neuro in the skin, brain, eyes and...

Journal: :Medical Journal Armed Forces India 2015

Journal: :Saudi medical journal 2006
Sule Yucetas Sedat Cetiner Tulin Oygur

This report represents the suspected familial case series of odontogenic keratocysts OKCs related to Gorlin Goltz syndrome GGS, a rare genetic disorder characterized mainly by multiple basal cell carcinomas, OKCs and other less frequent skeletal and neurological manifestations. Familial cases included grandmother's father, grandmother, father and son. Although they had all OKCs, father addition...

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