Leiomyomatous Hamartoma of Incisive Papilla with High Frenal Attachment: A Case Report.

Sujeet S Pal, Suleman A Khan, Saumya Navit, Kunal Sah, Shaifali Agrawal, Harshal Gaidhane
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Abstract

Aim: This case report aims to describe a rare congenital lesion of the incisive papilla with a high labial frenulum attachment, clinically mimicking congenital epulis but histopathologically diagnosed as an oral leiomyomatous hamartoma.

Background: Oral leiomyomatous hamartoma is a very rare congenital lesion, mainly appearing on the median anterior maxilla/incisive papilla and tongue.

Case description: This clinical paper is about a rare lesion in a 6-year-old female child whose parents reported to the department with the complaint of slow-growing soft tissue overgrowth between the front teeth of the upper jaw, present since birth. The soft tissue growth is now causing difficulty in biting food and is visible during smiling and speaking, causing an esthetically unpleasing appearance. The clinical examination also revealed a high labial frenulum attached to the lesion. The lesion was provisionally diagnosed as congenital epulis based on the clinical picture. However, after excisional biopsy and histologic evaluation with special stains, the lesion was finally diagnosed as leiomyomatous hamartoma.

Conclusion: Surgical excision of the lesion followed by frenectomy was performed with no postoperative complications.

Clinical significance: Owing to the rare occurrence and nature of mimicking congenital epulis, it is important for a dental practitioner to have knowledge about these types of lesions. The final diagnosis of such lesions can only be made after histopathological evaluation using special stains. This case report describes the clinical and histopathological features of a rare leiomyomatous hamartoma of the incisive papilla, along with high frenulum attachment and its management.

How to cite this article: Pal SS, Khan SA, Navit S, et al. Leiomyomatous Hamartoma of Incisive Papilla with High Frenal Attachment: A Case Report. Int J Clin Pediatr Dent 2024;17(6):717-722.

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具有高位膈肌附着的切迹乳头乳头状瘤(Liomyomatous Hamartoma of Incisive Papilla with High Frenal Attachment):病例报告
目的:本病例报告旨在描述一种罕见的切乳头先天性病变,该病变具有高唇裂附着,临床上类似于先天性外翻,但组织病理学诊断为口腔黏膜乳头状瘤:背景:口腔乳头状瘤是一种非常罕见的先天性病变,主要出现在上颌骨正中前方/incisive乳头和舌头上:这篇临床论文讲述的是一名 6 岁女婴的罕见病变,该患儿的父母向该科报告,主诉上颌前牙之间的软组织生长缓慢,自出生起就存在。现在,软组织增生导致咬食物困难,在微笑和说话时也能看到,造成了外观上的不美观。临床检查还发现,病变部位附着一个高唇系带。根据临床表现,病变被初步诊断为先天性外翻。然而,经过切除活检和特殊染色的组织学评估,病变最终被诊断为乳头状瘤:结论:手术切除病灶后进行了肾盂切除术,术后无并发症:临床意义:由于这类病变很少发生,且具有模仿先天性外翻的性质,因此牙科医生必须了解这类病变。此类病变的最终诊断只能在使用特殊染色剂进行组织病理学评估后才能做出。本病例报告描述了一个罕见的切乳头乳头状乳头状瘤的临床和组织病理学特征,以及高韧带附着及其处理:Pal SS, Khan SA, Navit S, et al:病例报告。Int J Clin Pediatr Dent 2024;17(6):717-722.
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CiteScore
1.20
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135
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