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一名患有轻度家族性腺瘤性息肉病(aFAP)的年轻患者的罕见牙源性腺样瘤病例报告及诊断与治疗:病例报告及5年随访

Diagnosis and treatment of a rare case of adenomatoid odontogenic tumor in a young patient affected by attenuated familial adenomatosis polyposis (aFAP): case report and 5 year follow-up.

作者信息

Marrelli M, Pacifici A, Di Giorgio G, Cassetta M, Stefanelli L V, Gargari M, Promenzio L, Annibali S, Cristalli M P, Chiaravalloti E, Pacifici L, Tatullo M

机构信息

Calabrodental Clinic, Oral and Maxillofacial Unit, Crotone, Italy.

出版信息

Eur Rev Med Pharmacol Sci. 2014;18(2):265-9.

Abstract

BACKGROUND

The adenomatoid odontogenic tumor (AOT) is a quite rare odontogenic tumor, with an incidence rate of approximately 12 cases/year worldwide. Attenuated familial adenomatous polyposis (aFAP) is a syndrome characterized by a significant risk to develop colon cancer. The aim of the paper is to describe a case never reported before in the literature: an AOT developed in a patient with aFAP; moreover, we want to show how it appears 5 years after surgery and after the regeneration of the eroded bone tissue, using the Platelet-Rich Fibrin (PRF) as filling material.

CASE PRESENTATION

We report the case of a female 18 years old patient, affected by aFAP; she comes to us with a swelling on the right hemi-face. We performed several radiological exams, and they showed a neoformation approximately 2 cm in diameter: this neoformation packed the upper right canine, therefore, we hypothesized a dentigerous cyst. We decided to proceed to open biopsy and enucleation of the lesion. An intra-operative endodontic treatment on the adjacent partially resorbed teeth was also performed. Finally, we performed a reconstruction of eroded bone tissue, by use of Platelet-Rich Fibrin as filling material. The samples fixed and embedded in paraffin have led to the diagnosis of AOT. After 5 years from the surgery, we did not find any clear sign of relapse, in addition, the use of PRF has favored an optimal osteogenesis at the surgical site.

CONCLUSIONS

Undoubtedly, a correct diagnosis of AOT allows to have a more performing clinical and surgical approach. Furthermore, this case could document a new manifestation of aFAP in extra-intestinal site. The onset of an AOT is quite rare in the general population, and this rarity could represent a critical point for its diagnosis; AOT onset in a patient with aFAP is a finding that could represent a new element of diagnosis and, therefore, the starting point to perform a more effective therapy.

摘要

背景

腺样牙源性肿瘤(AOT)是一种非常罕见的牙源性肿瘤,全球发病率约为每年12例。attenuated家族性腺瘤性息肉病(aFAP)是一种以患结肠癌风险显著为特征的综合征。本文的目的是描述一例文献中从未报道过的病例:一名患有aFAP的患者发生了AOT;此外,我们想展示使用富血小板纤维蛋白(PRF)作为填充材料,在手术后5年以及侵蚀性骨组织再生后的情况。

病例介绍

我们报告了一名18岁女性患者的病例,她患有aFAP;她因右半侧面部肿胀前来就诊。我们进行了多项影像学检查,结果显示有一个直径约2厘米的新生物:这个新生物包绕右上尖牙,因此,我们推测为含牙囊肿。我们决定进行开放性活检并摘除病变。还对相邻部分吸收的牙齿进行了术中牙髓治疗。最后,我们使用PRF作为填充材料对侵蚀性骨组织进行了重建。固定并石蜡包埋的样本诊断为AOT。手术后5年,我们未发现任何明显的复发迹象,此外,PRF的使用有利于手术部位的最佳骨生成。

结论

毫无疑问,对AOT的正确诊断有助于采取更有效的临床和手术方法。此外,该病例可能记录了aFAP在肠外部位的一种新表现。AOT在普通人群中的发病相当罕见,这种罕见性可能是其诊断的一个关键点;AOT在患有aFAP的患者中发病是一个可能代表新诊断要素的发现,因此是开展更有效治疗的起点。

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