نتایج جستجو برای: adenomatoid tumor

تعداد نتایج: 428516  

Journal: :Journal of Clinical and Experimental Dentistry 2011

Journal: :International Journal of Case Reports and Images 2014

2015
Won-Gyo Seo Chul-Hwan Kim Hae-Seo Park Jong-Won Jang Woo-Yeol Chung

Adenomatoid odontogenic tumor (AOT) is a rare, benign odontogenic tumor that predominantly appears in the second decade of life in female patients. Most AOTs occur in the anterior part of the maxilla and are usually associated with impacted anterior teeth. There are three types of AOT, follicular, extrafollicular, and peripheral, which are classified based on the location of the lesion and its ...

Journal: :Brazilian dental journal 2005
Sonu Nigam Sanjeev Kumar Gupta K Uma Chaturvedi

Adenomatoid odontogenic tumor (AOT) is an uncommon tumor of odontogenic origin, characterized histologically by the formation of ductlike structures with amyloid-like deposits. Histogenesis of AOT is still uncertain and it is often considered as a hamartomatous lesion rather than a true neoplasm. AOT has a benign behavior and conservative surgical enucleation or curettage is sufficient. We repo...

2011
Sunil S. Mishra Shirish S. Degwekar Mukta B. Motwani Ruchi M. Anand Sharad Pawar

The Adenomatoid Odontogenic Tumor (AOT) is a rare, slow growing, benign, odontogenic epithelial tumor with characteristic clinical and histological features; which usually arise in the second or third decade. It is a tumor composed of odontogenic epithelium in a variety of histoarchitectural patterns which are embedded in a mature connective tissue stroma. It is mostly encountered in young pati...

2016
Jose Martinez-Mas Alberto Miranda-Paanakker Paloma Gomez-Leal Patricia Navarro-Sanchez Andres Bueno-Crespo Juan Pedro Martinez-Cendan Manuel Remezal-Solano

Fetal lung masses are rare findings in prenatal ultrasound scanning in general population, of which congenital cystic adenomatoid malformation is the most commonly diagnosed type. This paper reports a single case of congenital cystic adenomatoid malformation detected at our hospital and the subsequent clinical follow-up using ultrasound scanning and fetal magnetic resonance imaging.

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