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一名3岁男孩的外周性成釉细胞纤维牙本质瘤:一例罕见病例报告。

Peripheral ameloblastic fibrodentinoma in a 3-year-old boy: Report of an unusual and rare case.

作者信息

Kaur Vaneet, Tilakraj T N

机构信息

Department of Pedodontics and Preventive Dentistry, Dr Syamala Reddy Dental College Hospital and Research Centre, Bengaluru, Karnataka, India.

出版信息

J Oral Maxillofac Pathol. 2018 Jan-Apr;22(1):112-115. doi: 10.4103/jomfp.JOMFP_118_17.

Abstract

We report a rare and unusual case of a Peripheral Ameloblastic Fibro-Dentinoma (PAFD) occurring in a 3 year old Indian boy. The boy presented to the hospital complaining of swelling in anterior maxillary region with a history of trauma. Periapical radiography of the area did not reveal any bone resorption. The entire mass was excised under local anesthesia, and the histological examination revealed a diagnosis of PAFD. The postoperative course was satisfactory and the excised area has remained free of recurrence for 9 months. PAFD is a rare entity and only 5 cases have been reported in literature. The present case is one of the youngest in the group. The mode of differentiation of the odontogenic lesion is a pointer in the diagnosis and histogenesis has been discussed.

摘要

我们报告了一例罕见的外周型成釉细胞纤维牙本质瘤(PAFD),发生在一名3岁的印度男孩身上。该男孩因上颌前部区域肿胀并伴有外伤史前来医院就诊。该区域的根尖片未显示任何骨质吸收。在局部麻醉下切除了整个肿物,组织学检查确诊为PAFD。术后过程顺利,切除部位9个月来未复发。PAFD是一种罕见的疾病,文献中仅报道过5例。本病例是该组中年龄最小的病例之一。本文讨论了该牙源性病变的分化方式在诊断中的意义及其组织发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cf5/5917518/ce8c52abed8e/JOMFP-22-112-g001.jpg

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