نتایج جستجو برای: nevoid basal cell carcinoma syndrome

تعداد نتایج: 2469788  

2013
Ivelina Yordanova Dimitar Gospodinov Veselin Kirov Verka Pavlova Galja Radoslavova

Gorlin-Goltz syndrome (GGS) also known as Nevoid Basal Cell Carcinoma Syndrome is a rare autosomal-dominant disorder characterized mainly by the presence of multiple basal cell carcinomas (BCC), odontogenic keratocysts of the jaw and palmar pits. This syndrome is associated with a wide spectrum of developmental anomalies and neoplasms. A case of familial Gorlin-Goltz syndrome with many of the c...

Journal: :acta medica iranica 0
h. a. nikpour

there is an impression that basal cell carcinomas (bcc) occurring in younger population may be of more invasive behavior in comparison to those arising in older patients. the purpose of this study was to investigate this hypothesis by comparing the histological types of bcc in a large cohort of young and old patients. a total of 287 histological reports and clinical records were evaluated. a co...

2014
Yeliz Bilir Erkan Gokce Banu Ozturk Faik Alev Deresoy Ruken Yuksekkaya Emel Yaman

Gorlin-Goltz syndrome or basal cell nevus syndrome is an autosomal dominant syndrome characterized by skeletal anomalies, numerous cysts observed in the jaw, and multiple basal cell carcinoma of the skin, which may be accompanied by falx cerebri calcification. Basal cell carcinoma is the most commonly skin tumor with slow clinical course and low metastatic potential. Its concomitance with Gorli...

Journal: :iranian journal of pathology 2015
oya n. sivrikoz gülşen kandiloğlu

background and objective: clinical behavior of basal cell carcinoma (bcc) is known to be different according to histological growth pattern and basosquamous cell carcinomas (bsc) are known with their aggressive behavior and metastatic capacity. in this study, we evaluated bcl-2 and cyclin d1 expressions in bcc and bsc cases comparatively, to explore their predictive value on the aggressive beha...

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2010

Journal: :iranian journal of otorhinolaryngology 0
seyed hosein fattahi masoum department of thoracic surgery, mashhad university of medical sciences, mashhad, iran. noorieh sharifi solid tumor treatment research center, faculty of medicine, mashhad university of medical sciences, mashhad, iran. shirin taraz jamshidi solid tumor treatment research center, faculty of medicine, mashhad university of medical sciences, mashhad, iran. alireza sharifian department of anesthesiology, mashhad university of medical sciences, mashhad, iran. reza rezaee department of thoracic surgery, mashhad university of medical sciences, mashhad, iran.

introduction: primary small cell carcinoma of theesophagus (pscec) associated with paraneoplastic sweating syndrome is a rare disease characterized with rapid growth rate, metastasis at the time of diagnosis, and poor prognosis. the lung is the most common site for small cell carcinoma but this malignancy includes 0.1% to 1% of all gastrointestinal and 0.8% to 2.7% of esophageal malignancies. s...

F. Haghighi Reza Ghaderi,

Background: The most frequently mutated tumor suppressor gene found in human cancer is p53. In a normal situation, p53 is activated upon the induction of DNA damage to either arrest the cell cycle or to induce apoptosis. However, when mutated, p53 is no longer able to properly accomplish these functions. The aim of this study was to investigate the expression of p53 gene in cases of skin cancer...

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