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一例婴儿外周骨化性纤维瘤罕见病例。

A Rare Case of Peripheral Ossifying Fibroma in an Infant.

作者信息

Singh Khushboo, Gupta Shikha, Hussain Itrat, Augustine Jeyaseelan, Ghosh Sujoy, Gupta Sunita

机构信息

Department of Oral Medicine and Radiology, Maulana Azad Institute of Dental Sciences, New Delhi, India.

Department of Oral and Maxillofacial Surgery, Maulana Azad Institute of Dental Sciences, New Delhi, India.

出版信息

Contemp Clin Dent. 2021 Jan-Mar;12(1):81-83. doi: 10.4103/ccd.ccd_364_20. Epub 2021 Mar 20.

Abstract

Peripheral ossifying fibroma (POF) associated with natal/neonatal teeth is extremely rare. In general, POF occurs as a soft-tissue gingival nodule occurring in young adults. We report an unusual and a rare case in a 5-month-old male child who had two, localized, soft-tissue growth over the mandibular anterior alveolar ridge. History revealed the presence of natal teeth in the same mandibular anterior region, which exfoliated at the age of 2 months. Intraoral periapical radiograph showed soft tissue density with evidence of calcifications that also corroborated with the histopathological finding of masses of mineralized areas. Excision of the lesions followed by histopathological examination proved the final diagnosis of POF. Inspite of being a benign reactive lesion, a high recurrence rate has been reported. Such lesions require long-term follow-up subsequent to excision with histopathological examination due to a high recurrence rate.

摘要

与 natal/neonatal 牙相关的外周骨化性纤维瘤(POF)极为罕见。一般来说,POF 表现为发生在年轻人中的软组织牙龈结节。我们报告了一例罕见的特殊病例,一名 5 个月大的男童下颌前牙槽嵴上有两处局限性软组织肿物。病史显示同一下颌前部区域存在 natal 牙,这些牙在 2 个月大时脱落。口内根尖片显示软组织密度影并有钙化迹象,这也与组织病理学发现的矿化区域团块相符。病变切除后经组织病理学检查确诊为 POF。尽管它是一种良性反应性病变,但据报道其复发率较高。由于复发率高,此类病变切除后需要长期随访并进行组织病理学检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a4e/8092083/0feb9c23b80c/CCD-12-81-g001.jpg

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