Histogenesis and Clinical Analysis of 2 Cases of Congenital Gingival Granular Cell Tumour
نویسندگان
چکیده
منابع مشابه
Congenital gingival granular cell tumor of newborn.
diagnosis and prediction of recovery. Among the various modalities of imaging, spinal ultrasound appears to be very promising and hence is recommended as the first modality of imaging(4). However, it should be remembered that changes are known to occur in the lesion over time and a single ultrasound may not pick up all lesions. Hence, it is not surprising that ultrasound of the cervical spine w...
متن کاملcongenital gingival granular cell tumor: a case report
the congenital gingival granular cell tumor (cgct), also as known as congenital epulis, is an unusual benign oral mucosal lesion in newborns. a two-day-old female patient was admitted to the department of pediatric dentistry at gulhane medical academy, ankara, turkey with her family, and an intraoral examination showed a cgct located in the buccal region of the maxillary right first primary mol...
متن کاملCongenital Gingival Granular Cell Tumor: A Case Report
Ceren Yıldırım, Tamer Zerener , Metin Şençimen , Özlem Martı Akgün , Hasan Ayberk Altuğ , Ali Fuat ÇİÇEK 3 1 Dept. of Pediatric Dentistry, University of Health Sciences, Gulhane Health Sciences Institute, Ankara, Turkey. 2 Dept. of Maxillofacial Surgery, University of Health Sciences, Gulhane Health Sciences Institute, Ankara, Turkey. 3 Dept. of Pathology, Gulhane Education and Research Hospita...
متن کاملCongenital gingival granular cell tumor. A case report.
Congenital gingival granular cell tumor is a rare benign lesion of uncertain origin, which has been found only in newborn infants. This article describes one such case. Our immunohistochemical study employing antibodies against S-100 protein, epithelial membrane antigen, carcinoembryonic antigen, wide-spectrum keratin, desmin and vimentin yielded data supporting the theory of a mesenchymal cell...
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ژورنال
عنوان ژورنال: JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH
سال: 2015
ISSN: 2249-782X
DOI: 10.7860/jcdr/2015/10048.5409