新生儿先天性颗粒细胞脓包1例,诊断、治疗及预后回顾。

IF 3.1 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Frontiers in oral health Pub Date : 2025-08-11 eCollection Date: 2025-01-01 DOI:10.3389/froh.2025.1548291
P C Guidone, Roberta Seccia, L A Fabrocini, G Troiano, G Maffei, Maria Carmela Pedicillo, Giuseppe Pannone, Lorenzo Lo Muzio, Rosanna Zamparese, Giorgio Mori, Ilenia Sara De Stefano
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引用次数: 0

摘要

摘要先天性颗粒细胞脓疱是一种罕见的良性肿瘤,通常在出生时出现,最常见于上颌牙槽嵴。病例介绍:我们报告一例5天大的女性,右侧上颌牙槽嵴有光滑的多分叶状肿块,导致进食困难。手术切除在镇静下进行。组织学和免疫组织化学分析证实了CGCE的诊断。随访1个月无复发。结论:早期诊断和手术治疗对避免功能损害至关重要。完全切除后预后良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Congenital granular cell epulis in a neonate: a case report and review of diagnosis, treatment, and prognosis.

Congenital granular cell epulis (CGCE) is a rare benign tumor typically presenting at birth and most commonly located on the maxillary alveolar ridge.

Case presentation: We report the case of a five-day-old female with a smooth, multilobulated mass on the right maxillary alveolar ridge causing feeding difficulties. Surgical excision was performed under sedation. Histological and immunohistochemical analysis confirmed the diagnosis of CGCE. No recurrence was observed at one-month follow-up.

Conclusion: Early diagnosis and surgical treatment of CGCE are essential to avoid functional impairment. The prognosis is excellent following complete excision.

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来源期刊
CiteScore
3.30
自引率
0.00%
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审稿时长
13 weeks
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